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Cromakalim, RP49356, pinacidil and minoxidil sulphate in the rat uterus and their antagonism by glibenclamide. Smooth Muscle Research Group.

作者信息

Piper I, Hollingsworth M

机构信息

Department of Physiological Sciences, University of Manchester, UK.

出版信息

Br J Pharmacol. 1989 Dec;98 Suppl:807P.

PMID:2514955
Abstract
摘要

相似文献

1
Cromakalim, RP49356, pinacidil and minoxidil sulphate in the rat uterus and their antagonism by glibenclamide. Smooth Muscle Research Group.
Br J Pharmacol. 1989 Dec;98 Suppl:807P.
2
Effects of several potassium channel openers and glibenclamide on the uterus of the rat.几种钾通道开放剂和格列本脲对大鼠子宫的影响。
Br J Pharmacol. 1990 Dec;101(4):901-7. doi: 10.1111/j.1476-5381.1990.tb14178.x.
3
Comparative effects of the K+ channel openers, pinacidil and cromakalim on vascular tone: sensitivity to glyburide and calcium.
Proc West Pharmacol Soc. 1992;35:97-102.
4
Vascular pharmacology of ATP-sensitive K+ channels: interactions between glyburide and K+ channel openers.ATP敏感性钾通道的血管药理学：格列本脲与钾通道开放剂之间的相互作用
J Vasc Res. 1993 Jan-Feb;30(1):2-12. doi: 10.1159/000158969.
5
Glibenclamide is a competitive antagonist of cromakalim, pinacidil and RP 49356 in guinea-pig pulmonary artery.格列本脲在豚鼠肺动脉中是克罗卡林、吡那地尔和RP 49356的竞争性拮抗剂。
Eur J Pharmacol. 1989 Jun 20;165(2-3):231-9. doi: 10.1016/0014-2999(89)90717-6.
6
Anti-ischemic effects of the potassium channel activators pinacidil and cromakalim and the reversal of these effects with the potassium channel blocker glyburide.钾通道激活剂吡那地尔和克罗卡林的抗缺血作用以及钾通道阻滞剂格列本脲对这些作用的逆转。
J Pharmacol Exp Ther. 1989 Oct;251(1):98-104.
7
Cross tolerance between cromakalim and RP49356 in the uterus of the rat in vivo and in vitro.
Eur J Pharmacol. 1992 Sep 4;219(3):347-53. doi: 10.1016/0014-2999(92)90474-i.
8
Hypoglycemic sulfonylureas antagonize the effects of cromakalim and pinacidil on 86Rb fluxes and contractile activity in the rat aorta.降血糖磺脲类药物可拮抗色满卡林和吡那地尔对大鼠主动脉86Rb通量及收缩活性的作用。
Pharmacology. 1990;41(1):36-48. doi: 10.1159/000138697.
9
Some degree of overlap exists between the K(+)-channels opened by cromakalim and those opened by minoxidil sulphate in rat isolated aorta.在大鼠离体主动脉中，由克罗卡林开启的钾离子通道与由硫酸米诺地尔开启的钾离子通道之间存在一定程度的重叠。
Naunyn Schmiedebergs Arch Pharmacol. 1991 Sep;344(3):351-9. doi: 10.1007/BF00183011.
10
Effects of glibenclamide on cromakalim-induced responses in rabbit isolated aorta.
Br J Pharmacol. 1989 Dec;98 Suppl:806P.

引用本文的文献

1
Effects of several potassium channel openers and glibenclamide on the uterus of the rat.几种钾通道开放剂和格列本脲对大鼠子宫的影响。
Br J Pharmacol. 1990 Dec;101(4):901-7. doi: 10.1111/j.1476-5381.1990.tb14178.x.
2
Comparison of the effects of the K(+)-channel openers cromakalim and minoxidil sulphate on vascular smooth muscle.钾通道开放剂克罗卡林和硫酸米诺地尔对血管平滑肌作用的比较。
Br J Pharmacol. 1991 May;103(1):1148-52. doi: 10.1111/j.1476-5381.1991.tb12315.x.