Luo Yue, Liu Chao-Qi, He Hai-Bo, Wang Ting, He Yu-Min, Zhang Chang-Cheng, Yuan Ding, Yuan Cheng-Fu
Hubei Key Laboratory of Tumor Microenvironment and Immunotheraphy, China Three Gorges University Yichang 443002, China.
College of Biology and Pharmaceuticals, China Three Gorges University Yichang 443002, China.
Zhongguo Zhong Yao Za Zhi. 2021 May;46(9):2260-2266. doi: 10.19540/j.cnki.cjcmm.20210201.401.
Non-alcoholic steatohepatitis(NASH) was induced by high-sugar and high-fat diet in mice to investigate the intervention effect of total saponins from Panax japonicus(TSPJ) and explore its possible mechanism. Mice were fed with high-sugar and high-fat diet to establish NASH model, and intervened with different doses of TSPJ(15, 45 mg·kg~(-1)). The animals were fed for 26 weeks. The histomorphology and pathological changes of liver tissues were observed by HE staining. The transcriptional expression levels of miR-199 a-5 p, autophagy related gene 5(ATG5) and inflammatory cytokines interleukin-6(IL-6), interleukin-1β(IL-1β) and tumor necrosis factor α(TNF-α) in mouse liver were measured by quantitative Real-time polymerase chain reaction(qRT-PCR). Western blot was used to detect the expression of autophagy-related proteins ATG5, P62/SQSTM1(P62), and microtubule-associated protein light chain 3(LC3)-I/Ⅱ proteins in mouse liver. The expression of P62 protein was detected by immunofluorescence staining. In order to verify the targeting regulation relationship between miR-199 a-5 p and ATG5, miR mimic/inhibitor NC and miR-199 a-5 p mimic/inhibitor were transfected into Hepa 1-6 cells, and the expression of ATG5 mRNA and protein was detected. pMIR-reportor ATG5-3'UTR luciferase reporter gene plasmid was constructed and co-transfected with miR mimic/inhibitor NC and miR-199 a-5 p mimic/inhibitor into Hepa 1-6 cells to detect luciferase activity. In vivo, HE staining in the model group showed typical fatty degeneration and inflammatory infiltration, with increased expression of miR-199 a-5 p and decreased expression of ATG5 mRNA and protein. The expression of autophagy-associated protein P62 increased significantly, the ratio of LC3Ⅱ/Ⅰ decreased, and the transcriptional expression of inflammatory factors increased significantly. After the intervention by TSPJ, the pathological performance of liver tissue was significantly improved, the expression of miR-199 a-5 p decreased and the expression of ATG5 mRNA and protein increased, the expression of autophagy-associated protein P62 decreased significantly, the ratio of LC3Ⅱ/Ⅰ increased, and the transcriptional expression of inflammatory cytokines IL-6, IL-1β and TNF-α decreased significantly. In vitro, it was found that the expression of ATG5 mRNA and protein and luciferase activity decreased significantly in miR-199 a-5 p overexpression cells, while after inhibition of miR-199 a-5 p expression, the expression level of ATG5 mRNA and protein and luciferase activity increased. The results showed that TSPJ can improve NASH in mice fed with high-sugar and high-fat diet, and its mechanism may be related to the regulation of miR-199 a-5 p/ATG5 signal pathway, the regulation of autophagy activity and the improvement of inflammatory response of NASH.
通过高糖高脂饮食诱导小鼠非酒精性脂肪性肝炎(NASH),以研究竹节参总皂苷(TSPJ)的干预作用并探讨其可能机制。用高糖高脂饮食喂养小鼠以建立NASH模型,并用不同剂量的TSPJ(15、45mg·kg⁻¹)进行干预。动物喂养26周。通过苏木精-伊红(HE)染色观察肝组织的组织形态学和病理变化。采用定量实时聚合酶链反应(qRT-PCR)检测小鼠肝脏中miR-199a-5p、自噬相关基因5(ATG5)以及炎性细胞因子白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子α(TNF-α)的转录表达水平。采用蛋白质免疫印迹法检测小鼠肝脏中自噬相关蛋白ATG5、P62/SQSTM1(P62)和微管相关蛋白轻链3(LC3)-Ⅰ/Ⅱ蛋白的表达。通过免疫荧光染色检测P62蛋白的表达。为验证miR-199a-5p与ATG5之间的靶向调控关系,将miR模拟物/抑制剂NC和miR-199a-5p模拟物/抑制剂转染至Hepa 1-6细胞中,检测ATG5 mRNA和蛋白的表达。构建pMIR-reportor ATG5-3'UTR荧光素酶报告基因质粒,并与miR模拟物/抑制剂NC和miR-199a-5p模拟物/抑制剂共转染至Hepa 1-6细胞中,检测荧光素酶活性。在体内,模型组HE染色显示典型的脂肪变性和炎性浸润,miR-199a-5p表达增加,ATG5 mRNA和蛋白表达降低。自噬相关蛋白P62表达显著增加,LC3Ⅱ/Ⅰ比值降低,炎性因子转录表达显著增加。TSPJ干预后,肝组织病理表现明显改善,miR-199a-5p表达降低,ATG5 mRNA和蛋白表达增加,自噬相关蛋白P62表达显著降低,LC3Ⅱ/Ⅰ比值增加,炎性细胞因子IL-6、IL-1β和TNF-α转录表达显著降低。在体外,发现miR-199a-5p过表达细胞中ATG5 mRNA和蛋白表达以及荧光素酶活性显著降低,而抑制miR-199a-5p表达后,ATG5 mRNA和蛋白表达水平以及荧光素酶活性增加。结果表明,TSPJ可改善高糖高脂饮食喂养小鼠的NASH,其机制可能与调控miR-199a-5p/ATG5信号通路、调节自噬活性以及改善NASH的炎性反应有关。