Chakrabarti Mrinmay, Haque Azizul, Banik Naren L, Nagarkatti Prakash, Nagarkatti Mitzi, Ray Swapan K
University of South Carolina School of Medicine, Department of Pathology, Microbiology, and Immunology, Columbia, SC 29209, USA.
Department of Microbiology and Immunology, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC 29425, USA.
Brain Res Bull. 2014 Oct;109:22-31. doi: 10.1016/j.brainresbull.2014.09.004. Epub 2014 Sep 20.
Recent results from laboratory investigations and clinical trials indicate important roles for estrogen receptor (ER) agonists in protecting the central nervous system (CNS) from noxious consequences of neuroinflammation and neurodegeneration. Neurodegenerative processes in several CNS disorders including spinal cord injury (SCI), multiple sclerosis (MS), Parkinson's disease (PD), and Alzheimer's disease (AD) are associated with activation of microglia and astrocytes, which drive the resident neuroinflammatory response. During neurodegenerative processes, activated microglia and astrocytes cause deleterious effects on surrounding neurons. The inhibitory activity of ER agonists on microglia activation might be a beneficial therapeutic option for delaying the onset or progression of neurodegenerative injuries and diseases. Recent studies suggest that ER agonists can provide neuroprotection by modulation of cell survival mechanisms, synaptic reorganization, regenerative responses to axonal injury, and neurogenesis process. The anti-inflammatory and neuroprotective actions of ER agonists are mediated mainly via two ERs known as ERα and ERβ. Although some studies have suggested that ER agonists may be deleterious to some neuronal populations, the potential clinical benefits of ER agonists for augmenting cognitive function may triumph over the associated side effects. Also, understanding the modulatory activities of ER agonists on inflammatory pathways will possibly lead to the development of selective anti-inflammatory molecules with neuroprotective roles in different CNS disorders such as SCI, MS, PD, and AD in humans. Future studies should be concentrated on finding the most plausible molecular pathways for enhancing protective functions of ER agonists in treating neuroinflammatory and neurodegenerative injuries and diseases in the CNS.
实验室研究和临床试验的最新结果表明,雌激素受体(ER)激动剂在保护中枢神经系统(CNS)免受神经炎症和神经退行性变的有害后果方面发挥着重要作用。包括脊髓损伤(SCI)、多发性硬化症(MS)、帕金森病(PD)和阿尔茨海默病(AD)在内的几种中枢神经系统疾病中的神经退行性过程与小胶质细胞和星形胶质细胞的激活有关,这些细胞驱动着局部神经炎症反应。在神经退行性过程中,活化的小胶质细胞和星形胶质细胞会对周围神经元产生有害影响。ER激动剂对小胶质细胞激活的抑制作用可能是延缓神经退行性损伤和疾病发生或进展的有益治疗选择。最近的研究表明ER激动剂可通过调节细胞存活机制、突触重组、对轴突损伤的再生反应和神经发生过程来提供神经保护作用。ER激动剂的抗炎和神经保护作用主要通过两种已知的ER,即ERα和ERβ介导。尽管一些研究表明ER激动剂可能对某些神经元群体有害,但ER激动剂增强认知功能的潜在临床益处可能会超过相关的副作用。此外,了解ER激动剂对炎症途径的调节活性可能会导致开发出在人类SCI、MS、PD和AD等不同中枢神经系统疾病中具有神经保护作用的选择性抗炎分子。未来的研究应集中在寻找最合理的分子途径,以增强ER激动剂在治疗中枢神经系统神经炎症和神经退行性损伤及疾病中的保护功能。