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Abstract This experiment evaluated the influence of creep feeding supplementation on productive and reproductive performance and on serum metabolome profile in Nelore (Bos indicus) heifers. Female calves were assigned to treatments: Creep (n = 190), with ad libitum access to a nutritional supplement from 70 to 220 days after birth, or Control (n = 140), without supplementation. After weaning (Day 220), both groups followed the same pasture and nutritional management. Body weight (BW) and backfat thickness (BFAT) were measured over time. Blood samples were collected at 220 and 360 days for LC–MS/MS targeted metabolomics. On day 408, during the synchronization timed artificial insemination (TAI) protocol, reproductive status (RS: diameter of uterine horn and largest follicle, and presence of CL) was assessed. Creep feeding increased BW and BFAT at weaning, but no differences in BW, BFAT, or RS after weaning were observed. Nonetheless, the pregnancy per AI (P/AI) for 1st service was 28.9% higher in the Creep group. On day 220, 11 significant metabolites influenced five metabolic pathways: Glucose-alanine cycle, alanine, glutathione, phenylalanine and tyrosine metabolism, and urea cycle. On day 360, 14 significant metabolites influenced eight metabolic pathways: Malate-aspartate shuttle, arginine and proline metabolism, urea cycle, aspartate, beta-alanine, glutamate metabolism, ammonia recycling and citric acid cycle. In conclusion, creep feeding supplementation improved calf performance and induced metabolic changes at weaning and 360 days of age. Although heifers had similar productive performance and reproductive status, when submitted to TAI, those supplemented with creep feeding had greater P/AI.

Objective Pregnant Nelore heifers (n = 417) were used to evaluate the effects of supplementation with monensin-molasses multinutrient block (B) during pre and/or postpartum on reproductive and progeny performance. Methods Heifers were allocated in four treatments: i) CC: heifers received control supplement (C) in loose meal form (0.06% of body weight [BW] offered daily before and after parturition; n = 108); ii) CB: received C before parturition and B (0.07% of BW offered weekly after parturition; n = 117); iii) BC: received B before and C after parturition (n = 103) and iv) BB: received B before and after parturition (n = 89). During pre and postpartum periods, concentration of metabolites/hormones and cow/calf performance was evaluated over time. Cows were synchronized twice for fixed timed artificial insemination (FTAI) using an estradiol/progesterone-based protocol. Data was analyzed by orthogonal contrasts (C). Results B increased pregnancy at first FTAI (p = 0.04) and overall pregnancy rate (C1: CC vs BB+BC+CB; p = 0.05). Supplemented cows had greater body condition score (BCS) only at parturition (D0; p = 0.04) and at D40 (p = 0.02). B increased BW (p = 0.03), glucose concentrations (p = 0.01) and subcutaneous fat thickness (p = 0.03) only at D40. Concentrations of insulin were higher in supplemented cows (p = 0.008). Calves born by cows supplemented before and after parturition (C2: BB vs BC+CB) were heavier at 80 (p

Development of new methods for early diagnosis of pregnancy can be important to increase the reproductive efficiency and profitability of dairy herds. The bovine conceptus secretes IFN-τ that stimulates the transcription of several genes in circulating immune cells and extrauterine tissues. The aims of this study were to evaluate the mRNA abundance for pregnancy predictability of a classic gene stimulated by IFN-τ (ISG15) and a novel potential pregnancy marker (LGALS3BP) in peripheral blood mononuclear cells (PBMC), total blood leukocytes (TBL) or milk leukocytes (TML), and cervical cells (CC) on d 20 after timed artificial insemination (TAI) in dairy cattle. Eighteen Holstein females (12 cows and 6 heifers) were submitted to an estrous synchronization protocol for TAI (d 0). On d 20 post-TAI, blood samples were collected from coccygeal vessels for isolation of PBMC and in Tempus Blood RNA tubes (Applied Biosystems) for TBL. Samples of CC were collected using a cytological brush, and the TML were isolated from milk samples collected before routine milking. Pregnancy diagnosis was performed on d 30 post-TAI using transrectal ultrasonography, and females were classified as pregnant (n = 8) or nonpregnant (n = 10). Total RNA was extracted and mRNA abundance of target genes (ISG15 and LGALS3BP) was quantified by reverse-transcription quantitative PCR and normalized in relation to reference genes. Data were analyzed by ANOVA using the MIXED procedure of SAS (SAS Institute Inc.). The mRNA abundance of ISG15 was greater in pregnant than in nonpregnant animals for PBMC, TBL, and CC. No difference was detected for TML based on pregnancy status. For LGALS3BP mRNA abundance, no difference was detected between pregnant and nonpregnant animals for PBMC, TBL, and TML, but a tendency for greater abundance in pregnant animals was observed for CC. The fold change for ISG15 in each pregnant cow related to the mean of nonpregnant animals was 2.73 ± 0.31, 3.40 ± 2.17, 1.64 ± 0.29, and 0.005 ± 0.002 for PBMC, CC, TBL, and TML, respectively. The fold change for LGALS3BP in each pregnant cow related to the mean of nonpregnant animals was 0.97 ± 0.38, 1.77 ± 0.39, 0.20 ± 0.08, and 0.70 ± 0.11 for PBMC, CC, TBL, and TML, respectively. The receiver operating characteristic curve analysis indicated that ISG15 abundance predicted pregnancy in PBMC (area under curve, AUC = 0.92) and CC (AUC = 0.77) but not in TBL (AUC = 0.72) or TML (AUC = 0.52). In conclusion, mRNA abundance for ISG15 in PBMC was the best predictor for pregnancy at d 20 post-TAI, whereas TBL and TML were not good predictors of pregnancy on d 20 post-TAI. The mRNA abundance of LGALS3BP was not associated with pregnancy status in any type of cell evaluated.

This study evaluated (a) the efficacy of an association between injectable antibiotic therapy and sealant (ATBS) on milk yield (MY), somatic cell count (SCC), and prevalence of intramammary infections (IMI); and (b) the efficacy of gonadotropin-releasing hormone (GnRH) on follicular cyst (FCs) resolution (cyclicity at the 45th day in milk; DIM) and cumulative pregnancy rate (CPR) in heifers submitted to a lactation induction protocol (LIP). A total of 114 crossbred (Holstein × Jersey) heifers, with 34.7 ± 4.8 months and 439 ± 56.35 kg were submitted to LIP. On the 5th day of the LIP, the heifers were assigned to (i) ATBS (n = 57) with 7 mg/kg of norfloxacin associated with sealant and (ii) Control 1 (n = 57; CONT1) with no treatments. Lactation began on the 21st day of LIP and the 15th DIM, FCs were diagnosed and 106 heifers were randomized into two treatment groups with 53 heifers each: (i) GnRH (5 mL injectable GnRH) and (ii) Control 2 (CONT2; no treatment). Of the 114 heifers initially induced, 83.33% (n = 95) responded to LIP with an average MY of 15.19 kg/milk/day during 22 weeks of lactation. In the first 14 DIM, the IMI prevalence was 18% and 28% for heifers ATBS and CONT1 treated, respectively. Additionally, coagulase-negative Staphylococcus was the most frequently isolated group of pathogens. Mammary quarters that received ATBS treatment had a lower risk of IMI and SCC than CONT1. The cyclicity at 45 DIM was 68% (ATBS) and 35% (CONT1), and 57% and 46% for animals in the GnRH and CONT2. CPR was 60% in the ATBS group and 89% in CONT1, but GnRH treatment did not affect the CPR. In conclusion, LIP was effective in stimulating MY in heifers, and the IMI prevalence decreased with ATBS treatment. Also, the use of GnRH did not affect the FC regression, cyclicity at 45 DIM, and CPR.

