Effect of stress on brain inflammation and multiple sclerosis

被引:106
作者
Karagkouni, Anna [1 ]
Alevizos, Michail [1 ]
Theoharides, Theoharis C. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Tufts Univ, Sch Med, Dept Mol Physiol & Pharmacol, Mol Immunopharmacol & Drug Discovery Lab, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Dept Biochem, Boston, MA 02111 USA
[3] Tufts Univ, Sch Med, Dept Internal Med, Boston, MA 02111 USA
[4] Tufts Med Ctr, Boston, MA USA
[5] Tufts Univ, Sch Med, Dept Psychiat, Boston, MA 02111 USA
关键词
Blood-brain barrier; Corticotropin-releasing hormone; Flavonoids; Neurotensin; Neuropeptides; Inflammation; Microglia; Mast cells; Multiple sclerosis; Stress; CORTICOTROPIN-RELEASING HORMONE; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; PITUITARY-ADRENAL AXIS; MYELIN BASIC-PROTEIN; HUMAN MAST-CELLS; THEILERS VIRUS-INFECTION; CENTRAL-NERVOUS-SYSTEM; LIFE EVENTS; RESTRAINT STRESS;
D O I
10.1016/j.autrev.2013.02.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Substantial evidence indicates that stress can precipitate or worsen symptoms of inflammation in general and more specifically in multiple sclerosis (MS), a demyelinating, autoimmune disease characterized by inflammation of the central nervous system (CNS). However, the mechanism of how stress affects MS is not well understood. We reviewed publications in PubMed since 1995 and propose that neuropeptides secreted under stress, such as corticotropin releasing hormone (CRH) and neurotensin (NT), activate microglia and mast cells to release inflammatory molecules. These lead to maturation and activation of T17 autoimmune cells, disruption of the blood-brain barrier (BBB) and T cell entry into the CNS, thus promoting brain inflammation and contributing to MS pathology. Reduction of stress and inhibition of these processes by select flavonoids could provide novel therapeutic approaches. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:947 / 953
页数:7
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