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重复给予氯丙嗪会增强大鼠对5-羟色胺受体刺激的行为反应。

Repeated chlorpromazine administration increases a behavioural response of rats to 5-hydroxytryptamine receptor stimulation.

作者信息

Green A R

出版信息

Br J Pharmacol. 1977 Feb;59(2):367-71. doi: 10.1111/j.1476-5381.1977.tb07501.x.

Abstract

1 The hyperactivity syndrome produced in rats by administration of tranylcypromine (20 mg/kg i.p.) followed 30 min later by L-tryptophan (50 mg/kg i.p.) is generally considered to be due to increased 5-hydroxytryptamine (5-HT) functional activity. It is inhibited by chlorpromazine (30 mg/kg i.p.) injected 60 min before the tranylcypromine. However, chlorpromazine injection for 4 days either at a dose of 30 mg/kg once daily or 5 mg/kg twice daily results in an enhanced hyperactivity response to tranylcypromine and L-tryptophan administration 24 h after the final dose of chlorpromazine. 2 One injection of chlorpromazine (30 mg/kg) did not produce enhancement 24 h later and the inhibition of the tranylcypromine/L-tryptophan hyperactivity observed after acute chlorpromazine injection was seen if the rats were given tranylcypromine and L-tryptophan 1 h after the fourth chlorpromazine (30 mg/kg) dose. 3 Chlorpromazine (30 mg/kg) once daily or 5 mg/kg twice daily for 4 days resulted in rats displaying enhanced behavioral responses to the suggested 5-HT agonist 5-methoxy N,N-dimethyltryptamine (2 mg/kg) on day 5. 4 Chlorpromazine (30 mg/kg) once daily for 4 days produces a slight increase in brain 5-hydroxytryptamine (5-HT) concentration on day 5, but no difference in the rate of brain 5-HT synthesis or the rate of 5-HT accumulation after tranylcypromine and L-tryptophan administration. 5. There is some evidence that chlorpromazine blocks 5-HT receptors. It has also been observed that several other neuroleptic drugs do not produce enhanced 5-HT responses after repeated administration. It is suggested therefore that the enhanced behavioural response to 5-HT receptor stimulation following repeated chlorpromazine administration may be because this drug blocks 5-HT receptors.

摘要
  1. 腹腔注射反苯环丙胺(20毫克/千克),30分钟后再腹腔注射L-色氨酸(50毫克/千克),由此在大鼠身上产生的多动综合征通常被认为是由于5-羟色胺(5-HT)功能活性增强所致。在反苯环丙胺注射前60分钟注射氯丙嗪(30毫克/千克,腹腔注射)可抑制该综合征。然而,以30毫克/千克的剂量每日注射一次氯丙嗪,或以5毫克/千克的剂量每日注射两次氯丙嗪,连续注射4天,在最后一剂氯丙嗪注射24小时后,大鼠对反苯环丙胺和L-色氨酸给药的多动反应会增强。2. 单次注射氯丙嗪(30毫克/千克)在24小时后不会产生增强作用,并且如果在第四次注射氯丙嗪(30毫克/千克)后1小时给大鼠注射反苯环丙胺和L-色氨酸,会观察到急性注射氯丙嗪后对反苯环丙胺/L-色氨酸多动的抑制作用。3. 氯丙嗪(30毫克/千克)每日一次或5毫克/千克每日两次,连续注射4天,会导致大鼠在第5天对建议的5-HT激动剂5-甲氧基-N,N-二甲基色胺(2毫克/千克)表现出增强的行为反应。4. 氯丙嗪(30毫克/千克)每日一次,连续注射4天,在第5天会使大脑5-羟色胺(5-HT)浓度略有增加,但在给予反苯环丙胺和L-色氨酸后,大脑5-HT合成速率或5-HT积累速率没有差异。5. 有一些证据表明氯丙嗪会阻断5-HT受体。还观察到其他几种抗精神病药物在重复给药后不会产生增强的5-HT反应。因此有人提出,氯丙嗪重复给药后对5-HT受体刺激的行为反应增强可能是因为这种药物阻断了5-HT受体。

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