The aim of this study was to determine whether buffalo heifers maintained at a constant live weight (LW) and body condition score (BCS) by a restricted diet show changes in reproductive function in response to changes in day length. Heifers were fed a low energy diet (86% daily intake recommended for the species) throughout the study, which involved an 8-week period of decreasing day length and a 7-week period of increasing day length. Weekly, LW, BCS and ovarian follicular/oocyte population were assessed. Blood and follicular fluid samples were taken at the time of ovum pick-up for hormone analyses and at 30-day intervals to measure metabolic substrates. Buffalo heifers maintained LW and BCS throughout the study and blood concentrations of the main metabolic hormones, such as GH, insulin, IGF-1 and thyroid hormones were not influenced by photoperiod. Likewise, there were no differences in metabolic substrates such as glucose, NEFA, triglycerides and HDL cholesterol, suggesting that the metabolic condition remained essentially the same. During increasing day length periods, the number of total follicles (8.4 ± 0.5 vs. 11.9 ± 0.6; p

In vitro embryo production and embryo transfer (ET) in buffaloes has been developed for decades. However, most studies are focused on the donor or laboratory improvements, and there is a lack of reports regarding the recipients. Therefore, our aim was to investigate factors associated to pregnancy (P/ET), pregnancy loss (PL), and calving rates in buffalo recipients. The studied factors were season, recipient parity, the synchronization protocol, the CL diameter, asynchrony between the embryo and the recipient, the day of the recipient estrous cycle, the embryo (fresh vs. vitrified), the day of embryo development, and the embryo stage. These retrospective data, from a program of in vitro produced embryos, were analyzed by logistic regression, and the odds ratio was also estimated. Two factors were related to P/ET and the calving rate: (1) progesterone associated to estradiol plus eCG protocol for fixed time ET tended to affect positively P/ET on day 30 (41.9 vs. 36.1%, respectively; P = 0.07; AOR = 1.28) and P/ET on day 60 (37.8 vs. 36.1%, respectively; P = 0.09; AOR = 1.08) compared to the Ovsynch protocol; and (2) the CL diameter (≥14.5 mm) at transfer increased P/ET on day 30 (47.4 vs. 32.5%; P < 0.01; AOR = 1.87) and on day 60 (45.3 vs. 27.7%; P < 0.01; AOR = 2.16), and also the calving rate (37.9 vs. 21.7%; P < 0.01; AOR = 2.20). PL was greater when ET was done in the nonbreeding season compared to the breeding season (PL 30–60: 12.8 vs. 0.0%, P = 0.01; AOR > 999.99; PL 60-calving: 26.8 vs. 3.6%, P = 0.03; AOR = 9.90; and PL 30-calving: 36.2 vs. 3.6%, P = 0.01; AOR = 15.30). In conclusion, the data of our study indicated that the synchronization protocol, the CL diameter, and ET during the breeding season impacted the reproductive efficiency of buffalo recipients.

ABSTRACT: The aim of this study was to evaluate different times for timed artificial insemination (TAI) in buffalo submitted to a P4/E2/eCG-based protocol. In this study, 204 buffaloes were distributed into one of two groups (TAI56, n=103 and TAI64, n=101). At a random stage of the oestrous cycle (Day 0 = D0), in the morning (TAI56, a.m.) or afternoon (TAI64, p.m.), buffaloes received an intravaginal progesterone device (P4; 1.0 g) plus EB (2.0 mg i.m.). On D9 a.m. (TAI56) or p.m. (TAI64), the P4 was removed and buffaloes received PGF2a (0.53 mg i.m. sodium cloprostenol) and eCG (400 IU i.m.). On D10 a.m. (TAI56) or p.m. (TAI64), 24 h after P4 removal, buffaloes were treated with EB (1.0 mg i.m.). Buffaloes from TAI56 and TAI64 were inseminated 56 and 64 h after P4 removal (D11, p.m. and D12, a.m., respectively). Ultrasound examinations were performed on D0 to ascertain ovarian follicular status, at TAI to measure the diameter of the dominant follicle (DF) and D42 for pregnancy diagnosis. The statistical analysis was performed using the GLIMMIX procedure of SAS®. There was no difference between TAI56 and TAI64 for the diameter of the DF at TAI and the pregnancy per TAI. It was concluded that TAI 56 or 64 h after P4 removal did not affect fertility in buffaloes submitted to the induction of ovulation with EB. The present research supports that is possible to perform TAI at any time throughout the day in buffalo synchronized during the non-breeding season.

Abstract Background This study evaluated the impact of hormonal modulation at the onset of proestrus on ovarian response and uterine gene expression of beef cows. Methods A total of 172 anestrous beef cows were assigned to one of four groups according to the treatment with estradiol cypionate (ECP) and/or equine chorionic gonadotropin (eCG) [CON (n = 43), ECP (n = 43), eCG (n = 44) and ECP + eCG (n = 42)]. Results ECP-treated cows (ECP and ECP + eCG groups) presented greater occurrence of estrus (44.6% vs. 65.4%; P = 0.01) and pregnancy per AI [47.1% vs. 33.3%; P = 0.07], but similar progesterone (P4) concentration at subsequent diestrus than cows not treated with ECP (CON and eCG groups). Nonetheless, eCG-treated cows (eCG and ECP + eCG groups) presented larger follicle at timed AI (12.6 ± 0.3 vs. 13.5 ± 0.3 mm; P = 0.03), greater ovulation rate (96.5% vs. 82.6%; P = 0.008) and greater P4 concentration at d 6 (3.9 ± 0.2 vs. 4.8 ± 0.2 ng/mL; P = 0.001) than cows not treated with eCG (CON and ECP groups). Next, cows with a new corpus luteum 6 d after TAI were submitted to uterine biopsy procedure. Uterine fragments [CON (n = 6), ECP (n = 6)] were analyzed by RNA-Seq and a total of 135 transcripts were differentially expressed between groups (73 genes up-regulated by ECP treatment). Subsequently, uterine samples were analyzed by qPCR (genes associated with cell proliferation). ECP treatment induced greater abundance of PTCH2 (P = 0.07) and COL4A1 (P = 0.02), whereas suppressed EGFR (P = 0.09) expression. Conversely, eCG treatment increased abundance of HB-EGF (P = 0.06), ESR2 (P = 0.09), and ITGB3 (P = 0.05), whereas it reduced transcription of ESR1 (P = 0.05). Collectively, supplementation with ECP or eCG at the onset of proestrous of anestrous beef cows influenced ovarian responses, global and specific endometrial gene expression. Conclusion Proestrus estradiol regulate the endometrial transcriptome, particularly stimulating proliferative activity in the endometrium.

Com o objetivo de verificar a influência do suplemento mineral consumido na concentração dos macro e microelementos no plasma seminal e nas características do sêmen de búfalos, 60 bezerros de 10 meses de idade foram mantidos sob lotação intermitente por 14 meses, consumindo, ad libitum, dois suplementos minerais distintos e divididos aleatoriamente em dois grupos: G-Bov (suplemento mineral convencional recomendado para bovinos; n=30) e G-Buf (suplemento mineral específico para búfalos; n=30). O consumo do suplemento mineral foi calculado a partir da diferença entre a quantidade de suplemento oferecido e a sobra mensal do cocho. Dos búfalos a partir dos 22 meses de idade foram realizadas oito colheitas de sêmen de cada animal. As médias das variáveis foram analisadas por meio do teste de Kruskal-Wallis, com nível de significância de 5%, também foi analisada a correlação de Pearson entre a concentração de minerais no plasma seminal e as características do ejaculado. Observou-se que os animais do G-Buf mesmo consumindo menos suplemento mineral (G-Bov = 83,18 vs. G-Buf = 77,14 g UA-1 dia-1; P < 0,05) obtiveram maior volume do ejaculado e melhores motilidade, vigor e turbilhonamento. Esta pesquisa apresenta as concentrações de macro e microelementos no plasma seminal de búfalos suplementados com diferentes formulações minerais. Além disso, concluiu-se que as características físicas e morfológicas do sêmen de búfalos jovens são influenciadas pelo tipo de suplementação mineral, apresentando sêmen de melhor qualidade em búfalos suplementados com suplementos específicos para a espécie. Dos minerais presentes no plasma seminal de búfalos, o fósforo é o elemento que mostra maior correlação positiva com as características seminais no ejaculado.

