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1.
Acta Physiol Lat Am ; 33(4): 293-8, 1983.
Artigo em Inglês | MEDLINE | ID: mdl-6430033

RESUMO

The release of 3H-catecholamines evoked by Black Widow spider venom gland extract (BW-GE) has been studied in the isolated rat hypothalamus (HT), occipital cortex (OC), preloaded with 3H-noradrenaline, and isolated caudate nucleus (CN) preloaded with 3H-dopamine. The BWGE at a concentration of 0.04 gland/ml increased significantly 3H-output in isolated slices of rat HT, OC and CN. This effect was markedly depressed when control calcium concentration in the medium (1.68 mM) was reduced (0-0.56 mM) or enhanced (3 mM), as well as in the presence of an organic Ca2+ antagonist, verapamil (10 microM), or ionophore A 23187 (40 microM), a substance that increases the influx of calcium into the cell. Morphine (up to 0.4 mM) evoked no effect upon 3H-noradrenaline release induced by BWGE. Morphine (10 microM), but not ionophore A 23187 or high Ca2+ (3 mM), reduced 3H-noradrenaline release induced by 20 mM K+. Low Ca2+ and verapamil produced similar effects than those observed for BWGE. Our results demonstrate differences between BWGE and potassium stimuli, and indicate that BWGE releases 3H-catecholamines by a calcium dependent process.


Assuntos
Venenos de Artrópodes/farmacologia , Cálcio/metabolismo , Catecolaminas/metabolismo , Núcleo Caudado/metabolismo , Córtex Cerebral/metabolismo , Hipotálamo/metabolismo , Venenos de Aranha/farmacologia , Animais , Viúva Negra , Calcimicina/farmacologia , Estimulação Elétrica , Masculino , Potássio/metabolismo , Ratos , Ratos Endogâmicos , Trítio/metabolismo , Verapamil/farmacologia
2.
Acta Physiol Lat Am ; 33(4): 293-8, 1983.
Artigo em Inglês | BINACIS | ID: bin-49817

RESUMO

The release of 3H-catecholamines evoked by Black Widow spider venom gland extract (BW-GE) has been studied in the isolated rat hypothalamus (HT), occipital cortex (OC), preloaded with 3H-noradrenaline, and isolated caudate nucleus (CN) preloaded with 3H-dopamine. The BWGE at a concentration of 0.04 gland/ml increased significantly 3H-output in isolated slices of rat HT, OC and CN. This effect was markedly depressed when control calcium concentration in the medium (1.68 mM) was reduced (0-0.56 mM) or enhanced (3 mM), as well as in the presence of an organic Ca2+ antagonist, verapamil (10 microM), or ionophore A 23187 (40 microM), a substance that increases the influx of calcium into the cell. Morphine (up to 0.4 mM) evoked no effect upon 3H-noradrenaline release induced by BWGE. Morphine (10 microM), but not ionophore A 23187 or high Ca2+ (3 mM), reduced 3H-noradrenaline release induced by 20 mM K+. Low Ca2+ and verapamil produced similar effects than those observed for BWGE. Our results demonstrate differences between BWGE and potassium stimuli, and indicate that BWGE releases 3H-catecholamines by a calcium dependent process.

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