实用医学杂志 ›› 2023, Vol. 39 ›› Issue (7): 827-832.doi: 10.3969/j.issn.1006⁃5725.2023.07.006

• 基础研究 • 上一篇    下一篇

白术内酯Ⅲ调节AMPK/SIRT1/NF⁃κB信号通路对脓毒症大鼠肝损伤的影响 

潘毅 陈军喜 闫智杰 夏芝辉    

  1. 南昌大学第四附属医院重症医学科(南昌 330000)

  • 出版日期:2023-04-10 发布日期:2023-04-10
  • 基金资助:
    江西省卫生计生委科技计划(编号:20195308)

Influence of Atractylide Ⅲ regulating AMPK/SIRT1/NF⁃κB signaling pathway on liver injury in septic rats

PAN Yi,CHEN Junxi,YAN Zhijie,XIA Zhihui.   

  1. Department of Critical Care Medicine,the Fourth Affiliated Hospi⁃ tal of Nanchang University,Nanchang 330000,China 

  • Online:2023-04-10 Published:2023-04-10

摘要:

目的 探究白术内酯Ⅲ(Atractylidene Ⅲ,Atr⁃Ⅲ)对脓毒症大鼠肝损伤的影响以及对腺苷酸 激活蛋白激酶(AMPK)/去乙酰化酶 1(SIRT1)/核因子⁃κB(NF⁃κB)信号通路的调节作用。方法 60 SPF SD 雄性大鼠分为假手术组、模型组、阳性组、Atr⁃Ⅲ低、高剂量组、Atr⁃Ⅲ高剂量+AMPK 抑制剂组。 检测大鼠血清中谷草转氨酶(AST)、谷丙转氨酶(ALT)水平;苏木素-伊红(HE)染色观察肝组织的病理变 化;TUNEL 染色检测肝细胞凋亡情况;ELISA 检测血清白细胞介素 1β(IL⁃1β)、白细胞介素 6(IL⁃6)、肿瘤坏死因子 α(TNF⁃α)水平;检测肝组织超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的活性;Western blot 测通路相关蛋白表达情况。结果 与假手术组相比,模型组大鼠肝细胞损伤严重,AST、ALT、IL⁃1β、IL⁃6 TNF⁃α 水平、细胞凋亡率、p65 NF⁃κB 磷酸化表达均升高,SOD、CAT 活性、AMPK 磷酸化、SIRT1 蛋白表达均 降低(P < 0.05);与模型组相比,阳性组和 Atr⁃Ⅲ组大鼠肝细胞形态恢复,AST、ALT、IL⁃1β、IL⁃6、TNF⁃α 平、细胞凋亡率、p65 NF⁃κB 磷酸化表达均降低,SOD、CAT 水平、AMPK 磷酸化、SIRT1 蛋白表达均升高 P < 0.05)。AMPK 抑制剂 BML⁃275 消除了高剂量 ATL⁃Ⅲ对脓毒症大鼠肝损伤的缓解作用。结论 Atr⁃Ⅲ 可以激活AMPK/SIRT1信号通路,抑制p65 NF⁃κB 活化,减轻脓毒症大鼠的肝损伤。

关键词: 白术内酯Ⅲ,  , AMPK/SIRT1/NF?κB , 通路,  , 脓毒症,  , 肝损伤,  , 炎症

Abstract:

Objective To explore the influence of Atractylidene Ⅲ(Atr⁃Ⅲ)on liver injury in septic rats and its regulation on AMP⁃activated protein kinase(AMPK)/ sirtuin 1(SIRT1)/nuclear factor kappa⁃B(NF⁃κB signaling pathway. Methods Eighty SPF SD male rats were randomly grouped into sham operation group,model group,positive group,low⁃dose,high⁃dose Atr⁃Ⅲ group,and high⁃dose Atr⁃Ⅲ+AMPK inhibitor group. The levels of aspartate aminotransferase(AST)and alanine aminotransferase(ALT)were detected in the serum of rats;HE staining was applied to observe the pathological changes of liver tissue;TUNEL staining was applied to detect hepa⁃ tocyte apoptosis;ELISA was applied to detect the levels of serum interleukin 1β(IL⁃1β),interleukin 6(IL⁃6), tumor necrosis factor α(TNF⁃α);the activities of superoxide dismutase(SOD)and catalase(CAT)liver tissue were detected;Western blot was used to detect the expression of related proteins. Results Compared with sham operation group,hepatocyte injury was severe in model group,the levels of AST,ALT,IL⁃1β,IL⁃6,TNF⁃α,the rate of apoptosis,and the ratio of p⁃p65 NF⁃κB/p65 NF⁃κB were all increased(P < 0.05),the levels of SOD CAT,the ratio of p⁃AMPK/AMPK,and the protein expression of SIRT1 were all decreased(P < 0.05). Compared with model group,the morphology of rat hepatocytes in positive group and Atr⁃Ⅲ low⁃dose and high⁃dose groups recovered,the levels of AST,ALT,IL⁃1β,IL⁃6,TNF⁃α,the rate of apoptosis,and phosphorylation of p65 NF⁃ κB were all increased(P < 0.05),the levels of SOD,CAT,phosphorylation of AMPK,and the protein expression of SIRT1 were all decreased(P < 0.05). The AMPK inhibitor BML⁃275 abrogated the attenuating effect of high⁃ dose ATL⁃Ⅲ on liver injury in septic rats. Conclusion Atr⁃Ⅲ can activate the AMPK/SIRT1 signaling pathway and inhibit the activation of p65 NF⁃κB,thereby reducing liver injury in septic rats. 

Key words:

Atractylenolide Ⅲ, AMPK/SIRT1/NF?κB pathway, sepsis, liver injury, inflammation