The present study examined whether priming with estradiol benzoate (EB) for 12 h increased both the peak and duration of LH release in response to kisspeptin (KISS1, KP) in cows. In a Latin square design, ovariectomized Nelore cows (n = 8) received: Control, i.m. 4 mL of 0.9% saline; KP, i.m. 4 mg murine KISS1-10; EBKP, i.m. 4 mg KISS1-10 + i.m. 2 mg EB simultaneously; EB12KP, i.m. 4 mg KISS1-10 + i.m. 2 mg EB 12 h before KISS1-10. Concentrations of LH were determined in blood samples obtained at time 0 (treatment), 20, 40, 60, 90, 120, 150, 180, 210 and 270 min. Concentrations of LH were analyzed by Proc GLIMMIX for repeated measures. In case of significance, the adjusted Tukey test was used to test for differences among treatments. GraphPad 8.0 PRISM® was used to determine the area under the LH-response curve (AUC) after injection of KISS1-10. Plasma LH remained relatively constant throughout sampling after treatment with saline. The peak in LH after injection of KISS1-10 occurred at 20 min in Groups KP and EBKP and at 40 min in Group EB12KP. The peak LH response (∆LH, ng/mL) was greater (p < 0.01) in Group EB12KP (5.6 ± 0.9) than in Groups KP (2.4 ± 0.9) and EBKP (3.5 ± 0.9), which did not differ. AUC (LH ng/mL*min) was greater (p = 0.02) in Group EB12KP (439 ± 73) than in Groups KP (176 ± 73) and EBKP (241 ± 73), with the latter two groups not differing. The findings indicated that 12 h priming with EB increased both the peak and duration of the LH response to treatment with KISS1. The incorporation of EB priming and KISS1 could improve the efficiency of estrus synchronization with fixed-time AI in cows. This would have an important practical application in assisted breeding in beef and dairy cattle.

Reproductive efficiency plays a major role in the long-term sustainability of livestock industries and can be improved through genetic and genomic selection. This study aimed to estimate genetic parameters (heritability and genetic correlation) and identify genomic regions and candidate genes associated with anti-Müllerian hormone levels (AMH) and antral follicle populations measured after estrous synchronization (AFP) in Nellore cattle. The datasets included phenotypic records for 1099 and 289 Nellore females for AFP and AMH, respectively, high-density single nucleotide polymorphism (SNP) genotypes for 944 animals, and 4129 individuals in the pedigree. The heritability estimates for AMH and AFP were 0.28 ± 0.07 and 0.30 ± 0.09, and the traits were highly and positively genetically correlated (rG = 0.81 ± 0.02). These findings indicated that these traits can be improved through selective breeding, and substantial indirect genetic gains are expected by selecting for only one of the two traits. A total of 31 genomic regions were shown to be associated with AMH or AFP, and two genomic regions located on BTA1 (64.9–65.0 Mb and 109.1–109.2 Mb) overlapped between the traits. Various candidate genes were identified to be potentially linked to important biological processes such as ovulation, tissue remodeling, and the immune system. Our findings support the use of AMH and AFP as indicator traits to genetically improve fertility rates in Nellore cattle and identify better oocyte donors.

We hypothesized that stimulatory and superovulatory treatments, using equine chorionic gonadotropin (eCG), modulate the expression of genes related to insulin, cellular modelling and angiogenesis signaling pathways in the bovine corpus luteum (CL). Therefore, we investigated: 1-the effect of these treatments on circulating insulin and somatomedin C concentrations and on gene and protein expression of INSR, IGF1 and IGFR1, as well as other insulin signaling molecules; 2-the effects of eCG on gene and protein expression of INSR, IGF1, GLUT4 and NFKB1A in bovine luteal cells; and 3-the effect of stimulatory and superovulatory treatments on gene and protein expression of ANG, ANGPT1, NOS2, ADM, PRSS2, MMP9 and PLAU. Serum insulin did not differ among groups (P = 0.96). However, serum somatomedin C levels were higher in both stimulated and superovulated groups compared to the control (P = 0.01). In stimulated cows, lower expression of INSR mRNA and higher expression of NFKB1A mRNA and IGF1 protein were observed. In superovulated cows, lower INSR mRNA expression, but higher INSR protein expression and higher IGF1, IGFR1 and NFKB1A gene and protein expression were observed. Expression of angiogenesis and cellular modelling pathway-related factors were as follows: ANGPT1 and PLAU protein expression were higher and MMP9 gene and protein expression were lower in stimulated animals. In superovulated cows, ANGPT1 mRNA expression was higher and ANG mRNA expression was lower. PRSS2 gene and protein expression were lower in both stimulated and superovulated animals related to the control. In vitro, eCG stimulated luteal cells P4 production as well as INSR and GLUT4 protein expression. In summary, our results suggest that superovulatory treatment induced ovarian proliferative changes accompanied by increased expression of genes providing the CL more energy substrate, whereas stimulatory treatment increased lipogenic activity, angiogenesis and plasticity of the extracellular matrix (ECM).

