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One hundred twenty crossbred steers were allotted to six weight blocks. Within each block, steers were allotted to one of four pens in a randomized complete block design (5 head per pen, 24 total pens). Treatments were low forage control diets (LFC) or high forage diets supplemented with soybean oil (HFO), without or with anabolic implant in 2 × 2 factorial arrangement. As compared with LFC, HFO reduced dry matter intake and average daily gain, without affecting the gain:feed ratio. Feeding HFO also decreased dressing yield and backfat thickness, with no impact on the longissimus dorsi area and Warner-Bratzler shear force. Meat from steers fed HFO contained greater relative proportion of cis-9, cis-12 18:2, cis-9, trans-11 18:2, and cis-9, cis-12, cis-15 18:3 as compared with LFC. Implanted steers had greater dry matter intake, average daily gain, and gain:feed ratio. Implants improved dressing yield, tended to increase the longissimus dorsi area, decreased backfat thickness, and increased meat Warner-Bratzler shear force. Meat from implanted steers contained greater relative concentration of cis-9, cis-12 18:2 and cis-9, cis-12, cis-15 18:3, without affecting cis-9, trans-11 18:2, as compared with non-implanted animals. No interaction of diet by implant was observed for these variables.

This study investigated the use of K2CO3 as dietary buffer to prevent or to recover from low milk fat production when early-lactating dairy goats are fed a high-starch, low-fiber (HSLF) diet. At kidding, 30 Alpine goats housed in pens with Calan gate feeders received a total mixed ration with a forage-to-concentrate ratio of 55:45 on a dry matter (DM) basis for a baseline period of 27 ± 4 d. Goats (milk yield, 4.14 ± 0.88 kg/d; milk fat, 4.28 ± 0.52%; mean ± SD) were then assigned to 1 of 10 blocks according to parity (first vs. second or more) and milk fat concentration, and fed a HSLF diet containing 45% forages and 55% concentrates for 2 experimental periods of 28 d. Treatments were identified as (1) control, in which the HSLF diet was fed throughout both periods; (2) preventive, in which the HSLF diet supplemented with K2CO3 (1.6% of DM) was fed during both periods; and (3) recovery, in which the HSLF diet was fed during the first period (P1) and the HSLF diet supplemented with K2CO3 was fed during the second period (P2). Data from P1 and P2 were analyzed separately. In P1, preplanned contrasts were used to evaluate the preventive effect of K2CO3 (control and recovery, both groups receiving the same diet during this period, vs. preventive), and in P2, to assess the potential of K2CO3 to alleviate an already existing state of low milk fat (control vs. recovery and preventive vs. recovery). Feeding the HSLF diet in P1 moderately decreased milk fat concentration (−16%) and yield (−13%) as compared with baseline. Dietary addition of K2CO3 decreased DM intake by 12 and 14% in P1 and P2, respectively. Ruminal pH was not different among treatments. There was also no significant difference in milk yield (4.13 and 3.71 kg/d on average in P1 and P2, respectively) for any tested contrasts. In P1, milk fat concentration and yield did not differ among goats fed control (3.58% and 151 g/d, respectively) and preventive (3.67% and 148 g/d, respectively) diets. In P2, milk fat concentration and yield did not differ among goats fed the control diet (3.38% and 137 g/d, respectively), and diets where K2CO3 was used as preventive (3.44% and 126 g/d, respectively) or recovery treatment (3.25% and 113 g/d, respectively). Supplementing a high-concentrate diet with 1.6% K2CO3 was therefore not effective in either preventing or suppressing already existing conditions of low milk fat production in dairy goats.

Six Holstein cows were used in a replicated 3 × 3 Latin Square design to investigate the effect of flaxseed meal on production performance and oxidative stability of milk enriched with n-3 fatty acids. Flaxseed oil was abomasally infused to all cows at 243 g·d−1 which increased milk concentration of α-linolenic acid from 3.08 (pretrial) up to 53.0 mg·g−1 fat. On a dry matter basis, dietary treatments were canola meal (CM; 165 g·kg−1), flaxseed meal (FM; 165 g·kg−1), and CM (165 g·kg−1) + vitamin E (VE; 300 IU·kg−1). Pre-planned contrasts were CM vs. FM and VE vs. FM. No difference was observed on dry matter intake, milk production, and yield of milk protein, and lactose for any of the contrasts evaluated. However, fat yield tended to be lower with FM relative to CM but was not different from VE. Milk enterolactone concentration was 6.8-fold greater with FM than with CM, whereas milk tocopherol was increased by 3.4-fold with VE relative to FM. Increased concentrations of enterolactone or tocopherol were not efficient to significantly modify the time course of appearance of propanal, hexanal, hept-cis-4-enal, and 1-octen-3-one in milk during storage evaluated for 10 d at 4 °C.

In high-yielding dairy cows, some fertility traits can be influenced by the fatty acid (FA) composition of the follicular fluid during early lactation. The first objective of the current study was to evaluate the potential of dietary supplements enriched in specific FA to influence the FA composition of follicular fluid lipid classes in early lactation dairy cows. The second objective was to determine the influence of the resulting follicular fluid FA composition on the folliculogenesis, lipid and energy metabolism of granulosa cells, as well as oocyte quality and embryo development. Twenty Holstein multiparous cows in late gestation were randomly assigned to 200 g/d of FA supplements enriched in (1) palmitic acid (control treatment; 82% 16:0; PA) in the rumen or (2) palmitoleic acid (sea buckthorn oil; 27% cis-9 16:1, 28% 16:0, 22% cis-9 18:1, and 11% cis-9,cis-12 18:2; SBT) in the abomasum. The treatment period ranged from 20 ± 5 d precalving to 67 ± 2 d postcalving. Cumulus-oocyte complexes, granulosa cells, and follicular fluid were recovered from 2 sequential sessions of ovum pick-up (OPU-1 and OPU-2) at 46 and 67 ± 2 d postcalving (mean ± standard deviation). On the same days, blood samples were collected. Milk performance was recorded, and feed and milk samples were collected from d 8 to 10 ± 3 (onset of lactation), d 35 to 37 ± 2 (before OPU-1), and d 63 to 65 ± 2 (before OPU-2). Treatments did not affect milk yield or fat concentration throughout the experimental trial. Compared with PA, SBT increased the cis-9 16:1 concentration in milk fat, in plasma esterified lipid classes (phospholipids, cholesterol esters, and triacylglycerols), and in follicular fluid phospholipids and cholesterol esters at OPU-1. Abundance of mRNA for stearoyl-CoA desaturase 1 and 5, and perilipin 2 in granulosa cells was not different between treatments, but an increase in the level of stearoyl-CoA desaturase 5 was observed between the 2 OPU periods. Treatments did not affect oocyte quality and developmental capacity or embryo lipid metabolism when cultivated in vitro. These results suggest that limited modifications in the FA composition of the oocyte microenvironment via dietary lipid supplements enriched in specific FA had no major effects on granulosa cell metabolism and oocyte developmental capacity in early lactation cows.

The objective of the current study was first to characterize lipid raft microdomains isolated as detergent-resistant membranes (DRM) from mammary gland tissue, and second to determine how dietary fatty acids (FA) such as conjugated linoleic acid (CLA), 19:1 cyclo, and long-chain n-3 polyunsaturated FA affect lipid raft markers of mammary cells, and to finally establish relationships between these markers and lactation performance in dairy cows. Eight Holstein cows were used in a replicated 4 × 4 Latin square design with periods of 28 d. For the first 14 d, cows received daily an abomasal infusion of (1) 406 g of a saturated FA supplement (112 g of 16:0 + 230 g of 18:0) used as a control; (2) 36 g of a CLA supplement (13.9 g of trans-10,cis-12 18:2) + 370 g of saturated FA; (3) 7 g of Sterculia fetida oil (3.1 g of 19:1 cyclo, STO) + 399 g of saturated FA; or (4) 406 g of fish oil (55.2 g of cis-5,cis-8,cis-11,cis-14,cis-17 20:5 + 59.3 g of cis-4,cis-7,cis-10,cis-13,cis-16,cis-19 22:6, FO). Mammary biopsies were harvested on d 14 of each infusion period and were followed by a 14-d washout interval. Cholera toxin subunit B, which specifically binds to ganglioside M-1 (GM-1), a lipid raft marker, was used to assess its distribution in DRM. Infusions of CLA, STO, and FO were individually compared with the control, and significance was declared at P ≤ 0.05. Milk fat yield was decreased with CLA and FO, but was not affected by STO. Milk lactose yield was decreased with CLA and STO, but was not affected by FO. Mammary tissue shows a strong GM-1-signal enrichment in isolated DRM from mammary gland tissue. Caveolin (CAV) and flotillin (FLOT) are 2 proteins considered as lipid raft markers and they are present in DRM from mammary gland tissue. Distributions of GM-1, CAV-1, and FLOT-1 showed an effect of treatments determined by their subcellular distributions in sucrose gradient fractions. Regardless of treatments, data showed positive relationships between the yield of milk fat, protein, and lactose, and the abundance GM-1 in DRM fraction. Milk protein yield was positively correlated with relative proportion of FLOT-1 in the soluble fraction, whereas lactose yield was positively correlated with relative proportion of CAV-1 in the DRM fractions. Infusion of CLA decreased mRNA abundance of CAV-1, FLOT-1, and FLOT-2. Regardless of treatments, a positive relationship was observed between fat yield and mRNA abundance of FLOT-2. In conclusion, although limited to a few markers, results of the current experiment raised potential links between variation in specific biologically active component of raft microdomains in bovine mammary gland and lactation performances in dairy cows.

