Contribution to Special Issue on Fast effects of steroids. The concept that the positive feedback effect of ovarian estradiol (E) results in GnRH and gonadotropin surges is a well-established principle. However, a series of studies investigating the rapid action of E in female rhesus monkeys has led to a new concept that neuroestradiol, synthesized and released in the hypothalamus, also contributes to regulation of the preovulatory GnRH surge. This unexpected finding started from our surprising observation that E induces rapid stimulatory action in GnRH neurons in vitro. Subsequently, we confirmed that a similar rapid stimulatory action of E occurs in vivo. Unlike subcutaneous injection of E benzoate (EB), a brief (10-20 min), direct infusion of EB into the median eminence in ovariectomized (OVX) female monkeys rapidly stimulates release of GnRH and E in a pulsatile manner, and the EB-induced GnRH and E release is blocked by simultaneous infusion of the aromatase inhibitor, letrozole. This suggests that stimulated release of E is of hypothalamic origin. To further determine the role of neuroestradiol we examined the effects of letrozole on EB-induced GnRH and LH surges in OVX females. Results indicate that letrozole treatment greatly attenuated the EB-induced GnRH and LH surges. Collectively, neuroestradiol released from the hypothalamus appears to be necessary for the positive feedback effect of E on the GnRH/LH surge.
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http://dx.doi.org/10.1016/j.yhbeh.2018.04.003 | DOI Listing |
Horm Behav
August 2018
Wisconsin National Primate Research Center, University of Wisconsin, Madison, WI 53715, United States; Department of Pediatrics, University of Wisconsin, Madison, WI 53706, United States. Electronic address:
Contribution to Special Issue on Fast effects of steroids. The concept that the positive feedback effect of ovarian estradiol (E) results in GnRH and gonadotropin surges is a well-established principle. However, a series of studies investigating the rapid action of E in female rhesus monkeys has led to a new concept that neuroestradiol, synthesized and released in the hypothalamus, also contributes to regulation of the preovulatory GnRH surge.
View Article and Find Full Text PDFJ Neurosci
December 2013
Wisconsin National Primate Research Center, and Department of Pediatrics, University of Wisconsin, Madison, Wisconsin 53715.
Release of gonadotropin releasing hormone (GnRH) from the medial basal hypothalamus (MBH)/median eminence region (S-ME) is essential for normal reproductive function. GnRH release is profoundly regulated by the negative and positive feedback effects of ovarian estradiol (E2). Here we report that neuroestradiol, released in the S-ME, also directly influences GnRH release in ovariectomized female monkeys, in which the ovarian source of E2 is removed.
View Article and Find Full Text PDFGend Med
September 2005
Department of Neurobiology and Physiology, Northwestern Universirty, Evanston, Illinois 60208, USA.
Background: Preovulatory gonadotropin-releasing hormone and luteinizing hormone (LH) surges depend on activation of estrogen-inducible progesterone receptors (PRs) in the hypothalamus. Although testosterone treatment can suppress LH secretion under some circumstances, how androgens affect the release of preovulatory hormone surges, and the cellular mechanisms by which androgens exert any such effects, remains unknown.
Objective: This study examined the hypothesis that testosterone can block the release of estrogen-induced gonadotropin surges via attenuation of estrogen's ability to induce PRs in the preoptic area (POA)-hypothalamus.
Neuroendocrinology
March 1998
Prince Henry's Institute of Medical Research, Clayton, Vic., Australia.
Endogenous opioid systems in the hypothalamus inhibit gonadotropin-releasing hormone (GnRH) secretion, and a reduction in this inhibitory input (disinhibition) is thought to be part of the neural mechanism of the preovulatory GnRH/luteinizing hormone (LH) surge. We showed previously that intracerebroventricular infusion of the highly specific opioid mu-receptor agonist DAMGO delayed the oestrogen-induced LH surge in ovariectomized (OVX) ewes, whereas both delta- and kappa-agonists were ineffective. The aim of the present study was to establish the anatomical site of this effect.
View Article and Find Full Text PDFCell Mol Neurobiol
June 1996
Department of Physiology, Faculty of Medicine, University of Córdoba, Spain.
1. Intact or ovariectomized (OVX) cyclic rats injected or not with RU486 (4 mg/0.2 ml oil) from proestrus onwards were bled at 0800 and 1800 h on proestrus, estrus and metestrus.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!