Effects and Mechanism of Oxymatrine Combined with Compound Yinchen Granules on the Apoptosis of Hepatocytes through the Akt/FoxO3a/Bim Pathway.

Xian Zhang,Yuanzi Wang,Haifeng Zhang,Bin Zhang,Wei Jiang,Jiajia Ge,Tongtong Xu,Xuejuan Zhu,Juliana Melgaço

doi:10.1155/2022/8644356

Abstract

The aim of the present study was to investigate the effects and mechanism of oxymatrine (OMT) combined with compound yinchen granules (CYG) on the apoptosis of hepatocytes through the Akt/FoxO3a/Bim pathway in rats with acute liver failure. The rat model of acute liver failure was established using lipopolysaccharide/D-galactosamine (LPS/D-GalN). The expression of proteins in rat liver tissues was detected by western blot analysis. The mRNA expression of FoxO3a, Bim, Bax, Bcl-2, and caspase-3 in rat liver tissues was detected by RT-qPCR. The apoptosis rate of rat hepatocytes was determined by flow cytometry. Western blots showed that when compared with the normal group, the expression of p-Akt and p-FoxO3a in the model group was decreased (P < 0.05), while the expression of Bim was increased (P < 0.01). Compared with the model group, the expression of p-Akt and p-FoxO3a in the OMT group and the OMT combined with CYG groups was increased (P < 0.05 or P < 0.01), while the expression of Bim was decreased (P < 0.05). The Bax/Bcl-2 ratio and caspase-3 protein expression in the model group were significantly higher than those in the normal group (P < 0.01). The Bax/Bcl-2 ratio and the expression of caspase-3 protein in the OMT group and the OMT combined with CYG groups were significantly lower than those in the model group (P < 0.01). The results of RT-qPCR were consistent with those of western blot. The results of flow cytometry showed that the apoptosis rate of hepatocytes in the OMT group and the OMT combined with CYG groups was significantly lower than that in the model group (P < 0.05 or P < 0.01). We concluded that LPS/D-GalN can induce apoptosis of hepatocytes in rats with acute liver failure through the Akt/FoxO3a/Bim pathway. OMT combined with CYG inhibits apoptosis of hepatocytes in rats with acute liver failure via the Akt/FoxO3a/Bim pathway.

Highlights

Hepatocyte apoptosis plays an important role in the pathogenesis of acute liver failure (ALF) [1,2,3]
Six rats died in the model group, one rat died in the OMT group, and no rats died in the OMT and Compound yinchen granules (CYG) groups
It has been found that apoptosis is one of the main forms of hepatocyte death in ALF, and the occurrence of ALF is closely related to apoptosis of hepatocytes [19, 20]

Summary

Introduction

Hepatocyte apoptosis plays an important role in the pathogenesis of acute liver failure (ALF) [1,2,3]. The mechanism of hepatocyte apoptosis in ALF is not yet fully understood. There are no effective drugs to inhibit the apoptosis of hepatocytes. It is important to identify effective therapeutic drugs and their targets. Due to the complicated etiology of hepatocyte apoptosis in ALF, it is unlikely to be treated by a single factor, and a multifactor comprehensive treatment is necessary. Oxymatrine (OMT) is an alkaloid extracted from the root of Sophora flavescens, Sophora, and Radix alopecuroides. Pharmacological and clinical trials have proved that OMT has anti-inflammatory, antiallergic, antifiber, antitumor, antiapoptosis, and other pharmacological effects [4,5,6,7,8]. Compound yinchen granules (CYG) are composed of yinchen (Herba artemisiae), danshen (Salvia miltiorrhiza), and dahuang (rhubarb)

Objectives

Methods

Results

Conclusion