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Endocrinology, Vol 133, 2453-2460, Copyright © 1993 by Endocrine Society


ARTICLES

Evidence for a protein-like factor from "rete testis" fluid that suppresses luteinizing hormone-releasing hormone (LHRH) pulses (LHRH statin): a new hormonal activity?

MR Blanc, JC Poirier, A Locatelli and A Caraty
Laboratoire de Neuroendocrinologie Sexuelle, Institut National de la Recherche Agronomique, Nouzilly, France.

Signals that modulate LH-releasing hormone (LHRH) pulse frequency are fundamental mechanisms for regulating important reproductive processes. Gonadal steroids are presently considered to account for the entire gonadal feedback mechanism that modulates LHRH secretion. However, we have previously suggested that a testicular protein(s) present in charcoal-treated rete testis fluid (ctRTF) can suppress LH pulsatility in the ram. The present experiments were aimed at determining whether the disappearance of LH pulses induced by ctRTF administration implicate a hypothalamic or a pituitary site of action. Thus, we have examined the effects of ctRTF peripheral administration on 1) the LH response to LHRH, 2) LHRH portal blood levels, and 3) LHRH content in hypothalamic tissue. Finally, the effects of ctRTF administered into the third ventricle on plasma LH levels were assessed. The present results show that a testicular protein(s) is able to suppress LHRH pulse frequency without affecting amplitude and without any effect on the LH response to LHRH (LHRH Statin). The observation that an active dose administered by the intracerebroventricular route is 0.0005 the active dose needed by the peripheral route reinforces this evidence. These data lead to the new concept that the testicular signals that govern LHRH pulse frequency may be not only steroids, but also proteins.


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C. Cariou-Guennoc, J.C. Poirier, B. Calas, A. Locatelli, J.L. Dacheux, and M.R. Blanc
Evidence That Luteinizing Hormone-Releasing Hormone Statin from Ovine Rete Testis Fluid Is Immunologically Related to {alpha}C Inhibin
Biol Reprod, June 1, 2000; 62(6): 1551 - 1563.
[Abstract] [Full Text]




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