Suppr超能文献

甘草酸通过抑制 HMGB1 磷酸化和炎症反应缓解马钱子碱诱导的神经毒性。

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

机构信息

Department of Pharmacy, the Second Xiangya Hospital, Central South University, Changsha, 410011, China.

Institute of Clinical Pharmacy, Central South University, Changsha, 410011, China.

出版信息

J Neuroimmune Pharmacol. 2024 May 21;19(1):21. doi: 10.1007/s11481-024-10128-8.

Abstract

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.

摘要

最近有几项临床病例报告显示马钱子具有神经毒性。因此,本研究旨在探讨高迁移率族蛋白 B1(HMGB1)在马钱子致神经毒性模型中的作用,并评估与 HMGB1 释放调节相关的甘草酸(GA)的潜在缓解作用。将 48 只 SD 大鼠腹腔注射马钱子提取物(175mg/kg),随后连续 4 天灌胃给予 GA(50mg/kg)。在 SS 和 GA 处理后,通过组织病理学检查观察神经元变性、凋亡和坏死。评估了炎症细胞因子(TNF-α和 IL-1β)、神经递质相关酶(MAO 和 AChE)、血清 HMGB1、核内和细胞质内 HMGB1/ph-HMGB1 以及 PP2A、PKC 和 HMGB1 之间的相互作用。还研究了 MAPK 通路的影响。结果表明,这种神经毒性的特征是神经元变性和凋亡、促炎细胞因子的诱导以及神经递质代谢酶的减少。相反,GA 治疗显著改善了上述作用并减轻了神经损伤。此外,马钱子促进了 HMGB1 的磷酸化及其在核和细胞质之间的易位,从而激活了 NF-κB 和 MAPK 通路,引发了各种炎症反应。我们的实验表明,GA 可以部分逆转这些作用。总之,GA 酸减轻了马钱子诱导的神经毒性,可能是通过抑制 HMGB1 的磷酸化并防止其从细胞中释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5145/11108907/c4e6037ec049/11481_2024_10128_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验