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Glycyrrhizin Attenuates Kainic Acid-Induced Neuronal Cell Death in the Mouse Hippocampus

机译:甘草甜素可减轻海藻酸诱导的小鼠海马神经元细胞死亡。

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摘要

Glycyrrhizin (GL), a triterpene that is present in the roots and rhizomes of licorice (Glycyrrhiza glabra), has been reported to have anti-inflammatory and anti-viral effects. Recently, we demonstrated that GL produced the neuroprotective effects with the suppression of microglia activation and proinflammatory cytokine induction in the postischemic brain with middle cerebral artery occlusion (MCAO) in rats and improved motor impairment and neurological deficits. In the present study, we investigated whether GL has a beneficial effect in kainic acid (KA)-induced neuronal death model. Intracerebroventricular (i.c.v.) injection of 0.94 nmole (0.2 µg) of KA produced typical neuronal death in both CA1 and CA3 regions of the hippocampus. In contrast, administration of GL (10 mg/kg, i.p.) 30 min before KA administration significantly suppressed the neuronal death, and this protective effect was more stronger at 50 mg/kg. Moreover, the GL-mediated neuroprotection was accompanied with the suppression of gliosis and induction of proinflammatory markers (COX-2, iNOS, and TNF-α). The anti-inflammatory and anti-excitotoxic effects of GL were verified in LPS-treated primary microglial cultures and in NMDA- or KA-treated primary cortical cultures. Together these results suggest that GL confers the neuroprotection through the mechanism of anti-inflammatory and anti-excitotoxic effects in KA-treated brain.
机译:甘草甜素(GL)是存在于甘草(甘草)根和根茎中的三萜,据报道具有抗炎和抗病毒作用。最近,我们证明GL可以通过抑制大鼠中脑动脉闭塞(MCAO)缺血后脑中的小胶质细胞活化和促炎性细胞因子的诱导而产生神经保护作用,并改善运动障碍和神经功能缺损。在本研究中,我们调查了GL在海藻酸(KA)诱导的神经元死亡模型中是否具有有益作用。脑室内(i.c.v.)注射0.94 nmole(0.2 µg)的KA在海马CA1和CA3区均产生典型的神经元死亡。相反,在KA施用前30分钟施用GL(10mg / kg,腹膜内)明显抑制神经元死亡,并且在50mg / kg时这种保护作用更强。此外,GL介导的神经保护作用与神经胶质的抑制和促炎性标志物(COX-2,iNOS和TNF-α)的诱导有关。在LPS处理的原代小胶质细胞培养物以及NMDA或KA处理的原代皮层培养物中证实了GL的抗炎和抗兴奋剂作用。这些结果共同表明,GL通过在KA治疗的大脑中发挥抗炎和抗兴奋毒性作用的机制来赋予神经保护作用。

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