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RESEARCH ARTICLE

226 Using a long-acting recombinant human follicle-stimulating hormone in cattle: 2. Superovulatory response

R. M. Moura A , L. P. Martins A , G. Passamani B , C. A. C. Fernandes C , L. G. B. Siqueira D , R. A. Figueiredo E and J. H. M. Viana A E
+ Author Affiliations
- Author Affiliations

A Universidade de Brasília, Brasilia, DF, Brazil

B Universidade Federal de Uberlândia, Uberlândia, MG, Brazil

C Universidade de Alfenas, Alfenas, MG, Brazil

D Embrapa Gado de Leite, Juiz de Fora, MG, Brazil

E Embrapa Recursos Genéticos e Biotecnologia, Brasília, DF, Brazil

Reproduction, Fertility and Development 36(2) 269 https://doi.org/10.1071/RDv36n2Ab226

© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing on behalf of the IETS

In a previous study, we demonstrated that long-acting human recombinant follicle-stimulating hormone (rhFSH) can be used to stimulate follicle growth in cattle. The aim of this study was to evaluate the superovulatory response to this rhFSH. Cycling Nelore heifers (n = 19) with an average 371.7 ± 5.7 kg bodyweight were subjected to a follicular wave synchronization protocol consisting of the insertion of an intravaginal progesterone-releasing device (1 g, Sincrogest, Ouro Fino, Brazil) and 2 mg of oestradiol benzoate (Sincrodiol, Ouro Fino) on Day −4, and were superovulated (Day 0) either using eight decreasing doses 12 h apart of pFSH (120 mg Folltropin-V, Vetoquinol, Brazil, n = 9) or with a single subcutaneous injection of 20 µg rhFSH (Corifollitropin Alpha, Shering-Plough, Brazil, n = 10). On Day 3 the progesterone (P4) devices were removed and luteolysis was induced with 26.3 mg cloprostenol sodium (Induscio, GlobalGen, Brazil). On Day 4, ovaries were scanned using an ultrasound equipped with a 7.5-MHz rectal probe (DP 30, Mindray, Brazil) and follicles were measured and classified according to diameter. On Day 5 ovulation was induced with 16 µg buserelin acetate (Maxrelin, GlobalGen) and heifers were inseminated twice, immediately after ovulation induction and 12 h later, with semen from a single Nelore sire. Seven days after the first AI, the number of corpora lutea (CL) was counted by ultrasound, blood samples were collected for P4 analysis, uterine flushing was carried out, and the number of ova and viable embryos recorded. Plasma P4 concentrations were evaluated by electrochemiluminescence (Immulite P4, Siemens, UK). Data were analysed using the Proc Glimmix of SAS. There was no difference in the number of follicles <4 mm (2.4 ± 0.6 vs 1.6 ± 0.5; P = 0.3017), from 5 to 6 mm (7.9 ± 1.1 vs 7.1 ± 0.8; P = 0.5780) or >7 mm (24.3 ± 4.3 vs 30.0 ± 5.1; P = 0.44) on Day 4 between groups pFSH and rhFSH, respectively. Plasma P4 concentrations on the day of embryo flushing did not differ between pFSH and rhFSH groups (54.4 ± 14.6 vs 66.5 ± 10.4 ng mL−1, respectively; P = 0.50). However, heifers receiving rhFSH presented greater mean follicle size on Day 4 (8.6 ± 0.1 vs 8.0 ± 0.1; P < 0.01), ovulation rate (61.3% vs 42.5%, P < 0.01), and number of CL (18.4 ± 2.5 vs 10.3 ± 1.6; P < 0.05), and a trend towards more ova (8.3 ± 1.4 vs 5.1 ± 0.9; P = 0.07) and viable embryos (2.5 ± 0.9 vs 0.6 ± 0.3; P = 0.06), when compared with those receiving pFSH. In summary, superovulation can be successfully induced in Nelore heifers with a single dose of a long-acting rhFSH.

Research was supported by CAPES, DPG UnB, and FAPDF 00193–00002307/2022–11.