Gilgun-Sherki Yossi, Melamed Eldad, Offen Daniel
Laboratory of Neuroscience, Felsenstein Medical Research Center and Department of Neurology, Rabin Medical Center- Beilinson Campus, The Sackler School of Medicine, Tel Aviv University, Petach Tikva 49100, Israel.
Curr Pharm Des. 2006;12(27):3509-19. doi: 10.2174/138161206778343091.
Increasing evidence indicates that inflammation is involved in the pathogenesis of many neurological, particularly neurodegenerative diseases. Even if inflammation is not a primary causative process, its presence may contribute to the continued loss of CNS neurons. Therefore, it seems reasonable to propose that use of anti-inflammatory drugs might diminish the cumulative effects of inflammation in the brain. Indeed, some epidemiological studies performed to date, especially in Alzheimer's disease, suggests that sustained use of anti-inflammatory drugs (AIDs) may prevent or slow down the progression of neurodegenerative diseases. However, small number of clinical trials carried out so far using AIDs, were minimal and equivocal in their outcome. Potential reasons for these mixed results include timing of AIDs administration, nonselective inhibition of cyclooxygenase (COX), inappropriate use of particular anti-inflammatory drugs for a given disease or disease progression/ severity, sub-optimal dose in target site, or limited penetration to the brain through the blood-brain barrier (BBB). Therefore, design of AIDs for the treatment of neurodegenerative diseases based upon better BBB penetration, and with minimal adverse events, would be appropriate. In addition, relevant genetic differences among patients should be considered planning new AIDs, for improved efficacy. Furthermore, due to the possible co-involvement of oxidative stress and excitotoxicity in the pathogenesis of these diseases, combination therapy with antioxidants or glutamate antagonists or a multi-potent drug might be much more effective in successfully treating neurodegenerative diseases.
越来越多的证据表明,炎症参与了许多神经疾病尤其是神经退行性疾病的发病机制。即使炎症不是主要的致病过程,其存在也可能导致中枢神经系统神经元的持续丧失。因此,提出使用抗炎药物可能会减轻大脑炎症的累积影响似乎是合理的。事实上,迄今为止进行的一些流行病学研究,尤其是在阿尔茨海默病方面的研究表明,持续使用抗炎药物(AIDs)可能预防或减缓神经退行性疾病的进展。然而,迄今为止使用AIDs进行的少数临床试验,其结果微乎其微且模棱两可。这些混合结果的潜在原因包括AIDs给药的时机、环氧化酶(COX)的非选择性抑制、针对特定疾病或疾病进展/严重程度使用不适当的抗炎药物、靶部位剂量不足,或通过血脑屏障(BBB)进入大脑的渗透性有限。因此,设计基于更好的BBB渗透性且不良事件最少的用于治疗神经退行性疾病的AIDs是合适的。此外,在规划新的AIDs时应考虑患者之间相关的基因差异,以提高疗效。此外,由于氧化应激和兴奋性毒性可能共同参与这些疾病的发病机制,联合使用抗氧化剂或谷氨酸拮抗剂或一种多效药物在成功治疗神经退行性疾病方面可能会更有效。