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潜在抗抑郁药物坦达明的临床药理学研究

Clinical pharmacological studies of tandamine, a potential antidepressive drug.

作者信息

Ehsanullah R S, Ghose K, Kirby M J, Turner P, Witts D

出版信息

Psychopharmacology (Berl). 1977 Mar 23;52(1):73-7. doi: 10.1007/BF00426603.

Abstract

Tandamine hydrochloride, a thiopyranoindole, was more active than desmethylimipramine in inhibiting the tyramine pressor response after single oral doses in human volunteers. When compared with a placebo, tandamine was found to possess significant anticholinergic activity, to reduce appetite and to produce sedation. Compared with clomipramine, it caused a smaller inhibition of 5-HT but a more marked inhibition of dopamine uptake into human platelets. Further clinical and pharmacological studies with tandamine may help to elucidate the respective roles of different monoamines in depression, sedation and appetite.

摘要

盐酸坦达明,一种硫代吡喃吲哚,在人类志愿者单次口服给药后,其在抑制酪胺升压反应方面比去甲丙咪嗪更具活性。与安慰剂相比,发现坦达明具有显著的抗胆碱能活性、能降低食欲并产生镇静作用。与氯米帕明相比,它对5-羟色胺的抑制作用较小,但对多巴胺摄入人血小板的抑制作用更为显著。对坦达明进行进一步的临床和药理学研究可能有助于阐明不同单胺在抑郁、镇静和食欲方面各自的作用。

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