Artigo Revisado por pares

Sex differences in the amphetamine stimulated release of catecholamines from rat striatal tissue in vitro

1981; Elsevier BV; Volume: 204; Issue: 2 Linguagem: Inglês

10.1016/0006-8993(81)90595-3

ISSN

1872-6240

Autores

Jill B. Becker, V.D. Ramírez,

Tópico(s)

Hormonal and reproductive studies

Resumo

Sex and estrous cycle-related differences in the amphetamine (AMT)-stimulated release (pg/mg/min) of catecholamines (CA) from rat striatal and mediobasal hypothalamus (MBH) fragments were measured in an in vitro perifusion system. In striatal tissue from intact males, AMT stimulated the release of both norepinephrine (NE) and dopamine (DA). The AMT-stimulated release of DA from striatal tissue obtained from intact females varied with the stage of the estrous cycle. This increase in DA release was lower in striatal tissue from proestrous females than from females in estrus(P < 0.05) or diestrus1 (P < 0.01). The NE release stimulated by AMT was greater than basal release only on estrus and diestrus 2. Following castration (CAST) or CAST plus 500 μg testosterone propionate (TP), daily for 4 days, striatal tissue fragments from male rats continued to release CA in response to AMT stimulation. In contrast, ovariectomy (OVX) severely attenuated the AMT-stimulated release of both CA. Treatment of OVX females with 5 μg estradiol benzoate (EB), daily for 4 days, or 1.2 mg progesterone (P) slightly increased the AMT-stimulated release of DA but not NE. Treatment of OVX females with 5 μg EB, daily for 4 days, plus 1.2 mg P completely restored the AMT-stimulated release of both CA. Interestingly, MBH fragments from intact of gonadectomized rats, with or without hormonal treatment, demonstrated a consistent AMT-stimulated release of DA regardless of the sex of the animal. The AMT-stimulated NE release from these MBH fragments was less consistent, but there were no significant differences between the groups. These results demonstrate that the AMT-stimulated release of DA from striatal tissue in vitro is sex, hormonal, and tissue dependent.

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