首页> 外文期刊>Japanese Journal of Pharmacology >A COMPARISON OF THE DIFFERENTIAL EFFECTS OF NITROGLYCERIN, NIFEDIPINE AND PAPAVERINE ON CONTRACTURES INDUCED IN VASCULAR AND INTESTINAL SMOOTH MUSCLE BY POTASSIUM AND LANTHANUM
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A COMPARISON OF THE DIFFERENTIAL EFFECTS OF NITROGLYCERIN, NIFEDIPINE AND PAPAVERINE ON CONTRACTURES INDUCED IN VASCULAR AND INTESTINAL SMOOTH MUSCLE BY POTASSIUM AND LANTHANUM

机译:硝酸甘油,奈非替定和帕帕汀对钾和镧诱导的血管和肠平滑肌收缩作用的不同作用比较

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References(33) Cited-By(15) To elucidate the mechanisms of smooth muscle relaxant effects of nitroglycerin, the effects of this substance on the potassium contracture (K+-contracture) and the lanthanum-induced contracture (La3+-contracture) were studied using smooth muscle preparations of the canine coronary artery and colon and the findings compared with the effects of nifedipine, a representative calcium antagonistic vasodilator. The effects of papaverine, a prototype smooth muscle relaxant, were also studied. La3+-contracture was induced in a calcium-free environment with the addition of lanthanum, an effective blocker of calcium influx. In the coronary artery, nitroglycerin produced a relaxation both of the La3+-contracture and the K+-contracture. However, neither La3+-contracture nor K-contracture in the colon was affected. Nifedipine did not relax the La3+-contracture in a range of doses at which K+-contracture of both types of smooth muscles was relaxed. Papaverine produced a relaxation of La3+-contracture as well as K+-contracture, in both types of smooth muscles. Unlike the mechanism related to the relaxant effects of nifedipine, which is generally admitted to be an inhibition of calcium influx, the relaxant effect of nitroglycerin was attributed to the suppression of calcium release from the intracellular store sites and/or stimulation of calcium uptake into the intracellular store-sites. Papaverine was assumed to produce a relaxation through augmentation of the calcium binding to the intracellular store sites for calcium as well as through inhibition of the calcium influx.
机译:参考文献(33)被引用者(15)为了阐明硝酸甘油对平滑肌松弛作用的机制,研究了该物质对钾挛缩(K +收缩)和镧诱导的挛缩(La3 +收缩)的作用。犬冠状动脉和结肠的平滑肌制剂,并将结果与​​代表性的钙拮抗血管扩张剂硝苯地平进行比较。罂粟碱(一种原型平滑肌松弛剂)的作用也得到了研究。在不含钙的环境中,通过添加镧(一种有效的钙流入阻滞剂)可以诱导La3 +收缩。在冠状动脉中,硝酸甘油使La3 +收缩和K +收缩均松弛。但是,结肠中的La3 +收缩和K收缩均不受影响。硝苯地平在使两种类型的平滑肌的K +收缩的剂量范围内都没有使La3 +收缩。罂粟碱在两种类型的平滑肌中均产生La3 +收缩和K +收缩。与硝苯地平的松弛作用相关的机制不同,后者通常被认为是抑制钙流入的机制,而硝酸甘油的松弛作用则归因于抑制钙从细胞内储存位点释放和/或刺激钙吸收进入细胞内。细胞内储存位点。罂粟碱被认为通过增加钙与细胞内钙储存位点的结合以及抑制钙内流而产生松弛作用。

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