Figure 2. ZLE had no detected cytotoxic effects on HepG2 cells. Cell morphology treated with different concentration of ZLE for 24 h (A) andCell viability of ZLE was detected by MTT assay (B). ZLE had no detected inhibition on proliferation of HepG2 cells in concentration of 100-1000 μg/mL. Values are presented as mean ± SE of three experiments. P < 0.05, vs control group

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High Anti-oxidative and Lipid-lowering Activities of Flavonoid Glycosides-rich Extract from the Leaves of Zanthoxylum bungeanum in Multi-system

Limei Ma, Ke Li, Dandan Wei, Hengyi Xiao, Hai Niu, Wen Huang

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