Early luteal development in Santa Inês ewes superovulated with reduced doses of porcine follicle‐stimulating hormone

2018 ◽  
Vol 54 (3) ◽  
pp. 456-463 ◽  
Author(s):  
Mariana Garcia Kako Rodriguez ◽  
Giovanna Serpa Maciel ◽  
Ricardo Andres Ramirez Uscategui ◽  
Victor José Correia Santos ◽  
Ricardo Perecin Nociti ◽  
...  
2012 ◽  
Vol 41 (3) ◽  
pp. 603-606 ◽  
Author(s):  
Bianor Matias Cardoso Neto ◽  
Larissa Pires Barbosa ◽  
Cristiane da Silva Aguiar ◽  
Rosiléia Silva Souza ◽  
Ana Lúcia Almeida Santana ◽  
...  

2015 ◽  
Vol 27 (1) ◽  
pp. 264
Author(s):  
M. E. F. Oliveira ◽  
M. A. R. Feliciano ◽  
L. G. Oliveira ◽  
J. F. Fonseca ◽  
W. R. R. Vicente

This study was designed to evaluate the follicular status at the 1st FSH injection in ewes superstimulated near the 1st follicular wave of the CIDR protocol during nonbreeding (NB), transition (T), and breeding (B) season, and thus to correlate them with the superovulatory response (SR). On Day 0, all females (30 Santa Ines ewes; n = 10 per season) received a progesterone (P4) device (CIDR®; Zoetis, Brazil) and 37.5 µg of d-cloprostenol. The superestimulation (ST) was initiated on Day 4, 4, and 6 of protocol in the NB, T, and B season, respectively. These follicular wave emergence days were defined in a previous study that evaluated the follicular dynamic in P4 protocol (Oliveira et al. 2011 Acta Scientiae Veterinariae, 38, 361). The ST consisted of 8 injections of pFSH administrated twice a day in descending order (40/30/20/ and 10 mg of pFSH; Folltropin-V, Bioniche, Canada). The P4 device was removed 2 days after the beginning of the FSH treatment and all ewes received another injection of 37.5 µg of d-cloprostenol and a dose of 200 IU of eCG at the same time. B-mode ultrasound of ovaries was performed immediately before the 1st FSH injection. The follicles were classified according to their diameters into categories based on physiological dynamics: (C1) 2–4.25 mm, representative of the population before dominance phase; (C2) 4.5–5 mm, initial dominance phase; (C3) 5.25–5.75 mm, middle dominance phase; and (C4) 6 mm, preovulatory phase. Data were analysed by GLIMMIX using SAS comparing mean values (± s.e.m.) between seasons (P < 0.05) and Pearson correlation was made. All ewes had small follicles (C1) at the beginning the ST; however, only one female had solely C1 follicles. The number of C1 follicles did not differ between seasons (12.9 ± 0.9, 12.8 ± 0.8, and 12.1 ± 0.5 follicles for the NB, T, and B season, respectively). One-half of the animals from NB and T seasons had no C3 and C4 follicles, whereas 40% of females in B season showed the same follicular status. The percentage of ewes that had no C4 follicles was 80, 100, and 50% for the NB, T, and B season, respectively. There were no difference between season in number of C2 follicles (1.8 ± 0.5, 1.7 ± 0.4, and 1.7 ± 0.4) and C3 follicles (0.3 ± 0.1, 0.6 ± 0.2, 0.1 ± 0.1) for NB, T, and B seasons, respectively. However, the number of C4 follicles was significantly higher (P < 0.05) in the NB (0.2 ± 0.13) and B (0.6 ± 0.2) season than T period, which had no follicles in this category. The SR did not differ between seasons (12.4 ± 0.9, 13.1 ± 2.3, and 17.0 ± 2.3 for the NB, T, and B season, respectively) and had no correlation to any follicular category. In conclusion, the ST started on a day when there was a large population of small follicles, regardless of the season, confirming proximity to follicular wave emergence. However, the ovarian population was not restricted to this category. Therefore, it is possible that wave emergence has already started in some ewes before the initiation of the ST.Financial support is from FAPESP and CNPq.


1991 ◽  
Vol 125 (3) ◽  
pp. 280-285 ◽  
Author(s):  
J. Alan Talbot ◽  
Ann Lambert ◽  
Robert Mitchell ◽  
Marek Grabinski ◽  
David C. Anderson ◽  
...  

Abstract We have investigated the role of Ca2+ in the control of FSH-induced estradiol secretion by Sertoli cells isolated from 8-10 days old rats. Exogenous Ca2+ (4-8 mmol/1) inhibited FSH-stimulated E2 secretion such that, with 8 mmol/l Ca2+ and FSH (8 IU/l) E2 secretion decreased from 2091±322 to 1480±84 pmol/l (p<0.002), whilst chelation of Ca2+ in the culture medium with EGTA (3 mmol/l) increased E2 secretion from 360±45 to 1242±133 pmol/l) in the absence of FSH. Further, EGTA (3 mmol/l) markedly potentiated FSH (8 IU/l), forskolin (1 μmol/l) and dibutyryl cAMP (1 mmol/l)-stimulated E2 secretion. Addition of the Ca2+ ionophores, ionomycin (2-5 μmol/l) and A23187 (2 μmol/l), inhibited FSH (8 IU/l)-stimulated E2 secretion by >80%. The effect of ionomycin was totally reversible, whereas that of A23187 was irreversible. Ionomycin (5 μmol/l) had no effect on EGTA-induced E2 secretion in the absence of FSH, but reduced EGTA-provoked E2 secretion by 59% in the presence of FSH (8 IU/l). Similarly, forskolin- and dibutyryl cAMP-provoked E2 production was inhibited 46-50% by ionomycin (5 μmol/l). We conclude that FSH-induced E2 secretion from immature rat Sertoli cells is modulated by intra- and extracellular Ca2+.


Sign in / Sign up

Export Citation Format

Share Document