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氧化阿米替林:与其他抗抑郁药物相比的受体结合情况

Amitriptylinoxide: receptor-binding profile compared with other antidepressant drugs.

作者信息

Borbe H O, Zierenberg O

出版信息

Pharmacopsychiatry. 1985 Sep;18(5):314-9. doi: 10.1055/s-2007-1017388.

Abstract

The interactions of amitriptylinoxide and various antidepressant drugs with different neurotransmitter and drug receptors were investigated by receptor binding studies. Amitriptylinoxide had less affinity than amitriptyline for most of the receptors studied. Half maximal inhibition of acetylcholine receptor binding occurred for amitriptylinoxide at 18 mumol/l (amitriptyline: 0.32 mumol/l). Comparing all studied antidepressants for muscarinic acetylcholine receptor binding, amitriptylinoxide had the weakest affinity of all tested tricyclic compounds. Also the affinity of amitriptylinoxide for alpha-receptor binding was about 60 fold less than that of amitriptyline. For all antidepressants investigated, the lowest affinities were found for benzodiazepine, opiate and beta-receptor binding. The weak affinities of amitriptylinoxide for various receptors may be responsible for its reduced side-effects, while it still retains potent antidepressant properties by stabilising the amitriptyline-level in the brain.

摘要

通过受体结合研究,对氧化阿米替林与各种抗抑郁药物和不同神经递质及药物受体之间的相互作用进行了研究。在大多数所研究的受体方面,氧化阿米替林的亲和力低于阿米替林。氧化阿米替林对乙酰胆碱受体结合产生半数最大抑制作用时的浓度为18 μmol/L(阿米替林为0.32 μmol/L)。在比较所有所研究的抗抑郁药物对毒蕈碱型乙酰胆碱受体的结合情况时,氧化阿米替林在所有测试的三环类化合物中亲和力最弱。氧化阿米替林对α受体结合的亲和力也比阿米替林低约60倍。在所研究的所有抗抑郁药物中,对苯二氮䓬、阿片和β受体结合的亲和力最低。氧化阿米替林对各种受体的弱亲和力可能是其副作用减少的原因,同时它通过稳定大脑中的阿米替林水平仍保留强效抗抑郁特性。

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