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S-亚硝基硫醇的体外血管舒张及体内心血管效应:与标准硝基血管扩张剂的比较及交叉耐受性

In vitro vasorelaxant and in vivo cardiovascular effects of S-nitrosothiols: comparison to and cross tolerance with standard nitrovasodilators.

作者信息

Smith M P, Humphrey S J, Kerr S W, Mathews W R

机构信息

Cardiovascular Diseases Unit, Upjohn Laboratories, Upjohn Company, Kalamazoo, MI.

出版信息

Methods Find Exp Clin Pharmacol. 1994 Jun;16(5):323-35.

PMID:7934311
Abstract

The in vitro vasorelaxant and in vivo cardiovascular effects of synthetic S-nitrosothiols (RSNOs) were compared to standard nitrovasodilators. S-Nitroso-glutathione (GSNO), S-nitroso-N-acetylcysteine (NACysNO), S-nitroso-galactopyranose (GPSNO), S-nitroso-thioglycerol (TGSNO) and S-nitroso-homocysteine (HCysNO) relaxed phenylephrine (PE) contracted rabbit aorta at 50% effective concentrations (EC50s) of 3-46 nM. While nitroglycerin (GTN) exhibited in vitro tolerance after preincubation, the RSNOs were considerably less cross tolerant to GTN. In conscious dogs, GSNO, NACysNO and GPSNO (1-20 mcg/kg/min i.v.) paralleled nitroprusside (SNP) in reducing mean arterial and central venous pressure (MAP; CVP) with mild tachycardia. GSNO, NACysNO and SNP were more hypotensive and more resistant to isosorbide dinitrate (ISDN) cross tolerance than GTN. NACysNO showed mild self tolerance with low infusion (2.5 mcg/kg/min x 4h x 3 days) and blunted GTN's hypotension. These studies demonstrate that GSNO and NACysNO are SNP-like vasodilators in conscious dogs, which exhibit less cross tolerance to ISDN than GTN. Further, RSNOs relax vascular smooth muscle seemingly independent of nitric oxide (NO) liberation, and nitrate tolerance may involve reduced RSNO formation or NO release rather than desensitized guanylate cyclase (GC).

摘要

将合成的S-亚硝基硫醇(RSNOs)的体外血管舒张作用和体内心血管效应与标准硝基血管扩张剂进行了比较。S-亚硝基谷胱甘肽(GSNO)、S-亚硝基-N-乙酰半胱氨酸(NACysNO)、S-亚硝基吡喃半乳糖(GPSNO)、S-亚硝基硫代甘油(TGSNO)和S-亚硝基高半胱氨酸(HCysNO)在50%有效浓度(EC50s)为3 - 46 nM时可使苯肾上腺素(PE)收缩的兔主动脉舒张。虽然硝酸甘油(GTN)在预孵育后表现出体外耐受性,但RSNOs对GTN的交叉耐受性明显较低。在清醒犬中,GSNO、NACysNO和GPSNO(静脉注射1 - 20 mcg/kg/min)在轻度心动过速的情况下,与硝普钠(SNP)相似,可降低平均动脉压和中心静脉压(MAP;CVP)。与GTN相比,GSNO、NACysNO和SNP的降压作用更强,对异山梨醇二硝酸酯(ISDN)交叉耐受性的抵抗力更强。NACysNO在低剂量输注(2.5 mcg/kg/min×4h×3天)时表现出轻度的自身耐受性,并减弱了GTN的降压作用。这些研究表明,在清醒犬中,GSNO和NACysNO是类似SNP的血管扩张剂,它们对ISDN的交叉耐受性低于GTN。此外,RSNOs舒张血管平滑肌似乎独立于一氧化氮(NO)的释放,并且硝酸盐耐受性可能涉及RSNO形成减少或NO释放减少,而不是鸟苷酸环化酶(GC)脱敏。

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