石杉碱A通过类视黄醇X受体α转录调节丙酮酸羧化酶的表达,从而调节阻塞性睡眠呼吸暂停的体内和体外实验。

Human & experimental toxicology Pub Date : 2025-01-01 Epub Date: 2025-05-19 DOI:10.1177/09603271251342572
Juan Huang, Hui Li, Qin Huang, Li Wang, Ying Wu, Xin Tan
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引用次数: 0

摘要

本研究探讨HuA通过类视黄醇X受体α (RXRA)影响丙酮酸羧化酶的表达,从而影响阻塞性睡眠呼吸暂停(OSA)进展的分子机制。方法进行生物信息学分析,筛选差异表达基因(DEGs),寻找RXRA下游靶基因。在慢性间歇性缺氧(CIH)小鼠模型中评估认知功能、神经元损伤、氧化应激和炎症。Morris水迷宫试验评估游泳路径长度、逃避潜伏期和穿越平台时间。采用H&E和尼氏染色观察脑组织病理变化及神经元计数。ELISA法检测氧化应激水平和炎症因子水平。采用染色质免疫沉淀法(ChIP)检测了CIH中丙酮酸羧化酶启动子区域RXRA的富集程度,采用双荧光素酶法分析了RXRA对丙酮酸羧化酶启动子活性的影响。结果rxra是HuA的潜在调控靶基因。丙酮酸羧化酶被确定为RXRA靶基因和OSA的重要DEG。cih诱导小鼠认知障碍、神经元损伤、氧化应激和炎症,而HuA治疗可减轻这些症状。在OSA中,抑制RXRA表达导致丙酮酸羧化酶表达降低。HuA处理可增强RXRA的表达,从而促进丙酮酸羧化酶的表达。HuA通过RXRA/丙酮酸羧化酶轴减轻cih诱导的认知障碍、神经元损伤、氧化应激和炎症。综上所述,HuA通过促进RXRA/丙酮酸羧化酶轴,减轻了cih诱导的认知障碍、神经元损伤、氧化应激和炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In silico and in vivo experiments of Huperzine A modulating the development of obstructive sleep apnea by transcriptionally regulating pyruvate carboxylase expression via retinoid X receptor alpha.

IntroductionThis study investigated the molecular mechanism by which HuA influences the expression of pyruvate carboxylase via retinoid X receptor alpha (RXRA), thereby affecting the progression of obstructive sleep apnea (OSA).MethodsBioinformatics analysis including screening of differentially expressed genes (DEGs) and searching the downstream target genes of RXRA were conducted. Cognitive function, neuronal damage, oxidative stress, and inflammation were evaluated in chronic intermittent hypoxia (CIH) mouse models. The Morris water maze test was used to assess swimming path length, escape latency, and platform crossing times. H&E and Nissl staining was performed to evaluate pathological changes and neuronal counts in brain tissue. ELISA was utilized to measure the oxidative stress levels and inflammatory cytokines. RXRA enrichment in the pyruvate carboxylase promoter region in CIH was assessed using Chromatin Immunoprecipitation (ChIP), and the effect of RXRA on pyruvate carboxylase promoter activity was analyzed using dual-luciferase assay.ResultsRXRA was identified as a potential regulatory target gene of HuA. Pyruvate carboxylase was identified as a RXRA target gene and a significant DEG in OSA. CIH-induced cognitive impairment, neuronal damage, oxidative stress, and inflammation in mice, while such symptoms were alleviated by HuA treatment. In OSA, suppression of RXRA expression led to reduced pyruvate carboxylase expression. HuA treatment enhanced RXRA expression, thereby promoting pyruvate carboxylase expression. HuA alleviated CIH-induced cognitive impairment, neuronal damage, oxidative stress, and inflammation via the RXRA/pyruvate carboxylase axis.ConclusionIn summary, HuA alleviates CIH-induced cognitive impairment, neuronal damage, oxidative stress, and inflammation by promoting the RXRA/pyruvate carboxylase axis.

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