Toktam Deylami, M. Sanati, G. Ahangari
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引用次数: 1

摘要

背景:多发性硬化症(MS)是一种慢性中枢神经系统炎症性自身免疫性疾病。全世界有近250万人患有多发性硬化症,女性的发病率是男性的两倍。自身免疫t细胞以中枢神经系统的髓鞘为目标,引起炎症、脱髓鞘并最终破坏神经元。材料和方法:本研究首先采用Ficoll-hypaque法从30名健康对照者和30名MS患者外周血单个核细胞(PBMC)分离。提取总RNA,合成cDNA。结论:根据既往研究5-HT3RA 5-羟色胺受体在MS患者中5-HT3RA神经递质功能及t细胞活化中的重要性以及5-HT3RA受体表达显著升高,血清素水平与MS的关系,可以得出该受体的过表达与MS的进展有显著相关性。另一方面,考虑到单胺氧化酶是神经系统中负责5 -羟色胺氧化的关键酶,可能MS患者体内无法维持该酶的正常水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Discernment of Pathophysiological Aspects of Multiple Sclerosis Based On Mono Amino Oxidase (MAO) and Ion Channel Receptor 5HT3RA as Activator of T-Cells
Background: Multiple sclerosis (MS) is a chronic, inflammatory and autoimmune disease of central nervous system. MS affects nearly 2.5 million people in the world and is twice more common in women than men. Autoimmune T-cells target the myelin sheath in central nervous system, causing inflammation, demyelination and eventual destruction of neurons. We examined changing expression of serotonin receptor (5-HT3RA) as well as monoamine oxidase (MAO-A) genes in peripheral blood mononuclear cells in MS patients. Materials and methods: In this study, peripheral blood mononuclear cells (PBMC) were first isolated from 30 healthy controls and 30 volunteers with MS using Ficoll-hypaque. Total RNA was extracted and cDNA was synthesized. In this process, mRNA concentration of 5-HT3RA and MAO-A as target genes as well as β-actin as reference gene was compared in PBMC of healthy subjects and patients using Real-time PCR. Results: After statistical analysis of resulting data, a significant increase was observed in the expression of 5-HT3RA receptor gene as well as MAO-A gene in PBMC of patients with multiple sclerosis (P=0.001). Conclusion: According to previous studies on the association between serotonin level with MS importance of 5-HT3RA serotonin receptor in the function of this neurotransmitter as well as T-cell activation along with significant increase in the expression of 5-HT3RA receptor in MS patients, it can be concluded that overexpression of this receptor has a significant correlation with MS progress. On the other hand, considering the fact that monoamine oxidase is a key enzyme responsible for oxidation of serotonin in the nervous system, perhaps the body is not capable of maintaining normal level of this enzyme in MS patients. Therefore, considerable increase in MAO level may be responsible for reduced level of serotonin in MS patients, which is a likely reason for depression in these patients.
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