Avaliaram-se os efeitos da remoção temporária de bezerros (RTB) ou da aplicação de gonadotrofina coriônica eqüina (eCG) na taxa de prenhez (TP) de vacas Nelore lactantes tratadas com um dispositivo intravaginal liberador de progesterona (DILP). No experimento 1, 83 vacas Nelore e 102 mestiças (Nelore × Red Angus) foram distribuídas em três grupos. Em dia aleatório do ciclo estral (D0), os animais do grupo 1 foram tratados com benzoato de estradiol (BE; 2,5 mg, IM, Estrogin®) e um DILP (1 g de progesterona, DIB®), removido no D9, quando também se administrou d-cloprostenol (150 µg, IM, Prolise®) e aproximadamente 12 horas após identificação do estro realizou-se a inseminação artificial. No grupo 2 (IATF), o tratamento foi semelhante ao aplicado no grupo 1, porém, administrou-se uma segunda dose de benzoato de estradiol (1 mg) no D10 e 30-36 horas mais tarde realizou-se a inseminação artificial em tempo fixo (IATF). No grupo 3 (IATF/RTB), os bezerros foram removidos a partir do D9 até a inseminação artificial com tempo fixo (IATF). As taxas de prenhez para as vacas Nelore e mestiças foram, respectivamente, de 7,69 e 41% (Controle); 23,52 e 59,57% (IATF); 69,44 e 55,81% (IATF/RTB). No experimento 2, 255 vacas Nelore lactantes foram distribuídas em três grupos. Os animais do grupo 4 (IATF) foram tratados com benzoato de estradiol (2 mg) e um DILP (1,9 g de progesterona, CIDR-B®) no D0 e no D8 sofreram remoção do DILP no D8 e administração de 25 mg de dinoprost (IM, Lutalyse®). No D9, foi aplicado benzoato de estradiol (1 mg) realizando-se a IATF 30-36 horas mais tarde. No grupo 5 (IATF/RTB), os bezerros foram removidos no D9 até a IATF. O grupo 6 (eCG) foi semelhante ao IATF, exceto pela aplicação de eCG no D9 (400 UI, IM, Novormon®). As taxas de prenhez foram de 50,57 (IATF), 53,57 (IATF/RTB) e 54,76% (eCG). A associação de RTB ao tratamento hormonal com DILP aumenta as taxas de prenhez, enquanto a adição de eCG ao tratamento não melhora as taxa de prenhez de vacas Nelore lactantes ciclando e em boa condição corporal.This study aimed to evaluate the effects of temporary calf removal (TCR) or eCG administration on pregnancy rates of milking Nelore cows treated with a intravaginal progesterone releasing device (IPRD). In the first experiment 83 Nelore and 102 Nelore vs. Red Angus crossbred cows were randomly allocated to 3 groups. Animals in Group 1 (CON) received estradiol benzoate (EB; 2.5 mg, i.m., Estrogin®) and an IPRD (1g progesterone, DIB®) in a random stage of the estrous cycle (D0). At D9 the IPRD was removed and the animals were treated with d-cloprostenol (150µg, i.m., Prolise®). The animals were artificially inseminated (AI) 12 h after estrus detection. Group 2 (FTAI) was similar to CON, except that another dose of EB (1mg) was administered at D10, and 30-36 hours later artificial insemination (FTAI) was performed at a fixed time. In Group 3 (FTAI/TCR) the calves were removed from D9 to the FTAI. Pregnancy rates for Nelore and crossbred cows were, respectively, 7.69 and 41% (CON); 23.52 and 59.57 (FTAI); 69.44 and 55.81 (FTAI/TCR). In the second experiment, 255 lactating Nelore cows were allocated to 3 groups. At D0, animals in Group 4 (FTAI) received EB (2 mg) and one IPRD (1.9g progesterone, CIDR-B®), which was removed at D8 when the cows received 25 mg of dinoprost (i.m., Lutalyse®). At D9 EB (1 mg) was administered and 30-36 hours later all animas were FTAI. In Group 5 (FTAI/TCR) the calves were removed from D9 to FTAI. The Group 6 (eCG) was similar to IATF except for the administration of eCC in D9 (400 IU, i.m., Novormon®). Pregnancy rates were: 50.57% (FTAI), 53.57% (FTAI/TCR) and 54.76% (eCG). These results indicated that TCR associated with IPRD increase pregnancy rates, whereas the addition of eCG to IPRD do not improve pregnancy rates in Nelore cows which are cycling and in lactation with good body condition.

Recent advances in the field of animal assisted reproduction have allowed faster dissemination of animals with superior genetics. In cattle, the development of some biotechnologies such as the in vitro production (IVP) of embryos optimized the use of oocytes, which represents a great improvement in embryo production world-wide. Therefore, females with high net merit can be multiplied more efficiently to maximize the number of their offspring. The use of ultrasound-guided transvaginal follicle aspiration combined with IVP allowed wide commercial transfer of IVP-embryos with satisfactory pregnancy results. Yet, there are a number of unanswered areas including the level of repeatability and predictability in IVP systems. Thus, the aim of this study was to evaluate the repeatability of some variables related to IVP of bovine embryos from Nellore breed. The study was conducted from 2011 to 2012 using 42 Nellore cows housed at the Centro APTA Bovinos de Corte located in Sertãozinho-SP, Brazil. Donors were kept under the same management throughout the entire experimental period. All animals underwent a total of 25 transvaginal ultrasound-guided follicular aspiration sections. Oocytes were retrieved and handled similarly by Sexing Technologies using semen from 11 sires. Repeatability was evaluated in the following variables: total number of oocytes, embryos and viable oocytes, viable oocyte rate (number of viable oocytes divided by the total number of oocytes), and the embryo rate (total number of embryos divided by the number of viable oocytes). Statistical analyzes were performed with the PROC GLIMMIX (SAS Inst., Inc., Cary, NC). Resulting repeatability for the above mentioned variables were: total number of oocytes = 0.72; numbers of viable oocytes = 0.73; number of embryos = 0.65, rate of viable oocytes = 0.14 and embryo rate = 0.18. It was observed that variables having poisson distribution such as total oocytes, number of oocytes and viable embryos showed high repeatability over time. Interestingly, variables reported as percentages as for viable oocyte rate and embryo rate did not show high repeatability. As a result, donors who had high numbers of viable oocytes didn’t necessarily yield a consistent percentage of good quality embryos throughout the IVP sessions. In conclusion, among all studied variables, the total number of oocytes, number of viable oocytes and number of embryos showed high repeatability in Nellore cows.

Several factors can influence the recovery of the amount of oocytes for in vitro embryo production (IVEP), including the age of the donor, the time and the frequency at which the animal is collected and climate station year. Another factor is the individual variation of each animal in the number of oocytes and embryos. Thus, the aim of this work was to evaluate the effect of the number of aspirations and the influence of the months of the year in the amount of total and viable oocytes in Nellore cows. The date was collected from January 2011 to December 2012. Non-lactating, cycling Nellore cows (n = 42) of high genetic value were used as oocyte donors. The procedures were carried out in a farm in southeast Brazil (21°8’16”S/48°58’2”W), located in humid tropical climate. All the donors were maintained on pasture consisting of guinea grass (Panicum maximum and Urochloa brizantha), getting protein mineral supplement energy and water ad libitum daily. The analyzes were performed by proc GLIMMIX of SAS 9.3 (SAS Inst., Inc., Cary, NC). The amount of total oocytes (P=0.16) and viable (P=0.11) did not influenced by the number of aspirations. However, the months of the year have an effect on the amount of total and viable (P

Estudou-se a involução uterina durante o período pós-parto de 32 (trinta e duas) fêmeas bubalinas da raça Murrah com idades variando entre 3 e 12 anos, em boa condição corporal e sem problemas reprodutivos aparentes durante o exame ginecológico. Os animais pertenciam ao Instituto de Zootecnia, Estação Experimental de Zootecnia do Vale do Ribeira, município de Registro-SP. A completa involução anatômica do útero, verificada por palpação retal duas vezes por semana, ocorreu, em média, 25,23 ± 5,41 dias após o parto. Não foram observadas diferenças estatísticas (p > 0,05) entre o tempo de involução uterina (em dias) e o mês do parto, o peso da búfala ao parto, a ordem de partos, a idade da búfala, o sexo do bezerro, a produção leiteira, o reinício da atividade ovariana, o primeiro cio após-parto e o período de serviço. Verificou-se uma correlação positiva (r = 0,41; p < 0,05) entre o tempo (em dias) para a ocorrência da involuçãi uterina e o peso do bezerro ao nascer.

Estudou-se a involução uterina durante o período pós-parto de 32 (trinta e duas) fêmeas bubalinas da raça Murrah com idades variando entre 3 e 12 anos, em boa condição corporal e sem problemas reprodutivos aparentes durante o exame ginecológico. Os animais pertenciam ao Instituto de Zootecnia, Estação Experimental de Zootecnia do Vale do Ribeira, município de Registro-SP. A completa involução anatômica do útero, verificada por palpação retal duas vezes por semana, ocorreu, em média, 25,23 ± 5,41 dias após o parto. Não foram observadas diferenças estatísticas (p > 0,05) entre o tempo de involução uterina (em dias) e o mês do parto, o peso da búfala ao parto, a ordem de partos, a idade da búfala, o sexo do bezerro, a produção leiteira, o reinício da atividade ovariana, o primeiro cio após-parto e o período de serviço. Verificou-se uma correlação positiva (r = 0,41; p < 0,05) entre o tempo (em dias) para a ocorrência da involuçãi uterina e o peso do bezerro ao nascer.

