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二乙胺/一氧化氮(DEA/NO)复合物与S-亚硝基-N-乙酰青霉胺(SNAP)在体内的静脉与动脉作用

Venous versus arterial actions of diethylamine/nitric oxide (DEA/NO) complex and S-nitroso-N-acetylpenicillamine (SNAP) in vivo.

作者信息

Ng S S, Pang C C

机构信息

Department of Pharmacology and Therapeutics, Faculty of Medicine, The University of British Columbia, Vancouver, Canada.

出版信息

Br J Pharmacol. 1998 Nov;125(6):1247-51. doi: 10.1038/sj.bjp.0702175.

Abstract

We studied the effects of diethylamine/NO complex (DEA/NO) and S-nitroso-N-acetylpenicillamine (SNAP), relative to those of sodium nitroprusside (SNP) and nitroglycerin (NTG), on mean arterial pressure (MAP), mean circulatory filling pressure (MCFP), arterial resistance (Ra), venous resistance (Rv), heart rate (HR), cardiac output (CO) and stroke volume (SV) in groups of Inactin-anaesthetized rats pre-treated with i.v. mecamylamine (3.7 micromol kg(-1)) and noradrenaline (6.8 nmol kg(-1) min(-1)). Doses of each that reduced MAP by 30%, 80% and the lowest dose that maximally reduced MAP were examined to allow a comparison of the compounds' dilator actions at equivalent effective depressor doses. DEA/NO (4, 32 and 256 microg kg(-1) min(-1)), SNAP (4, 32 and 256 microg kg(-1) min(-1)) and SNP (8, 32 and 128 microg kg(-1) min(-1)) caused similar dose-dependent reductions in MAP and Ra, and increases in CO and SV. NTG (0.2, 0.8 and 6.4 microg kg(-1) min(-1)) dose-dependently reduced Ra, and increased CO and SV, but lowered MAP only at the highest dose. DEA/NO, SNAP and SNP but not NTG lowered MCFP with efficacy: DEA/NO > SNAP > SNP. All four drugs reduced Rv with efficacy: DEA/NO approximately equal to SNAP > SNP approximately equal to NTG. Therefore, all compounds lowered Ra and Rv. DEA/NO, SNAP and SNP but not NTG reduced MCFP. The pharmacological profiles of DEA/NO and SNAP resemble SNP more than NTG.

摘要

我们研究了二乙胺/一氧化氮复合物(DEA/NO)和S-亚硝基-N-乙酰青霉胺(SNAP)相对于硝普钠(SNP)和硝酸甘油(NTG),对预先经静脉注射美加明(3.7微摩尔/千克)和去甲肾上腺素(6.8纳摩尔/千克·分钟)处理的Inactin麻醉大鼠组的平均动脉压(MAP)、平均循环充盈压(MCFP)、动脉阻力(Ra)、静脉阻力(Rv)、心率(HR)、心输出量(CO)和每搏输出量(SV)的影响。研究了每种药物使MAP降低30%、80%时的剂量以及最大程度降低MAP的最低剂量,以便在等效有效降压剂量下比较这些化合物的扩张血管作用。DEA/NO(4、32和256微克/千克·分钟)、SNAP(4、32和256微克/千克·分钟)和SNP(8、32和128微克/千克·分钟)引起MAP和Ra类似的剂量依赖性降低,以及CO和SV增加。NTG(0.2、0.8和6.4微克/千克·分钟)剂量依赖性降低Ra,增加CO和SV,但仅在最高剂量时降低MAP。DEA/NO、SNAP和SNP而非NTG降低MCFP,其效能为:DEA/NO > SNAP > SNP。所有四种药物降低Rv的效能为:DEA/NO约等于SNAP > SNP约等于NTG。因此,所有化合物均降低Ra和Rv。DEA/NO、SNAP和SNP而非NTG降低MCFP。DEA/NO和SNAP的药理学特征与SNP更相似,而非NTG。

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