Literature DB >> 318993

Effects of testosterone implants and hypothalamic lesions on luteinizing hormone regulation in the castrated male rat.

C Y Cheung, J M Davidson.   

Abstract

The effects of intrahypothalamic and subcutaneous implants of testosterone (T) and those of hypothalamic lesions on resting levels of circulating LH and pituitary responsiveness to exogenous LHRH were studied in castrated male rats to elucidate hypothalamic and pituitary regulation of LH secretion. Two hundred mug implants of testosterone propionate (TP) in the median eminence region suppressed plasma LH titers before evidence of direct inhibition of pituitary function (as indicated by testing with LHRH) was found. Such implants release appreciable amounts of T into the peripheral circulation in the immediate post-operative period, and SC Silastic (constant release) capsules containing T have similar effects. The findings suggest that, regardless of the site of implant, the initial negative feedback inhibition of LH by T is not dependent on direct action at the pituitary levels but rather appears to be a hypothalamic effect. In the days following exposure to hypothalamic or peripheral implantation of T, however, a progressively developing decline in the response to exogenous LHRH was observed. In order to determine whether this effect results from suppression of endogenous LHRH release, the median eminence-arcuate region was destroyed to remove the source of LHRH. In these animals, the suppression of plasma LH was evident on the first day after the lesion, but pituitary responsiveness to LHRH was unaffected until after one week. When Sialastic capsules were implanted SC into lesioned animals, a more rapid (less than 1 week) inhibition of pituitary responsivity ensued. Suprachiasmatic lesions did not affect basal LH secretion or pituitary responses to LHRH. The data provide evidence for a dual feedback action of T on LH in castrated male rats: an initial inhibitory effect presumably due to hypothalamic inhibition (commencing at around 6h after hypothalamic of SC implantation of T), and a subsequent suppression of pituitary responisveness (after one day) presumably due to direct action of T on the pituitary. In addition to these phenomena, findings in rats bearing median eminence-arcurate lesions suggest that the removal of endogenous LHRH by itself leads to an eventual decline in pituitary responsiveness (greater than one week postoperatively).

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Year:  1977        PMID: 318993     DOI: 10.1210/endo-100-2-292

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  4 in total

1.  Administration of gonadal steroids to the castrated male rat prevents a decrease in the release of gonadotropin-releasing hormone from the incubated hypothalamus.

Authors:  R S Rudenstein; H Bigdeli; M H McDonald; P J Snyder
Journal:  J Clin Invest       Date:  1979-02       Impact factor: 14.808

2.  Pituitary gonadotropin-releasing hormone receptors. Effects of castration, steroid replacement, and the role of gonadotropin-releasing hormone in modulating receptors in the rat.

Authors:  M S Frager; D R Pieper; S A Tonetta; J A Duncan; J C Marshall
Journal:  J Clin Invest       Date:  1981-03       Impact factor: 14.808

3.  Sex steroid modulation of fatty acid utilization and fatty acid binding protein concentration in rat liver.

Authors:  R K Ockner; N Lysenko; J A Manning; S E Monroe; D A Burnett
Journal:  J Clin Invest       Date:  1980-05       Impact factor: 14.808

4.  Testosterone replacement does not normalize carcass composition in chronically decerebrate male rats.

Authors:  Ruth B S Harris; Emily W Kelso; William P Flatt; Harvey J Grill; Timothy J Bartness
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-04-15       Impact factor: 3.619

  4 in total

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