Huo Xiaowei, Sun Xiaoke, Cao Zepeng, Qiao Jingzhe, Yang Sa, Meng Xiangbo, Zhao Yanyan
College of Pharmaceutical Science, Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Hebei University, Baoding, Hebei 071002, P.R. China.
Oncology Department, Hebei Yiling Hospital, Shijiazhuang, Hebei 050091, P.R. China.
Exp Ther Med. 2019 Jul;18(1):172-178. doi: 10.3892/etm.2019.7572. Epub 2019 May 10.
The glycyrrhizic acid (GA) epimers 18α- and 18β-GA exert anti-inflammatory and hepatoprotective activities, which may help to protect against alcoholic liver disease, particularly alcoholic hepatitis (AH). The aim of the present study was to investigate the optimal ratio of 18α- and 18β-GA for preventing AH in rats. Different groups of rats were administered seven different ratios of 18α- and 18β-GA (10:0, 8:2, 6:4, 5:5, 4:6, 2:8 and 0:10; 10.83 mg/kg), vehicle control, or silymarin (22.75 mg/kg) as a positive control, followed by administration of 40% alcohol (10 ml/kg) once a day for four weeks. Subsequently, livers were isolated and routinely processed for histological examination. The serum levels of 23 cytokines and chemokines associated with AH were examined with a Bio-Plex 200 Luminex assay. It was revealed that all ratios of 18α- and 18β-GA prevented alcohol-induced liver injury, as evidenced by a lesser degree of histopathological changes in the liver as compared with those in the model group. Furthermore, the levels of 15 cytokines/chemokines were significantly altered after alcohol administration, which was significantly inhibited by, pre-treatment with different proportions of 18α- and 18β-GA, particularly at a ratio of 4:6, for most cytokines/chemokines associated with AH, including tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-2, IL-4, IL-5, IL-7, IL-6, monocyte chemotactic protein 1 (MCP-1), macrophage inflammatory protein (MIP)-1α, MIP-3α, macrophage- and granulocyte macrophage colony-stimulating factor, chemokine (C-X-C motif) ligand 1(GRO/KC), vascular endothelial growth factor and C-C motif chemokine ligand 5 (RANTES). Taken together, based on these results the optimal ratio of 18α- and 18β-GA to prevent AH in model rats was considered to be 4:6.
甘草酸(GA)的差向异构体18α - GA和18β - GA具有抗炎和保肝活性,这可能有助于预防酒精性肝病,尤其是酒精性肝炎(AH)。本研究的目的是探讨18α - GA和18β - GA预防大鼠AH的最佳比例。将不同组的大鼠给予七种不同比例的18α - GA和18β - GA(10:0、8:2、6:4、5:5、4:6、2:8和0:10;10.83毫克/千克)、溶剂对照或水飞蓟宾(22.75毫克/千克)作为阳性对照,随后每天给予一次40%酒精(10毫升/千克),持续四周。随后,分离肝脏并进行常规处理以进行组织学检查。使用Bio - Plex 200 Luminex检测法检测与AH相关的23种细胞因子和趋化因子的血清水平。结果显示,所有比例的18α - GA和18β - GA均能预防酒精诱导的肝损伤,与模型组相比,肝脏组织病理学变化程度较轻即可证明。此外,酒精给药后15种细胞因子/趋化因子的水平发生了显著改变,用不同比例的18α - GA和18β - GA预处理可显著抑制这种改变,特别是对于与AH相关的大多数细胞因子/趋化因子,在比例为4:6时,包括肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β、IL - 2、IL - 4、IL - 5、IL - 7、IL - 6、单核细胞趋化蛋白1(MCP - 1)、巨噬细胞炎性蛋白(MIP)-1α、MIP - 3α、巨噬细胞和粒细胞巨噬细胞集落刺激因子、趋化因子(C - X - C基序)配体1(GRO/KC)、血管内皮生长因子和C - C基序趋化因子配体5(RANTES)。综上所述,基于这些结果,18α - GA和18β - GA预防模型大鼠AH的最佳比例被认为是4:6。