PURPOSE: To examine the intra- and inter-individual variability in fatty acid composition of follicular fluid (FF) of 23 patients undergoing assisted reproductive treatment. METHODS: The average coefficient of variation within each patient (CV(w)) and intra-class correlation coefficient (ICC) values of FF fatty acid composition as well as correlation between the fatty acid composition of individual, pooled or first-punctured follicles, were assessed. RESULTS: The proportions of 16:0, 18:0, cis-9 18:1, 18:2n-6, 20:5n-3, total MUFA and n-3 PUFA showed good reproducibility (CV(w)

The aim of the present study was to compare the effects of post-ruminally infused fat supplements, varying in fatty acid (FA) chain length, on animal performance, metabolism and milk FA. Eleven multiparous Holstein dairy cows were used in a replicated incomplete 3 × 3 Latin square design with 7-d periods, separated by 7-d washouts. Treatments were administered as abomasal infusions of enrichments providing 280 g/d of FA: (1) palmitic acid (98·4 % 16 : 0; PA), (2) caprylic and capric acids (56·2 % 8 : 0, 43·8 % 10 : 0; medium-chain TAG (MCT)) and (3) stearic acid (99·0 % 18 : 0; SA). Relative to PA, SA decreased the efficiency of fat-corrected milk production, which was associated with a tendency for higher DM intake and lower FA absorption with SA, whereas MCT was not different from PA for these variables. Milk fat concentration and yield were increased by PA relative to SA, but only fat yield tended to be greater relative to MCT. Relative to PA, MCT increased milk fat concentration of FA < 16 C, whereas SA increased FA > 16 C. Expression of mammary stearoyl-coA desaturase 1 was lower with SA than with PA. Relative to PA, liver expression of adenosine monophosphate-activated protein kinase-1 and pyruvate kinase was increased with MCT, whereas expression of these genes tended to be increased by SA. The mechanism of increased fat secretion with PA does not seem to be related to a modulation of the expression of lipogenesis-related genes, but rather to increased substrate availability as reflected by milk FA profile.

The objective of the experiment was to determine if factors such as endosperm type (floury vs. vitreous) and particle size (fine vs. medium) of dry corn grain, known to affect starch digestibility in the rumen, modify apparent ruminal synthesis and duodenal flow of B vitamins in lactating dairy cows. Eight lactating multiparous Holstein cows equipped with rumen and duodenal cannulas were assigned randomly to a treatment sequence according to a 2 × 2 factorial arrangement in duplicate 4 × 4 Latin square design experiment. Duration of each experimental period was 21 d. When expressed per unit of dry matter intake (DMI), floury treatments increased duodenal flow and apparent ruminal synthesis of niacin and folates but tended to increase apparent degradation of thiamin in the rumen. Duodenal flow of thiamin, riboflavin, niacin, folates, and vitamin B12, expressed per unit of DMI, decreased with an increase in particle size. Similarly, apparent degradation of thiamin and riboflavin was greater and apparent synthesis of niacin, folates, and vitamin B12 was reduced when cows were fed coarser dry corn grain particles. Neither endosperm type nor particle size had an effect on duodenal flow and apparent ruminal synthesis of vitamin B6. Apparent ruminal syntheses, expressed per unit of DMI, of all studied B vitamins but thiamin were negatively correlated with apparent ruminal digestibility of neutral detergent fiber. Duodenal flow of microbial N was positively correlated with apparent ruminal synthesis of riboflavin, niacin, vitamin B6, and folates. Under the conditions of the present experiment, except for thiamin, the effects of factors increasing starch digestibility of dry corn grain in the rumen on the amounts of B vitamins available for absorption by the dairy cow seem to be mediated through differences on ruminal digestibility of neutral detergent fiber and, to a lesser extent, on duodenal microbial N flow.

Several experiments were conducted over the past few years to evaluate the feeding value of flax seed and oil in dairy cow diets. The current meta-analysis and meta-regression was undertaken to assess the overall effect of different forms of flax, as a source of trienoic (cis-9,cis-12,cis-15 18:3) fatty acids (FA), on lactation performance and on transfer efficiency of its constituent n-3 FA from diet to milk fat. Comparisons were first conducted with nonsupplemented controls or with diets containing either saturated (mainly 16:0 or 18:0 or both), monoenoic (mainly cis-9 18:1), or dienoic (mainly cis-9,cis-12 18:2) FA. Results indicate that supplementing flax seed and oil decreased dry matter intake, as well as actual and energy-corrected milk yield without affecting the efficiency of utilization of dietary dry matter or energy as compared with nonsupplemented iso-energetic controls. When compared with the other 3 types of dietary fat evaluated, flax rich in trienoic FA supported a yield of energy-corrected milk similar to supplements rich in saturated, monoenoic, or dienoic FA. Greater milk fat concentration and feed efficiency were observed with saturated supplements. However, milk fat concentration and yield were lower with dienoic FA than with flax supplements. Further analyses were conducted to compare the effect of different forms of flax oil, seed, or fractions of seed. Among the 6 categories evaluated, mechanically processed whole seed (rolled or ground) allowed the greatest yield of energy-corrected milk and the best feed efficiency when compared with free oil, intact or extruded whole seed, protected flax, and flax hulls. Feeding protected flax and flax hulls allowed the greatest milk fat concentration of cis-9,cis-12,cis-15 18:3. Moreover, the greatest transfer efficiencies of this fatty acid from diet to milk were recorded with the same 2 treatments, plus the mechanically processed whole seed. These results make this last category the most suitable treatment, among the 6 flax forms evaluated, to combine optimum lactation performance and protection of flax constituent cis-9,cis-12,cis-15 18:3.

Apparent ruminal synthesis and duodenal flow of thiamin, riboflavin, niacin, vitamin B6, folates, and vitamin B12 were evaluated in an experiment using 15 ruminally and duodenally cannulated lactating Holstein cows fed a basal diet, according to a crossover design, supplemented or not with 56 g/d of Saccharomyces cerevisiae fermentation product. Duration of the treatment period was 28 d. The basal ration had 28% neutral detergent fber, 30% starch and 16.5% crude protein; forages were corn silage (67% of forage dry matter) and alfalfa silage (33% of forage dry matter). Concentrations of B vitamins were analyzed in feed and duodenal digesta. Apparent ruminal synthesis of each B vitamin was calculated as the duodenal flow minus the intake. Under the present experimental conditions, a dietary supplement of Saccharomyces cerevisiae fermentation product had no effect apparent synthesis of B vitamins in the rumen or on the amounts of these vitamins reaching the duodenum and available for absorption by the dairy cow.

The objective of this study was to compare the effects of ground corn or liquid molasses fed as the sole supplemental nonstructural carbohydrate (NSC) source on production performance, milk fatty acid (FA) profile, grazing behavior, and N metabolism in grazing dairy cows. A strip-grazing management system was used, with cows offered a new strip of fresh herbage after each milking, resulting in approximately 16 h of access to pasture daily. Animals were fed a diet formulated to yield an 86:14 forage-to-concentrate ratio consisting [dry matter (DM) basis] of 74% mixed grass-legume herbage, 12% mixed-mostly legume baleage, 12% NSC source, and 2% mineral-vitamin premix. Twenty Jersey cows averaging (mean ± standard deviation) 121 ± 73 d in milk in the beginning of the study were randomly assigned to 1 of 2 herbage supplementation treatments: (1) baleage plus ground corn (B+GC) or (2) baleage + liquid molasses (B+LM). Both NSC sources were fed at a flat rate of 1.6 kg of DM/cow daily. The study lasted from June to September for a total of 15 wk with data and sample collection conducted in wk 3, 7, 12, and 15. Milk samples for FA analysis were collected in wk 2, 4, 6, 8, 9, 11, and 13. Data were analyzed using the MIXED procedure of SAS (SAS Institute Inc., Cary, NC) for a randomized complete block design with repeated measures over time. Treatment × week interactions were observed for supplement DM intake, milk urea N, bite rate, urinary excretion of uric acid, and milk FA (e.g., 17:0, 18:0, cis-9,trans-11 18:2). Supplement DM intake was greatest in cows fed B+LM in wk 7, 12, and 15. Compared with cows fed B+GC, those fed B+LM had lower concentrations of milk urea N in wk 7 and 15. Milk yield, concentrations and yields of milk components, and plasma concentrations of essential AA, except Met, which was lowest with feeding B+LM, were not affected by supplementation. The plasma concentration of urea N was lowest with feeding B+LM. Cows fed B+GC spent more time grazing than those fed B+LM. Feeding B+GC increased cis-9 18:1 FA and most trans-18:1 FA in milk, whereas B+LM increased Σ odd-chain FA, Σ n-3 FA, and the trans-11 18:1 to trans-10 18:1 ratio, and decreased the n-6 to n-3 ratio. Based on current results, B+LM can entirely replace B+GC without negatively affecting milk yield or yields and concentrations of milk fat and true protein, while decreasing milk urea N, plasma urea N, and the milk trans-11 18:1 to trans-10 18:1 ratio, and increasing Σ n-3 FA.

