Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo, Buffalo, New York 14214, USA.
J Pharm Sci. 2013 Sep;102(9):3070-81. doi: 10.1002/jps.23550. Epub 2013 May 13.
This review summarizes the major advances that had been reported since the outstanding contributions that Professor Benet and his group had made in the 1980s and 1990s concerning the metabolism and pharmacologic action of organic nitrates (ORNs). Several pivotal studies have now enhanced our understanding of the metabolism and the bioactivation of ORNs, resulting in the identification of a host of cysteine-containing enzymes that can carry out this function. Three isoforms of aldehyde dehydrogenase, all of which with active catalytic cysteine sites, are now known to metabolize, somewhat selectively, various members of the ORN family. The existence of a long-proposed but unstable thionitrate intermediate from ORN metabolism has now been experimentally observed. ORN-induced thiol oxidation in multiple proteins, called the "thionitrate oxidation hypothesis," can be used not only to explain the phenomenon of nitrate tolerance, but also the various consequences of chronic nitrate therapy, namely, rebound vasoconstriction, and increased morbidity and mortality. Thus, a unifying biochemical hypothesis can account for the myriad of pharmacological events resulting from nitrate therapy. Optimization of the future uses of ORN in cardiology and other diseases could benefit from further elaboration of this unifying hypothesis.
这篇综述总结了自 20 世纪 80 年代和 90 年代以来,Benet 教授及其团队在有机硝酸盐(ORN)代谢和药理作用方面的杰出贡献之后,所报道的主要进展。几项关键研究现在增强了我们对 ORN 代谢和生物活化的理解,从而确定了一系列可以发挥此功能的含半胱氨酸的酶。现已发现三种醛脱氢酶同工型,它们都具有活性催化半胱氨酸位点,可选择性地代谢 ORN 家族的各种成员。ORN 代谢中存在先前提出但不稳定的亚硝硫醇中间产物的假设,现在已经通过实验观察到。ORN 诱导的多种蛋白质中的硫醇氧化,称为“亚硝硫醇氧化假说”,不仅可以解释硝酸盐耐受现象,还可以解释慢性硝酸盐治疗的各种后果,即反弹血管收缩,发病率和死亡率增加。因此,一个统一的生化假设可以解释硝酸盐治疗引起的无数药理学事件。进一步阐述这一统一假设可能会使 ORN 在心脏病学和其他疾病中的未来用途得到优化。