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米诺环素治疗减轻兴奋性纹状体损伤后的白质损伤。

Minocycline treatment reduces white matter damage after excitotoxic striatal injury.

机构信息

Edmond and Lily Safra International Institute of Neuroscience of Natal, Natal/RN, Brazil.

出版信息

Brain Res. 2010 May 6;1329:182-93. doi: 10.1016/j.brainres.2010.03.007. Epub 2010 Mar 11.

Abstract

We investigated the protective effects of minocycline following white matter damage (WMD) in the rat striatum. Excitotoxic lesions were induced by N-Methyl-d-Aspartate (NMDA) microinjections and caused striatal damage, concomitant with microglial/macrophage activation. The excitotoxic lesion both damaged oligodendrocytes (Tau-1(+) cells) and caused a decrease in tissue reactivity for myelin basic protein (MBP) after post-lesional day 3 (PLD). Treatment with the semi-synthetic tetracycline antibiotic minocycline, however, led to oligodendrocyte preservation and decreased myelin impairment. Taken together, these results suggest that white matter damage (WMD) is an important component of the physiopathology of acute striatal damage and that microglial/macrophage activation contributes to this pathological phenomenon.

摘要

我们研究了米诺环素在大鼠纹状体白质损伤(WMD)后的保护作用。通过 N-甲基-D-天冬氨酸(NMDA)微注射诱导兴奋性毒性损伤,导致纹状体损伤,同时伴有小胶质细胞/巨噬细胞激活。兴奋性损伤不仅损伤少突胶质细胞(Tau-1(+)细胞),而且在损伤后第 3 天(PLD)后导致髓鞘碱性蛋白(MBP)的组织反应性降低。然而,用半合成四环素抗生素米诺环素治疗可导致少突胶质细胞保存和减少髓鞘损伤。总之,这些结果表明,白质损伤(WMD)是急性纹状体损伤病理生理学的一个重要组成部分,小胶质细胞/巨噬细胞的激活有助于这一病理现象。

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