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Pyruvate blocks blood-brain barrier disruption lymphocyte infiltration and immune response in excitotoxic brain injury

机译:丙酮酸阻断兴奋性中毒性脑损伤中的血脑屏障破坏淋巴细胞浸润和免疫反应

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摘要

The effects of pyruvate, the end metabolite of glycolysis, on blood-brain barrier (BBB) impairment and immune reactivity were examined in the quinolinic acid (QA)-injected rat striatum. Extensive disruption of BBB was observed at 7 d post QA-injection as demonstrated by increased immunohistochemical staining using antibody against immunoglobulin G (IgG). Animals receiving pyruvate administration (500 mg/kg) with QA-injection exhibited reduced lgG immunoreactivity (by 45%) relative to QA alone. QA intrastriatal injection also resulted in marked increases in the number of infiltrating T-lymphocytes (by 70-fold) and expression of major histocompatibility complex (MHC-class II) (by 45-fold) relative to unlesioned control. Treatment with pyruvate significantly reduced infiltration of T-cells (by 68%) and MHC class II expression (by 48%) induced by QA. These results indicate that QA injection into rat striatum leads to impairment in BBB function with pyruvate administration reducing immune response and BBB leakiness in excitotoxic injury.
机译:在注射喹啉酸(QA)的大鼠纹状体中检查了丙酮酸(糖酵解的最终代谢产物)对血脑屏障(BBB)损伤和免疫反应性的影响。 QA注射后第7天观察到BBB的广泛破坏,这是通过使用针对免疫球蛋白G(IgG)的抗体进行的免疫组织化学染色增强所证实的。相对于单独的QA,接受QA注射接受丙酮酸(500 mg / kg)给药的动物表现出降低的IgG免疫反应性(降低45%)。相对于无损对照,QA纹状体内注射还导致浸润性T淋巴细胞数量显着增加(增加了70倍)和主要组织相容性复合物(II类MHC)的表达(增加了45倍)。丙酮酸处理可显着降低QA诱导的T细胞浸润(减少68%)和MHC II类表达(减少48%)。这些结果表明,向大鼠纹状体注射QA会导致BBB功能受损,丙酮酸给药会降低免疫反应和兴奋性毒性损伤中的BBB渗漏。

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