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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of Chronic Oral Administration of Isosorbide Dinitrate on In Vitro Contractility of Rat Arterial Smooth Muscle
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Effects of Chronic Oral Administration of Isosorbide Dinitrate on In Vitro Contractility of Rat Arterial Smooth Muscle

机译:长期口服异山梨醇酯对大鼠动脉平滑肌体外收缩力的影响

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References(36) Cited-By(3) In this study, we examined the effects of in vitro and in vivo treatment with isosorbide dinitrate (ISDN) on the in vitro response of isolated rat aorta. The in vitro treatment of isolated aorta with ISDN (100 μM) for 2 hr had no effect on the ISDN-induced relaxation of norepinephrine-induced contraction. In the aorta isolated from the rats treated with a high dose (90 mg/kg) of ISDN for 7-14 days, in contrast, the relaxant effect of ISDN was significantly reduced. However, the relaxant effect of sodium nitroprusside was only slightly attenuated by the treatment with a high dose of ISDN for 14 days; and the relaxant effects of 8-bromo-cGMP, levcromakalim and verapamil were unchanged. These results suggest that tolerance to ISDN was obtained only after the in vivo chronic treatment with a high dose of ISDN. ISDN may desensitize the nitric oxide-generating step rather than inactivate guanylate cyclase or the downstream pathways.
机译:参考文献(36)Cited-By(3)在本研究中,我们研究了硝酸异山梨酯(ISDN)体外和体内治疗对离体大鼠主动脉的体外反应的影响。用ISDN(100μM)体外处理离体主动脉2小时对ISDN诱导的去甲肾上腺素引起的收缩没有影响。相反,在从用高剂量(90 mg / kg)ISDN处理7-14天的大鼠中分离出的主动脉中,ISDN的松弛作用显着降低。但是,用高剂量的ISDN治疗14天后,硝普钠的松弛作用仅被稍微减弱了。 8-溴-cGMP,左旋克罗卡林和维拉帕米的松弛作用没有变化。这些结果表明,仅在用高剂量的ISDN进行体内慢性治疗后才获得对ISDN的耐受性。 ISDN可能会使一氧化氮生成步骤不敏感,而不是使鸟苷酸环化酶或下游通路失活。

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