Institute of Liver Diseases, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China ; Key Laboratory of Liver and Kidney Diseases, Ministry of Education, of Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Evid Based Complement Alternat Med. 2012;2012:234987. doi: 10.1155/2012/234987. Epub 2012 Oct 21.
Kudzu (Pueraria lobata) is one of the earliest medicinal plants used to treat alcohol abuse in traditional Chinese medicine for more than a millennium. However, little is known about its effects on chronic alcoholic liver injury. Therefore, the present study observed the effects of puerariae radix extract (RPE) on chronic alcoholic liver injury as well as Kupffer cells (KCs) activation to release tumor necrosis factor alpha (TNF-α) induced by gut-derived endotoxin in rats and macrophage cell line. RPE was observed to alleviate the pathological changes and lipids deposition in liver tissues as well as the serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), and hepatic gamma-glutamyl transpeptidase (GGT) activity. Meanwhile, RPE inhibited KCs activation and subsequent hepatic TNF-α expression and downregulated the protein expression of endotoxin receptors, lipopolysaccharide binding protein (LBP), CD14, Toll-like receptor (TLR) 2, and TLR4 in chronic alcohol intake rats. Furthermore, an in vitro study showed that RPE inhibited the expression of TNF-α and endotoxin receptors, CD14 and TLR4, induced by LPS in RAW264.7 cells. In summary, this study demonstrated that RPE mitigated liver damage and lipid deposition induced by chronic alcohol intake in rats, as well as TNF-α release, protein expression of endotoxin receptors in vivo or in vitro.
野葛(Pueraria lobata)是传统中药中治疗酒精滥用的最早药用植物之一,已有一千多年的历史。然而,对于其对慢性酒精性肝损伤的作用知之甚少。因此,本研究观察了野葛根提取物(RPE)对慢性酒精性肝损伤以及肠源性内毒素诱导的库普弗细胞(KCs)激活释放肿瘤坏死因子-α(TNF-α)的作用,在大鼠和巨噬细胞系中。RPE 可减轻肝组织的病理变化和脂质沉积,以及血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)和肝γ-谷氨酰转肽酶(GGT)活性。同时,RPE 抑制 KCs 激活和随后的肝 TNF-α表达,并下调慢性酒精摄入大鼠内毒素受体、脂多糖结合蛋白(LBP)、CD14、Toll 样受体(TLR)2 和 TLR4 的蛋白表达。此外,体外研究表明,RPE 抑制 LPS 诱导的 RAW264.7 细胞中 TNF-α和内毒素受体、CD14 和 TLR4 的表达。综上所述,本研究表明 RPE 减轻了大鼠慢性酒精摄入引起的肝损伤和脂质沉积,以及体内或体外 TNF-α释放和内毒素受体蛋白表达。