scholarly journals Effects of gonadotrophin-releasing hormone and prostaglandin F-2  on corpus luteum function and timing of the subsequent ovulation in the mare

Reproduction ◽  
1988 ◽  
Vol 83 (2) ◽  
pp. 545-551 ◽  
Author(s):  
A. L. Johnson ◽  
S. E. Becker ◽  
M. L. Roma
1986 ◽  
Vol 108 (3) ◽  
pp. 323-328 ◽  
Author(s):  
T. A. Bramley ◽  
G. S. Menzies ◽  
D. T. Baird

ABSTRACT The effects of a number of analogues of gonadotrophin-releasing hormone (GnRH) on the binding of a radiolabelled GnRH agonist (GnRH-A; d-Ser(But)6, des Gly10]GnRH-ethylamide) to homogenates of human corpus luteum (CL) and rat pituitary tissue were compared. Specific binding was inhibited by GnRH and GnRH-like peptides only. Both the C-terminal amide and N-terminal region of the GnRH molecule were required for binding in both tissues. However, amino acid substitutions at position 6 markedly enhanced, and at position 8 markedly reduced, binding potencies in rat pituitary tissue compared with human CL binding sites. These results indicate that GnRH-binding sites of rat pituitary and human luteal tissue have a similar degree of specificity for GnRH-like peptides, and a similar requirement for both N- and C-terminal regions of the peptide, but that differences in specificity related to the mid-chain region of GnRH exist between human luteal and rat pituitary binding sites. J. Endocr. (1985) 000, 000–000


1984 ◽  
Vol 101 (3) ◽  
pp. 365-370 ◽  
Author(s):  
B. J. McLeod ◽  
W. Haresign

ABSTRACT Oestrus was synchronized in 15 naturally cyclic ewes by the administration of a prostaglandin F2α analogue. Groups of five ewes were then treated i.v. with either small doses of gonadotrophin releasing hormone (GnRH; 125 or 250 ng/injection) or saline, at 2-h intervals from day 14 of the subsequent cycle until 24 h after the onset of oestrus. Treatment with GnRH induced episodic LH release which continued until the onset of a preovulatory LH surge. Mean plasma LH concentrations over this period were significantly (P< 0·001) higher in animals receiving 250 ng GnRH (2·44±0·11 μg/l) than in those receiving either 125 ng GnRH (1·17±0·06 μg/l) or saline (1·14±0·05 μg/l). However, GnRH treatment did not influence the timing of oestrus or mean ovulation rates. J. Endocr. (1984) 101, 365–370


1987 ◽  
Vol 115 (2) ◽  
pp. 273-282 ◽  
Author(s):  
A. S. McNeilly ◽  
H. M. Fraser

ABSTRACT Continuous infusion of a gonadotrophin-releasing hormone (GnRH) agonist (buserelin) by osmotic minipump from day 1 of the luteal phase in five Welsh ewes resulted in a sustained suppression of plasma concentrations of FSH which increased three- to eightfold within 2 days after the end of infusion 29 days later. Plasma concentrations of LH increased three- to eightfold over the first 5 days of infusion and then became basal and non-pulsatile until 1 day after the end of infusion. Duration of the luteal phase and plasma concentrations of progesterone were not significantly different in control and treated ewes. Pulses of LH in control ewes were followed by increases in concentrations of progesterone in samples collected at 10-min intervals for 7 h on days 10 and 14 of the luteal phase. However, progesterone was also released in a pulsatile manner in the absence of LH pulses in both control and GnRH agonist-treated ewes. After natural luteolysis, no ovulation or corpus luteum function occurred in treated ewes up to 15 days after the end of treatment on day 29, even though oestrus, indicating follicular development and oestrogen secretion, had occurred 8–11 days after treatment ended. After 30 days of infusion the ovaries of GnRH agonist-treated ewes contained no follicles > 2·5 mm in diameter. In follicles of 1–2 mm in diameter the basal and LH-stimulated production of oestradiol and testosterone in vitro were similar in both control and GnRH agonist-treated ewes, and a similar proportion of these follicles was oestrogenic (> 370 mol oestradiol per follicle) in GnRH agonist-treated and control ewes. These results show (1) that progesterone secretion by the corpus luteum of the ewe can be sustained in the presence of basal concentrations but absence of pulsatile secretion of LH, and progesterone is released in a pulsatile manner whether or not LH pulses are present, (2) that follicular development beyond 2·5 mm in diameter in the ewe is dependent upon adequate stimulation by both LH and FSH and (3) that the continuous infusion of GnRH agonist is a simple method for providing reproducible suppression of LH and FSH and follicular development in the ewe to allow the study of gonadotrophin action on the ovary in vivo. J. Endocr. (1987) 115, 273–282


2018 ◽  
Vol 30 (3) ◽  
pp. 507 ◽  
Author(s):  
Ryan R. Witt ◽  
John J. Rodger ◽  
John C. Rodger

Lucrin Depot (AbbVie), a 1-month microsphere gonadotrophin-releasing hormone (GnRH) agonist preparation, was investigated as a potential agent to synchronise cycling in the fat-tailed dunnart (Sminthopsis crassicaudata). Forty-eight randomly selected females were treated with 5 or 10 mg kg−1 Lucrin Depot (n = 24 per dose). Eighteen females per treatment had their reproductive activity scored at 4, 8, 12 and 16 weeks using two ovarian (Graafian follicle and corpus luteum status) and two reproductive tract (uterine and vaginal muscularity and vascularity) parameters that formed a reproductive activity score. Six females per treatment were paired with a male at 4 weeks. Fertility was assessed between 8 and 16 weeks by pouch check, and thereafter by dissection. The effects of the 5 and 10 mg kg−1 doses were statistically equivalent. Females showed suppression at 4–8 weeks, an increase in reproductive activity at 8–12 weeks and all were cycling normally at 16 weeks. Six pouch young were born at 12 weeks to two females treated with the 5 mg kg−1 dose. Nine embryos were recovered at 16 weeks from two females treated with the 10 mg kg−1 dose. In conclusion, Lucrin Depot can suppress breeding, and fertile mating can occur in subsequent cycles in the dunnart. There is potential for Lucrin Depot to be used as an assisted breeding tool, but it may need to be combined with ovarian stimulation treatment to achieve practical levels of synchronisation in the fat-tailed dunnart.


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