The effect and mechanism of highland barley β-glucan in improving liver regeneration after partial hepatectomy

被引:2
|
作者
Liu, Qinhui [1 ,2 ]
Tang, Qin [1 ]
Liu, Xinchun [2 ]
Tian, Min [2 ]
Jing, Xiandan [1 ]
Feng, Zongyun [2 ,5 ]
Yang, Xuping [3 ,4 ]
机构
[1] Sichuan Univ, Inst Metab Dis & Pharmacotherapy, West China Hosp, Chengdu 610041, Peoples R China
[2] Sichuan Agr Univ, Coll Agron, State Key Lab Crop Gene Explorat & Utilizat Southw, Chengdu 611130, Peoples R China
[3] Southwest Med Univ, Dept Pharm, Affiliated Hosp, Luzhou 646000, Peoples R China
[4] Southwest Med Univ, Dept Pharm, Affiliated Hosp, 25 Taiping St, Luzhou 646000, Peoples R China
[5] Sichuan Agr Univ, Coll Agron, State Key Lab Crop Gene Explorat & Utilizat Southw, 211 Huimin Rd, Chengdu 611130, Peoples R China
基金
中国国家自然科学基金;
关键词
beta-glucan; Highland barley; Hepatocyte proliferation; Liver regeneration; Partial hepatectomy; CELL-CYCLE; APOPTOSIS; INJURY; MICE; PROLIFERATION; SURVIVAL; MASS; AKT; D1;
D O I
10.1016/j.jff.2023.105631
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Studies have shown the beneficial effect of highland barley ss-glucan (HBBG) on multiple acute and chronic liver diseases, however, whether it can improve liver regeneration following 2/3 partial hepatectomy (PH) is yet unknown. This study investigated the positive effect of ss-glucan on liver regeneration in acute liver injury after PH. Before PH or CCl4 administration, mice were fed either a chow diet or that containing 5 or 10% HBBG for two weeks. The experimental mice were weighed on days 0, 1, and 2 after PH or CCl4 treatment, and the serum and liver tissue were collected. qRT-PCR, Western blotting, TUNEL staining, and immunostaining analysis were performed to measure the associated indices of proliferation and apoptosis of hepatocytes. We found that 5% HBBG promoted hepatocyte proliferation and liver regeneration and increased the liver/body weight ratio at 1 and 2 days after PH in mice. Mechanistically, HBBG activated the STAT3-CyclinD1 signaling pathway to increase hepatocyte proliferation, accelerating their transition from the G0 to S phase. Additionally, the HBBG intervention decreased hepatocyte apoptosis in the CCl4-induced liver injury model of mice. Concisely, HBBG can promote hepatocyte proliferation and liver regeneration via the STAT3-CyclinD1 signaling pathway in acute liver injury or PH.
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页数:9
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