Oocytes from dairy cattle and buffaloes have severely compromised developmental competence during summer. While analysis of gene expression is a powerful technique for understanding the factors affecting developmental hindrance in oocytes, analysis by real-time reverse transcription PCR (RT-PCR) relies on the correct normalization by reference genes showing stable expression. Furthermore, several studies have found that genes commonly used as reference standards do not behave as expected depending on cell type and experimental design. Hence, it is recommended to evaluate expression stability of candidate reference genes for a specific experimental condition before employing them as internal controls. In acknowledgment of the importance of seasonal effects on oocyte gene expression, the aim of this study was to evaluate the stability of expression levels of ten well-known reference genes (ACTB, GAPDH, GUSB, HIST1H2AG, HPRT1, PPIA, RPL15, SDHA, TBP and YWHAZ) using oocytes collected from different categories of dairy cattle and buffaloes during winter and summer. A normalization factor was provided for cattle (RPL15, PPIA and GUSB) and buffaloes (YWHAZ, GUSB and GAPDH) based on the expression of the three most stable reference genes in each species. Normalization of non-reference target genes by these reference genes was shown to be considerably different from normalization by less stable reference genes, further highlighting the need for careful selection of internal controls. Therefore, due to the high variability of reference genes among experimental groups, we conclude that data normalized by internal controls can be misleading and should be compared to not normalized data or to data normalized by an external control in order to better interpret the biological relevance of gene expression analysis.

O presente estudo foi realizado para verificar se a elevação das concentrações plasmáticas de estradiol durante os tratamentos superovulatórios afeta o transporte dos oócitos em fêmeas bubalinas, bem como se a qualidade inferior dos oócitos de búfalos e/ou alguma diferença funcional no oviduto destes animais é responsável pela baixa taxa de recuperação de embriões em búfalas superovuladas quando comparadas a vacas submetidas ao mesmo tratamento. Foram utilizados 10 ovidutos de búfalas e 15 de vacas, tratadas para a indução de ovulação única. Os ovidutos foram colocados em placas de Petri e receberam os seguintes tratamentos: sem E2 e inseridos com 5 oócitos de búfalas (G-BufBuf e G-BovBuf); sem E2 e com 5 oócitos de vacas (G-BufBov e G-BovBov); com E2 e com 5 oócitos de búfalas (G-BufE2Buf e G-BovE2Buf); e com E2 e com 5 oócitos de vacas (G-BufE2Bov e G-BovE2Bov; fatorial 2x2x2). Posteriormente, foram incubados por 24h e, após esse período, foram lavados para a recuperação e contagem dos oócitos. Como não foi verificado efeito de interação, foram analisados os efeitos principais. O número e a taxa de recuperação de oócitos foi maior em ovidutos de vacas que de búfalas (1,4±0,3/35,0±8,6% vs. 0,5±0,2/10,0±4,6%; P0,05). Não foi verificada diferença no número de oócitos de búfalas ou de vacas recuperados (1,4±0,4 e 0,6±0,2; P>0,05). Observou-se também que houve tendência (P=0,07) de maior taxa de recuperação de oócitos de búfalas que de vacas (35,2±9,2% vs. 12,9±5,4%). Os dados são indicativos de que o transporte de oócitos pelo oviduto de búfalas e de vacas independe da espécie do oócito e não é influenciado pelo E2.

O objetivo desse estudo foi avaliar o efeito da redução da primeira dose de GnRH (10 vs 20 µg) e do tipo de protocolo de sincronização para a IATF (Ovsynch e Heatsynch) na taxa de prenhez de vacas holandesas de alta produção sincronizadas para IATF (n = 581). Os animais foram distribuídos entre os tratamentos e alocados em arranjo fatorial 2x2, sendo: Trat 1- Ovsynch (20 µg GnRH no D0; PGF no D7; 10 µg GnRH no D9 e IATF no D10; n = 141), Trat 2- ½ Ovsynch (10 µg GnRH no D0; PGF no D7; 10 µg GnRH no D9 e IATF no D10; n = 159), Trat 3- Heatsynch (20 µg GnRH no D0; PGF no D7; 1 mg BE no D8 e IATF no D10; n = 147) e Trat 4- ½ Heatsynch (10 µg GnRH no D0; PGF no D7; 1 mg BE no D8 e IATF no D10; n = 134). O Grupo Ovsynch (Trat 1 e 2) apresentou maior taxa de prenhez que o grupo Heatsynch (Trat 3 e 4) aos 28 dias (45,7% (137/300) e 39,9% (112/281), respectivamente; P = 0,07) e aos 56 dias de gestação (41,0% (123/300) e 34,2% (96/281), respectivamente; P = 0,06). A dose de GnRH, não influenciou (P >; 0.10)a taxa de prenhez aos 28 dias (44,4% (128/288) vs 41,3% (121/293); P = 0,50) e aos 56 dias (38,2% (110/288) vs 37,2% (109/293); P = 0,68) entre os grupos tratados com 10 µg ou 20 µg de acetato de buserelina. As perdas gestacionais (ente 28 e 56 dias) nγo diferiram entre os protocolos para IATF e dose de GnRH (P >; 0,10). Conclui-se que, protocolo Ovsynch apresentou maior taxa de prenhez à IATF que o Heatsynch e a administração de 10 µg de Acetato de Buserelina no início dos tratamentos de sincronização não comprometeu a eficiência do protocolo de sincronização para IATF em vacas holandesas de alta produção.

Este estudo objetivou comparar as taxas de concepção, em vacas de corte no período pós-parto (PPP), tratadas com Gonadotrofina Coriônica Eqüina (eCG) ou Benzoato de Estradiol (BE), após o uso de Norgestomet submetidas à inseminação artificial em tempo fixo (IATF). A hipótese é que a administração de eCG ou BE aumenta as taxas de concepção. Vacas Nelore (n=138) e Brangus (n=63), lactantes, entre 26 e 118 dias do PPP, foram divididas em três grupos homogêneos e dentro de cada grupo subdivididas em dois blocos, um com um PPP < 45 dias (PPP1; n=107) e outro >; 45 dias (PPP2; n=94). Todas as fêmeas receberam um implante auricular contendo 3mg de Norgestomet (Crestar®), seguido pela administração de 5mg de Valerato de Estradiol. Os implantes auriculares foram mantidos durante 10 dias. Na retirada dos implantes, as fêmeas receberam 1mL de solução fisiológica (n=68; Grupo Controle) ou 500UI de eCG (Folligon®; n=67; Grupo eCG) ou 1mg de Benzoato de Estradiol (Index; n=66; Grupo BE) 24 horas após a retirada do implante. A IATF foi realizada 54 horas após a retirada do implante. O diagnóstico de gestação foi realizado por ultra-sonografia 30 dias após a IATF. Houve interação entre os tratamentos e o PPP. No PPP1, a taxa de concepção foi maior no grupo eCG comparado ao BE (47,22% vs. 15,38%; P

Doze carneiros machos adultos mestiços Santa Inês de mesma idade e porte semelhante foram empregados em um delineamento inteiramente casualizado, por um período experimental de 60 dias. Os animais foram distribuídos para três tratamentos: A. 100% das exigências em proteína degradável no rúmen (controle); B. 100% das exigências em proteína degradável no rúmen + 3% de uréia + enxofre (99% S) e C. 100% das exigências em proteína degradável no rúmen + 3% de uréia + enxofre quelatado (21,5% S). Semanalmente foram colhidas amostras de sêmen obtidas com emprego de vagina artificial e de sangue para determinação da concentração de nitrogênio uréico plasmático, assim como realizadas pesagens dos animais e aferições de circunferência escrotal. No sêmen foram analisados: volume e turbilhonamento; vigor, motilidade e concentração espermática; total de espermatozóides e total de espermatozóides viáveis no ejaculado; integridade de membrana e de acrossoma; morfologia espermática e concentração de nitrogênio uréico no plasma seminal. Os animais suplementados com uréia apresentaram níveis de N-uréico no plasma sanguíneo e seminal significativamente maiores que os encontrados nos do tratamentos controle (p

