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兴奋性氨基酸拮抗剂可减弱可卡因对伏隔核细胞外多巴胺的作用。

Excitatory amino acid antagonists attenuate the effects of cocaine on extracellular dopamine in the nucleus accumbens.

作者信息

Pap A, Bradberry C W

机构信息

Department of Psychiatry, Yale University School of Medicine, Connecticut, USA.

出版信息

J Pharmacol Exp Ther. 1995 Jul;274(1):127-33.

PMID:7616389
Abstract

The effect of N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate excitatory amino acid antagonists on systemic cocaine-induced increases in extracellular dopamine was examined. The alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate receptor subtype antagonist, 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), and N-methyl-D-aspartate receptor antagonists, 2-amino-5-phosphonovalerate and dizocilpine, were infused via a microdialysis probe placed in the nucleus accumbens. The local infusion of 2-amino-5-phosphonovalerate (500 microM), dizocilpine (50 microM) and CNQX (100 microM), started 80 min before cocaine injection, significantly inhibited the cocaine-induced increase in extracellular dopamine. The CNQX blockade was dose-dependent with respect to both CNQX concentration infused and dose of cocaine administered. Simultaneous infusion of the two antagonists (500 microM 2-amino-5-phosphonovalerate and 100 microM CNQX) did not lead to further reductions in the effects of cocaine when compared to either antagonist alone. Our results suggest that both N-methyl-Daspartate and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate subtypes of excitatory amino acid antagonist receptors may contribute to the stimulatory effect of cocaine on extracellular dopamine in the nucleus accumbens.

摘要

研究了N-甲基-D-天冬氨酸和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸/海人藻酸兴奋性氨基酸拮抗剂对全身可卡因诱导的细胞外多巴胺增加的影响。通过置于伏隔核的微透析探针注入α-氨基-3-羟基-5-甲基异恶唑-4-丙酸/海人藻酸受体亚型拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)以及N-甲基-D-天冬氨酸受体拮抗剂2-氨基-5-磷酸戊酸和地佐环平。在注射可卡因前80分钟开始局部注入2-氨基-5-磷酸戊酸(500微摩尔)、地佐环平(50微摩尔)和CNQX(100微摩尔),可显著抑制可卡因诱导的细胞外多巴胺增加。CNQX的阻断作用在注入的CNQX浓度和给予的可卡因剂量方面均呈剂量依赖性。与单独使用任何一种拮抗剂相比,同时注入两种拮抗剂(500微摩尔2-氨基-5-磷酸戊酸和100微摩尔CNQX)并未导致可卡因作用的进一步降低。我们的结果表明,兴奋性氨基酸拮抗剂受体的N-甲基-D-天冬氨酸和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸/海人藻酸亚型可能均有助于可卡因对伏隔核中细胞外多巴胺的刺激作用。

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