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Cromakalim, nicorandil and pinacidil: novel drugs which open potassium channels in smooth muscle.

作者信息

Hamilton T C, Weston A H

机构信息

Beecham Pharmaceuticals Research Division, Medicinal Research Centre, Harlow, Essex, U.K.

出版信息

Gen Pharmacol. 1989;20(1):1-9. doi: 10.1016/0306-3623(89)90052-9.

DOI:10.1016/0306-3623(89)90052-9
PMID:2523328
Abstract
摘要

相似文献

1
Cromakalim, nicorandil and pinacidil: novel drugs which open potassium channels in smooth muscle.克罗卡林、尼可地尔和平尼地尔：可使平滑肌钾通道开放的新型药物。
Gen Pharmacol. 1989;20(1):1-9. doi: 10.1016/0306-3623(89)90052-9.
2
Effects of pinacidil, cromakalim, and nicorandil on potassium currents of rat basilar artery smooth muscle.吡那地尔、克罗卡林和尼可地尔对大鼠基底动脉平滑肌钾电流的影响。
Adv Exp Med Biol. 1991;304:531-41. doi: 10.1007/978-1-4684-6003-2_47.
3
Comparative effects of K+ channel blockade on the vasorelaxant activity of cromakalim, pinacidil and nicorandil.钾通道阻断对克罗卡林、匹那地尔和尼可地尔血管舒张活性的比较影响。
Eur J Pharmacol. 1988 Aug 2;152(3):331-9. doi: 10.1016/0014-2999(88)90728-5.
4
Effect of three novel K+ channel openers, cromakalim, pinacidil and nicorandil on allergic reaction and experimental asthma.三种新型钾通道开放剂（克罗卡林、匹那地尔和尼可地尔）对过敏反应和实验性哮喘的影响。
Jpn J Pharmacol. 1991 May;56(1):13-21. doi: 10.1254/jjp.56.13.
5
Analysis of cromakalim-, pinacidil-, and nicorandil-induced relaxation of the 5-hydroxytryptamine precontracted rat isolated basilar artery.克罗卡林、吡那地尔和尼可地尔对5-羟色胺预收缩的大鼠离体基底动脉舒张作用的分析。
Naunyn Schmiedebergs Arch Pharmacol. 1991 Apr;343(4):377-83. doi: 10.1007/BF00179042.
6
Cromakalim, a potassium channel activator: a comparison of its cardiovascular haemodynamic profile and tissue specificity with those of pinacidil and nicorandil.克罗卡林，一种钾通道激活剂：其心血管血流动力学特征及组织特异性与匹那地尔和尼可地尔的比较
J Cardiovasc Pharmacol. 1988;12(5):535-42.
7
Effects of putative activators of K+ channels in mouse pancreatic beta-cells.钾通道假定激活剂对小鼠胰腺β细胞的影响。
Br J Pharmacol. 1989 Nov;98(3):957-65. doi: 10.1111/j.1476-5381.1989.tb14626.x.
8
Vasodilatation of canine cerebral arteries by nicorandil, pinacidil and lemakalim.尼可地尔、匹那地尔和雷马卡林对犬脑动脉的血管舒张作用。
Gen Pharmacol. 1992 Mar;23(2):197-201. doi: 10.1016/0306-3623(92)90009-9.
9
[Advance in pharmacology of potassium channels in cardiovascular system and their clinical use].
Zhonghua Yi Xue Za Zhi. 1992 Mar;72(3):180-3.
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Interaction of potassium channel openers and blockers in canine atrial muscle.钾通道开放剂与阻滞剂在犬心房肌中的相互作用。
Br J Pharmacol. 1989 Jul;97(3):753-62. doi: 10.1111/j.1476-5381.1989.tb12013.x.

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Potassium channel agonists modify the local anaesthetic activity of bupivacaine in mice.钾通道激动剂可改变布比卡因在小鼠体内的局部麻醉活性。
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Cromakalim inhibits electrically-evoked [3H]acetylcholine release from a tube-preparation of the rat isolated trachea by an epithelium-dependent mechanism.克罗卡林通过一种依赖上皮的机制抑制大鼠离体气管管段制备物中电诱发的[3H]乙酰胆碱释放。
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