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解毒化瘀颗粒对急性肝衰竭大鼠模型肝再生的促进作用:miRNA-mRNA表达分析

Jie-Du-Hua-Yu Granules Promote Liver Regeneration in Rat Models of Acute Liver Failure: miRNA-mRNA Expression Analysis.

作者信息

Wang Tingshuai, Wang Na, Zhang Rongzhen, Huang Shaodong, Qiu Hua, Long Fuli, Wang Minggang, Mao Dewen

机构信息

School of Chinese Medicine, Hunan University of Traditional Chinese Medicine, Changsha, Hunan 410208, China.

Department of Hepatology, The First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning, Guangxi 530023, China.

出版信息

Evid Based Complement Alternat Med. 2020 Dec 30;2020:8180959. doi: 10.1155/2020/8180959. eCollection 2020.

Abstract

PURPOSE

Jie-Du-Hua-Yu (JDHY) granules are a traditional Chinese medicine with known therapeutic effects for the treatment of acute liver failure (ALF). This study explored the potential molecular mechanism(s) of JDHY granules in promoting liver regeneration and preventing ALF.

METHODS

Rat models of ALF were constructed through administration of D-galactosamine (D-GalN) (600 mg/kg) and lipopolysaccharides (LPS) (20 g/kg). Rats were gavaged with JDHY granules, and serum and liver samples were collected at 12 h post-D-GalN/LPS administration. The degree of liver injury was evaluated through hepatic pathology and alanine/aspartate aminotransferase (ALT/AST) activity. miRNA chips were used to detect the miRNA expression profiles of rat models. Bioinformatics analysis was used to identify the biological processes and cell signaling pathways mediating the therapeutic effects of JDHY. Real-time PCR (RT-PCR) and western blotting were used to validate the data.

RESULTS

JDHY granules could effectively decrease the levels of ALT and AST, relieve D-GalN/LPS-induced liver injury, and improve hepatic function. JDHY granules were found to regulate the expression of 20 miRNAs and 19 mRNAs, which influenced 21 biological processes and 9 signaling pathways. Upon analysis of the therapeutic mechanism(s) governing the effects of JDHY granules on liver regeneration, enhanced DNA replication and an improved cholesterol metabolic ratio were identified. JDHY granules were also found to increase the expression of MCM3, CDK4, and TC, confirming the involvement of these pathways. Moreover, JDHY granules were found to promote hepatocyte mitosis and inhibit the progression of ALF.

CONCLUSION

JDHY granules protect against D-GalN/LPS-induced ALF in rats by promoting liver regeneration through enhanced DNA replication and an improved cholesterol metabolic ratio.

摘要

目的

解毒化瘀颗粒是一种对急性肝衰竭(ALF)具有已知治疗效果的中药。本研究探讨了解毒化瘀颗粒促进肝再生和预防ALF的潜在分子机制。

方法

通过给予D-半乳糖胺(D-GalN)(600mg/kg)和脂多糖(LPS)(20μg/kg)构建ALF大鼠模型。给大鼠灌胃解毒化瘀颗粒,并在给予D-GalN/LPS后12小时收集血清和肝脏样本。通过肝脏病理学和丙氨酸/天冬氨酸转氨酶(ALT/AST)活性评估肝损伤程度。使用miRNA芯片检测大鼠模型的miRNA表达谱。生物信息学分析用于鉴定介导解毒化瘀颗粒治疗作用的生物学过程和细胞信号通路。使用实时PCR(RT-PCR)和蛋白质印迹法验证数据。

结果

解毒化瘀颗粒可有效降低ALT和AST水平,减轻D-GalN/LPS诱导的肝损伤,并改善肝功能。发现解毒化瘀颗粒调节20种miRNA和19种mRNA的表达,影响21个生物学过程和9条信号通路。在分析解毒化瘀颗粒对肝再生作用的治疗机制时,发现DNA复制增强和胆固醇代谢率改善。还发现解毒化瘀颗粒增加MCM3、CDK4和TC的表达,证实了这些通路的参与。此外,发现解毒化瘀颗粒促进肝细胞有丝分裂并抑制ALF的进展。

结论

解毒化瘀颗粒通过增强DNA复制和改善胆固醇代谢率促进肝再生,从而保护大鼠免受D-GalN/LPS诱导的ALF。

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