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1.
Physiol Behav ; 51(5): 961-8, 1992 May.
Artigo em Inglês | MEDLINE | ID: mdl-1319590

RESUMO

Male Wistar rats living in colonies of 4 males plus 4 females were compared to noncolony males, cohabitating with a female. Irreversible dominance relationships developed between one dominant male (D) and three subordinates (S). Dominants developed high basal testosterone levels and large preputial glands. Subordinates had reduced preputial glands despite normal testicle weights and normal basal testosterone levels. Basal corticosterone was elevated in both ranks, in S more so than in D, while in acute encounters both ranks showed a similar increase in the corticosterone-to-ACTH ratio. They also underwent a similar reduction in thymus weight, while an increase in adrenal weight was more pronounced in D. In D-S-I encounters, during which D simultaneously attacked S and an intruder (I) for 20 minutes, both defenders showed a 3-4 fold increase in plasma prolactin, while in the offensive dominant the level remained low. Similar, but weaker hormonal contrasts between offence and defence were found for beta-endorphin, ACTH, and corticosterone, while alpha-MSH and testosterone did not discriminate. In our view, the marked hyporesponsiveness of prolactin to acute offence may be associated with a specific offensive setting of dopaminergic inhibitory and beta-adrenergic stimulatory influences.


Assuntos
Comportamento Agonístico/fisiologia , Nível de Alerta/fisiologia , Hormônios/sangue , Predomínio Social , Meio Social , Hormônio Adrenocorticotrópico/sangue , Agressão/fisiologia , Animais , Corticosterona/sangue , Dominação-Subordinação , Masculino , Sistema Hipófise-Suprarrenal/fisiologia , Prolactina/sangue , Ratos , Ratos Endogâmicos , Testosterona/sangue , alfa-MSH/sangue , beta-Endorfina/sangue
2.
Physiol Behav ; 46(5): 779-85, 1989 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-2516908

RESUMO

Gonadotropin secretion in immature male rats was inhibited by administration of a potent LHRH antagonist (LHRH-A): from 6 to 15 days of age (early onset/short-term treatment), from 6 to 48 days of age (early onset/long-term treatment) or from 22 to 31 days of age (late onset/short-term treatment). Balano-preputial separation was retarded by 9 or 13 days (short-term treatments) or by about 40 days (long-term treatment). Adult testicular weight was lowered and plasma FSH was increased after early, but not after late onset of LHRH-A treatment. Plasma LH and testosterone levels were not affected by any of the LHRH-A treatments. Fertility was diminished after early onset LHRH-A administration only. Adult precopulatory and copulatory behavior were severely affected after early onset of LHRH-A treatment. Intensity of precopulatory anogenital inspection was increased. The copulatory pattern was incomplete with absence of ejaculatory behavior during sexual behavior tests. Sexual behavior was not affected after late onset of LHRH-A treatment. Thus, administration of LHRH-A to immature male rats delays balano-preputial separation irrespective of the age of onset of LHRH-A treatment. In contrast, effects on adult FSH levels, testicular weight, fertility and sexual behavior depend on age and duration of LHRH-A administration.


Assuntos
Fertilidade/efeitos dos fármacos , Hormônio Liberador de Gonadotropina/análogos & derivados , Comportamento Sexual Animal/efeitos dos fármacos , Maturidade Sexual/efeitos dos fármacos , Animais , Esquema de Medicação , Hormônio Foliculoestimulante/sangue , Hormônio Liberador de Gonadotropina/administração & dosagem , Hormônio Liberador de Gonadotropina/farmacologia , Hormônio Luteinizante/sangue , Masculino , Tamanho do Órgão/efeitos dos fármacos , Ratos , Ratos Endogâmicos , Testículo/anatomia & histologia , Testosterona/sangue
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