Abstract

We examined the effects of physiological concentrations of estradiol (E2) and progesterone (P) on plasma LH, FSH, and prolactin (PRL) and on LHRH concentrations in several microdissected brain regions in ovariectomized (OVX) rats. One week after ovariectomy (Day 0), rats received Silastic capsules containing only sesame oil or 37.5, 75.0 or 150 μg E2/ml of oil s.c. The E2 capsules produced plasma estrogen concentrations of 7.0, 9.6, or 15.4 pg/ml, respectively, on Day 2 whereas oil-treated controls had 5.4 pg/ml of E2 in plasma. All three E2 -treated groups of rats had LH surges of comparable magnitude during the afternoon of Day 2. Two Silastic capsules of P (50 mg/ml) were implanted at 0900 h on Day 2 into E2 -treated rats. In animals in which E2 levels were 7.0 or 9.6 pg/ml, P only moderately amplified the LH surges. However, when plasma E2 concentrations reached 15 pg/ml, P treatment evoked a massive release of LH and advanced the time of release by 1 h. In contrast, the stress of inserting oil capsules into ether-anesthetized E2-treated rats at 0900 h on Day 2 had no effect on afternoon LH surges in these animals. FSH surges occurred only in rats receiving both E2 and P. PRL surges were induced using the highest concentrations of E2 and were advanced in time by P. When the highest dose of E2 was used, LHRH concentrations in the median eminence (ME) increased prior to and decreased during the E2 P-induced surge. These changes were not paralleled by any changes in the other anterior brain regions we examined (suprachiasmatic preoptic nucleus, suprachiasmatic nucleus, medial preoptic nucleus, anterior hypothalamic nucleus, and retrochiasmatic area). No changes in LHRH concentrations were observed under any other steroid treatment regimen. Higher plasma E2 concentrations induced by the 150μ g/ml E2 capsule were correlated with higher LHRH concentraions in the median eminence concomitant with a parallel trend in some of the anterior brain areas: MPN (P<0.06), SPN (P<0.06), and RCA (P<0.03).

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.