The objective of the current study was to assess the effects of particle size of dietary Ca salts of fatty acids (FA) on their inertness in the rumen, animal performance and transfer efficiency of polyunsaturated FA from diet to milk fat. Commercially produced CS of unsaturated FA (166 g/kg c 9 18:1, 105 g/kg c 9 c 12 18:2, 317 g/kg c 9 c 12 c 15 18:3) were sieved through a 1.9-mm screen, and the retained particles were identified as coarse CS. The small particles were ground through a 0.864-mm sieve, and identified as fine CS. A mixture of unprotected FA, as triacylglycerols (TG), with a composition similar to that of the CS served as control. Eight Holstein cows were used in a 4 × 4 Latin square design. Treatments were administration of FA at the rate of 600 g/d in the form of: (1) coarse CS in the rumen; (2) fine CS in the rumen; (3) TG in the rumen; and (4) TG in the abomasum for 14 days. Pre-planned contrasts were used to compare coarse CS with: (i) fine CS (effect of particle size); (ii) TG in the rumen (negative control); and (iii) TG in the abomasum (positive control). Actual milk yield was lower with abomasal infusion of TG (26.3 kg/d), but was not affected by ruminal supplies of TG (29.7 kg/d) or fine CS (29.5 kg/d) as compared with coarse CS (30.4 kg/d). Milk fat yield was similar with coarse CS (1.05 kg/d) and abomasal infusion of TG (1.02 kg/d), but was lower with ruminal supply of fine CS (0.95 kg/d; tendency) and TG (0.89 kg/d). Accordingly, milk fat concentrations of t 10 c 12 18:2 were similar with coarse CS (0.35 g/kg) and abomasal infusion of TG (0.33 g/kg), but were greater with ruminal supply of fine CS and TG (0.59 g/kg for both treatments). The apparent transfer efficiency of c 9 c 12 c 15 18:3, from diet and lipid supplements to milk fat, varied from 0.017 to 0.264 g secreted/g consumed with ruminal and abomasal infusions of TG, respectively. The recovery of c 9 c 12 c 15 18:3 in milk was greater with coarse CS (0.084 g/g) than with fine CS (0.042 g/g). Results confirm the hypothesis that large particles of CS improved protection against ruminal biohydrogenation of unsaturated FA and milk performance in lactating dairy cows.

Previous studies reported that addition of K 2 CO 3 to high-concentrate diets improved milk fat synthesis, although the mechanism is yet to be established. The objective of the current experiment was to investigate the effects of dietary cation-anion difference (DCAD), cation source, and buffering ability of the mineral supplement on rumen biohydrogenation of fatty acids and production performance in dairy cows fed a high-concentrate diet. Thirty-five early-lactation Holstein cows (25 multiparous ruminally fistulated and 10 primiparous nonfistulated) were used in a randomized complete block design (7 blocks) with 33-d periods, including a 5-d pre-treatment collection period used as a covariate. Diets were (1) control, a basal diet [47% nonfibrous carbohydrates, DCAD (Na + K – Cl – S) = 65 mEq/kg of dry matter (DM)] containing 40% forage (including 60% corn silage) and 60% concentrate, (2) K 2 CO 3 (control + K 2 CO 3 , 1.8% of DM, DCAD=326 mEq/kg of DM), (3) KHCO 3 (control + KHCO 3 , 2.6% of DM, DCAD=324 mEq/kg of DM), (4) KCl (control + KCl, 2.0% of DM, DCAD=64 mEq/kg of DM), and (5) Na 2 CO 3 (control + Na 2 CO 3 , 1.4% of DM, DCAD=322 mEq/kg of DM). Pre-planned orthogonal contrasts were used to assess the effects of K 2 CO 3 (control vs. K 2 CO 3 ), buffering ability (K 2 CO 3 vs. KHCO 3 ), DCAD (K 2 CO 3 vs. KCl), and cation type (K 2 CO 3 vs. Na 2 CO 3 ). Supplementing K 2 CO 3 in a high-concentrate diet did not improve milk fat yield or 4% fat-corrected milk yield. Milk fat concentration was greater in cows fed K 2 CO 3 compared with control (4.03 vs. 3.26%). Milk yield tended to decrease (34.5 vs. 38.8 kg/d) and lactose yield decreased in cows fed K 2 CO 3 as compared with KCl (1.64 vs. 1.87 kg/d). Milk fat concentration of trans -10 18:1 was increased when cows were fed Na 2 CO 3 as compared with K 2 CO 3 . A positive relationship was observed between concentrations of anteiso 15:0 and trans -10, cis -12 18:2 in milk fat from cows receiving K 2 CO 3 . Milk Na concentration was increased, whereas milk Cl was decreased with K 2 CO 3 as compared with KHCO 3 or KCl. A positive relationship was established between milk Cl concentration and milk yield (R 2 = 0.34) across all dietary treatments. Cation-anion difference (Na + K – Cl – S) in ruminal fluid was increased with K 2 CO 3 as compared with control or KCl. Blood pH tended to decrease in cows fed KCl compared with K 2 CO 3 . Our results suggest that mineral supplementation tends to affect milk and milk fat synthesis and that factors other than DCAD, potassium ion, or buffer ability may be implicated. The variations observed in mineral composition of milk suggest an allostatic process to maintain an ionic equilibrium in mammary epithelial cells in response to mineral composition of the diet.

Polyphenol oxidase in red clover (RC) silage reduces lipolysis and consequently protects its constituent fatty acids (FA) against biohydrogenation by ruminal microorganisms. Fatty acid biohydrogenation could be further inhibited by reducing the nitrogen (N) supply to ruminal bacteria. To compare the effects of RC and alfalfa (AL) silage fed in diets differing in rumen-degradable protein supply on the transfer efficiency of polyunsaturated FA from diet to milk, and on the resulting FA profile of milk fat, 8 multiparous Holstein dairy cows (72 ± 17 days in milk) were used in a replicated 4 × 4 Latin square design (21-day periods including 14 days of adaptation). Four treatments were compared in a 2 × 2 factorial arrangement with AL or RC fed in diets formulated to provide 100% (RDP‐100) or 85% (RDP‐85) of calculated rumen-degradable protein requirements. Rumen-degradable protein concentrations were adjusted by varying the supplies of ground vs. steam-flaked corn grains, and untreated vs. heat-treated soybean meals. Feeding RC, as compared with AL diets, decreased ruminal ammonia-N concentration as well as urea-N in plasma and milk. Intakes of c 9 c 12 18:2 and c 9 c 12 c 15 18:3 were lower for cows fed RC, but their secretion in milk and their apparent transfer efficiency from diet were greater as compared to cows fed AL. As a result, feeding RC increased the concentrations of c 9 c 12 18:2 and c 9 c 12 c 15 18:3, but decreased the proportions of t 11 18:1, c 9 t 11 18:2, and t 11 c 15 18:2 in milk fat. These results are consistent with the lower effective ruminal disappearance of c 9 c 12 18:2 and c 9 c 12 c 15 18:3 in RC as determined by a 96 h in sacco incubation, and the lower abundance of ruminal bacteria capable of hydrolyzing dietary lipids and hydrogenating polyunsaturated FA ( Ruminococcus albus and Ruminococcus flavefaciens ) in the rumen content. The apparent transfer efficiency of c 9 c 12 18:2 from diet to milk was further increased by feeding RDP‐85 as compared with RDP‐100 diet. Feeding RC decreased concentrations of linear odd-chain FA (11:0, 13:0, 15:0, 17:0, and c 9 17:1) and increased proportions of branched-chain FA (iso13:0, iso14:0, iso15:0, iso16:0, iso17:0, anteiso15:0, and anteiso17:0) in milk fat as compared with AL. In conclusion, as compared with AL, cows fed RC produced milk with greater concentrations of major forage FA ( c 9 c 12 18:2 and c 9 c 12 c 15 18:3) and lower proportions of intermediates in ruminal biohydrogenation of these FA. Variations in milk fat concentrations of odd- and branched-chain FA, which are synthesized in the rumen by various microbial populations, may be reflecting the effects of forage source on ruminal fermentation.

The concept of Rumen Unsaturated Fatty Acid Load (RUFAL) has been proposed to reflect the supply of dietary unsaturated fatty acids in relation with their potential to disturb ruminal fermentation and trigger milk fat depression in lactating dairy cows. The objective of this study was to assess this concept, and its relationship with milk fat concentration, using data available in a DHI database. Data from Holstein cows recorded over 3 yr by Valacta (Sainte-Anne-de-Bellevue, QC, Canada) were used for the analysis. The fatty acid concentrations in feed were obtained from CNCPS V6.1, INRA-AFZ Tables of Feed Composition, and peer-reviewed articles. Multiple regression analyses were performed at 2 stages of lactation (early: 1–100 DIM; and established: 101–350 DIM) using the MIXED procedure of SAS. Estimated breeding value was also included to account for the effect of genetics on milk fat concentration. Results show that RUFAL has a negative and significant relationship with milk fat concentration at each stage of lactation (P

