大理大学学报 ›› 2023, Vol. 8 ›› Issue (8): 49-53.

• 基础医学 • 上一篇    下一篇

Ghrelin减轻高糖所致肝细胞损伤的作用研究

叶圣莹,王鑫瑞,高靖雯,秦 燕*   

  1. (大理大学基础医学院,云南大理 671000)

  • 收稿日期:2022-10-22 修回日期:2022-12-12 出版日期:2023-08-15 发布日期:2023-07-11
  • 通讯作者: 秦燕,教授,E-mail:lantingxun@126.com。
  • 作者简介:叶圣莹,硕士研究生,主要从事高糖致肝细胞损伤机制研究。
  • 基金资助:
    云南省教育厅科学研究基金项目(2022Y815)

The Protective Effect of Ghrelin on High Glucose-Induced Hepatocellular Injury

Ye Shengying, Wang Xinrui, Gao Jingwen, Qin Yan*   

  1. (Pre-clinical College, Dali University, Dali, Yunnan 671000,China)

  • Received:2022-10-22 Revised:2022-12-12 Online:2023-08-15 Published:2023-07-11

摘要: 目的:观察Ghrelin对高糖所致肝细胞损伤的保护作用,初步探讨其作用机制。方法:建立高糖所致肝细胞损伤模型,给予Ghrelin(10-7 mmol /L)干预。随机分为空白对照组、Ghrelin+空白对照组、高糖组、Ghrelin+高糖组,检测细胞增殖率及丙氨酸转氨酶(ALT)、丙二醛(MDA)、超氧化物歧化酶(SOD)含量;实时荧光定量聚合酶链反应检测含半胱氨酸的天冬氨酸蛋白水解酶-1(Caspase-1)、白细胞介素-18(IL-18)和白细胞介素-1β(IL-1β)mRNA表达水平;免疫荧光技术检测消皮素D(GSDMD)蛋白表达量。结果:Ghrelin能够降低ALT、MDA含量,增加SOD含量,显著降低焦亡相关因子Caspase-1、IL-18、IL-1β mRNA和GSDMD蛋白的表达水平。结论:Ghrelin对高糖所致肝细胞损伤具有保护作用,其作用机制之一可能是通过减轻氧化应激,进而抑制Caspase-1介导的细胞焦亡而实现的。

关键词: font-family:Times New Roman, ">Ghrelinfont-family:Times New Roman, ">;高糖;细胞损伤;氧化应激;焦亡

Abstract: Objective: To observe the protective effect of Ghrelin on high glucose-induced hepatocellular injury and preliminarily explore its mechanism. Methods: A high glucose-induced hepatocellular injury model was established and Ghrelin(10-7 mmol / L) was used for intervention. The experiment were randomly divided into blank control group, Ghrelin + blank control group, high glucose group and Ghrelin + high glucose group. The cell proliferation rate and expression levels of alanine aminotransferase(ALT), malondialdehyde(MDA) and superoxide dismutase(SOD) were detected. The mRNA expression levels of cysteinyl aspartate specific proteinase(Caspase-1), interleukin-18(IL-18) and interleukin-1β(IL-1β) were determined by real-time fluorescence quantitative polymerase chain reaction, and the expression of gasdermin D(GSDMD) protein was detected by immunofluorescence technique. Results: Ghrelin could decrease the content of ALT and MDA, increas the SOD content, and significantly reduce the expression levels of pyroptosis-related factors Caspase-1, IL-18, IL-1β mRNA and GSDMD protein. Conclusion: Ghrelin has a protective effect on high glucose-induced hepatocellular injury, and one of its mechanisms may be to relieve oxidative stress and inhibit Caspase-1-mediated pyroptosis.

Key words: font-family:Times New Roman, ">Ghrelinfont-family:Times New Roman, ">;font-family:Times New Roman, "> high glucosefont-family:Times New Roman, ">;font-family:Times New Roman, "> cell injuryfont-family:Times New Roman, ">;font-family:Times New Roman, "> oxidative stressfont-family:Times New Roman, ">;font-family:Times New Roman, "> pyroptosis

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