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儿茶酚胺能参与苯丙胺异构体对癫痫易感性的影响。

Catecholaminergic involvement in the effects of amphetamine isomers on seizure susceptibility.

作者信息

Gerald M C, Gupta T K

出版信息

Eur J Pharmacol. 1977 Jan 21;41(2):231-4. doi: 10.1016/0014-2999(77)90215-1.

Abstract

The (+)-amphetamine (2.5 mg/kg) increase in pentylenetetrazol seizure was abolished by pretreatment with reserpine, alpha-methyltyrosine methyl ester (alpha-MT), FLA-63 or 6-hydroxydopa. All treatments except reserpine antagonized the increase in seizure threshold produced by (-)-amphetamine (4 mg/kg). Only reserpine +alpha-MT antagonized the decrease in seizure threshold produced by (+)-amphetamine (15 mg/kg). These results indicate that amphetamine alterations in PTZ seizure susceptibility are mediated indirectly via the release of newly synthetized and/or granular stores of catecholamines.

摘要

利血平、α-甲基酪氨酸甲酯(α-MT)、FLA-63或6-羟基多巴预处理可消除(+)-苯丙胺(2.5毫克/千克)引起的戊四氮惊厥增加。除利血平外,所有处理均拮抗了(-)-苯丙胺(4毫克/千克)引起的惊厥阈值升高。只有利血平+α-MT拮抗了(+)-苯丙胺(15毫克/千克)引起的惊厥阈值降低。这些结果表明,苯丙胺对戊四氮惊厥易感性的改变是通过新合成的和/或颗粒状儿茶酚胺储存的释放间接介导的。

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