| Literature DB >> 25797347 |
Chen-Wei Pan1, Guang-Yao Zhou1, Wei-Lai Chen2, Lu Zhuge1, Ling-Xiang Jin1, Yi Zheng1, Wei Lin1, Zhen-Zhen Pan3.
Abstract
Forsythiaside A, an active constituent isolated from air-dried fruits of Forsythia suspensa, has been reported to have multiple pharmacological activities including anti-inflammatory, anti-oxidant, and antioxidant activities. In the present study, the hepatoprotective effect of forsythiaside A was investigated in lipopolysaccharide (LPS)/d-galactosamine (GalN)-induced acute liver injury in mice. Mice acute liver injury model was induced by LPS (50μg/kg)/GalN (800mg/kg). Forsythiaside A was administrated 1h prior to LPS/GalN exposure. The results showed that forsythiaside A attenuated hepatic pathological damage, malondialdehyde (MDA) content, and serum ALT, and AST levels induced by LPS/GalN. Moreover, forsythiaside A inhibited NF-κB activation, serum TNF-α and hepatic TNF-α levels induced by LPS/GalN. Furthermore, we found that forsythiaside A up-regulated the expression of Nrf2 and heme oxygenase-1. Our results showed that forsythiaside A protected against LPS/GalN-induced liver injury through activation of Nrf2 and inhibition of NF-κB activation.Entities:
Keywords: Acute liver injury; Forsythiaside; Lipopolysaccharide (LPS); NF-κB; Nrf2
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Year: 2015 PMID: 25797347 DOI: 10.1016/j.intimp.2015.03.009
Source DB: PubMed Journal: Int Immunopharmacol ISSN: 1567-5769 Impact factor: 4.932