Importance of Apolipoprotein A-I in Multiple Sclerosis

被引:21
作者
Gardner, Lidia A. [1 ,2 ]
Levin, Michael C. [1 ,2 ,3 ]
机构
[1] VA Med Ctr, Res Serv, Memphis, TN 38104 USA
[2] Univ Tennessee, Hlth Sci Ctr, Dept Neurol, Memphis, TN USA
[3] Univ Tennessee, Hlth Sci Ctr, Neurosci Inst, Memphis, TN USA
关键词
HDL; ApoA-I; multiple sclerosis; CNS; ATP- binding cassette transporter A1; sphingosine; 1; phosphate; FTY720; (fingolimod; Gilenya); HIGH-DENSITY-LIPOPROTEIN; SCAVENGER RECEPTOR BI; PPAR-GAMMA AGONISTS; CHOLESTEROL HOMEOSTASIS; ALZHEIMERS-DISEASE; ORAL FINGOLIMOD; SR-BI; INTRAMUSCULAR INTERFERON; CEREBROSPINAL-FLUID; FTY720; FINGOLIMOD;
D O I
10.3389/fphar.2015.00278
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Jean-Martin Charcot has first described multiple sclerosis (MS) as a disease of the central nervous system (CNS) over a century ago. MS remains incurable today, and treatment options are limited to disease modifying drugs. Over the years, significant advances in understanding disease pathology have been made in autoimmune and neurodegenerative components. Despite the fact that brain is the most lipid rich organ in human body, the importance of lipid metabolism has not been extensively studied in this disorder. In MS, the CNS is under attack by a person's own immune system. Autoantigens and autoantibodies are known to cause devastation of myelin through up regulation of T-cells and cytokines, which penetrate through the blood-brain barrier to cause inflammation and myelin destruction. The anti-inflammatory role of high-density lipoproteins (HDLs) has been implicated in a plethora of biological processes: vasodilation, immunity to infection, oxidation, inflammation, and apoptosis. However, it is not known what role HDL plays in neurological function and myelin repair in MS. Understanding of lipid metabolism in the CNS and in the periphery might unveil new therapeutic targets and explain the partial success of some existing MS therapies.
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页数:8
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