Miller Mark R, Wadsworth Roger M
Department of Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Br J Pharmacol. 2009 Jun;157(4):565-7. doi: 10.1111/j.1476-5381.2009.00193.x.
The organic nitrate drugs, such as glyceryl trinitrate (GTN; nitroglycerin), are clinically effective in angina because of their dilator profile in veins and arteries. The exact mechanism of intracellular delivery of nitric oxide (NO), or another NO-containing species, from these compounds is not understood. However, mitochondrial aldehyde dehydrogenase (mtALDH) has recently been identified as an organic nitrate bioactivation enzyme. Nitrate tolerance, the loss of effect of organic nitrates over time, is caused by reduced bioactivation and/or generation of NO-scavenging oxygen-free radicals. In a recent issue of the British Journal of Pharmacology, Wenzl et al. show that guinea-pigs, deficient in ascorbate, also have impaired responsiveness to GTN, but nitrate tolerance was not due to ascorbate deficiency that exhibited divergent changes in mtALDH activity. Thus, the complex function of mtALDH appears to be the key to activation of GTN, the active NO species formed and the induction of tolerance that can limit clinical effectiveness of organic nitrate drugs.
有机硝酸盐药物,如三硝酸甘油酯(GTN;硝酸甘油),因其在静脉和动脉中的扩张特性而在临床上对心绞痛有效。目前尚不清楚这些化合物中一氧化氮(NO)或其他含NO物质的细胞内传递的确切机制。然而,线粒体醛脱氢酶(mtALDH)最近已被确定为一种有机硝酸盐生物活化酶。硝酸盐耐受性,即有机硝酸盐的效果随时间丧失,是由生物活化降低和/或NO清除性氧自由基的产生所致。在最近一期的《英国药理学期刊》中,温兹尔等人表明,缺乏抗坏血酸的豚鼠对GTN的反应性也受损,但硝酸盐耐受性并非由于抗坏血酸缺乏,抗坏血酸缺乏表现为mtALDH活性的不同变化。因此,mtALDH的复杂功能似乎是GTN激活、形成活性NO物质以及诱导耐受性的关键,而耐受性会限制有机硝酸盐药物的临床疗效。