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基于网络药理学和动物实验验证白藜芦醇通过下调ATF4/Chop/Bcl-2/Bax信号通路抑制肠道衰老

Verification of Resveratrol Inhibits Intestinal Aging by Downregulating ATF4/Chop/Bcl-2/Bax Signaling Pathway: Based on Network Pharmacology and Animal Experiment.

作者信息

Liu Tian-Hao, Tu Wan-Qing, Tao Wen-Cong, Liang Qiu-Er, Xiao Ya, Chen Li-Guo

机构信息

College of Chinese Medicine, Jinan University, Guangzhou, China.

出版信息

Front Pharmacol. 2020 Jul 10;11:1064. doi: 10.3389/fphar.2020.01064. eCollection 2020.

Abstract

Resveratrol is one of the most well-known drugs used in the treatment of aging. However, the potential mechanisms of resveratrol on intestinal aging have not yet been fully investigated. Herein, we aimed to further explore the pharmacological mechanisms of resveratrol as a therapy for intestinal aging. We performed network construction and enrichment analysis network pharmacology. Then a further animal experimental validation containing 20 female C57BL/6J (wild type, WT) and 16 female (knock down, KD) naturally aging mice and oral supplementary resveratrol (44 mg/kg/day) for 30 days were conducted. The expression of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT), linear alkylethoxylate (AE), and malondialdehyde (MDA) were measured by ELISA, the observation of pathological changes and apoptosis in intestinal tissue were performed by HE, PAS, and TUNEL staining, the ATF4/Chop/Bcl-2/Bax signaling pathway-related proteins and mRNAs expression were measured by western blotting and real-time PCR. The network pharmacology showed 132 targets of resveratrol on aging. The enrichment analysis showed resveratrol antiaging involved mainly included protein heterodimerization activity, apoptosis, etc. Then ATF4/Chop/Bcl-2/Bax signaling pathway in biological process of apoptosis was selected to verify the potential mechanisms. Animal studies showed resveratrol upregulated the relative expression of SOD, GSH-Px, CAT, AE, whereas it downregulated the relative expression of MDA in intestine compared with the control group. There was also higher relative expression of SOD, GSH-Px, CAT, AE, and lower relative expression of MDA in KD mice than that in WT mice. Moreover, there was higher relative expression of SOD, GSH-Px, CAT, AE, and lower relative expression of MDA in KD mice than that in WT mice after resveratrol treatment. Decreased ATF4, Chop, Bax but increased Bcl-2 proteins and mRNAs expression were determined after resveratrol treatment compared with the control group; lower ATF4, Chop, Bax but higher Bcl-2 proteins and mRNAs expression were found in KD mice than that in WT mice. Additionally, lower relative proteins and mRNAs expression of ATF4, Chop, Bax and higher relative expression of Bcl-2 in KD mice than that in WT mice after resveratrol treatment. These findings demonstrated that resveratrol substantially inhibited intestinal aging downregulating ATF4/Chop/Bcl-2/Bax signaling pathway.

摘要

白藜芦醇是治疗衰老最著名的药物之一。然而,白藜芦醇对肠道衰老的潜在机制尚未得到充分研究。在此,我们旨在进一步探索白藜芦醇作为肠道衰老治疗药物的药理机制。我们进行了网络构建和富集分析——网络药理学。然后进行了进一步的动物实验验证,将20只雌性C57BL/6J(野生型,WT)和16只雌性(敲除,KD)自然衰老小鼠口服补充白藜芦醇(44毫克/千克/天)30天。通过酶联免疫吸附测定法测量超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(CAT)、线性烷基乙氧基化物(AE)和丙二醛(MDA)的表达,通过苏木精-伊红(HE)、过碘酸-雪夫(PAS)和末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)染色观察肠道组织的病理变化和细胞凋亡,通过蛋白质印迹法和实时聚合酶链反应测量激活转录因子4(ATF4)/C/EBP同源蛋白(Chop)/B细胞淋巴瘤-2(Bcl-2)/Bax信号通路相关蛋白和信使核糖核酸的表达。网络药理学显示白藜芦醇在衰老方面有132个靶点。富集分析表明白藜芦醇抗衰老主要涉及蛋白质异二聚化活性、细胞凋亡等。然后选择细胞凋亡生物学过程中的ATF4/Chop/Bcl-2/Bax信号通路来验证潜在机制。动物研究表明,与对照组相比,白藜芦醇上调了肠道中SOD、GSH-Px、CAT、AE的相对表达,而下调了MDA的相对表达。KD小鼠中SOD、GSH-Px、CAT、AE的相对表达也高于WT小鼠,MDA的相对表达低于WT小鼠。此外,白藜芦醇治疗后,KD小鼠中SOD、GSH-Px、CAT、AE的相对表达高于WT小鼠,MDA的相对表达低于WT小鼠。与对照组相比,白藜芦醇治疗后测定的ATF4、Chop、Bax蛋白和信使核糖核酸表达降低,但Bcl-2增加;KD小鼠中ATF4、Chop、Bax蛋白和信使核糖核酸表达低于WT小鼠,但Bcl-2高于WT小鼠。此外,白藜芦醇治疗后,KD小鼠中ATF4、Chop、Bax的相对蛋白和信使核糖核酸表达低于WT小鼠,Bcl-2的相对表达高于WT小鼠。这些发现表明,白藜芦醇通过下调ATF4/Chop/Bcl-2/Bax信号通路显著抑制肠道衰老。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0341/7366860/d1437a55d9f0/fphar-11-01064-g001.jpg

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