Eight ruminally fistulated, multiparous Holstein cows were arranged in a double 4×4 Latin square with 14-d periods to investigate the effects of lipid supplementation on performance, rumen parameters, the milk odd- and branched-chain fatty acid (OBCFA) profile, and the relationships between milk OBCFA and rumen parameters. Lipid supplementation is known to inhibit microbial growth in the rumen, decrease de novo microbial fatty acid synthesis, and increase the uptake of circulating fatty acids by the mammary gland; treatments were selected to isolate these effects on the milk OBCFA profile. The 4 treatments were (1) a lipid-free emulsion medium infused in the rumen (CTL), (2) soybean oil as a source of polyunsaturated fatty acids infused in the rumen (RSO), (3) saturated fatty acids (38% 16:0, 40% 18:0) infused in the rumen (RSF), and (4) saturated fatty acids infused in the abomasum (ASF). Fat supplements were provided continuously as emulsions at a rate of 450g/d. Preplanned contrasts compared CTL to RSO, RSO to RSF, and RSF to ASF. Infusing RSO slightly decreased ruminal pH, but did not affect volatile fatty acids profile and milk fat concentration as compared with CTL. The yields of energy-corrected milk, fat, and protein were greater with RSF compared with RSO. The concentration of odd-chain fatty acids was decreased by RSO, whereas even-chain iso fatty acids were not affected. Milk fat concentration of 17:0 + cis-9 17:1 was higher for RSF than for RSO, due to the saturated fatty acids supplement containing 2% 17:0 + cis-9 17:1. Limited differences were observed in the milk OBCFA profile between RSF and ASF. A multiple regression analysis yielded the following equation for predicting rumen pH based on milk fatty acids: pH=6.24 - (0.56×4:0) + (1.67 × iso 14:0) + (4.22 × iso 15:0) + (9.41×22:0). Rumen propionate concentration was negatively correlated with milk fat concentration of iso 14:0 and positively correlated with milk 15:0, whereas the acetate-to-propionate ratio gave the opposite correlations with milk iso 14:0 and 15:0. Milk fat concentration of 17:0 + cis-9 17:1 was not related to rumen propionate or to acetate-to-propionate ratio, due to the presence of 17:0 and cis-9 17:1 in the saturated fatty acids supplement. The results suggest that although lipid supplementation can affect the profile of milk OBCFA, the promise remains of using these milk fatty acids to evaluate rumen function.

Fertilization with Se improves forage organic Se concentration, but comparisons with other forms of Se supplementation in feeding lactating dairy cows are scarce. Our objective was to compare the effect of Se-enriched forages to dietary sources of inorganic and organic Se. Digestibility, retention, and balance were assessed by measuring Se concentrations in feces, urine, milk, and blood. The resulting effect on antioxidant status and lactation performance of dairy cows was also determined. High-Se silages [1.72 mg of Se/kg of dry matter (DM)] were produced following a spring application of 2.5 kg/ha of Selcote Ultra, whereas low-Se silages (0.05 mg of Se/kg of DM) were produced in the Se-unfertilized portion of the same fields. After a 77±17 d period of Se depletion, 33 late-lactation primiparous Holstein cows were blocked and randomly assigned for 43 d to 1 of 4 experimental total mixed rations fed for ad libitum intake in an unbalanced randomized block design. Treatments consisted of 4 diets: control with low-Se silages, without Se supplement (0.12±0.04 mg of Se/kg of DM); ISe with low-Se silages and inorganic Se (0.80±0.14 mg of Se/kg of DM); YSe with low-Se silages and organic Se from yeast (0.70±0.11 mg of Se/kg of DM); and FSe with high-Se silages, without Se supplement (0.79±0.14 mg of Se/kg of DM). Organic Se, either as YSe or FSe, was more available and more effective to increase blood and milk Se concentrations than ISe. Moreover, FSe was more available than YSe, as cows fed FSe excreted 16 and 22% less Se (as percentage of intake) in feces and urine, respectively, had higher Se apparent absorption (17%), retention (37%), and balance (45%), and had greater concentration of Se in serum (16%) and milk (11%) than cows fed YSe. Antioxidant status (whole blood and plasma glutathione peroxidase, and milk thioredoxin reductase and malondialdehyde) was not affected by treatments. Dry matter intake, yield of actual, energy-corrected, and fat-corrected milk, as well as milk fat and lactose concentrations, were not affected by the dietary treatments. Cows fed ISe had lower milk protein concentration (3.44%) than cows fed YSe (3.58%) or FSe (3.51%). Cows fed Se-supplemented diets had a lower milk somatic cell count than cows fed the control diet. Results from the current study showed that the production of Se-enriched forages is an effective method to supplement dairy cows in Se as it was more available than YSe, and did not alter antioxidant status and performances of lactating dairy cows.

Given its elevated content of carotenoids, alfalfa protein concentrates (APC) have the potential to prevent oxidation of milk enriched in polyunsaturated fatty acids. The effects of feeding APC or supplemental vitamin E on production, composition, and oxidative stability of milk enriched in polyunsaturated fatty acids were evaluated using 6 lactating Holstein cows (224±18d in milk) in a replicated 3×3 Latin square (21-d periods, 14d for adaptation). Treatment diets contained (dry matter basis) (1) 9% soybean meal (control, CTL); (2) 9% soybean meal + 300 IU of vitamin E/kg (VitE treatment); or (3) 9% APC (APC treatment). Cows received a continuous abomasal infusion of 450g/d of linseed oil. As a result, milk fat content of cis-9,cis-12 18:2 increased from 1.08±0.13 to 3.9±0.40% (mean ± SD), whereas cis-9,cis-12,cis-15 18:3 increased from 0.40±0.04 to 14.27±1.81% during the experimental period compared with the pretrial period. Milk yield tended to be higher for APC (14.7kg/d) compared with CTL (13.4kg/d), and was greater than that for VitE (13.0kg/d). Protein yield was higher in cows fed APC (518g/d) compared with VitE (445g/d) but was not different from that in cows fed CTL (483g/d). These effects resulted in improved milk N efficiency in cows fed APC (26.1% of N intake secreted in milk) compared with CTL (23.0%) and VitE (22.9%). Feeding APC increased milk fat content of lutein (252μg/g) compared with CTL (204μg/g) and VitE (190μg/g). Milk fat content of vitamin E was higher for APC (34.5μg/g) compared with CTL (19.0μg/g) and tended to be lower than that with VitE (44.9μg/g). Redox potential of fresh milk from cows fed APC (152mV) was similar to that of VitE (144mV), but lower than that of CTL (189mV). Treatments had no effect on fresh milk contents of dissolved oxygen (8.1±1.5mg/L), and conjugated diene hydroperoxides (2.7±0.5mmol/L). The concentrations of volatile lipid oxidation products (propanal, hexanal, hept-cis-4-enal, 1-octen-3-one) tended to be decreased by APC relative to CTL, whereas similar values were observed for VitE, except for hexanal, which was reduced by 40% in VitE. In conclusion, feeding APC to lactating dairy cows could serve as a source of dietary protein that improves dietary N utilization efficiency, and also as a preharvest technology to increase natural antioxidant levels in milk to limit oxidation.

Effects of forage family (legume vs. grass) on apparent ruminal synthesis (ARS) and postruminal supply of B vitamins were evaluated in 2 experiments. Diets containing either alfalfa (AL) or orchardgrass (OG) silages as the sole forage were offered to ruminally and duodenally cannulated lactating Holstein cows in crossover design experiments. Experiment 1 compared diets containing AL and OG [~23% forage neutral detergent fiber (NDF) and ~27% total NDF] offered to 8 cows in two 15-d treatment periods. Experiment 2 compared diets containing AL and OG (~25% forage NDF and ~30% total NDF) offered to 13 cows in two 18-d treatment periods. Thiamin, riboflavin, niacin, vitamin B6, folates, and vitamin B12 were analyzed in feeds and duodenal digesta. Apparent ruminal synthesis was calculated as the duodenal flow of each vitamin minus its intake. Forage family affected B vitamin intakes, duodenal flow, and ARS. In both experiments, AL diets increased vitamin B6 and decreased folate intakes. In experiment 1, riboflavin and niacin intakes were greater with the OG diet, whereas in experiment 2 thiamin intake was greater but riboflavin intake was smaller with the OG diet. In spite of the low contribution of either silage to the dietary folate content, folate intake was greater with OG diets than AL due to the difference in soybean meal contribution between diets. Niacin and folate ARS were not affected by the forage family. Duodenal microbial nitrogen flow was positively correlated with ARS of riboflavin, niacin, vitamin B6, folates, and vitamin B12, but tended to be negatively correlated with thiamin ARS. Apparent ruminal synthesis of folates and vitamin B12 appear to be related to microbial biomass activity. Changes in nutrient composition of the diets likely affected the microbial population in the rumen and their B vitamin metabolism.