O presente estudo teve como objetivo traçar o perfil de gonadotrofinas em 12 novilhas Nelore, a fim de testar a hipótese de que há declínio nas concentrações de FSH e elevação transitória nos níveis de LH durante a seleção folicular. A partir da ovulação (D0) foram colhidas amostras de sangue da veia jugular a cada 12 horas até o D5, para a dosagem de FSH e LH plasmáticos. Empregou-se o método de radioimunoensaio de duplo anticorpo. A sensibilidade do ensaio de LH foi de 0,02ng/ml e a de FSH de 0,005ng/ml. Os coeficientes de variação intra-ensaio foram 13,6% e 18,8%, respectivamente. Os dados (média±EPM) foram normalizados para o momento da divergência folicular e, posteriormente, analisados por ANOVA e por regressão linear, cúbica e quadrática. Também foi empregado o Teste t para comparação entre o ponto mais alto e o mais baixo da curva. Não se verificou efeito de tempo sobre as concentrações plasmáticas de FSH e de LH quando se utilizou análise de variância e de regressão. Entretanto, através do Teste t pontual, o FSH atingiu as menores concentrações plasmáticas 36 (0,40±0,05ng/ml) e 60 horas (0,42±0,04ng/ml) após a divergência, comparativamente às 36 horas anteriores ao desvio, quando as concentrações foram máximas (0,63±0,08ng/ml). Conclui-se, portanto, que há declínio nas concentrações plasmáticas de FSH, contudo, não foi comprovada elevação transitória nas concentrações de LH próximo ao momento do desvio folicular em fêmeas Nelore.

O objetivo desse estudo foi avaliar a liberação de LH durante os protocolos de sincronização da ovulação em bubalinos. Para tanto, quinze búfalas multíparas receberam 25 mg de Lecirelina no Dia 0, e 150 mg de D-Cloprostenol no Dia 7. No Dia 8, foi aplicado benzoato de estradiol nas búfalas do Grupo 1 (0,5 mg, n = 5) e do Grupo 2 (1,0 mg, n = 5). No Dia 9, os animais receberam 25mg de Lecirelina (Controle, n = 5). Para mensuração das concentrações plasmáticas de LH foram colhidas amostras de sangue da veia jugular no Dia 7, e em seguida em intervalos de 3 horas até completar 72 horas após a aplicação de PGF2a. Para avaliação da liberação de LH foram comparados os momentos de ocorrência do pico LH em relação à PGF2a, as durações, as amplitudes e a área sob o pico de pré-ovulatório de LH. As búfalas dos Grupos Controle, 1 e 2 apresentaram picos pré-ovulatórios de LH em 51 + 0,0 horas, 47,3 + 2,7 horas e 47,0 + 3,8 horas após a aplicação da PGF2a, respectivamente (P>;0,05). A duração do pico de LH foi menor no Controle (7,8 + 1,5 horas) do que nos Grupos 1 e 2 (10,5 + 1,5 horas vs. 10,8 + 2,4 horas, respectivamente; P < 0,05). A amplitude média dos picos pré-ovulatórios de LH foram de 4,5 + 0,4 ng/mL, 4,0 + 0,4 ng/mL e 4,3 + 0,8 ng/mL para os Grupos Controle, 1 e 2, respectivamente (P >; 0,05). A área sob o pico de LH no Controle (4,8 ± 0,7) foi menor do que as áreas dos Grupos 1 e 2 (8,8 ± 2,5 vs. 8,7 ± 2,2, respectivamente; P < 0,05). Em resumo, a aplicação de benzoato de estradiol proporcionou maior duração e área do pico pré-ovulatório de LH do que a administração de GnRH em protocolos Ovsynch em bubalinos.

O objetivo do presente experimento foi avaliar a performance reprodutiva e as características de estros em novilhas cruzadas de corte (Bos taurus indicus x Bos taurus taurus) tratadas com o protocolo MGA/Prostaglandina (PG) em associação a outros hormônios. No dia 0 (Dia 0 = início da ingestão do MGA) as novilhas foram distribuídas ao acaso para receber 2mL de solução salina (grupo Salina), 2500UI de hCG (grupo hCG), 20µg de acetato de buserelina (grupo GnRH) ou 5mg de 17²-estradiol + 100mg de progesterona (grupo 17²-E2+P4). Amostras de sangue foram colhidas nos dias - 7, 0, 7 e 10 para a mensuração das concentrações plasmáticas de progesterona. Independentemente do tratamento, todas as novilhas receberam 0,5mg MGA/animal/dia durante 8 dias (Dia 0 ao 7) e PG (Dia 7). Os estros foram observados durante 120h, a partir da injeção de PG, pelo sistema "Heat-Watch". As novilhas foram inseminadas 12 horas após o início dos estros ou 72h depois da injeção de PG. O diagnóstico de gestação foi realizado 35 dias após a última inseminação, por ultra-sonografia. As respostas em estros foram de 50,0%, 22,2%, 59,5% e 71,8% para os grupos Salina, hCG, GnRH e 17²-E2+P4, respectivamente (P

O objetivo desse estudo foi avaliar a eficiência da meia dose de PGF2alfa no protocolo de sincronização da ovulação (GnRH/PGF2alfa/GnRH) para inseminação artificial em tempo fixo em bubalinos. Foram utilizadas 262 búfalas (³ 40 dias pós-parto), divididas em dois grupos (Grupo 1, n = 125, GnRH/ ½ dose de PGF2alfa/GnRH; Grupo Controle, n = 137, GnRH/PGF2alfa/GnRH). Os animais do Grupo 1 receberam 25 mg de GnRH IM (Lecirelina, Gestran-plus®) e, após sete dias, receberam 75mg de PGF2alfaIM (d-cloprostenol, Preloban®). Dois dias após a aplicação da PGF2alfa, esses animais receberam 25mg de GnRH IM (Lecirelina). Os animais do Grupo Controle receberam o mesmo tratamento, à exceção da dose de PGF2alfa (150mg de d-cloprostenol, Preloban®). Todos os animais foram inseminados em tempo fixo 16 horas após a segunda aplicação de GnRH. Foram colhidas amostras de sangue de 35 búfalas do Grupo 1 e de 30 do Grupo Controle nos dias da aplicação de PGF2alfa e da segunda dose de GnRH. As colheitas de sangue foram realizadas para avaliar as concentrações plasmáticas de progesterona. Os resultados demonstraram que a taxa de concepção não foi influenciada pela dose de PGF2alfa (P>;0,05). As taxas de concepção dos Grupos 1 e Controle foram de 48,00% (60/125) e 40,90% (56/137), respectivamente. Observou-se que 88,60% (n = 35) das búfalas do Grupo 1 e 90,00% (n = 30) do Grupo Controle apresentaram luteólise 48 horas após a aplicação de PGF2alfa (P>;0,05). Em conclusão, os resultados indicaram que ambos tratamentos proporcionaram aceitáveis taxas de concepção. Dessa forma, a dose recomendada de PGF2alfa pode ser reduzida pela metade no protocolo de sincronização da ovulação para inseminação artificial em tempo fixo em bubalinos.

