Feng Shuaixia, Tang Jie, Wei Xia, Lu Zou, Xu Ying, Zhang Tong, Han Han
School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201210, China.
School of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 201210, China.
J Ethnopharmacol. 2025 Jan 30;337(Pt 3):118956. doi: 10.1016/j.jep.2024.118956. Epub 2024 Oct 17.
Swertia cincta is a traditional remedy for cholestasis commonly utilised in Yunnan, China. Despite its widespread use, the specific active components and underlying mechanisms of action remain poorly understood.
This study aimed to investigate the therapeutic properties, mechanisms, and active compounds of Swertia cincta in an animal model of cholestasis induced by alpha-naphthylisothiocyanate (ANIT).
UHPLC/Q-TOF-MS and high-performance liquid chromatography (HPLC) were utilised to analyse the blood components of Swertia cincta. An ANIT-induced cholestatic liver injury animal model was established, and metabolomics was employed to explore the potential mechanisms of Swertia cincta in treating cholestatic liver injury. Hepatocellular injury induced by taurochenodeoxycholic acid was evaluated in vitro, and key bioactive components of Swertia cincta for cholestatic liver injury treatment were identified and confirmed using the ANIT-induced mouse model.
The established HPLC method demonstrates good specificity and reproducibility, enabling the simultaneous determination of six components in Swertia cincta. Results from serum biochemical indicators and liver pathology analysis indicated that Swertia cincta exhibits promising anti-cholestasis liver injury effects. Specifically, gentiopicroside, loganic acid, and isoorientin were identified as key active ingredients in treating cholestatic liver injury. Their mechanism of action primarily involves regulating PPAR-α, FXR, CYP3A4, NTCP, CAR, and CPT2. By modulating PPAR-α and bile acid metabolism-related proteins, reducing pro-inflammatory factors, enhancing bile acid transport, and promoting fatty acid oxidation to reduce lipid accumulation, Swertia cincta exerts protective and therapeutic effects against cholestatic liver injury. Notably, gentian bitter glycosides appear to be the most critical components for this effect.
Swertia cincta may improve cholestatic liver injury by activating the peroxisome proliferator-activated receptor alpha pathway, and the key active compounds were gentiopicroside, loganic acid, and isoorientin.
环叶獐牙菜是中国云南常用于治疗胆汁淤积的一种传统药物。尽管其应用广泛,但其具体活性成分和潜在作用机制仍知之甚少。
本研究旨在研究环叶獐牙菜在α-萘异硫氰酸酯(ANIT)诱导的胆汁淤积动物模型中的治疗特性、作用机制和活性化合物。
采用超高效液相色谱/四极杆飞行时间质谱联用仪(UHPLC/Q-TOF-MS)和高效液相色谱(HPLC)分析环叶獐牙菜的血液成分。建立ANIT诱导的胆汁淤积性肝损伤动物模型,并采用代谢组学方法探讨环叶獐牙菜治疗胆汁淤积性肝损伤的潜在机制。体外评估牛磺鹅去氧胆酸诱导的肝细胞损伤,并使用ANIT诱导的小鼠模型鉴定和确认环叶獐牙菜治疗胆汁淤积性肝损伤的关键生物活性成分。
所建立的HPLC方法具有良好的特异性和重现性,能够同时测定环叶獐牙菜中的六种成分。血清生化指标和肝脏病理分析结果表明,环叶獐牙菜具有显著的抗胆汁淤积性肝损伤作用。具体而言,龙胆苦苷、马钱子酸和异荭草苷被确定为治疗胆汁淤积性肝损伤的关键活性成分。其作用机制主要涉及调节过氧化物酶体增殖物激活受体α(PPAR-α)、法尼醇X受体(FXR)、细胞色素P450酶家族3亚家族A成员4(CYP3A4)、钠-牛磺胆酸共转运多肽(NTCP)、组成型雄烷受体(CAR)和肉碱棕榈酰转移酶2(CPT2)。通过调节PPAR-α和胆汁酸代谢相关蛋白,减少促炎因子,增强胆汁酸转运,并促进脂肪酸氧化以减少脂质蓄积,环叶獐牙菜对胆汁淤积性肝损伤发挥保护和治疗作用。值得注意的是,龙胆苦味苷似乎是发挥此作用的最关键成分。
环叶獐牙菜可能通过激活过氧化物酶体增殖物激活受体α途径改善胆汁淤积性肝损伤,关键活性化合物为龙胆苦苷、马钱子酸和异荭草苷。