[基于HGF/PI3K/Akt信号轴的芍药配伍乌药促进慢性急性肝衰竭肝细胞再生的机制]

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2024-08-01 DOI:10.19540/j.cnki.cjcmm.20240412.707
Xiao-Ling Tian, Yu Zhang, Shan DU, Meng-Si Wu, Nian-Hua Tan, Bin Chen
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引用次数: 0

摘要

本研究基于肝细胞生长因子(HGF)/磷脂酰肌醇3-激酶(PI3K)/蛋白激酶B(Akt)信号转导轴,探讨了芍药配伍乌药(PRR-ALRP)对急性慢性肝衰竭(ACLF)大鼠的治疗作用及其对肝细胞再生的影响。通过皮下和尾静脉注射牛血清白蛋白并腹腔注射脂多糖(LPS)+D-半乳糖胺(D-GalN),建立急性慢性肝衰竭大鼠模型。大鼠分为正常对照(NC)组、模型(载体)组、PRR-ALRP(5.85 g-kg~(-1))组和肝细胞生长因子颗粒(HGFG,4.05 g-kg~(-1))组。血红素-伊红(HE)染色用于观察大鼠肝组织的病理变化。使用自动生化分析仪检测血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和总胆红素(TBIL)。白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)是通过酶联免疫吸附法检测的炎症因子。免疫荧光染色法检测增殖细胞核抗原(PCNA)、单克隆抗体鉴定抗原(Ki67)和细胞周期蛋白 B1(CyclinB1)的阳性表达。采用实时荧光定量聚合酶链反应(RT-qPCR)和 Western 印迹法检测 HGF、生长因子受体结合蛋白 1(Gab1)、PI3K、Akt、磷酸化 PI3K(p-PI3K)和磷酸化 Akt(p-Akt)的 mRNA 和蛋白表达水平。结果显示,与载体组相比,PRR-ALRP组肝脏组织病理评分降低,肝功能改善,炎症反应减轻,PCNA、Ki67和CyclinB1荧光表达增强。此外,与模型组相比,PRR-ALRP 组的 HGF 和 Gab1 蛋白表达上调,PI3K 和 Akt 磷酸化活化。这些研究结果表明,PRR-ALRP中药对通过减轻肝细胞炎症损伤和促进肝细胞再生来发挥抗肝功能衰竭的作用,其特定的调节机制可能与激活HGF/PI3K/Akt信号通路有关。
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[Mechanism of Paeoniae Radix Rubra and Aconiti Lateralis Radix Praeparata herbal pair in promoting hepatocellular regeneration in chronic acute liver failure based on HGF/PI3K/Akt signaling axis].

Based on the hepatocyte growth factor(HGF)/phosphatidylinositol 3-kinase(PI3K)/protein kinase B(Akt) signaling axis, this study investigated the therapeutic effect of Paeoniae Radix Rubra and Aconiti Lateralis Radix Praeparata(PRR-ALRP) her-bal pair on acute-on-chronic liver failure(ACLF) rats and its impact on hepatocellular regeneration. The rat model of ACLF was constructed by subcutaneous and tail vein injection of bovine serum albumin combined with intraperitoneal injection of lipopolysaccharides(LPS)+D-galactosamine(D-GalN). The rats were divided into normal control(NC) group, model(vehicle) group, PRR-ALRP(5.85 g·kg~(-1)) group, and hepatocyte growth factor granules(HGFG, 4.05 g·kg~(-1)) group. Hematoxylin-eosin(HE) staining was used to observe pathological changes in rat liver tissues. Serum alanine aminotransferase(ALT), aspartate transaminase(AST), and total bilirubin(TBIL) were detected using an automatic biochemical analyzer. The levels of interleukin-1β(IL-1β) and tumor necrosis factor-α(TNF-α) inflammatory factors were detected by ELISA. Immunofluorescence staining was used to detect the positive expression of proliferating cell nuclear antigen(PCNA), antigen identified by monoclonal antibody(Ki67), and cell cycle protein B1(CyclinB1). Real-time fluorescence-based quantitative polymerase chain reaction(RT-qPCR) and Western blot were used to detect the mRNA and protein expression levels of HGF, growth factor receptor-bound protein 1(Gab1), PI3K, Akt, phosphorylated PI3K(p-PI3K), and phosphorylated Akt(p-Akt). The results showed that compared with the vehicle group, the PRR-ALRP group had reduced liver tissue pathological scores, improved liver function, and reduced inflammatory response, with enhanced PCNA, Ki67, and CyclinB1 fluorescence expression. Furthermore, compared with the model group, the PRR-ALRP group showed upregulated expression of HGF and Gab1 proteins, as well as activation of PI3K and Akt phosphorylation. These findings suggest that PRR-ALRP herbal pair exerts anti-liver failure effects by alleviating hepatocyte inflammatory damage and promoting hepatocellular regeneration, and its specific regulatory mechanism may be related to the activation of the HGF/PI3K/Akt signaling pathway.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
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