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RX 77368的神经药理学评估——促甲状腺激素释放激素(TRH)的一种稳定类似物。

Neuropharmacological evaluation of RX 77368--a stabilised analogue of thyrotropin-releasing hormone (TRH).

作者信息

Metcalf G, Dettmar P W, Fortune D, Lynn A G, Tulloch I F

出版信息

Regul Pept. 1982 Mar;3(3-4):193-206. doi: 10.1016/0167-0115(82)90125-2.

Abstract

L-Pyroglutamyl-L-histidyl-L-2,3-dimethylprolineamide (Pyr-His-Dmp . NH2; RX 77368) a stabilised analogue of thyrotropin-releasing hormone (TRH) has been examined for neuropharmacological effects in animal tests. The compound was more potent than either TRH or clinically established drugs in four animal tests of antidepressant potential (reserpine reversal, clonidine antagonism, tremorine reversal and learned immobility). RX 77368 also antagonised barbiturate sleeping time. Given by itself to rats the peptide produced arousal as characterised by EEG and EMG measurements and delayed the onset of sleep. The arousal induced was not accompanied by increases in locomotor activity. The profile of pharmacological activity for RX 77368 did not correspond to the profiles of tricyclic antidepressants, psychic-stimulants or analeptic drugs. The possible clinical uses for such a molecule are discussed.

摘要

L-焦谷氨酰-L-组氨酰-L-2,3-二甲基脯氨酰胺(Pyr-His-Dmp.NH2;RX 77368)是促甲状腺激素释放激素(TRH)的一种稳定类似物,已在动物试验中对其神经药理学作用进行了研究。在四项抗抑郁潜力动物试验(利血平逆转、可乐定拮抗、震颤素逆转和习得性不动)中,该化合物比TRH或临床常用药物更有效。RX 77368还拮抗巴比妥类药物的睡眠时间。单独给大鼠注射该肽会引起以脑电图和肌电图测量为特征的觉醒,并延迟睡眠的开始。所诱导的觉醒并不伴有运动活动的增加。RX 77368的药理活性特征与三环类抗抑郁药、精神兴奋剂或兴奋药的特征不相符。讨论了这种分子可能的临床用途。

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