1983
DOI: 10.1038/301062a0
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β-Endorphin regulates lordosis in female rats by modulating LH-RH release

Abstract: Several lines of evidence have implicated the endogenous opioid peptides in the regulation of masculine sexual behaviour. However, although the opioid related peptides alpha-melanocyte stimulating hormone (alpha-MSH) and adrenocorticotropin (ACTH) have been shown to affect lordosis behaviour in the female rat, there is as yet no evidence for a role of the endogenous opiates in the regulation of female sexual behaviour. We present here evidence that the endogenous opiates in the mesencephalic central grey (MCG)… Show more

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Cited by 115 publications
(13 citation statements)
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“…Gallo and Block (1991) observed increased P4 secretion during estrous cycles and pregnancy when rbGH was injected and speculated that these effects may have been caused by an increase in IGF-I production stimulated by the rbGH treatment (Spicer et al 1990). However, the length and regularity of estrous cycles were not affected by rbGH treatment in the study by Gallo and Block (1991) (Sirinathsinghji et al 1983). No data are available which demonstrate effects of rbGH or milk yield on p-endorphin production and all of the above listed possibilities require investigation.…”
Section: Effects Of Growth Hormone On Body Conditionmentioning
confidence: 70%
“…Gallo and Block (1991) observed increased P4 secretion during estrous cycles and pregnancy when rbGH was injected and speculated that these effects may have been caused by an increase in IGF-I production stimulated by the rbGH treatment (Spicer et al 1990). However, the length and regularity of estrous cycles were not affected by rbGH treatment in the study by Gallo and Block (1991) (Sirinathsinghji et al 1983). No data are available which demonstrate effects of rbGH or milk yield on p-endorphin production and all of the above listed possibilities require investigation.…”
Section: Effects Of Growth Hormone On Body Conditionmentioning
confidence: 70%
“…These studies clearly indicate that EOPs can regulate reproductive function by inhibiting the secretion of GnRH at the level of the central nervous system (CNS) (26,28,34) (Figure 2). …”
Section: Hormonal Control Of Reproductive Function By the Opioid Systemmentioning
confidence: 99%
“…The main function of FSH is to stimulate the proliferation of Sertoli cells during puberty, whereas LH regulates the synthesis of testosterone in the adult testes (24). Administration of morphine is associated with a suppression of LH release, whereas opioid antagonists such as naloxone and naltrexone produce increased serum levels of LH in humans and many animal species (25,26). The opioid-induced inhibition of LH release is mediated by a hypothalamic action because, on the one hand, opioid receptors have been described in purified gonadotrophs and, on the other hand, in vivo treatment with GnRH antagonists completely blocked the release of GnRH induced by naloxone (27)(28)(29).…”
Section: Hormonal Control Of Reproductive Function By the Opioid Systemmentioning
confidence: 99%
“…Central injections of either NPY or ␤-END inhibit reproductive behavior in rats and hamsters when primed with estradiol and progesterone (Sirinathsinghji et al, 1983;Wiesner and Moss, 1984;Clark et al, 1985;Gorzalka et al, 1997;Torii et al, 1999;Corp et al, 2001). Furthermore, infusion of ␤-END into the MPN inhibited lordosis (Sirinathsinghji, 1986), suggesting that ␤-END is an endogenous ligand of the -opioid receptor (MOR) in this nucleus.…”
Section: Introductionmentioning
confidence: 99%