Wang Ellen Q, Lee Woo-In, Brazeau Daniel, Fung Ho-Leung
Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, SUNY, Buffalo, NY 14260-1200, USA.
AAPS PharmSci. 2002;4(2):E10. doi: 10.1208/ps040210.
Vascular nitrate tolerance is often accompanied by changes in the activity and/or expression of a number of proteins. However, it is not known whether these changes are associated with the vasodilatory properties of nitrates, or with their tolerance mechanisms. We examined the hemodynamic effects and vascular gene expressions of 2 nitric oxide (NO) donors: nitroglycerin (NTG) and S-nitroso-N-acetylpenicillamine (SNAP). Rats received 10 microg/min NTG, SNAP, or vehicle infusion for 8 hours. Hemodynamic tolerance was monitored by the maximal mean arterial pressure (MAP) response to a 30-microg NTG or SNAP bolus challenge dose (CD) at various times during infusion. Gene expression in rat aorta after NTG or SNAP treatment was determined using cDNA microarrays, and the relative differences in expression after drug treatment were evaluated using several statistical techniques. MAP response of the NTG CD was attenuated from the first hour of NTG infusion (P <.001, analysis of variance [ANOVA]), but not after SNAP (P >.05, ANOVA) or control infusion (P >.05, ANOVA). Student t-statistics revealed that 447 rat genes in the aorta were significantly altered by NTG treatment (P <.05). An adjusted t-statistic approach using resampling techniques identified a subset of 290 genes that remained significantly different between NTG treatment vs control. In contrast, SNAP treatment resulted in the up-regulation of only 7 genes and the down-regulation of 34 genes. These results indicate that continuous NTG infusion induced widespread changes in vascular gene expression, many of which are consistent with the multifactorial and complex mechanisms reported for nitrate tolerance.
血管性硝酸酯耐受性常伴有多种蛋白质活性和/或表达的变化。然而,尚不清楚这些变化是与硝酸酯的血管舒张特性相关,还是与它们的耐受机制相关。我们研究了两种一氧化氮(NO)供体:硝酸甘油(NTG)和S-亚硝基-N-乙酰青霉胺(SNAP)的血流动力学效应和血管基因表达。大鼠接受10微克/分钟的NTG、SNAP或溶媒输注8小时。在输注期间的不同时间,通过对30微克NTG或SNAP推注挑战剂量(CD)的最大平均动脉压(MAP)反应来监测血流动力学耐受性。使用cDNA微阵列测定NTG或SNAP处理后大鼠主动脉中的基因表达,并使用多种统计技术评估药物处理后表达的相对差异。NTG CD的MAP反应从NTG输注的第一小时开始减弱(方差分析[ANOVA],P<.001),但SNAP输注后(ANOVA,P>.05)或对照输注后(ANOVA,P>.05)未减弱。学生t检验显示,NTG处理使主动脉中的447个大鼠基因发生显著改变(P<.05)。使用重采样技术的调整t统计方法确定了290个基因的子集,这些基因在NTG处理与对照之间仍存在显著差异。相比之下,SNAP处理仅导致7个基因上调和34个基因下调。这些结果表明,持续输注NTG会引起血管基因表达的广泛变化,其中许多变化与报道的硝酸酯耐受性的多因素和复杂机制一致。