Neuroprotective and anti-inflammatory effects of estrogen receptor ligand treatment in mice

[摘要] Demyelination and neurodegeneration is a major contributor in the progression of disability in multiple sclerosis (MS). Thus, the development of therapies that are neuroprotective has elicited considerable interests. Estrogens and estrogen receptor (ER) ligand treatments are promising treatments to prevent MS-induced neurodegeneration and a multicenter phase II clinical trial of estriol as a beneficial therapy in MS is underway. Here, we discuss studies performed in Our laboratory that examined the effects of ER ligands in the inflammatory/demyelinating disorder experimental autoimmune encephalomyelitis (EAE), a model of MS. Administration of estriol or 17 beta-estradiol reduced clinical severity and this clinical disease improvement was associated with favorable changes in cytokine production. There was a significant decrease of neuronal pathology in gray matter along with myelin and axon preservation in white matter of spinal cords of mice with EAE. In subsequent experiments, we contrasted the results of ER alpha versus ER beta ligand treatment. While ER alpha ligand treatment was anti-inflammatory, ER beta ligand treatment was not. ER beta ligand treatment nevertheless reduced demyelination and preserved axon numbers in white matter and prevented neuronal abnormalities in gray matter. Clinically, ER alpha ligand treatment abrogated the disease at the onset, while ER beta ligand treatment had no effect at disease onset, but promoted recovery. Thus, unlike ER alpha ligand treatment, ER beta ligand treatment was protective at the level of the target organ, independent of anti-inflammatory effects in the peripheral immune system. ER beta ligand treatment should be considered as a potential neuroprotective agent for MS and other neurodegenerative diseases, particularly since breast and uterine cancer are mediated through ER alpha. Published by Elsevier B.V.

[发布日期] 2009-11-15

[效力级别]  Proceedings Paper

[关键词] Estrogen receptor ligands;Anti-inflammation;Neuroprotection;EAE