Singh Randhir, Kishore Lalit, Kaur Navpreet
M.M. College of Pharmacy, Maharishi Markandeshwar University, Mullana-Ambala, Haryana 133207, India.
M.M. College of Pharmacy, Maharishi Markandeshwar University, Mullana-Ambala, Haryana 133207, India.
Pharmacol Res. 2014 Feb;80:21-35. doi: 10.1016/j.phrs.2013.12.005. Epub 2013 Dec 25.
Diabetic neuropathy is a heterogeneous group of disorders with extremely complex pathophysiology and affects both somatic and autonomic components of the nervous system. Neuropathy is the most common chronic complication of diabetes mellitus. Metabolic disruptions in the peripheral nervous system, including altered protein kinase C activity, and increased polyol pathway activity in neurons and Schwann cells resulting from hyperglycemia plays a key role in the development of diabetic neuropathy. These pathways are related to the metabolic and/or redox state of the cell and are the major source of damage. Activation of these metabolic pathways leads to oxidative stress, which is a mediator of hyperglycemia induced cell injury and a unifying theme for all mechanisms of diabetic neuropathy. The therapeutic intervention of these metabolic pathways is capable of ameliorating diabetic neuropathy but therapeutics which target one particular mechanism may have a limited success. Available therapeutic approaches are based upon the agents that modulate pathogenetic mechanisms (glycemic control) and relieve the symptoms of diabetic neuropathy. This review emphasizes the pathogenesis, presently available therapeutic approaches and future directions for the management of diabetic neuropathy.
糖尿病性神经病变是一组病理生理学极其复杂的异质性疾病,会影响神经系统的躯体和自主神经成分。神经病变是糖尿病最常见的慢性并发症。外周神经系统的代谢紊乱,包括蛋白激酶C活性改变,以及高血糖导致神经元和施万细胞中多元醇途径活性增加,在糖尿病性神经病变的发展中起关键作用。这些途径与细胞的代谢和/或氧化还原状态相关,是损伤的主要来源。这些代谢途径的激活会导致氧化应激,氧化应激是高血糖诱导细胞损伤的介质,也是糖尿病性神经病变所有机制的共同主题。对这些代谢途径的治疗性干预能够改善糖尿病性神经病变,但针对某一特定机制的治疗可能效果有限。现有的治疗方法基于调节致病机制(血糖控制)和缓解糖尿病性神经病变症状的药物。本综述着重阐述糖尿病性神经病变的发病机制、目前可用的治疗方法以及未来的治疗方向。