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脑啡肽降解肽酶抑制剂可增强丙咪嗪和茚满二氮卓对小鼠的抗抑郁作用。

Antidepressant action of imipramine and iprindole in mice is enhanced by inhibitors of enkephalin-degrading peptidases.

作者信息

de Felipe M C, Jiménez I, Castro A, Fuentes J A

机构信息

Department of Pharmacology, School of Medicine, Univesidad Complutense, Madrid, Spain.

出版信息

Eur J Pharmacol. 1989 Jan 10;159(2):175-80. doi: 10.1016/0014-2999(89)90702-4.

Abstract

The implication that opioid peptides are involved in the action of the antidepressants imipramine and iprindole was investigated in mice by using the forced swimming test as an experimental model of depression. Both the drugs were found to shorten the immobility time in this test. This effect of imipramine and iprindole was reversed by the opiate antagonist naloxone. Moreover, when subeffective doses of either imipramine or iprindole were given together with an intracerebroventricular injection of an inhibitor of their degradation (thiorphan or bestatin), the immobility time was again decreased. Interestingly, the reduction of the time of immobility was found to be not related to the effect of the drugs on locomotor activity. These data might be taken as further evidence for the involvement of opioid peptides in the pharmacological action of antidepressant drugs.

摘要

以强迫游泳试验作为抑郁症的实验模型,在小鼠中研究了阿片肽参与抗抑郁药丙咪嗪和茚满二酮作用的情况。在该试验中发现这两种药物均能缩短不动时间。丙咪嗪和茚满二酮的这种作用被阿片拮抗剂纳洛酮逆转。此外,当给予亚有效剂量的丙咪嗪或茚满二酮并同时脑室内注射其降解抑制剂(硫醇苯丙氨酸或贝司他汀)时,不动时间再次减少。有趣的是,发现不动时间的减少与药物对运动活性的影响无关。这些数据可作为阿片肽参与抗抑郁药物药理作用的进一步证据。

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