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Made available in DSpace on 2013-09-27T14:54:12Z (GMT). No. of bitstreams: 1 WOS000288627700007.pdf: 187475 bytes, checksum: f44a03d706cf45e64484e91ab7b27272 (MD5) Previous issue date: 2011-02-01 Made available in DSpace on 2013-09-30T18:36:09Z (GMT). No. of bitstreams: 1 WOS000288627700007.pdf: 187475 bytes, checksum: f44a03d706cf45e64484e91ab7b27272 (MD5) Previous issue date: 2011-02-01 Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-20T13:42:31Z No. of bitstreams: 1 WOS000288627700007.pdf: 187475 bytes, checksum: f44a03d706cf45e64484e91ab7b27272 (MD5) Made available in DSpace on 2014-05-20T13:42:31Z (GMT). No. of bitstreams: 1 WOS000288627700007.pdf: 187475 bytes, checksum: f44a03d706cf45e64484e91ab7b27272 (MD5) Previous issue date: 2011-02-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) The objectives of this study were to determine the interval from ovulation to deviation and the diameter of the dominant (DF) and largest subordinate (SF) follicles at deviation in buffalo (Bubalus bubalis) heifers. Two methods of evaluation (observed vs. calculated) were used. FSH and LH profiles encompassing follicle deviation (Experiment 1), and the follicular diameter when the DF acquired ovulatory capacity (Experiment 2) were also determined. The time of deviation and the diameter of the of and the largest SF at deviation did not differ between observed and calculated methods. Overall, follicle deviation occurred 2.6 +/- 0.2 d (mean SEM) after ovulation, and the diameters of the DF and SF at deviation were 7.2 +/- 0.2 and 6.4 +/- 0.2 mm, respectively. No changes in plasma levels of FSH or LH were observed (P= 0.32 and P= 0.96, respectively). Experiment 2 was conducted in two phases according to the diameter of the of during the first wave of follicular development at the time of LH challenge (25 mg of pLH). In the first phase, follicles ranging from 5.0 to 6.0 mm (n = 7), 6.1 to 7.0 mm (n = 11), or 7.1 to 8.0 mm (n= 9) were used, and in the second phase, follicles ranging from 7.0 to 8.4 mm (n=10), 8.5 to 10.0 mm (n = 10), or 10.1 to 12.0 mm (n = 9) of diameter were used. After the pLH treatment, the of was monitored by ultrasonography every 12 h for 48 h. No ovulations occurred in heifers in the first phase. However, in the second phase, an effect of follicular diameter was observed on ovulation rate [7.0-8.4 mm (0.0%, 0/10), 8.5-10.0 mm (50.0%, 5/10), and 10.0-12.0 mm (55.6%, 5/9)]. In summary, follicle deviation occurred 2.6d after ovulation in buffalo (B. bubalis) heifers, when the diameters of the DF and SF were 7.2 and 6.4 mm, respectively. No significant changes in plasma concentrations of FSH or LH were detected. Finally, the acquisition of ovulatory capacity occurred when the of reached 8.5 mm in diameter. (C) 2010 Elsevier B.V. All rights reserved. FMVZ USP, Dept Anim Reprod, BR-05508270 São Paulo, Brazil APTA Registro, Registro, SP, Brazil Autonomous Veterinarian, Vicosa, MG, Brazil UFMA, Ctr Ciencias Agr & Ambientais, Chapadinha, MA, Brazil IB UNESP, Dept Bioestatist, Botucatu, SP, Brazil IB UNESP, Dept Farmacol, Botucatu, SP, Brazil Lab Endocrinol UNESP, Dept Apoio & Prod Saúde Anim, Aracatuba, SP, Brazil Univ Saskatchewan, Western Coll Vet Med, Saskatoon, SK S7N 0W0, Canada IB UNESP, Dept Bioestatist, Botucatu, SP, Brazil IB UNESP, Dept Farmacol, Botucatu, SP, Brazil Lab Endocrinol UNESP, Dept Apoio & Prod Saúde Anim, Aracatuba, SP, Brazil FAPESP: 03/10203-4

In Holstein cows, the diameter of the dominant follicle (DF) at the time of follicle deviation is 8.5 mm and the subordinate follicle (SF) is 7.2 mm (Ginther et al. 1996 Biol. Reprod. 55, 1187–1194). However, follicular responsiveness to an ovulatory treatment occurs only with 10.0-mm-diameter follicles (Sartori et al. 2001 Biol. Reprod. 65, 1403–1409). The current study tested the hypothesis that, in Bos indicus (Nelore and crossbred Nelore � Gir) females, the follicular diameters at the time of deviation and ovulation responsiveness are smaller than those in Holstein cows. The experiment was performed in two phases. In the first phase, 12 Nelore heifers were previously synchronized with a protocol using progestagen and estradiol benzoate. After implant removal, all heifers were evaluated by transrectal ultrasonography (Aloka SSD-500, Tokyo, Japan) every 12 h until Day 5 of the estrous cycle (Day 0 = Day of the ovulation) to assess the time of ovulation, the time of follicle deviation, and the follicular diameter at the deviation. In the second phase, 29 Bos