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基质金属蛋白酶-9和NADPH氧化酶在实验性自身免疫性脑脊髓炎小鼠组织和血浆中的表达及激活

Expression and activation of matrix metalloproteinase-9 and NADPH oxidase in tissues and plasma of experimental autoimmune encephalomyelitis in mice.

作者信息

Kandagaddala Lakshmi Devi, Kang Min-Jung, Chung Bong Chul, Patterson Tucker A, Kwon Oh-Seung

机构信息

Toxicology Laboratory, Korea Institute of Science and Technology, Sungbuk-gu, Seoul 136-791, Republic of Korea.

出版信息

Exp Toxicol Pathol. 2012 Jan;64(1-2):109-14. doi: 10.1016/j.etp.2010.07.002. Epub 2010 Aug 31.

Abstract

Experimental autoimmune encephalomyelitis (EAE) is a widely used animal model for multiple sclerosis (MS) that can be induced by immunization with myelin antigens such as myelin oligodendrocyte glycoprotein (MOG). The objective of this study was (i) to investigate how matrix metalloproteinase-9 (MMP-9) and NADPH oxidase enzymes are affected in the EAE mouse model and (ii) to know whether peripheral organs also express these enzymes in the EAE model. MOG(33-55) was administered subcutaneously on two sites over the back. Pertussis toxin was administered intraperitoneally immediately after MOG and again two days later. A significant difference was observed in body weights and clinical signs of EAE-induced mice. MMP-9 and NADPH oxidase enzymes were measured in central nervous system (CNS) tissues, peripheral tissues and plasma of EAE-induced mice. The primary findings include the distribution pattern of MMP-9 in CNS and peripheral tissues, and alterations in the enzymatic expression of MMP-9 and NADPH oxidase in the CNS tissues, spleen and plasma of EAE-induced mice. From these results, it can be considered that the spleen as well as the CNS can act as target organs in EAE disease, and plasma MMP-9 and NADPH oxidase may contribute to the pathogenesis of the disease.

摘要

实验性自身免疫性脑脊髓炎(EAE)是一种广泛应用于多发性硬化症(MS)研究的动物模型,可通过用髓鞘抗原如髓鞘少突胶质细胞糖蛋白(MOG)进行免疫诱导产生。本研究的目的是:(i)探究基质金属蛋白酶-9(MMP-9)和NADPH氧化酶在EAE小鼠模型中的变化情况;(ii)了解在EAE模型中周围器官是否也表达这些酶。将MOG(33-55)皮下注射到背部的两个部位。在注射MOG后立即腹腔注射百日咳毒素,两天后再注射一次。在EAE诱导小鼠的体重和临床症状方面观察到显著差异。对EAE诱导小鼠的中枢神经系统(CNS)组织、外周组织和血浆中的MMP-9和NADPH氧化酶进行了检测。主要发现包括MMP-9在CNS和外周组织中的分布模式,以及EAE诱导小鼠的CNS组织、脾脏和血浆中MMP-9和NADPH氧化酶的酶表达变化。从这些结果可以认为,脾脏以及CNS在EAE疾病中可作为靶器官,血浆中的MMP-9和NADPH氧化酶可能参与了该疾病的发病机制。

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