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Biol Reprod ; 66(1): 251-7, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11751289

RESUMO

We investigated the mechanism of estradiol-17beta (E2) action on stimulation of LH (=gonadotropin II) release in the black porgy fish (Acanthopagrus schlegeli Bleeker) using an in vivo approach and primary cultures of dispersed pituitary cells in vitro. In vivo, E2 but not androgens (testosterone [T] and 11-ketotestosterone [11-KT]) significantly stimulated plasma LH in a dose-dependent manner. Estradiol-17beta also increased brain content of seabream GnRH. GnRH antagonist prevented E2 stimulation of LH release in vivo, indicating that the effect of E2 on LH was mediated by GnRH. In vitro, sex steroids (E2, T, 11-KT) alone had no effect on basal LH release in the cultured pituitary cells, but GnRH significantly stimulated LH release. Estradiol-17beta potentiated GnRH stimulation of LH release, an effect that was inhibited by GnRH antagonist, and 11-KT, but not T, also potentiated GnRH stimulation of LH release. The potentiating effect of 11-KT on GnRH-induced LH release in vitro was stronger than that of E2. These data suggest that E2 triggers LH release in vivo by acting both on GnRH production at the hypothalamus and on GnRH action at the pituitary. In contrast, 11-KT may only stimulate GnRH action at the pituitary. The E2) induction of LH release, through multiple interactions with GnRH control, supports a possible central role of E2in the sex change observed in the protandrous black porgy.


Assuntos
Estradiol/farmacologia , Hormônio Liberador de Gonadotropina/efeitos dos fármacos , Hormônio Luteinizante/metabolismo , Perciformes/metabolismo , Animais , Química Encefálica/efeitos dos fármacos , Células Cultivadas , Relação Dose-Resposta a Droga , Hormônio Liberador de Gonadotropina/antagonistas & inibidores , Hormônio Liberador de Gonadotropina/metabolismo , Técnicas In Vitro , Hormônio Luteinizante/sangue , Masculino , Hipófise/citologia , Hipófise/efeitos dos fármacos , Hipófise/metabolismo
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