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美西律对大鼠肠系膜阻力动脉的血管舒张作用。

Vasorelaxant effect of mexiletine in mesenteric resistance arteries of rats.

作者信息

Dohi Y, Kojima M, Sato K

机构信息

Second Department of Internal Medicine, Nagoya City University Hospital, Japan.

出版信息

Br J Pharmacol. 1994 Mar;111(3):673-80. doi: 10.1111/j.1476-5381.1994.tb14790.x.

Abstract
  1. The vascular action of mexiletine, a class Ib antiarrhythmic agent, was investigated in the mesenteric resistance arteries of rats. 2. The second order branch of the mesenteric artery was cut into rings and changes in isometric tension were recorded. 3. Mexiletine (10(-6) -10(-3) M) evoked concentration-dependent, endothelium-independent relaxations in arteries contracted with noradrenaline. 4. Mexiletine (10(-4) M) did not affect the contraction induced by noradrenaline in Ca(2+)-free solution, while the compound inhibited the contraction induced by CaCl2 in noradrenaline-activated arteries. 5. The relaxation induced by mexiletine was less pronounced in arteries contracted with high KCl than in those contracted with noradrenaline. 6. Mexiletine induced identical relaxations in arteries contracted with noradrenaline in high KCl solution containing verapamil and in Krebs solution. 7. Thus, mexiletine induces relaxations by inhibiting transmembrane Ca2+ movement, but not Ca2+ release from the intracellular store site in mesenteric resistance arteries of rats. It is speculated that mexiletine possesses greater inhibitory effects against noradrenaline-activated, verapamil-insensitive (receptor-operated) Ca2+ channels than against verapamil-sensitive (voltage-dependent) channels.
摘要
  1. 对Ib类抗心律失常药物美西律的血管作用在大鼠肠系膜阻力动脉中进行了研究。2. 将肠系膜动脉的二级分支切成环并记录等长张力的变化。3. 美西律(10⁻⁶ - 10⁻³ M)在去甲肾上腺素收缩的动脉中引起浓度依赖性、非内皮依赖性舒张。4. 美西律(10⁻⁴ M)在无钙溶液中不影响去甲肾上腺素诱导的收缩,而该化合物在去甲肾上腺素激活的动脉中抑制氯化钙诱导的收缩。5. 美西律在高钾收缩的动脉中诱导的舒张不如在去甲肾上腺素收缩的动脉中明显。6. 美西律在含维拉帕米的高钾溶液和Krebs溶液中对去甲肾上腺素收缩的动脉诱导相同的舒张。7. 因此,美西律通过抑制跨膜Ca²⁺移动而非抑制大鼠肠系膜阻力动脉细胞内储存部位的Ca²⁺释放来诱导舒张。推测美西律对去甲肾上腺素激活的、维拉帕米不敏感(受体操作)的Ca²⁺通道的抑制作用比对维拉帕米敏感(电压依赖性)通道的抑制作用更强。

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