甘草酸通过抑制HMGB1磷酸化和炎症反应减轻精囊炎诱发的神经毒性

IF 6.2
Changwei Yu, Yalan Xiang, Min Zhang, Jing Wen, Xiaoyu Duan, Lu Wang, Gongying Deng, Pingfei Fang
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引用次数: 0

摘要

最近有几例临床病例报道了思密达的神经毒性。因此,本研究旨在探讨 HMGB1 在思密达诱导的神经毒性模型中的作用,并评估与调节 HMGB1 释放有关的甘草酸(GA)的潜在缓解作用。对48只SD大鼠腹腔注射Semen Strychni提取物(175毫克/千克),然后口服GA(50毫克/千克),连续四天。经 SS 和 GA 治疗后,通过组织病理学检查可观察到神经元变性、凋亡和坏死。对炎性细胞因子(TNF-α和IL-1β)、神经递质相关酶(MAO和AChE)、血清HMGB1、核和细胞质HMGB1/ph-HMGB1以及PP2A、PKC和HMGB1之间的相互作用进行了评估。此外,还研究了 MAPK 通路的影响。结果发现,这种神经毒性的特点是神经元变性和凋亡、诱导促炎细胞因子以及神经递质代谢酶的减少。相比之下,GA 治疗能明显改善上述影响,减轻神经损伤。此外,Semen Strychni 还能促进 HMGB1 的磷酸化及其在细胞核和细胞质之间的转位,从而激活 NF-κB 和 MAPK 通路,引发各种炎症反应。我们的实验证明,GA 可以部分逆转这些效应。总之,GA 酸减轻了思密达诱导的神经毒性,可能是通过抑制 HMGB1 磷酸化并阻止其从细胞中释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Glycyrrhizic Acid Alleviates Semen Strychni-Induced Neurotoxicity Through the Inhibition of HMGB1 Phosphorylation and Inflammatory Responses.

Glycyrrhizic Acid Alleviates Semen Strychni-Induced Neurotoxicity Through the Inhibition of HMGB1 Phosphorylation and Inflammatory Responses.

The neurotoxicity of Semen Strychni has been reported recently in several clinical cases. Therefore, this study was conducted to investigate the role of HMGB1 in a model of neurotoxicity induced by Semen Strychni and to assess the potential alleviating effects of glycyrrhizic acid (GA), which is associated with the regulation of HMGB1 release. Forty-eight SD rats were intraperitoneally injected with Semen Strychni extract (175 mg/kg), followed by oral administration of GA (50 mg/kg) for four days. After treatment of SS and GA, neuronal degeneration, apoptosis, and necrosis were observed via histopathological examination. Inflammatory cytokines (TNF-α and IL-1β), neurotransmitter associated enzymes (MAO and AChE), serum HMGB1, nuclear and cytoplasmic HMGB1/ph-HMGB1, and the interaction between PP2A, PKC, and HMGB1 were evaluated. The influence of the MAPK pathway was also examined. As a result, this neurotoxicity was characterized by neuronal degeneration and apoptosis, the induction of pro-inflammatory cytokines, and a reduction in neurotransmitter-metabolizing enzymes. In contrast, GA treatment significantly ameliorated the abovementioned effects and alleviated nerve injury. Furthermore, Semen Strychni promoted HMGB1 phosphorylation and its translocation between the nucleus and cytoplasm, thereby activating the NF-κB and MAPK pathways, initiating various inflammatory responses. Our experiments demonstrated that GA could partially reverse these effects. In summary, GA acid alleviated Semen Strychni-induced neurotoxicity, possibly by inhibiting HMGB1 phosphorylation and preventing its release from the cell.

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