O objetivo desse estudo foi avaliar eficiência do protocolo de sincronização da ovulação (GnRH/PGF2alfa/GnRH) para inseminação artificial em tempo fixo em bubalinos. No Experimento 1, trinta e três búfalas com 60 dias pós-parto, foram separadas em dois grupos para avaliação da dinâmica folicular (Grupo 1, n = 16, 10mg de GnRH/15mg de PGF2alfa/10mg de GnRH; Grupo 2, n = 17, 20mg de GnRH/PGF2alfa/10mg de GnRH). Exames ultra-sonográficos foram realizados de 12 em 12 horas para verificar a resposta ovariana à primeira aplicação de GnRH. Outras avaliações foram realizadas nos dias da aplicação da PGF2alfa e do segundo GnRH. Em seguida, foram realizados exames de 6 em 6 horas até o momento da ovulação. Foram colhidas amostras de sangue nos dias das aplicações para avaliar as concentrações de progesterona no momento das administrações hormonais. No Experimento 2, foi verificada a eficiência da sincronização da ovulação para inseminação artificial em tempo fixo (16 horas após o segunda dose de GnRH, n=1053), durante as estações reprodutiva favorável e desfavorável, nos anos de 1998 e 1999. Os animais receberam 20mg de GnRH/PGF2alfa/10mg de GnRH. Ainda, foi analisada a influência da condição corporal, ordem de partos, período pós-parto ao início do tratamento, ano e a estação reprodutiva (favorável ou desfavorável), sobre a taxa de concepção. No Experimento 1, verificou-se que 33,0 ± 8,3h após a primeira aplicação de GnRH, 60,60% dos animais ovularam (Grupo 1 = 70,5 vs. Grupo 2 = 50,00%; P>;0,05). A dose de GnRH (10mg vs. 20mg) e a concentração de progesterona no início do tratamento não interferiu na ovulação (P>;0,05). Os animais que ovularam (n = 20) após a primeira aplicação de GnRH apresentaram maior diâmetro folicular (P;0,05). No Experimento 2, observou-se taxa de concepção de 45,40% (n = 1053). Animais sincronizados durante a estação reprodutiva favorável apresentaram melhores taxas de concepção quando comparados ao período desfavorável (48,80% vs. 6,90%; P < 0,05). A taxa de concepção foi influenciada pela condição corporal dos animais e pela ordem de partos durante a estação reprodutiva favorável (P;0,05). Em conclusão, os Experimentos indicaram que a utilização da sincronização da ovulação para inseminação artificial em tempo fixo, durante a estação reprodutiva favorável, apresenta resultados satisfatórios em bubalinos, podendo ainda ser melhorados quando utilizadas búfalas multíparas com bom estado corporal no início do tratamento.

Objetivou-se avaliar a eficiência da sincronização da ovulação para inovulação em tempo fixo em novilhas Bos taurus indicus x Bos taurus taurus receptoras de embrião. No Experimento 1, a dinâmica folicular foi acompanhada durante o protocolo "Ovsynch" (G1; n=35) e após a aplicação de PGF2alfa (G2; n=34). No Experimento 2, os mesmos tratamentos foram realizados a campo em 168 (G1) e 177 (G2) novilhas. No D6, colheu-se sangue para dosagem de P4 e se realizaram exames ultra-sonográficos. No D7, realizou-se a inovulação. No Experimento 1, 45,7% dos animais ovularam após o 1º GnRH (P;0,05). Ao final, a taxa de prenhez no Gl foi de 35,7% e no G2 de 25,4% (P

O uso de protocolos de sincronização da ovulação em bubalinos é bastante vantajoso, em virtude de certas peculiaridades apresentadas pela espécie que podem prejudicar programas de inseminação artificial, como a baixa incidência de comportamento homossexual e relações de dominância entre os animais. Com o objetivo de verificar a eficácia da Lecirelina como agonista de GnRH no protocolo GnRH/PGF2alfa/GnRH, 270 búfalas, com período pós-parto entre 45 e 60 dias, mantidas a pasto em duas propriedades, foram submetidas a dois tratamentos de sincronização da ovulação. Os animais do Grupo 1 (n = 132) receberam, em dia desconhecido do ciclo estral, 20 µg de Buserelina IM, sendo aplicados, 7 dias mais tarde, 15 mg de prostaglandina (PGF2a). Dois dias após a administração da PGF2alfa, os animais receberam 10 µg de Buserelina, IM. As fêmeas do Grupo 2 (n = 138) foram tratadas seguindo o mesmo protocolo, com a diferença de que, na primeira e na terceira administrações hormonais, se aplicaram, respectivamente, 50 µg e 25 µg de Lecirelina, IM. A inseminação artificial foi efetuada em tempo fixo, 16 horas após a terceira administração hormonal, em ambos os grupos. O diagnóstico de gestação foi realizado por ultra-sonografia, 30 dias após a inseminação artificial. As taxas de concepção foram semelhantes [47,0% (62/132) e 50,0% (69/138) nos Grupos 1 e 2 (P >; 0,05)]. Não foi observado efeito da propriedade (P >; 0,05) nas taxas de concepção. Os resultados demonstram que é possível utilizar Lecirelina para promover a sincronização da ovulação de bubalinos, com resultados satisfatórios.

Mensurações pélvicas internas e externas foram realizadas in vivo em 255 búfalas mestiças. Para a pelvimetria interna, utilizou-se o pelvímetro de Menissier-Vissac. Os resultados foram confrontados com a idade, perímetro torácico, peso, altura e comprimento. Para comparação das medidas pélvicas, os animais foram divididos equitativamente em 3 grupos (n=85), segundo a ocorrência e freqüência de partos (nulíparas, primíparas e multíparas). Os diâmetros pélvicos internos: biilíacos superior e inferior (horizontais) e sacropúbico (vertical) apresentaram respectivamente as seguintes médias e desvios padrões: 17,1 ± 2,17 cm; 15,7 ± 2,11 cm e 22,3 ± 2,51 cm; e os externos: biilíaco, biisquiático e ilioisquiático, da mesma maneira: 59,8 ± 6,13 cm; 32,4 ± 3,56 cm e 44,5 ± 3,31 cm. Correlações positivas significantes (p < 0,01) foram verificadas entre todas as medidas, porém, dentre as medidas corpóreas gerais, o perímetro torácico revelou o mais alto índice de correlações com as medidas pélvicas internas e externas. Diferenças significativas (p < 0,05) entre os 3 grupos foram observadas em relação à pelvimetria interna, quando comparados através das médias ajustadas em função do perímetro torácico, porém em relação à pelvimetria externa somente entre as nulíparas e os demais grupos para os diâmetros biilíaco e ilioisquiático. Para o diâmetro biisquiático externo nenhum dos grupos revelou tais diferenças. A pelvimetria interna em relação à externa mostrou-se menos correlacionada com o desenvolvimento corpóreo e mais nitidamente influenciada pela ocorrência dos sucessivos partos.

O desempenho de um ELISA comercial (Bovine Rhinotracheitis virus antibody test Kit, Herdcheck®, IDEXX Laboratories Inc., USA) para a identificação de anticorpos anti-herpesvírus bovino tipo 1 (BHV-1), em soro bovino, foi avaliado em 133 amostras de soro de búfalos (Bubalus bubalis), sem histórico de vacinação para IBR, da Região do Vale do Ribeira, Estado de São Paulo. Tomando-se a técnica de soroneutralização como referência, o ELISA indireto apresentou sensibilidade e especificidade relativa de 97,14 e 46,03%, respectivamente. A concordância estimada pelo índice kappa, entre os dois métodos, foi de 0,44 IC (0,29-0,59), utilizando um intervalo de confiança de 95%.

