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扎普司特对猫肺血管床血管张力和血管舒张反应的影响。

Influence of Zaprinast on vascular tone and vasodilator responses in the cat pulmonary vascular bed.

作者信息

McMahon T J, Ignarro L J, Kadowitz P J

机构信息

Department of Pharmacology, Tulane University School of Medicine, New Orleans, Louisiana 70112.

出版信息

J Appl Physiol (1985). 1993 Apr;74(4):1704-11. doi: 10.1152/jappl.1993.74.4.1704.

Abstract

The influence of Zaprinast (M&B 22948), a guanosine 3',5'-cyclic monophosphate (cGMP)-specific phosphodiesterase inhibitor, was investigated in the pulmonary vascular bed of the cat under conditions of controlled blood flow and constant left atrial pressure. Under baseline conditions, injections of Zaprinast into the perfused lobar artery produced small decreases in lobar arterial pressure without altering systemic arterial or left atrial pressure. When tone was increased with U-46619, Zaprinast caused larger dose-dependent decreases in lobar arterial pressure without altering left atrial pressure. The decreases in lobar arterial pressure were reduced significantly by treatment with the nitric oxide (NO) synthesis inhibitor NG-nitro-L-arginine methyl ester (L-NAME) or the guanylate cyclase inhibitor methylene blue. Under elevated tone conditions, efferent vagal stimulation and intralobar injections of acetylcholine, substance P, NO solution, and the S-nitrosothiols [S-nitroso-N-acetylpenicillamine (SNAP) and S-nitroso-L-cysteine (CysNO)] decreased lobar arterial pressure in a frequency-dependent and dose-related manner. After treatment with Zaprinast, the decreases in lobar arterial pressure in response to efferent vagal stimulation, the endothelium-dependent vasodilators, and the nitrovasodilators were not changed, whereas the duration of the vasodilator responses as measured by the half times was increased significantly. Vasodilator responses to adenosine, albuterol, and pinacidil were not altered by Zaprinast. These data suggest that cGMP hydrolysis in the lung is rapid and that endothelium-derived NO is important in stimulating basal cGMP production and in regulating vascular tone.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在血流受控和左心房压力恒定的条件下,研究了鸟苷3',5'-环磷酸(cGMP)特异性磷酸二酯酶抑制剂扎普司特(M&B 22948)对猫肺血管床的影响。在基线条件下,向灌注的叶动脉注射扎普司特会使叶动脉压力略有下降,而不会改变体动脉或左心房压力。当用U-46619增加张力时,扎普司特会导致叶动脉压力出现更大的剂量依赖性下降,而不会改变左心房压力。用一氧化氮(NO)合成抑制剂NG-硝基-L-精氨酸甲酯(L-NAME)或鸟苷酸环化酶抑制剂亚甲蓝治疗可显著减轻叶动脉压力的下降。在高张力条件下,传出迷走神经刺激以及叶内注射乙酰胆碱、P物质、NO溶液和S-亚硝基硫醇[S-亚硝基-N-乙酰青霉胺(SNAP)和S-亚硝基-L-半胱氨酸(CysNO)]会以频率依赖性和剂量相关的方式降低叶动脉压力。用扎普司特治疗后,对传出迷走神经刺激、内皮依赖性血管舒张剂和硝基血管舒张剂的叶动脉压力下降没有改变,而通过半衰期测量的血管舒张反应持续时间显著增加。扎普司特对腺苷、沙丁胺醇和匹那地尔的血管舒张反应没有改变。这些数据表明,肺中cGMP的水解很快,并且内皮衍生的NO在刺激基础cGMP产生和调节血管张力方面很重要。(摘要截短于250字)

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