Institute of Cardiovascular Sciences, St. Boniface Hospital Research, Faculty of Medicine, Department of Physiology, University of Manitoba, Winnipeg, Manitoba, R2H 2A6 Canada.
Clin Chem Lab Med. 2013 Mar 1;51(3):535-43. doi: 10.1515/cclm-2012-0553.
Although vitamin B6 and its metabolite, pyridoxal 5'-phosphate (PLP), have been shown to exert beneficial effects in ischemic heart disease, the mechanisms of their action are not fully understood. Some studies have shown that ventricular arrhythmias and mortality upon the occlusion of coronary artery were attenuated by pretreatment of animals with PLP. Furthermore, ischemia-reperfusion-induced abnormalities in cardiac performance and defects in sarcoplasmic reticular Ca2+-transport activities were decreased by PLP. The increase in cardiac contractile activity of isolated heart by ATP was reduced by PLP, unlike propranolol, whereas that by isoproterenol was not depressed by PLP. ATP-induced increase in [Ca2+]i, unlike KCl-induced increase in [Ca2+]i in cardiomyocytes was depressed by PLP. Both high- and low-affinity sites for ATP binding in sarcolemmal membranes were also decreased by PLP. These observations support the view that PLP may produce cardioprotective effects in ischemic heart disease by attenuating the occurrence of intracellular Ca2+ overload due to the blockade of purinergic receptors.
虽然维生素 B6 及其代谢物 5′-磷酸吡哆醛(PLP)已被证明对缺血性心脏病具有有益作用,但它们的作用机制尚不完全清楚。一些研究表明,PLP 预处理可减轻动物冠状动脉闭塞后的室性心律失常和死亡率。此外,PLP 可降低缺血再灌注引起的心脏功能异常和肌浆网 Ca2+转运活性缺陷。与普萘洛尔不同,PLP 降低了分离心脏中由 ATP 引起的收缩活性增加,但不降低由异丙肾上腺素引起的增加。与 KCl 诱导的心肌细胞内 [Ca2+]i 增加不同,PLP 降低了由 ATP 诱导的 [Ca2+]i 增加。PLP 还降低了肌浆膜上高亲和和低亲和 ATP 结合位点。这些观察结果支持这样一种观点,即 PLP 通过阻断嘌呤能受体来减轻由于细胞内 Ca2+超载而引起的心肌缺血性心脏病的发生,从而产生心脏保护作用。