Milk fatty acid (FA) profile has been previously used as a predictor of enteric CH4output in dairy cows fed diets supplemented with plant oils, which can potentially impact ruminal fermentation. The objective of this study was to investigate the relationships between milk FA and enteric CH4 emissions in lactating dairy cows fed different types of forages in the context of commonly fed diets. A total of 81 observations from three separate 3×3 Latin square design (32-day periods) experiments including a total of 27 lactating cows (96±27 days in milk; mean±SD) were used. Dietary forages were included at 60% of ration dry matter and were as follows: (1) 100% corn silage, (2) 100% alfalfa silage, (3) 100% barley silage, (4) 100% timothy silage, (5) 50 : 50 mix of corn and alfalfa silages, (6) 50 : 50 mix of barley and corn silages and (7) 50 : 50 mix of timothy and alfalfa silages. Enteric CH4output was measured using respiration chambers during 3 consecutive days. Milk was sampled during the last 7 days of each period and analyzed for components and FA profile. Test variables included dry matter intake (DMI; kg/day), NDF (%), ether extract (%), milk yield (kg/day), milk components (%) and individual milk FA (% of total FA). Candidate multivariate models were obtained using the Least Absolute Shrinkage and Selection Operator and Least-Angle Regression methods based on the Schwarz Bayesian Criterion. Data were then fitted into a random regression using the MIXED procedure including the random effects of cow, period and study. A positive correlation was observed between CH4 and DMI (r=0.59,P0.19). Milk FA profile and DMI can be used to predict CH4emissions in dairy cows across a wide range of dietary forage sources

The objective of the current study was to compare the effects of feeding corn dried distillers’ grains with solubles (DDGS), camelina expeller (CE), whole camelina seeds (WCS), or whole flax seeds (WFS) on milk yield and composition of lactating dairy cows. Four Holstein cows were used in a 4 × 4 Latin square design with 21-d periods, including 14 d of adaptation followed by 7 d of sampling. Four isoproteic and isolipidic dietary treatments were formulated as follows: 1) 18 % DDGS; 2) 9.5 % CE; 3) 4.2 % WCS; and 4) 4.7 % WFS (dry matter basis). Pre-planned contrasts were established to compare: 1) the two by-products (DDGS rich in cis-9, cis-12 18:2 vs. CE rich in cis-9, cis-12, cis-15 18:3); 2) the two forms of camelina (CE vs. WCS); and 3) the two whole seeds (WCS vs. WFS). Differences were declared at P ≤ 0.05. Contrasts did not reveal any significant differences in dry matter intake ( x ¯ =24.6 kg/d). Actual milk yield was greater for cows fed WCS (36.5 kg/d) compared with WFS (35.6 kg/d). Moreover, yield of fat-corrected milk was lower with CE (29.8 kg/d) than with DDGS (35.3 kg/d) or WCS (33.5 kg/d). These effects are in line with lower milk fat concentration when cows received CE (27.1 g/kg) as compared with DDGS (36.3 g/kg) or WCS (34.8 g/kg). Lower milk fat observed with CE could be explained by a shift from the trans-11 to the trans-10 pathway of biohydrogenation, leading to the production of more intermediates known to inhibit milk fat synthesis, i.e., milk fat concentration of trans-10, cis-12 18:2 was greater with CE (0.078 mg/g) than with DDGS (0.045 mg/g) or WCS (0.041 mg/g). The transfer efficiency, from the diet to milk fat (g secreted/g consumed), of total n-3 fatty acids was lower with CE (0.082 g/g) compared with DDGS (0.109 g/g) or WCS (0.106 g/g), but was not different between WCS and WFS (0.110 g/g). Finally, the transfer efficiency of cis-13 22:1 was twice greater with CE than with WCS (0.198 vs. 0.105 g/g). In conclusion, feeding CE had a negative impact on lactation performance, and more specifically on milk fat yield; an effect that could be explained by the great accessibility of the residual oil contained in this by-product and its consequent interference with lipid metabolism in the rumen. Comparison of WCS with WFS reveals that both oilseeds support similar production efficiency and gross milk composition.

Microbial protein synthesis in the rumen would be optimized when dietary carbohydrates and proteins have synchronized rates and extent of degradation. The aim of this study was to evaluate the effect of varying ruminal degradation rate of energy and nitrogen sources on intake, nitrogen balance, microbial protein yield, and kinetics of nutrients in the rumen of growing kids. Eight Boer goats (38.2 ± 3.0 kg) were used. The treatments were arranged in a split-plot Latin square design with grain sources (barley or corn) forming the main plots (squares). Grain processing methods and levels of protein degradability formed the subplots in a 2 × 2 factorial arrangement for a total of 8 dietary treatments. The grain processing method was rolling for barley and cracking for corn. Levels of protein degradability were obtained by feeding untreated soybean meal (SBM) or heat-treated soybean meal (HSBM). Each experimental period lasted 21 d, consisting of a 10-d adaptation period, a 7-d digestibility determination period, and a 4-d rumen evacuation and sampling period. Kids fed with corn had higher purine derivatives (PD) excretion when coupled with SBM compared with HSBM and the opposite occurred with barley-fed kids ( ≤ 0.01). Unprocessed grain offered with SBM led to higher PD excretion than with HSBM whereas protein degradability had no effect when processed grain was fed ( ≤ 0.03). Results of the current experiment with high-concentrate diets showed that microbial N synthesis could be maximized in goat kids by combining slowly fermented grains (corn or unprocessed grains) with a highly degradable protein supplement (SBM). With barley, a more rapidly fermented grain, a greater microbial N synthesis was observed when supplementing a low-degradable protein (HSBM).

The effect of fat supplements (FS) providing different proportions of saturated (SFA) and unsaturated (UFA) fatty acids on supply, apparent ruminal synthesis (ARS), and duodenal flow (DF) of some B vitamins (thiamine, riboflavin, niacin, vitamin B6, folates, and vitamin B12) were evaluated in an experiment using 8 ruminally and duodenally cannulated lactating Holstein cows. The experiment was a replicated 4 × 4 Latin square design with 21-d treatment periods. The 4 treatments were a control diet without fatty acid supplement and 3 diets with 2.5% additional fatty acids from supplements containing (1) SFA, (2) an intermediate mixture of SFA and UFA, or (3) UFA. All diets were served as a total mixed ration once daily at 115% of the expected intake. B-vitamin concentrations were analyzed in feed and duodenal digesta. Apparent ruminal synthesis of each B vitamin was calculated as the DF minus the intake. B-vitamin concentrations were similar among the 4 treatments; consequently, daily intake of the vitamins followed the same pattern as dry matter intake. Adding FS decreased B-vitamin intakes (except vitamin B12), as did increasing the proportion of UFA. Riboflavin and niacin DF and ARS, expressed as total daily amount or per unit of dry matter intake, were not affected by FS, but increasing the proportion of UFA decreased riboflavin and niacin DF and ARS. Fat supplements decreased DF of vitamin B6, expressed either as total daily amount or per unit of dry matter intake. No treatment effects were observed on total daily folate DF and ARS. However, when expressed per unit of dry matter intake, folate DF and ARS were greater when cows were fed FS and they increased linearly with the proportion of UFA in the supplement. Inclusion of fat supplements into the dairy cow diet had a limited effect on the fate of most B vitamins in the rumen although increasing the proportion of UFA in the FS linearly decreased apparent synthesis of riboflavin and niacin in the rumen and the amounts of these vitamins reaching the small intestine.

Potassium carbonate supplementation is known to improve milk fat synthesis and to modify milk mineral composition in dairy cows. The objective of the current experiment was to evaluate the effect of K2CO3 on production performance, biohydrogenation of fatty acids (FA), and mineral composition of milk in early-lactation dairy cows fed a high-concentrate diet with or without soybean oil (SBO), as a source of polyunsaturated FA. Twenty-eight ruminally fistulated Holstein cows were used in a randomized complete block design. The experiment lasted 33 d, including a 5-d pretreatment collection period used as a covariate. Experimental treatments were arranged as a 2 × 2 factorial with 0 or 1.5% K2CO3 and with 0 or 2% SBO, and balanced to contain 40% forage (57% corn silage + 43% grass silage) and 60% concentrate. Preplanned orthogonal contrasts were used to assess the effects of K2CO3, SBO, and their interaction. Feeding K2CO3 did not affect milk yield, but tended to increase 4% fat-corrected milk and fat yield when combined with SBO. However, adding SBO to diets increased milk yield. Dietary K2CO3 supplementation did not affect milk fat concentration of trans-10 18:1 or any other identified biohydrogenation intermediates. Soybean oil supplementation decreased milk fat concentration of C16 and de novo synthesized FA, and increased preformed FA. Among the other effects of SBO supplementation observed, concentrations of cis-9,trans-11 18:2 increased, as well as most of the cis and trans isomers of 18:1 and 18:0. Milk urea N decreased in cows fed K2CO3 as compared with unsupplemented diets. A positive relation was established between milk Cl concentration and milk yield, suggesting that the equilibrium of this ion is linked to the efficiency of lactogenesis. The effect of K2CO3 on this mineral equilibrium in the mammary gland remains to be established. Overall, results have shown that potential effect of K2CO3 on milk fat synthesis is dependent on the levels of dietary polyunsaturated FA.

The objective of this study was to examine the effects of whole flax seed (FS) and flax oil (FO) supplementation on digestion, ruminal fermentation, and milk fatty acid (FA) profile of dairy cows fed high-forage (HF) or high-concentrate (HC) diets. Four ruminally lactating cows were used in a 4 × 4 Latin square design with dietary treatments arranged as a 2 × 2 factorial. High forage and HC basal diets were formulated by varying the proportions of grass and corn silages, as well as those of corn grain and soybean meal. The basal diets were fed for ad libitum intake, and supplemented with either FS or FO at the feeding rate of 2.0 and 0.7 kg/d, respectively. The forage:concentrate (F:C) ratios of the total diets (including top dressed FS or FO) were 700:300 and 300:700 on a dry matter (DM) basis for HF and HC, respectively. Increasing the concentrate proportion in the diet reduced ruminal pH, shifted volatile fatty acid (VFA) pattern toward more propionate and less acetate, and decreased protozoal numbers. These changes in ruminal fermentation resulted in a decrease of in sacco effective ruminal degradability (ERD) of acid detergent fiber (ADF) and neutral detergent fiber (aNFD) of grass silage. Despite alterations in rumen function, no interactions occurred between the proportion of concentrate in the diet and flax supplementation. Replacing FS with FO in the diet had no effect on dry matter intake (DMI) and ruminal fermentation characteristics, but increased organic matter (OM) digestibility and milk yield. An interaction between F:C and flax supplement was observed for the milk fat ratio of trans -11 18:1 to trans -10 18:1, which increased when FO replaced FS in HF diets, while the opposite was observed with HC diets. Feeding FS increased milk fat content and transfer efficiency of cis -9, cis -12, cis -15 18:3, the major FA present in flax, and decreased the concentration of trans intermediates of ruminal biohydrogenation as compared with FO.

