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某些血管舒张剂对离体人手部静脉的作用。

Actions of some vasodilators on isolated human hand veins.

作者信息

Arner M, Högestätt E D

出版信息

Acta Physiol Scand. 1987 Aug;130(4):671-7. doi: 10.1111/j.1748-1716.1987.tb08191.x.

Abstract

Vasospasm is a well recognized complication during microvascular surgery of the hand. In the search for new spasmolytic drug therapies, the effects of papaverine, nitroprusside, nimodipine and lidocaine on isolated human hand veins contracted by several postulated mediators of vasospasm were examined. Mechanical activity was recorded isometrically in ring segments of the vessels. Potassium ions, noradrenaline (NA), 5-hydroxytryptamine (5-HT) and prostaglandin F2 alpha (PGF2 alpha) all produced strong contractions that were highly dependent on the presence of extracellular Ca2+. Papaverine acted as a nonselective vasodilator, as it produced an almost identical inhibition of contractile responses to all examined stimulants. Nitroprusside inhibited contractions induced by agonists more than those evoked by K+, whereas the opposite was found for nimodipine. Nitroprusside also seemed to display a certain degree of selectivity among the agonist-induced responses (NA greater than PGF2 alpha greater than 5-HT). Lidocaine increased the contractile response to K+ and at high concentrations (greater than 10(-5) M) produced a contraction per se. The clinical efficacy of lidocaine as a vasodilator after topical application therefore seems to reflect an inhibitory action on vasoconstrictor nerves. Papaverine, nitroprusside, nimodipine and lidocaine differ considerably in their profiles of action and therefore deserve to be further evaluated in the treatment of vasospasm during microvascular surgery.

摘要

血管痉挛是手部微血管手术中一种公认的并发症。在寻找新的解痉药物疗法的过程中,研究了罂粟碱、硝普钠、尼莫地平和利多卡因对由几种假定的血管痉挛介质引起收缩的离体人手部静脉的影响。通过等长记录血管环段的机械活动。钾离子、去甲肾上腺素(NA)、5-羟色胺(5-HT)和前列腺素F2α(PGF2α)均产生强烈收缩,且高度依赖细胞外Ca2+的存在。罂粟碱作为一种非选择性血管扩张剂,因为它对所有检测的刺激物产生的收缩反应抑制作用几乎相同。硝普钠对激动剂诱导的收缩的抑制作用大于对钾离子诱导的收缩的抑制作用,而尼莫地平则相反。硝普钠在激动剂诱导的反应中似乎也表现出一定程度的选择性(NA>PGF2α>5-HT)。利多卡因增加了对钾离子的收缩反应,并且在高浓度(>10^(-5) M)时本身会产生收缩。因此,局部应用后利多卡因作为血管扩张剂的临床疗效似乎反映了其对血管收缩神经的抑制作用。罂粟碱、硝普钠、尼莫地平和利多卡因的作用模式有很大差异,因此在微血管手术中治疗血管痉挛方面值得进一步评估。

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