indicus heifers (Nelore and crossbred Nelore � Gir) were previously synchronized with the same protocol as cited above. After the ovulations (Day 0), the follicles were evaluated by transrectal ultrasonography every 24 h, until they reached the diameter of 7.0–8.4 mm (n = 9); 8.5–10.0 mm (n = 10); and >10.0 mm (n = 10). In order to assess the ovulatory capacity, all animals were treated with 25 mg of LH (Lutropin-V�; Bioniche Animal Health, Inc., Belleville, Ontario, Canada) at these follicle diameter ranges. After the LH treatment, all animals were monitored by ultrasonography every 12 h for 48 h. ANOVA, Bartlett, and chi-square tests were used in the statistical analyses. In the first phase, the diameters of the DF and SF at the time of follicular deviation (61.9 � 4.9 h after ovulation) were 6.2 � 0.2 and 5.8 � 0.2 mm, respectively. In the second phase, the the average follicular diameters at the time of LH administration in the groups 7.0–8.4 mm, 8.5–10.0 mm, and >10.0 mm were 7.6a � 0.1 mm, 9.6b � 0.1 mm, and 10.9c � 0.2 mm; and their ovulation rates were 33.3%a (3/9), 80.0%b (8/10), and 90.0%b (9/10), respectively (P < 0.05). The interval from LH treatment to ovulation was 38.0 � 4.0 h, 31.5 � 2.7 h, and 30.0 � 2.0 h, respectively (P > 0.05). In conclusion, in Bos indicus heifers, follicle deviation occurred with smaller diameters than previously reported in Bos taurus breeds. In addition, Bos indicus heifers are able to ovulate in response to 25 mg of LH with smaller diameters compared to those of Bos taurus breeds. Moreover, in Bos indicus heifers, ovulatory capacity is acquired by follicles as small as 7.0–8.4 mm, but this responsiveness significantly increases after follicles reach 8.5–10.0 mm. This work was supported by FAPESP (Proc:03/10203-4); Bioniche Animal Health, Inc., Belleville, Ontario, Canada; and Tecnopec, S�o Paulo, Brazil.

There is evidence that the deleterious effects of heat stress (HS) on fertility are less pronounced in Bos indicus than in B. taurus breeds, due primarily to differences in their thermoregulatory capacity. In the present work, the resistance to heat stress of Nelore embryos (B. indicus) was compared to either a breed not adapted (Angus; B. taurus) or adapted to high temperatures (Bonsmara; 5/8 B. indicus × 3/8 B. taurus). In Experiments (Exp.) 1 (Nelore vs. Angus) and 2 (Nelore vs. Bonsmara), oocytes obtained by ovum pickup OPU (during autumn) were matured (TCM-199), fertilized, and cultured (SOFaaci) in vitro. Ninety-six hours post-insemination (hpi), embryos with more than 16 cells were randomly allocated in two main groups: Group Control (embryos were maintained at 39°C all of the time) and Group HS (embryos were maintained at 41°C during 12 h and afterwards returned to 39°C). Blastocyst rates were determined on the 7th day of culture. In Exp. 1, 294 oocytes from Nelore and 144 from Angus cows had a cleavage rate of 67.9 and 59.4%, respectively. Ninety-six-hpi embryos (>16 cells) were distributed in four groups: Nelore Control (n = 97), Nelore HS (n = 95), Angus Control (n = 34) and Angus HS (n = 25). The blastocyst rates were 39/97 (40.2%), 23/95 (24.2%), 19/34 (55.9%), and e 8/25 (32.0%), respectively. The difference in rate of blatocyst formation caused by heat stress on Nelore (16.0%) and Angus (23.9%) was not significantly different (P < 0.05), and suggests, from oocytes obtained by OPU, that Nelore embryos may be more tolerant to HS than Angus embryos. However, it is necessary to increase the number of blastocysts per group in order to better characterize the effects of heat stress on these embryos. In Exp. 2, 294 oocytes from Nelore and 101 from Bonsmara cows had a cleavage rate of 41.2 and 51.2%, respectively. Ninety-six-hpi embryos (>16 cells) were distributed in four groups: Nelore Control (n = 44), Nelore HS (n = 49), Bonsmara Control (n = 22), and Bonsmara HS (n = 22). The blastocyst rates were 35/44 (79.5%), 30/49 (61.2%), 10/22 (45.5%), and 6/22 (27.3%), respectively. In spite of the fact that Bonsmara embryos had a lower blastocyst rate as compared to Nelore, the decline on blastocyst rate caused by HS was very similar in Nelore (18.3%) and Bonsmara embryos (18.2%). Additional OPU are underway to test the hypothesis that thermotolerance of Nelore embryos is similar to that in embryos from a breed adapted to high temperatures (Bonsmara), and superior to embryos from a non adapted breed (Angus). E. S. S., R. A. S., and M. F. G. N. were supported by a fellowship from FAPESP, and A. C. Z. B. by a fellowship from CAPES of Brazil.