Rumen bypass of flax oil (FO), which is rich in omega-3 fatty acids (FA), contributes to increase polyunsaturated FA proportion in milk fat. Flax meal (FM) is a source of antioxidants, which may reduce oxidative damage in cows given omega-3 FA. The aim of this study was to investigate the effects of dietary FM supplement on performance and antioxidant status in dairy cows infused with FO in the abomasum. Eight rumen fistulated lactating Holstein cows were assigned to a double 4×4 Latin square design with a 2×2 factorial arrangement of treatments: (1) control diet with no FM (CO); (2) diet containing 124 g/kg FM in the dry matter (DM); (3) CO and 250 g FO/d infused in the abomasum; and (4) FM and 250 g FO/d infused in the abomasum. Intake of DM and total DM input (including abomasally infused oil) were increased for cows fed FM and reduced for cows infused with FO. Milk production and milk composition did not differ among treatments except for lactose concentration that was increased with FO infusion. Milk fat from cows fed FM had lower omega-6 FA proportions. Abomasal infusion of FO increased proportions of polyunsaturated, omega-6 and omega-3 FA in milk fat. Cows fed CO with no FO infusion showed higher omega-6/omega-3 FA ratio in milk fat compared with the other treatments, whereas no difference was observed between CO and FM when FO was infused in the abomasum. Feeding FM did not change plasma and milk thiobarbituric acid reactive substances concentrations, whereas FO increased them. Infusion of FO in the abomasum increased the peroxidizability index, the maximal conjugated diene (CD) production and rate of CD production, whereas lag time and time to reach maximum amount of CD were reduced. Plasma antioxidant capacity before feeding was increased when cows received dietary FM or FO abomasal infusion, whereas no differences were observed 3 h postfeeding. Results suggest that FM supplementation to dairy cows receiving a source of polyunsaturated FA that bypasses the rumen does not provide any benefits for protecting cows and milk against lipoperoxidation.

The purpose of this study was to determine the effects of conjugated linoleic acid (CLA), Sterculia foetida oil (STO), and fish oil (FO) on milk yield and composition, milk FA profile, Δ(9)-desaturation activity, and mammary expression of 2 isoforms of stearoyl-coenzyme A desaturase (SCD-1 and SCD-5) in lactating dairy cows. Eight multiparous Holstein cows (69 ± 13 d postpartum) were used in a double 4 × 4 Latin square design with 28-d periods. For the first 14 d of each period, cows received an abomasal infusion of (1) 406 g of a saturated fatty acid (SFA) supplement (112 g of 16:0 + 230 g of 18:0) used as a control (CTL), (2) 36 g of a CLA supplement (13.9 g of trans-10,cis-12 18:2) + 370 g of SFA, (3) 7 g of STO (3.1g of 19:1 cyclo) + 399 g of SFA, or (4) 406 g of FO (55.2 g of cis-5,-8,-11,-14,-17 20:5 + 59.3 g of cis-4,-7,-10,-13,-16,-19 22:6). Infusions were followed by a 14-d washout interval. Compared with CTL, STO decreased milk yield from 38.0 to 33.0 kg/d, and increased milk fat concentration from 3.79 to 4.45%. Milk fat concentration was also decreased by CLA (2.23%) and FO (3.34%). Milk fat yield was not affected by STO (1,475 g/d) compared with CTL (1,431 g/d), but was decreased by CLA (774 g/d) and FO (1,186 g/d). Desaturase indices for 10:0, 12:0, and 20:0 were decreased, whereas the extent of desaturation of 14:0, 16:0, 17:0, and 18:0 was not affected by CLA treatment compared with CTL. Infusion of STO significantly decreased all calculated desaturase indices compared with CTL; the 14:0 index was reduced by 80.7%. Infusion of FO decreased the desaturase indices for 10:0, 14:0, 20:0, trans-11 18:1, and 18:0. The effect of FO on the 14:0 index indicates a decrease in apparent Δ(9)-desaturase activity of 30.2%. Compared with CTL, mammary mRNA abundance of SCD-1 was increased by STO (+30%) and decreased by CLA (-24%), whereas FO had no effect. No effect was observed on mRNA abundance of SCD-5. In conclusion, abomasal infusion of CLA, STO, and FO were shown to exhibit varying and distinct effects on desaturase indices, an indicator of apparent SCD activity, and mammary mRNA abundance of SCD-1.

Nutrient composition and organoleptic properties of milk can be influenced by cow diets. The objective of this study was to evaluate the forage type effects on volatile organic compounds, fatty acid (FA) profile, and organoleptic properties of milk. Timothy grass was fed as hay, pasture, or silage during a period of 27 d to a group of 21 cows in a complete block design based on days in milk. Each cow also received 7.2 kg/d of a concentrate mix to meet their nutrient requirements. Forage dry matter intake averaged 13.9 kg/d and was not different among treatments. Milk yield was higher for cows fed pasture, intermediate for cows fed silage, and lowest for cows fed hay. However, milk fat content was higher for cows fed hay and silage, compared with cows fed pasture. As a result, fat-corrected milk and fat yield were not different among treatments. Increasing the supply of dietary cis-9,cis-12 18:2 (linoleic acid) and cis-9,cis-12,cis-15 18:3 (α-linolenic acid) when feeding pasture enhanced the concentration of these 2 essential FA in milk fat compared with feeding hay or silage. Moreover, the ratio of 16:0 (palmitic acid) to cis-9 18:1 (oleic acid), which is closely related to the melting properties of milk fat, was lower in milk from cows on pasture than in milk from cows fed hay or silage. Cows fed hay produced milk with higher levels of several free FA and γ-lactones, but less pentanal and 1-pentanol. More dimethyl sulfone and toluene were found in milk of cows on pasture. Cows fed silage produced milk with higher levels of acetone, 2-butanone, and α-pinene. Results from a sensory evaluation showed that panelists could not detect a difference in flavor between milk from cows fed hay compared with silage. However, a significant number of assessors perceived a difference between milk from cows fed hay compared with milk from cows fed pasture. In a sensory ranking test, the percentage of assessors ranking for the intensity of total (raw milk, fresh milk, and farm milk), sweet (empyreumatic, vanilla, caramel, and sugar), and grassy (grass, leafy vegetable, and plant) flavors was higher for milk from cows fed pasture compared with hay and silage. Using timothy hay, pasture, or silage harvested at a similar stage of development, the current study shows that the taste of milk is affected by the forage type fed to cows. More research is, however, needed to establish a link between the sensory attributes of milk and the observed changes in volatile organic compounds and FA profile.

International audience; The objective of this study was to examine the effects of including corn dried distillers grains with solubles (DDGS) in the diet at the expense of corn and soybean meal on enteric CH4 emissions, ruminal fermentation characteristics, digestion (in sacco and apparent total-tract digestibility), N balance, and milk production of dairy cows. Twelve lactating Holstein cows were used in a triplicated 4×4 Latin square design (35-d periods) and fed (ad libitum intake) a total mixed ration containing (dry matter basis) 0, 10, 20, or 30% DDGS. Dry matter intake increased linearly, whereas apparent-total tract digestibility of dry matter and gross energy declined linearly as DDGS level in the diet increased. Increasing the proportion of DDGS in the diet decreased the acetate:propionate ratio, but this decrease was the result of reduced acetate concentration rather than increased propionate concentration. Milk yield increased linearly (up to +4kg/d) with increasing levels of DDGS in the diet and a tendency was observed for a quadratic increase in energy-corrected milk as the proportion of DDGS in the diet increased. Methane production decreased linearly with increasing levels of DDGS in the diet (495, 490, 477, and 475 g/d for 0, 10, 20, and 30% DDGS diets, respectively). When adjusted for gross energy intake, CH4 losses also decreased linearly as DDGS proportion increased in the diet by 5, 8, and 14% for 10, 20, and 30% DDGS diets, respectively. Similar decreases (up to 12% at 30% DDGS) were also observed when CH4 production was corrected for digestible energy intake. When expressed relative to energy-corrected milk, CH4 production declined linearly as the amount of DDGS increased in the diet. Total N excretion (urinary and fecal; g/d) increased as the amount of DDGS in the diet increased. Efficiency of N utilization (milk N secretion as a proportion of N intake) declined linearly with increasing inclusion of DDGS in the diet. However, productive N increased linearly with increasing proportions of DDGS in the diet, suggesting better efficiency of N use by the animal. Results from this study show that feeding DDGS to dairy cows can help to mitigate enteric CH4 emissions without negatively affecting intake and milk production.

