Wang Zhong-Yu, Liu Ying-Yi, Liu Guo-Hui, Lu Hai-Bin, Mao Cui-Ying
Department of Cardiology, China-Japan Union Hospital, Jilin University, Changchun, PR China.
Department of Anesthesia, China-Japan Union Hospital, Jilin University, Changchun, PR China.
Life Sci. 2018 Feb 1;194:88-97. doi: 10.1016/j.lfs.2017.12.015. Epub 2017 Dec 11.
Cardiovascular disease (CVD) is a key cause of deaths worldwide, comprising 15-17% of healthcare expenditure in developed countries. Current records estimate an annual global average of 30 million cardiac dysfunction cases, with a predicted escalation by two-three folds for the next 20-30years. Although β-blockers and angiotensin-converting-enzymes are commonly prescribed to control CVD risk, hepatotoxicity and hematological changes are frequent adverse events associated with these drugs. Search for alternatives identified endogenous cofactor l-carnitine, which is capable of promoting mitochondrial β-oxidation towards a balanced cardiac energy metabolism. l-Carnitine facilitates transport of long-chain fatty acids into the mitochondrial matrix, triggering cardioprotective effects through reduced oxidative stress, inflammation and necrosis of cardiac myocytes. Additionally, l-carnitine regulates calcium influx, endothelial integrity, intracellular enzyme release and membrane phospholipid content for sustained cellular homeostasis. Carnitine depletion, characterized by reduced expression of "organic cation transporter-2" gene, is a metabolic and autosomal recessive disorder that also frequently associates with CVD. Hence, exogenous carnitine administration through dietary and intravenous routes serves as a suitable protective strategy against ventricular dysfunction, ischemia-reperfusion injury, cardiac arrhythmia and toxic myocardial injury that prominently mark CVD. Additionally, carnitine reduces hypertension, hyperlipidemia, diabetic ketoacidosis, hyperglycemia, insulin-dependent diabetes mellitus, insulin resistance, obesity, etc. that enhance cardiovascular pathology. These favorable effects of l-carnitine have been evident in infants, juvenile, young, adult and aged patients of sudden and chronic heart failure as well. This review describes the mechanism of action, metabolism and pharmacokinetics of l-carnitine. It specifically emphasizes upon the beneficial role of l-carnitine in cardiomyopathy.
心血管疾病(CVD)是全球死亡的主要原因,在发达国家占医疗保健支出的15 - 17%。目前的记录估计全球每年平均有3000万例心脏功能障碍病例,预计在未来20 - 30年将增加两到三倍。尽管β受体阻滞剂和血管紧张素转换酶常用于控制心血管疾病风险,但肝毒性和血液学变化是与这些药物相关的常见不良事件。寻找替代药物发现了内源性辅因子左旋肉碱,它能够促进线粒体β氧化,实现心脏能量代谢的平衡。左旋肉碱促进长链脂肪酸进入线粒体基质,通过减少心肌细胞的氧化应激、炎症和坏死发挥心脏保护作用。此外,左旋肉碱调节钙内流、内皮完整性、细胞内酶释放和膜磷脂含量,以维持细胞内环境稳定。肉碱缺乏症以“有机阳离子转运体-2”基因表达降低为特征,是一种代谢性常染色体隐性疾病,也常与心血管疾病相关。因此,通过饮食和静脉途径给予外源性肉碱是一种合适的保护策略,可预防心室功能障碍、缺血再灌注损伤、心律失常和中毒性心肌损伤,这些都是心血管疾病的显著特征。此外,肉碱还能降低高血压、高脂血症、糖尿病酮症酸中毒、高血糖、胰岛素依赖型糖尿病、胰岛素抵抗、肥胖等加重心血管病理的因素。左旋肉碱的这些有益作用在婴儿、青少年、青年、成年和老年的急性和慢性心力衰竭患者中也很明显。本综述描述了左旋肉碱的作用机制、代谢和药代动力学。它特别强调了左旋肉碱在心肌病中的有益作用。