Vitamin C alleviates alcoholic liver injury by suppressing neutrophil infiltration in senescence marker protein 30-knockout mice irrespective of its antioxidant effects

酒精性肝病 维生素 抗氧化剂 渗透(HVAC) 维生素C 内科学 内分泌学 化学 维生素E 基因剔除小鼠 乙醇 肝损伤 生物化学 医学 肝硬化 物理 受体 热力学
作者
Su-Min Baek,Seoung-Woo Lee,Young‐Jin Lee,Seong‐Kyoon Choi,Hee-Yeon Kim,Min‐Soo Seo,Soo‐Eun Sung,A-Rang Lee,Tae–Un Kim,Se‐Hyeon Han,Jun‐Hyeok Son,Sang‐Joon Park,Tae‐Hwan Kim,Kyu‐Shik Jeong,Jin‐Kyu Park
出处
期刊:Life Sciences [Elsevier BV]
卷期号:297: 120228-120228 被引量:13
标识
DOI:10.1016/j.lfs.2021.120228
摘要

Alcoholic liver disease (ALD) comprises an important component in chronic liver diseases, and its clinical significance has increased due to the high consumption of alcohol worldwide. Vitamin C is a potent antioxidant, and several previous studies have suggested that its therapeutic role in ALD is derived from its antioxidant role. However, its anti-inflammatory role in ALD remains to be elucidated. Especially, the relationship between vitamin C and infiltration of neutrophils in ALD has not been discussed to date. For the reason, the present study investigated the precise role of vitamin C in neutrophil infiltration in ALD.In the present study, wild-type C57BL/6 and vitamin C-deficient senescence marker protein 30-knockout mice were pair-fed with a Lieber-DeCarli control or ethanol diet. Ethanol-fed groups were fed with increasing concentrations of EtOH (Lieber-DeCarli control diet for 5 days, 3% EtOH diet for a week, and 5% diet for 2 weeks) with or without vitamin C supplementation.Vitamin C dramatically attenuated the ethanol-mediated liver disease in the vitamin C-deficient ethanol-fed mice group by suppressing the infiltration of neutrophils accompanied by less CD68-positive cell infiltration. This attenuating role of vitamin C in neutrophil infiltration in the liver is associated with its protective effect for the ethanol-mediated intestinal damage in vitamin C-deficient ethanol-fed mice.This study provides a novel possibility of vitamin C to be used as an anti-inflammatory therapeutic agent associated with neutrophil infiltration in ALD, thereby helping to establish strategies for attenuating ALD.
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