Objective: Pregnant Nelore heifers (n = 417) were used to evaluate the effects of supplementation with monensin-molasses multinutrient block (B) during pre and/or postpartum on reproductive and progeny performance., Methods: Heifers were allocated in four treatments: i) CC: heifers received control supplement (C) in loose meal form (0.06% of body weight [BW] offered daily before and after parturition; n = 108); ii) CB: received C before parturition and B (0.07% of BW offered weekly after parturition; n = 117); iii) BC: received B before and C after parturition (n = 103) and iv) BB: received B before and after parturition (n = 89). During pre and postpartum periods, concentration of metabolites/hormones and cow/calf performance was evaluated over time. Cows were synchronized twice for fixed timed artificial insemination (FTAI) using an estradiol/progesterone-based protocol. Data was analyzed by orthogonal contrasts (C)., Results: B increased pregnancy at first FTAI (p = 0.04) and overall pregnancy rate (C1: CC vs BB+BC+CB; p = 0.05). Supplemented cows had greater body condition score (BCS) only at parturition (D0; p = 0.04) and at D40 (p = 0.02). B increased BW (p = 0.03), glucose concentrations (p = 0.01) and subcutaneous fat thickness (p = 0.03) only at D40. Concentrations of insulin were higher in supplemented cows (p = 0.008). Calves born by cows supplemented before and after parturition (C2: BB vs BC+CB) were heavier at 80 (p<0.001), 120 (p<0.001), 170 (p = 0.002) and 210 (p = 0.02) days old., Conclusion: Regardless of period of treatment, block supplementation increased pregnancy at first FTAI and overall pregnancy rate. Additionality, block supplementation during both pre and postpartum periods improved progeny weight until weaning. Block supplementation can be a tool to optimize fertility and calf performance in Nelore primiparous cows.

This study evaluated the association between plasma anti-Mullerian hormone (AMH) concentration and fertility in Nelore (Bos indicus) heifers submitted to timed artificial insemination (TAI). At the onset of the synchronization protocol, heifers (n = 289) received a subcutaneous P4 ear implant (3 mg) and 2 mg of oestradiol benzoate. Eight days later, the P4 implant was removed and 0.5 mg of oestradiol cypionate, prostaglandin (0.265 mg, i.m.) and equine chorionic gonadotropin (300 UI, i.m.) was administered, and TAI was performed 48 hr after ear implant removal. Ovarian ultrasound evaluations were performed to measure number of ovarian follicles, dominant follicle size and ovulation response. Pregnancy diagnosis was performed by ultrasound 30 days after AI. Heifers with greater circulating AMH had more antral follicles, a smaller dominant follicle near timed ovulation and lower ovulation response to the timed AI protocol compared to heifers with lower circulating AMH. Although AMH and pregnancy outcome had a quadratic-shaped pattern, AMH was not significantly associated with fertility. In conclusion, heifers with lower AMH had larger follicles towards the end of the synchronization protocol and greater ovulation responses, whereas greater circulating AMH was unrelated to conception success., (© 2020 Blackwell Verlag GmbH.)

Introduction: Endometritis is a condition marked by inflammation of the endometrium that affects dairy cows from 21 days after parturition, causing damage to herd fertility and economic losses on farms. The use of active compounds obtained from plant sources has gained importance as disease treatment agents in farm animals due to the high resistance rates currently observed against traditional antibiotics commonly used. The study was carried out to examine the chemical composition and to investigate the antibacterial activity of rosemary, cinnamon, cloves, eucalyptus, lemon, oregano and thyme essential oils against the reference strain of Escherichia coli (ATCC 25922), Fusobacterium necrophorum (ATCC 25286), Trueperella pyogenes (ATCC 19411) and Staphylococcus aureus (ATCC 29213), considered as typical bacteria causing endometritis., Methodology: The chemical composition of the seven essential oils were analyzed by GC-MS and their antibacterial activity was evaluated by the disc diffusion method., Results: Thirty-six components were identified in total using GC-MS analyzes. The main compounds were cinnamaldehyde (86.5% for cinnamon essential oil), eugenol (85.7% for clove essential oil), 1,8-cineol (80% for eucalyptus and 47.8% rosemary essential oils), limonene (65.5% for lemon essential oil), carvacrol (72.1% for oregano essential oil) and thymol (48.8% for thyme essential oil). The disc diffusion assay revealed that cinnamon, clove, oregano, and thyme essential oils showed the best results compared to the other three essential oils, showing the largest zone of inhibition against all bacteria evaluated., Conclusions: These findings indicated that essential oils are a potential agent to be used as an alternative for bovine endometritis treatment., Competing Interests: No Conflict of Interest is declared, (Copyright (c) 2020 Renan Braga Paiano, Jeannine Bonilla, Ricardo Luiz Moro de Sousa, Andrea Micke Moreno, Pietro Sampaio Baruselli.)

The uterus plays an essential role in mammalian reproduction and is a target of several hormonal protocols used to improve fertility in cattle. Many studies highlighted the importance of eCG treatment following fixed-time artificial insemination in improving follicular growth, ovulation and pregnancy rates in cattle. Moreover, eCG has been implicated in angiogenesis, leading to important changes in uterine blood flow and vascularisation. However, there is still a lack of information regarding the specific alterations induced by eCG upon glandular and vascular characteristics of bovine uterus. To investigate the influence of eCG on: uterine thickness and area; uterine artery diameter and area; uterine vascular and gland density; and the expression of the VEGFA-system, the uteri of crossbred beef cows were collected. All cows were submitted to follicular wave emergence synchronization. On day four of protocol, cows submitted to superovulation (n = 6) received 2000 IU eCG, on day eight, after expected follicular deviation, cows submitted to stimulatory treatment (n = 5) received 400 IU eCG. Control cows (n = 5) did not receive eCG. On day five po cows were subjected to ultrassonographic evaluation and slaughtered for uterine tissue sampling on day six po. Uterine vessels and glands were quantified by the counting point stereological method. The VEGFA-system was localized in different cellular types, showing no qualitative or quantitative differences in the site of expression or the intensity of the positive signal among the groups. Vascular density was decreased in the endometrium of stimulated and myometrium of superovulated cows compared with the control ones, which showed higher vascular density in the myometrium and endometrium of the ipsilateral uterine horn. The uterine gland density was higher in superovulated compared with stimulated and control cows. Thus, we can infer that stimulatory or superovulatory treatments with eCG influence the vascular density in the endometrium and myometrium in cattle., (© 2014 Blackwell Verlag GmbH.)

Ovulation induction (OI) is a cornerstone of human assisted reproduction treatments (ART). Current OI protocols are based on the human follicular dynamics model known as propitious moment theory (PMT), by which follicles continuously grow from the primordial pool without any pattern, and follicular fate depend on the occurrence of a gonadotropin surge. Recently, a new paradigm of human follicular dynamics called follicular waves was revealed using sequential ultrasound examination of 1 interovulatory interval. Instead of random growth, follicles develop in coordinated groups or waves, occurring 2 to 3 times during an interovulatory interval. Follicular waves are common in several other mono-ovulatory species, like equines and bovines. In fact, this model was applied to the development of several OI protocols in veterinary medicine, especially in cows. It has been shown that synchronization of OI with the emergence of a follicular wave increases substantially success rates in animals, even with single embryo transfer. Veterinarians have already developed mechanisms to control wave emergence through mechanical or chemical ablation of the dominant follicle or corpus luteum. Considering the follicular dynamics similarities between humans and bovines regarding the follicular wave phenomenon, we hypothesize that synchronization of follicular wave emergence with ovarian stimulation produces more competent oocytes and embryos and will enhance ART efficiency in humans. At the end of this article, we propose 2 theoretical approaches to induce the emergence of a follicular wave in women: (1) a mechanical strategy by aspiration of the dominant follicle and (2) a pharmacological strategy by administering estradiol and progesterone.