scholarly journals Reproductive endocrine effects of intranasal administration of norethisterone to adult female rhesus monkeys (Macaca mulatta)

Reproduction ◽  
1986 ◽  
Vol 76 (1) ◽  
pp. 215-220 ◽  
Author(s):  
V. Puri ◽  
G. F. X. David ◽  
A. K. Dubey ◽  
C. P. Puri ◽  
T. C. A. Kumar
1985 ◽  
Vol 110 (4) ◽  
pp. 461-468 ◽  
Author(s):  
G. F. X. David ◽  
V. Puri ◽  
A. K. Dubey ◽  
C. P. Puri ◽  
T. C. Anand Kumar

Abstract. Adult female rhesus monkeys exhibiting normal ovulatory menstrual cycles were treated with progesterone nasal sprays. Animals in group A (n = 9) were treated with the solvent only (controls). Animals in groups B (n = 6), C (n = 17) and D (n = 7), respectively, were treated with a daily dose of 0.4, 2 and 10 μg of progesterone and the spraying was done between days 5–14 of the cycle. Ovulation was monitored by laparoscopy on day 20. The serum endocrine profile throughout the treated menstrual cycle was studied with respect to oestradiol and progesterone. Bioactive luteinizing hormone (bLH) was studied in blood samples taken on the day of the mid-cycle oestradiol peak, 2 days before, and 2 days after. The menstrual cycle was divided into two phases with respect to the mid-cycle oestradiol peak: phase I was taken to include day 1 of the cycle to the day of the oestradiol peak, and the remaining part of the menstrual cycle was considered to be phase II. The serum-endocrine profile in the controls was similar to that observed in normal ovulatory menstrual cycles. However, in the progesterone-treated groups three types of menstrual cycles were discernable on the basis of the serum endocrine profile. In the type I menstrual cycle, observed only in group C (n = 10), the mid-cycle bLH peak was abolished and the progesterone levels remained low throughout the cycle. Laparoscopy revealed these to be anovulatory cycles. In the type II menstrual cycle, seen in the 3 animals of group B, 2 animals of group C, and in all the 7 animals of group D, the mid-cycle bLH peak was abolished and the progesterone levels during phase II of the cycle were significantly lower than in the controls, indicative of poor luteal function. In the type III menstrual cycle seen in the remaining monkeys, the serum endocrine profile did not differ from that seen in the controls. Thus, the present studies indicate that the intranasal administration of progesterone shows a dose-response effect with respect to the suppression of the oestradiol induced mid-cycle surge of bLH. Suppression of the mid-cycle bLH peak resulted in anovulatory cycles or ovulatory cycles with poor luteal function.


1971 ◽  
Vol 51 (4) ◽  
pp. 751-761 ◽  
Author(s):  
T. M. PLANT ◽  
V. H. T. JAMES ◽  
R. P. MICHAEL

SUMMARY Labelled progesterone was administered intravenously to five, adult female rhesus monkeys and urine and faeces were collected every 24 h. Excretion of radioactivity in urine occurred most rapidly in the first 24-h period and then declined exponentially. The excretion of radioactivity in faeces reached maxima during the 2nd, 3rd or 4th 24-h periods depending on the animal studied. 76–94% (mean 86%) of the radioactivity administered was recovered within 9 days, but small quantities continued to be excreted in urine up to 16 days after injection. Generally, greater amounts of radioactivity were recovered from faeces (41–57%) than from urine (26–48%). Using different hydrolytic and extraction procedures, some 50% of the radioactivity in urine was recovered in the neutral extracts. The major metabolite in urine was androsterone which accounted for 1·1–12·2% (mean 6·0%) of the progesterone administered. Pregnanediol was not an important urinary catabolite in this species. Differences in the extent to which progesterone is metabolized to C-19 compounds in macaques, baboons, great apes and man may reflect the phylogeny of a catabolic desmolase system in anthropoid primates.


2013 ◽  
Vol 100 (3) ◽  
pp. S338
Author(s):  
C.V. Bishop ◽  
W.K. McGee ◽  
E. Galbreath ◽  
M.B. Zelinski ◽  
J.L. Cameron ◽  
...  

1975 ◽  
Vol 4 (2) ◽  
pp. 120-128 ◽  
Author(s):  
Beverly Y. Cockrell ◽  
M.G. Valerio ◽  
W.F. Loeb

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