Schmeer Christian, Kretz Alexandra, Isenmann Stefan
Department of Neurology, Neuroregeneration Laboratory, University of Jena Medical School, Jena, Germany.
CNS Neurol Disord Drug Targets. 2007 Aug;6(4):282-7. doi: 10.2174/187152707781387260.
3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, generically termed statins, are widely prescribed for their cholesterol-lowering properties. In addition to lipid-lowering properties, statins have pleiotropic effects including anti-inflammatory, anti-apoptotic, and antiproliferative effects. Recently, data from experimental and observational studies have indicated that statins could also become a treatment option for diseases of the central nervous system (CNS). Many neurodegenerative diseases particularly affect the retina and other ocular structures and are the cause for blindness. This review, focused on recent clinical and experimental data, discusses known and putative mechanisms of statin actions underlying neuroprotective effects in relevant retinal and eye diseases. In addition, it presents evidence for the role of heat shock proteins (Hsps) as target of statin-mediated neuroprotective effects in ocular diseases.
3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂,通常称为他汀类药物,因其降胆固醇特性而被广泛处方。除了降脂特性外,他汀类药物还具有多效性作用,包括抗炎、抗凋亡和抗增殖作用。最近,实验和观察性研究的数据表明,他汀类药物也可能成为中枢神经系统(CNS)疾病的一种治疗选择。许多神经退行性疾病特别影响视网膜和其他眼部结构,是导致失明的原因。本综述聚焦于近期的临床和实验数据,讨论了他汀类药物在相关视网膜和眼部疾病中发挥神经保护作用的已知和推测机制。此外,还提供了热休克蛋白(Hsps)作为他汀类药物介导的眼部疾病神经保护作用靶点的证据。