Corn silage (CS) is associated with a reduction in milk fat content. The fact that CS is constituted of a grain and a forage fraction could explain this effect. This experiment evaluated the effect of grain fraction of CS on rumen fermentation, production performance and milk composition. Earless CS (ECS) was harvested after manually removing corn ears from the plant. Whole CS (WCS) was harvested from the same field on the same day. Eight (four ruminally fistulated) multiparous Holstein cows (84 days in milk) were utilized in a double 4 × 4 Latin square with 21-day periods. Treatments were (dry matter (DM) basis) (1) 23.0% WCS; (2) 12.4% ECS plus 10.6% high moisture corn (HMC) to obtain reconstituted CS (RCS); (3) 23.0% ECS; and (4) 23.0% timothy silage (TS). Diets were formulated to be isonitrogenous and were fed as total mixed ration once a day. DM intake (DMI), milk yield, 4.0% fat-corrected milk (FCM), as well as protein concentration and yield were higher for WCS than ECS. Compared with WCS, cows tended to eat less with RCS, and produced less milk and milk protein. However, yield of FCM was similar between WCS and RCS. Milk fat concentration and yield, as well as the specific ratio of t11 18:1 to t10 18:1 in milk fat did not differ among diets. Milk urea-N tended to be higher for ECS than WCS and TS, whereas ruminal NH3-N was higher with ECS than TS. Rumen pH decreased linearly with time after feeding but was not different between treatments. Higher acetate and lower propionate concentration resulted in greater acetate to propionate ratio with ECS compared with WCS. In conclusion, removing grain fraction from CS decreased milk production and modified rumen fermentation without affecting milk fat concentration and yield. Moreover, despite some differences in DMI and total ruminal volatile fatty acid concentration between WCS and RCS, the restoration of FCM yield, using HMC in RCS diets, to a level of production similar to WCS highlights the importance of energy and nutrients supplied by the grain fraction of CS to support milk yield.

Effects of plant maturity on apparent ruminal synthesis and post-ruminal supply of B vitamins were evaluated in two feeding trials. Diets containing alfalfa (Trial 1) or orchardgrass (Trial 2) silages harvested either (1) early cut, less mature (EC) or (2) late cut, more mature (LC) as the sole forage were offered to ruminally and duodenally cannulated lactating Holstein cows in crossover design experiments. In Trial 1, conducted with 16 cows (569±43 kg of empty BW (ruminal content removed) and 43.7±8.6 kg/day of 3.5% fat-corrected milk yield; mean±SD) in two 17-day treatment periods, both diets provided ~22% forage NDF and 27% total NDF, and the forage-to-concentrate ratios were 53 : 47 and 42 : 58 for EC and LC, respectively. In Trial 2, conducted with 13 cows (588±55 kg of empty BW and 43.7±7.7 kg/day of 3.5% fat-corrected milk yield; mean±SD) in two 18-day treatment periods, both diets provided ~25% forage NDF and 31% total NDF; the forage-to-concentrate ratios were 58 : 42 and 46 : 54 for EC and LC, respectively. Thiamin, riboflavin, niacin, vitamin B6, folates and vitamin B12 were measured in feed and duodenal content. Apparent ruminal synthesis was calculated as the duodenal flow minus the intake. Diets based on EC alfalfa decreased the amounts of thiamin, niacin and folates reaching the duodenum, whereas diets based on EC orchardgrass increased riboflavin duodenal flow. Daily apparent ruminal synthesis of thiamin, riboflavin, niacin and vitamin B6 were correlated negatively with their intake, suggesting a microbial regulation of their concentration in the rumen. Vitamin B12 apparent ruminal synthesis was correlated negatively with total volatile fatty acids concentration, but positively with ruminal pH and microbial N duodenal flow.

Nitrogen efficiency (milk N/dietary N; NE) can be used as a tool for the nutritional, economic, and environmental management of dairy farms. The aim of this study was to identify the characteristics of herds with varying NE and assess the effect on farm profitability. One hundred dairy herds located in Quebec, Canada, comprising on average 42 ± 18 cows in lactation were visited from October 2014 to June 2015. Feed intake was measured over 24 h. Samples of each feedstuff were taken and sent to a commercial laboratory for analysis of chemical composition. Feeding management and feed prices were recorded. Milk yield was recorded and milk samples were collected over 2 consecutive milkings. Fat, protein, and milk urea N were analyzed. Balances of metabolizable protein (MP; MP supply - MP requirements) and rumen degradable protein (RDP; RDP supply - RDP requirement) were calculated. A hierarchical cluster analysis was conducted and allowed grouping the farms by their NE. Four clusters were identified with an average NE of 22.1 (NE22), 26.9 (NE27), 30.0 (NE30), and 35.8% (NE36). Herds in clusters NE30 and NE36 were fed diets with greater concentrations of starch, net energy for lactation, and nonfiber carbohydrates than those in the other 2 clusters. Moreover, the average proportion of corn silage was lower for herds in cluster NE22 compared with NE30 and NE36 (8.23 vs. 31.8 and 31.3% of total forages, respectively). In addition, crude protein of the diets declined from an average of 16.0 to 14.9% with increasing NE among clusters. Average dry matter intake declined from 26.1 to 22.5 kg/d as NE of clusters increased. Herds in cluster NE22 had lower yields of milk (28.7 vs. 31.8 kg/d), fat (1.15 vs. 1.29 kg/d), and protein (0.94 vs. 1.05 kg/d) than the other clusters. Also, milk urea N was greater for farms in cluster NE22 (13.2 mg/dL) than for farms in the other clusters (11.4 mg/dL). Furthermore, MP and RDP balances decreased from 263.2 to -153.7 g/d and from 594.7 to 486.9 g/d, respectively, with increasing NE among clusters. Income over feed cost increased from $14.3 to $17.3/cow per day (Can$) as NE among clusters augmented. Results from this study showed that some farms were able to achieve high NE by using lower levels of dietary N and having cows with lower DMI while maintaining milk performance. These farms had a potentially lower environmental impact, and they were more profitable.

Effects of particle length of silages on apparent ruminal synthesis (ARS) and postruminal supply of B vitamins were evaluated in 2 feeding trials. Diets containing alfalfa (trial 1) or orchardgrass (trial 2) silages, chopped to either 19mm (long cut, LC) or 10mm (short cut, SC) theoretical particle length, as the sole forage were offered to ruminally and duodenally cannulated lactating Holstein cows in crossover design experiments. Forages chopped to a theoretical particle length of 19 and 10mm had mean particles sizes of 14.1 and 8.1mm, respectively, in trial 1, and 15.3 and 11.3mm, respectively, in trial 2. Trial 1 was conducted with 13 multiparous cows in two 19-d treatment periods; both diets contained approximately 20% forage neutral detergent fiber (NDF), 25% total NDF, and forage-to-concentrate ratios were approximately 47:53. Trial 2 was conducted with 15 cows in two 18-d treatment periods; both diets contained approximately 23% forage NDF, 28% total NDF, and had a forage-to-concentrate ratio of 50:50. Thiamine, riboflavin, niacin, vitamin B6, folates, and vitamin B12 were measured in feed and duodenal content. Daily ARS was calculated as the duodenal flow minus the intake. In trial 1, daily intake of individual B vitamins was increased with the LC diet, but ARS of thiamine, riboflavin, vitamin B6, and folates was reduced. In trial 2, except for folates, intakes of the other B vitamins were decreased with the LC diets, whereas ARS of riboflavin, niacin, and vitamin B6 was increased. Daily ARS of thiamine, riboflavin, niacin, and vitamin B6 were correlated negatively with their intake, suggesting that ruminal bacteria reduced their synthesis when dietary supply increased. Microbial activity could have also reduced degradation of thiamine, riboflavin, and niacin, which is supported by (1) the negative correlation between ARS of these vitamins and ruminal pH or microbial N duodenal flow; and (2) the positive correlation between ARS and ruminal concentrations of volatile fatty acids. Folate ARS followed the opposite correlation pattern. Nevertheless, in spite of differences in intake and ARS, with both forages, decreasing particle length of silages had limited effects on the amounts of B vitamins reaching the sites of absorption in the small intestine of dairy cows.

Four ruminally cannulated primiparous lactating cows were used in a 4 × 4 Latin square design experiment (28 d periods) with a 2 × 2 factorial arrangement of treatments to examine effects of eugenol supplementation, concentrate proportion of the diet and their interaction on digestion, ruminal fermentation, microbial populations, milk production and milk composition, including milk fatty acid (FA) profile. Cows were fed for ad libitum intake a low (LC) or high (HC) concentrate total mixed ration (TMR) without or with eugenol (50 mg/kg of dry matter (DM) intake. The forage:concentrate ratio was (DM basis) 650:350 and 350:650 for LC and HC, respectively. Adding eugenol to the diets had no effects on DM intake, digestion, ruminal fermentation, rumen microbial populations of bacteria and protozoa and milk performance. Increasing the concentrate proportion of the diet resulted in changes typical of cows fed high starch diets ( i.e. , lower ruminal pH and acetate:propionate ratio; shift in bacterial populations; lower milk fat and higher milk protein concentrations). The ratio t -11 18:1 to t -10 18:1 was not affected by dietary treatments, indicating no changes in the pathway of biohydrogenation of FA in the rumen. Despite the alteration of rumen function due to increasing the proportion of the concentrate of the diet, adding eugenol to these high or low concentrate diets did not modify digestion, ruminal fermentation and microbial populations, suggesting that the effect ( i.e. , antimicrobial) of eugenol is neither pH nor diet dependant. The lack of efficacy of eugenol at the dosage rate evaluated under the experimental conditions of this study suggests that this essential oil may have low potential for use as feed additive in dairy cow nutrition.

