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白亚君, 杜艳彬, 袁心柱, 等. 大黄酚介导TLR4/NF-κB通路对IgA肾病大鼠肾损伤和免疫反应的调控作用[J]. 四川大学学报(医学版), 2019, 50(6): 840-846.
引用本文: 白亚君, 杜艳彬, 袁心柱, 等. 大黄酚介导TLR4/NF-κB通路对IgA肾病大鼠肾损伤和免疫反应的调控作用[J]. 四川大学学报(医学版), 2019, 50(6): 840-846.
BAI Ya-jun, DU Yan-bin, YUAN Xin-zhu, et al. Regulation of Chrysophanol-mediated TLR4/NF-κB Pathway on Renal Injury and Immune Response in IgA Nephropathy Rats[J]. Journal of Sichuan University (Medical Sciences), 2019, 50(6): 840-846.
Citation: BAI Ya-jun, DU Yan-bin, YUAN Xin-zhu, et al. Regulation of Chrysophanol-mediated TLR4/NF-κB Pathway on Renal Injury and Immune Response in IgA Nephropathy Rats[J]. Journal of Sichuan University (Medical Sciences), 2019, 50(6): 840-846.

大黄酚介导TLR4/NF-κB通路对IgA肾病大鼠肾损伤和免疫反应的调控作用

Regulation of Chrysophanol-mediated TLR4/NF-κB Pathway on Renal Injury and Immune Response in IgA Nephropathy Rats

  • 摘要:
      目的  探讨大黄酚(CP)对IgA肾病大鼠肾损伤和免疫反应的调控作用。
      方法  将大鼠随机分为5组:对照组, IgA肾病模型(IgA)组, IgA+CP低、中、高剂量(2.5、5、10 mg/kg)组,除对照组外,其余组的大鼠采用脂多糖+牛血清蛋白+四氯化碳法建立IgA肾病模型,造模完成后,IgA+CP组腹腔注射不同剂量的大黄酚,对照组和模型组给予等容生理盐水,每天1次,连续给药4周。留取24 h尿液检测尿蛋白含量,取血检测血清肌酐和尿素氮;肾脏组织HE染色和TUNEL染色检测各组大鼠病理损伤和细胞凋亡;RT-PCR和Western blot检测肾组织Caspase-3和Caspase-9表达水平;酶联免疫吸附实验(ELISA)检测丙二醛(MDA)、过氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(Gpx)含量;ELISA和Western blot检测血清和肾组织白介素-1β、-6 (IL-1β、IL-6)和肿瘤坏死因子-α(TNF-α)蛋白表达;并采用RT-PCR和Western blot检测Toll样受体4(TLR4)、核转录因子-κB P65(NF-κB P65)表达水平和下游血管细胞黏附分子-1(VCAM-1)蛋白表达水平。
      结果  CP能剂量依赖性的降低IgA肾病大鼠尿蛋白、血清肌酐和尿素氮水平(P < 0.01);改善模型大鼠肾脏组织病理损伤、降低细胞凋亡率(P < 0.01),降低凋亡相关蛋白Caspase-3和Caspase-9的mRNA及蛋白表达水平(P < 0.01);抑制MDA产生的同时,增加抗氧化酶Gpx、SOD活性(P < 0.01);降低IL-1β、IL-6、TNF-α的血清水平和蛋白表达水平(P < 0.01);下调TLR4、NF-κB P65和VCAM-1的表达水平(P < 0.01)。
      结论  大黄酚对IgA肾病大鼠起到保护作用,其机制可能是通过TLR4/NF-κB P65信号通路调节IgA肾病的免疫反应,减轻肾损伤。

     

    Abstract:
      Objective  To investigate the regulatory effect and its mechanism of chrysophanol (CP) on renal injury and immune response in immunoglobin A (IgA) nephropathy rats.
      Methods  IgA nephropathy rat model was established by the method of lipopolysaccharide + bovine serum protein + carbon tetrachloride. Then the rats were randomly divided into 5 groups: control group, IgA group, IgA+low, medium and high dose of CP groups(2.5, 5 and 10 mg/kg for each group respectively). IgA+CP groups were intraperitoneally injected with different doses of chrysophanol once a day for 4 weeks, and the control group and IgA group were given isovolumetric saline. Urine protein content, serum creatinine and urea nitrogen were detected at 24 h after the administration of drugs. Kidney histopathological damage and apoptosis were measured by HE and TUNEL staining. The expression levels of Caspase-3 and Caspase-9 were detected by RT-PCR and Western blot; The contents of malondialdehyde (MDA), superoxide dismutase (SOD) and (glutathione peroxidase, Gpx) were detected by enzyme-linked immunosorbent assay (ELISA). The expression of interleukin-1β, -6 (IL-1β, IL-6) and tumor necrosis factor (TNF-α) in serum and kidney tissue were measured by ELISA and Western blot, respectively. The mRNA and protein expression levels of toll-like receptro 4 (TLR4), nuclear factor-κB P65 (NF-κB P65) were also detected by RT-PCR and Western blot, and vascular cell adherin molecule (VCAM-1) protein level was deteted by Western blot.
      Results  In IgA nephropathy rats, the administration of CP reduced proteinuria, serum creatinine and urea nitrogen in a dose-dependent manner (P < 0.01). It also improved the pathological damage of kidney tissue, reduced the apoptosis rate (P < 0.01), and decreased the mRNA and protein expression levels of apoptosis-related proteins Caspase-3 and Caspase-9 (P < 0.01). CP inhibited MDA production while increased the activities of antioxidant enzymes Gpx and SOD (P < 0.01), and decreased the levels of serum and protein expression of IL-1β, IL-6 and TNF-α (P < 0.01), as well as the expression levels of TLR4, NF-κB P65 and VCAM-1 (P < 0.01).
      Conclusion  Chrysophanol could play a protective role in IgA nephropathy rats, and its mechanism may be related to alleviating kidney injury and regulating immune response.

     

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