Vallianou Natalia, Evangelopoulos Angelos, Koutalas Pavlos
Department of Internal Medicine, Polykliniki General Hospital, 3 Pireos Str., 10552 Athens, Greece.
Rev Diabet Stud. 2009 Winter;6(4):230-6. doi: 10.1900/RDS.2009.6.230. Epub 2009 Dec 30.
Diabetic neuropathy presents a major public health problem. It is defined by the symptoms and signs of peripheral nerve dysfunction in diabetic patients, in whom other causes of neuropathy have been excluded. Pathogenetic mechanisms that have been implicated in diabetic neuropathy are: a) increased flux through the polyol pathway, leading to accumulation of sorbitol, a reduction in myo-inositol, and an associated reduced Na+-K+-ATPase activity, and b) endoneurial microvascular damage and hypoxia due to nitric oxide inactivation by increased oxygen free radical activity. Alpha-lipoic acid seems to delay or reverse peripheral diabetic neuropathy through its multiple antioxidant properties. Treatment with alpha-lipoic acid increases reduced glutathione, an important endogenous antioxidant. In clinical trials, 600 mg alpha-lipoic acid has been shown to improve neuropathic deficits. This review focuses on the relationship of alpha-lipoic acid and auto-oxidative glycosylation. It discusses the impact of alpha-lipoic acid on hyperglycemia-induced oxidative stress, and examines the role of alpha-lipoic acid in preventing glycation process and nerve hypoxia.
糖尿病神经病变是一个重大的公共卫生问题。它由糖尿病患者外周神经功能障碍的症状和体征所定义,且已排除其他导致神经病变的原因。与糖尿病神经病变相关的发病机制有:a)多元醇途径通量增加,导致山梨醇蓄积、肌醇减少以及相关的钠钾ATP酶活性降低;b)由于氧自由基活性增加使一氧化氮失活,导致神经内膜微血管损伤和缺氧。α-硫辛酸似乎通过其多种抗氧化特性延缓或逆转糖尿病外周神经病变。α-硫辛酸治疗可增加还原型谷胱甘肽,这是一种重要的内源性抗氧化剂。在临床试验中,已证明600毫克α-硫辛酸可改善神经病变缺陷。本综述重点关注α-硫辛酸与自身氧化糖基化的关系。它讨论了α-硫辛酸对高血糖诱导的氧化应激的影响,并研究了α-硫辛酸在预防糖基化过程和神经缺氧中的作用。