Endogenous dopamine differently affects N-[1-(2-benzo(b)thiophenyl)cyclohexyl]piperidine and cocaine binding to the dopamine uptake complex.

T Maurice, G Barbanel, J Vignon
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引用次数: 10

Abstract

1. [3H]N-[1-(2-Benzo(b)thiophenyl)cyclohexyl]piperidine ([3H]BTCP) labels in vivo the dopamine uptake complex in the mouse striatum. 2. In mice treated with gamma-butyrolactone (GBL, 400 mg/kg), [3H]BTCP specific binding was increased and ID50 values of BTCP and cocaine for the prevention of [3H]BTCP binding were significantly lowered. 3. In GBL-treated mice, cocaine (5 mg/kg, s.c.) had no effect on the BTCP ID50 value, whereas GBR 12783 (2 mg/kg, s.c.) increased it significantly. 4. Thus in vivo, endogenous dopamine and cocaine are competitive and non-competitive inhibitors, respectively, of the binding of [3H]BTCP.

内源性多巴胺不同程度地影响N-[1-(2-苯并(b)噻吩基)环己基]哌啶和可卡因与多巴胺摄取复合物的结合。
1. [3H]N-[1-(2-苯并(b)噻吩基)环己基]哌啶([3H]BTCP)在体内标记小鼠纹状体多巴胺摄取复合物。2. γ -丁内酯(GBL, 400 mg/kg)使小鼠[3H]BTCP特异性结合增加,BTCP与可卡因预防[3H]BTCP结合的ID50值显著降低。3.在gbl处理的小鼠中,可卡因(5 mg/kg, s.c)对BTCP ID50值没有影响,而GBR 12783 (2 mg/kg, s.c)显著增加了BTCP ID50值。4. 因此,在体内,内源性多巴胺和可卡因分别是[3H]BTCP结合的竞争性和非竞争性抑制剂。
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