Literature DB >> 3701707

Opioid modulation of LH secretion in the ewe.

A N Brooks, G E Lamming, P D Lees, N B Haynes.   

Abstract

Administration of opioid agonists and antagonists and measurement of resulting hormone changes were used to study the possible effects of opioids on reproductive function in the ewe. Intravenous administration of the long-acting methionine-enkephalin analogue FK33-824 (250 micrograms/h for 12 h) to 3 ewes during the follicular phase of the oestrous cycle depressed episodic LH secretion. This effect was reversed by administration of the opiate antagonist naloxone (25 mg/h) in combination with the FK33-824 treatment; in fact LH secretion was enhanced by the combined regimen. Naloxone (25 mg/h for 12 h) administered alone to 3 ewes in the follicular phase also enhanced LH secretion. In 3 animals treated with FK33-824 during the follicular phase, progesterone remained basal for 14 days after treatment, suggesting that ovulation was blocked. Jugular venous infusion of naloxone (25, 50 or 100 mg/h for 8h) into 5 ewes during the early and mid-luteal phase of the cycle resulted overall in a significant increase in mean plasma LH concentrations and LH episode frequency. To investigate whether endogenous opioids suppress LH release in seasonally anoestrous sheep, naloxone was infused intravenously into mature (25, 50 or 100 mg/h for 8 h) and yearling ewes (12 . 5, 25 or 50 mg/h for 8 h) during early, mid- and late anoestrus and plasma LH concentrations were measured. In the mature ewes, there was a trend for naloxone to increase LH values during the early anoestrous period but naloxone was without effect during mid- and late anoestrus. In the yearlings, naloxone infusion consistently increased plasma LH concentrations as a result of a significant increase in LH episode frequency. These experiments indicate that endogenous opioid peptides probably modulate gonadotrophin secretion during both the follicular and luteal phases of the oestrous cycle. However, the follicular phase of the sheep cycle is of short duration, and there may be residual effects of luteal-phase progesterone during this period. Secondly, there may be an age-dependent effect of naloxone on LH secretion during seasonal anoestrus in the ewe, with opioids playing a part in the suppression of LH in young but not in mature animals.

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Year:  1986        PMID: 3701707     DOI: 10.1530/jrf.0.0760693

Source DB:  PubMed          Journal:  J Reprod Fertil        ISSN: 0022-4251


  6 in total

1.  The negative feedback actions of progesterone on gonadotropin-releasing hormone secretion are transduced by the classical progesterone receptor.

Authors:  D C Skinner; N P Evans; B Delaleu; R L Goodman; P Bouchard; A Caraty
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

2.  κ-Opioid Receptor Is Colocalized in GnRH and KNDy Cells in the Female Ovine and Rat Brain.

Authors:  Peyton W Weems; Christine F Witty; Marcel Amstalden; Lique M Coolen; Robert L Goodman; Michael N Lehman
Journal:  Endocrinology       Date:  2016-04-11       Impact factor: 4.736

3.  Fasting-induced suppression of LH secretion does not require activation of ATP-sensitive potassium channels.

Authors:  Wenyu Huang; Maricedes Acosta-Martínez; Teresa H Horton; Jon E Levine
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-10-07       Impact factor: 4.310

4.  Evidence that orphanin FQ mediates progesterone negative feedback in the ewe.

Authors:  Casey C Nestor; Lique M Coolen; Gail L Nesselrod; Miro Valent; John M Connors; Stanley M Hileman; Guanliang Cheng; Michael N Lehman; Robert L Goodman
Journal:  Endocrinology       Date:  2013-08-08       Impact factor: 4.736

Review 5.  Importance of neuroanatomical data from domestic animals to the development and testing of the KNDy hypothesis for GnRH pulse generation.

Authors:  M N Lehman; L M Coolen; R L Goodman
Journal:  Domest Anim Endocrinol       Date:  2020-01-24       Impact factor: 2.290

Review 6.  Opioidergic pathways and kisspeptin in the regulation of female reproduction in mammals.

Authors:  Yoshihisa Uenoyama; Hitomi Tsuchida; Mayuko Nagae; Naoko Inoue; Hiroko Tsukamura
Journal:  Front Neurosci       Date:  2022-08-11       Impact factor: 5.152

  6 in total

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