Effect of Fangjihuangqi Decoction on Proliferation of Hepatic Stellate Cells in Lipopolysaccharide-intervented Rats
Yang Li
Abstract
Yang Li
Abstract
Objective:To evaluate the effect of Fangjihuangqi decoction on proliferation of hepatic stellate cells(HSC) in rats with lipopolysaccharide(LPS) intervention.Methods:HSC-T6 cells were cultured with high glucose DMEM(containing 10% FBS) with 1 EIU/mL LPS.The cells were then divided into 5 groups:blank control group,LPS group,and low-,medium-,and high-dose of Fangjihuangqi decoction groups.MMT assay was used to consecutively determine the absorbance for 5 days.ELISA method was used to detect the secration of MMP-2,TIMP-1,and TGF-β1 in the HSC-cultured supernatant after 48 h.Results:Fangjihuangqi decoction inhibited the proliferation of HSC,more obvious in the high-dose group.Compared with the LPS group,the high-dose test drug significantly increased the level of MMP-2 and decreased the level of TIMP-1 and TGF-β1(P0.01).Conclusion:Fangjihuangqi decoction can inhibit the proliferation of HSC by upregulating MMP-2 and downregulating TIMP-1 and TGF-β1 in LPS-intervented rats.
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Objective:To evaluate the effect of Fangjihuangqi decoction on proliferation of hepatic stellate cells(HSC) in rats with lipopolysaccharide(LPS) intervention.Methods:HSC-T6 cells were cultured with high glucose DMEM(containing 10% FBS) with 1 EIU/mL LPS.The cells were then divided into 5 groups:blank control group,LPS group,and low-,medium-,and high-dose of Fangjihuangqi decoction groups.MMT assay was used to consecutively determine the absorbance for 5 days.ELISA method was used to detect the secration of MMP-2,TIMP-1,and TGF-β1 in the HSC-cultured supernatant after 48 h.Results:Fangjihuangqi decoction inhibited the proliferation of HSC,more obvious in the high-dose group.Compared with the LPS group,the high-dose test drug significantly increased the level of MMP-2 and decreased the level of TIMP-1 and TGF-β1(P0.01).Conclusion:Fangjihuangqi decoction can inhibit the proliferation of HSC by upregulating MMP-2 and downregulating TIMP-1 and TGF-β1 in LPS-intervented rats.
Key concepts: Decoction, Lipopolysaccharide, Medicine, Hepatic stellate cell, Transforming growth factor, Pharmacology, Traditional medicine, Internal medicine