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肿瘤坏死因子-α 中和通过抑制短暂性局灶性脑缺血后基质金属蛋白酶的产生减轻脑水肿。

Tumor necrosis factor-alpha neutralization reduced cerebral edema through inhibition of matrix metalloproteinase production after transient focal cerebral ischemia.

作者信息

Hosomi Naohisa, Ban Camelia R, Naya Takayuki, Takahashi Tsutomu, Guo Peng, Song Xiao-yu R, Kohno Masakazu

机构信息

Second Department of Internal Medicine, Division of Stroke, Kagawa University School of Medicine, Ikenobe, Miki-cho, Kagawa, Japan.

出版信息

J Cereb Blood Flow Metab. 2005 Aug;25(8):959-67. doi: 10.1038/sj.jcbfm.9600086.

Abstract

After focal cerebral ischemia, tumor necrosis factor-alpha deteriorates cerebral edema and survival rate. Therefore, tumor necrosis factor-alpha neutralization could reduce cerebral microvascular permeability in acute cerebral ischemia. Left middle cerebral artery occlusion for 120 mins followed by reperfusion was performed with the thread method under halothane anesthesia in Sprague-Dawley rats. Antirat tumor necrosis factor-alpha neutralizing monoclonal antibody with a rat IgG Fc portion (15 mg/kg) was infused intravenously right after reperfusion. Stroke index score, infarct volume, cerebral specific gravity, and the endogenous expression of tumor necrosis factor-alpha, matrix metalloproteinase (MMP)-2, MMP-9, and membrane type 1-MMP in the brain tissue were quantified in the ischemic and matched contralateral nonischemic hemisphere. In the antitumor necrosis factor-alpha neutralizing antibody-treated rats, infarct volume was significantly reduced (P=0.014, n=7; respectively), and cerebral specific gravity was dramatically increased in the cortex and caudate putamen (P<0.001, n=7; respectively) in association with a reduction in MMP-9 and membrane type 1-MMP upregulation. Tumor necrosis factor-alpha in the brain tissue was significantly elevated in the ischemic hemisphere 6 h after reperfusion in the nonspecific IgG-treated rats (P=0.021, n=7) and was decreased in the antitumor necrosis factor-alpha neutralizing antibody-treated rats (P=0.001, n=7). Postreperfusion treatment with antirat tumor necrosis factor-alpha neutralizing antibody reduced brain infarct volume and cerebral edema, which is likely mediated by a reduction in MMP upregulation.

摘要

局灶性脑缺血后,肿瘤坏死因子-α会使脑水肿加重并降低存活率。因此,中和肿瘤坏死因子-α可降低急性脑缺血时脑微血管的通透性。在氟烷麻醉下,采用线栓法对Sprague-Dawley大鼠进行大脑中动脉闭塞120分钟后再灌注。再灌注后立即静脉注射含大鼠IgG Fc段的抗大鼠肿瘤坏死因子-α中和单克隆抗体(15毫克/千克)。对缺血半球和与之匹配的对侧非缺血半球脑组织中的卒中指数评分、梗死体积、脑比重以及肿瘤坏死因子-α、基质金属蛋白酶(MMP)-2、MMP-9和膜型1-MMP的内源性表达进行定量分析。在接受抗肿瘤坏死因子-α中和抗体治疗的大鼠中,梗死体积显著减小(P = 0.014,n = 7;分别表示),皮质和尾状核的脑比重显著增加(P < 0.001,n = 7;分别表示),同时MMP-9和膜型1-MMP的上调也有所减少。在非特异性IgG治疗的大鼠中,再灌注6小时后缺血半球脑组织中的肿瘤坏死因子-α显著升高(P = 0.021,n = 7),而在接受抗肿瘤坏死因子-α中和抗体治疗的大鼠中则降低(P = 0.001,n = 7)。抗大鼠肿瘤坏死因子-α中和抗体再灌注后治疗可减少脑梗死体积和脑水肿,这可能是通过减少MMP上调来介导的。

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