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通过自主神经系统递质对前列腺素诱导的人体肠道运动进行调节。

Modulation of the prostaglandin-induced intestinal motility in humans through the transmitters of the vegetative nervous system.

作者信息

Schmidt E, Bruch H P, Laven R, Hockerts T

出版信息

Eur Surg Res. 1978;10(5):329-35. doi: 10.1159/000128023.

Abstract

Research was done on the reciprocity between adrenergic and cholinergic stimulating or inhibiting pharmaceuticals and the prostaglandin-induced intestinal motility. By cholinergic activation, the amplitudes of the prostaglandin-dependent rhythmical contractions of human taenia coli were intensified. There was very little influence on the frequency of contractions, however. Simultaneous stimulation of adrenergic beta-receptors by increasing doses of adrenaline or noradrenaline caused the contraction amplitude and frequency to decrease continually until the contractions were completely eliminated. The cholinergic effect could be suppressed with atropine, the adrenergic-stimulated reaction was reversed by the blockage of beta-receptors. It was completely abolished by simultaneous addition of alpha- and beta-receptor-blocking drugs.

摘要

对肾上腺素能和胆碱能刺激或抑制药物与前列腺素诱导的肠道运动之间的相互作用进行了研究。通过胆碱能激活,人结肠带中依赖前列腺素的节律性收缩幅度增强。然而,对收缩频率的影响很小。通过增加肾上腺素或去甲肾上腺素的剂量同时刺激肾上腺素能β受体,会导致收缩幅度和频率持续下降,直到收缩完全消除。胆碱能效应可用阿托品抑制,肾上腺素能刺激反应可通过β受体阻断而逆转。同时加入α和β受体阻断药物可使其完全消除。

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