The aim of this study was to evaluate the effects of dietary supplementation with different fish oils (rich in PUFA) vs. hydrogenated animal fat (SFA) on semen production and quality, fatty acid composition, and preservation properties in boars under controlled and commercial conditions. In Exp. 1 (in a research station), 44 boars, allocated to 4 dietary treatments, received daily 2.5 kg of basal diet with a supplement of 1) 62 g of hydrogenated animal fat (AF, n = 12); 2) 60 g of menhaden oil containing 18% docosahexanoic acid (DHA) and 15% eicosapentanoic acid (EPA; MO, n = 11); 3) 60 g of tuna oil containing 33% DHA and 6.5% EPA (TO, n = 11); and 4) 60 g of menhaden oil and 2 mg/kg of biotin (MO+B, n = 10). Biotin is a critical factor in the elongation of PUFA. Semen was collected according to 3 successive phases: phase 1 (twice per week for 4 wk); phase 2 (daily collection for 2 wk); and phase 3 (twice per week for 10 wk). Experiment 2 was conducted in commercial conditions; 222 boars were randomly allocated to AF, MO, and TO treatments. Semen was collected twice weekly over a 6-mo period. All diets were balanced to be iso-energetic and provided an equivalent of 989 mg of vitamin E per day. Classical measurements of sperm quantity and quality were done for both experiments. Experiment 1 showed, after 28 wk of supplementation, a massive transfer of n-3 PUFA into sperm from boars fed fish oil diets (MO and TO). No differences were observed among dietary treatments for libido (P > 0.30), sperm production (P > 0.20), or percentage of motile cell (P > 0.20). Unexpectedly, MO+B diet reduced the percentage of normal sperm compared with the other treatments (P < 0.03). In conclusion, although it modified the fatty acid composition of sperm, supplementation of boars with dietary fish oils, rich in long chain n-3 fatty acids, did not influence semen production or quality postejaculation.

It has previously been established that supplementation of trans-10, cis-12 18:2 reduces milk fat content and fat deposition in several species. The objectives of the study were 1) to examine whether potential mechanisms by which trans-10, cis-12 18:2 is reported to affect lipid metabolism in adipose tissue of different species could be partly responsible for the inhibition in milk fat synthesis in lactating dairy cows; and 2) to investigate the effects of trans-10, cis-12 18:2 on the expression of a newly identified isoform of stearoyl-coenzyme A desaturase (SCD) in bovine mammary tissue. Four primiparous Holstein cows in established lactation, fitted with indwelling jugular catheters, were used in a balanced 2 x 2 crossover design. For the first 5 d of each period, cows were infused intravenously with a 15% lipid emulsion providing 10 g/d of either cis-9, cis-12 18:2 (control) or trans-10, cis-12 18:2 (conjugated linoleic acid; CLA). On d 5 of infusion, mammary gland biopsies were performed and tissues were analyzed for mRNA expression of acetyl-coenzyme A carboxylase, fatty acid synthetase, lipoprotein lipase, SCD1, SCD5, sterol regulatory element-binding protein-1, IL6, IL8, and tumor necrosis factor-alpha by real-time PCR. Compared with the control treatment, CLA reduced milk fat concentration and yield by 46 and 38%, respectively, and increased the trans-10, cis-12 18:2 content in milk fat from 0.05 to 3.54 mg/g. Milk yield, milk protein, and dry matter intake were unaffected by treatment. Infusion of the CLA treatment reduced the mRNA expression of acetyl-coenzyme A carboxylase and fatty acid synthetase by 46 and 57%, respectively, and tended to reduce the expression of SCD1 and lipoprotein lipase. Abundance of mRNA for sterol regulatory element-binding protein-1 was reduced by 59% in the CLA treatment group. However, infusing trans-10, cis-12 18:2 did not affect the expression of transcripts for SCD5, tumor necrosis factor-alpha, IL6, and IL8. Results from the current study corroborate the idea that effects of trans-10, cis-12 18:2 reported on adipose tissue in animal models and humans are not part of the response in the inhibition of milk fat synthesis in lactating dairy cows. They also support the hypothesis that SCD1 and SCD5 present important differences in their regulation and physiological roles.

Decreasing the dietary cation-anion difference (DCAD) by using anion sources before calving reduces hypocalcemia in cows at calving. Reduced DCAD from CaCl2-fertilized timothy hay achieves similar results, but the effects of feeding low-DCAD forage as silage have not been determined. The objective of this study was to evaluate the effect of low-DCAD timothy silage on dry cows. Six nonlactating and nonpregnant Holstein cows were used in a replicated 3 x 3 Latin square. Treatments were 1) control diet (DCAD = 232 mEq/kg of dry matter, DM); 2) low-DCAD diet using a low-DCAD timothy silage (LDTS; DCAD = -21 mEq/kg of DM); and 3) low-DCAD diet using a fermentation by-product (LDBP; DCAD = -32 mEq/kg of DM). Differences between dietary treatments were considered statistically significant at Por = 0.05 and tendencies were noted when 0.05P0.10. Compared with the control, feeding LDTS tended to decrease DM intake (10.6 vs. 12.5 kg/d) and decreased urinary pH (6.15 vs. 8.18) as well as apparent digestibility of DM (67 vs. 69%). Blood pH (7.37 vs. 7.42), HCO3- (25.3 vs. 27.5 mM), and base excess (0.4 vs. 3.1 mM) were decreased, and blood Cl- (29.6 vs. 29.1 mg/dL) was increased. Apparently absorbed Na and Cl were higher and apparently absorbed K, P, and digested ADF were lower for LDTS compared with the control. Both LDTS and LDBP resulted in similar DM intake. Urinary pH tended to be higher (6.15 vs. 5.98) and percentage of digested DM was lower (67 vs. 70%) with LDTS compared with LDBP. Blood ionized Ca (5.3 vs. 5.4 mg/dL) tended to be lower and blood Cl- (29.6 vs. 30.1 mg/dL) was lower, whereas blood pH (7.37 vs. 7.33), HCO3- (25.3 vs. 21.5 mM), and base excess (0.4 vs. -3.8 mM) were higher with LDTS compared with LDBP. Apparent absorption of Na, Cl, S, and P, as well as apparent digestion of acid detergent fiber, neutral detergent fiber, and N were lower, and K, Cl, S, P, Mg, and N were less retained with LDTS compared with LDBP. Results confirm that low-DCAD timothy silage can be used to produce a compensated metabolic acidosis by decreasing the DCAD of rations served to nonlactating dairy cows.

It has been previously established that trans -10, cis -12 conjugated linoleic acid plays an important role in milk fat depression (MFD). However, in many situations of dietary induced MFD, the reduction in milk fat synthesis is much greater than what would be predicted based on the milk fat concentration of trans -10, cis -12 18:2. These observations suggest that other biohydrogenation intermediates could be implicated in MFD. The objective of this study was to evaluate the effects on milk fat synthesis of an intravenous administration of 2 conjugated diene 18:3 isomers ( cis -9, trans -11, cis -15 and cis -9, trans -13, cis -15 18:3), which are intermediates in ruminal biohydrogenation of α-linolenic acid. Three multiparous Holstein dairy cows (days in milk=189±37 d; body weight=640±69kg; mean±standard deviation), fitted with indwelling jugular catheters, were randomly assigned to a 3×3 Latin square design. For the first 5 d of each period, cows were infused intravenously with a 15% lipid emulsion providing 1) cis -9, trans -11, cis -15 18:3+ cis -9, trans -13, cis -15 18:3+ trans -10, cis -12 18:2 (CD18:3+CLA); 2) cis -9, cis -12, cis -15 18:3+ cis -9, cis -12 18:2 as a control (ALA+LA); or 3) cis -9, cis -12, cis -15 18:3+ trans -10, cis -12 18:2, as a positive control (ALA+CLA). Milk production was recorded, and milk was sampled daily at each milking for analyses of fat, protein, lactose, milk urea nitrogen, and somatic cell count. Dry matter intake, milk yield, and milk protein were not affected by treatment. Over the experimental period, milk fat content was decreased by 7% for cows that received either ALA+CLA or CD18:3+CLA compared with ALA+LA. The temporal pattern of milk fat content showed a linear decrease during the infusion period for ALA+CLA and CD18:3+CLA treatment groups. The transfer efficiencies of conjugated diene 18:3 isomers into milk fat averaged 39 and 32% for cis -9, trans -11, cis -15 18:3 and cis -9, trans -13, cis -15 18:3, respectively. The CD18:3+CLA treatment had no effect on milk fat concentration beyond that attributable to its trans -10, cis -12 18:2 content. In conclusion, results from the current study offered no support for a role of either cis -9, trans -11, cis -15 18:3 or cis -9, trans -13, cis -15 in MFD.

The concentration of CLA in adipose tissue can be increased in ruminants by feeding pasture and extruded soybeans. The objective of this study was to evaluate maternal supplementation of raw (RS) or extruded (ES) soybeans on the concentrations of CLA in milk fat of cows and s.c. adipose tissue of suckling calves. Thirty-two spring-calving cows (BW 624 +/- 76 kg; BCS 3.5 +/- 0.4; mean +/- SD) and calves (BW 127 +/- 15 kg) were separated into 2 groups. Cows were distributed to have 8 calves of each sex in both groups. When animals were turned out to pasture, dams received 2 kg/d of either RS or ES. Dietary treatments had no effect on average milk intake (P = 0.22) and pasture forage intake (P = 0.13) for calves over the course of the grazing season. As a result, no effect of treatments was observed on ADG (P = 0.26). At weaning, milk fat content of CLA reached 15.4 and 24.2 mg/g of total fatty acids for cows fed RS and ES, respectively (P = 0.02). The CLA concentrations in adipose tissue were 16.9 and 25.0 mg/g of total fatty acids for calves suckling dams fed RS and ES, respectively (P < 0.001). Overall, results demonstrated supplementing grazing cows with ES increased CLA content in milk and adipose tissue of suckling calves.