临床肝胆病杂志2024，Vol.40Issue(1)：121-128,8.DOI:10.12449/JCH240121
四烯甲萘醌(MK-4)对CCl4诱导的急性肝损伤小鼠模型的保护作用分析
Menaquinone-4 exerts a protective effect against carbon tetrachloride-induced acute liver injury in mice by alleviating ferroptosis
摘要
Abstract
Objective To investigate whether menaquinone-4(MK-4)can exert a protective effect against carbon tetrachloride(CCl4)-induced acute liver injury(ALI)in mice by alleviating ferroptosis.Methods After adaptive feeding,adult male ICR mice,aged 8 weeks,were divided into Control group,MK-4 group,CCl4 model group(6-hour,12-hour,and 24-hour),and MK-4+CCl4 group(6-hour,12-hour,and 24-hour),with 6 mice in each group.The mice in the Control group were given intraperitoneal injection of an equal dose of corn oil;the mice in the MK-4 group were given intraperitoneal injection of 40 mg/kg MK-4 solution,followed by an equal dose of corn oil after 1 hour;the mice in the MK-4+CCl4 group(6-hour,12-hour,and 24-hour)were given intraperitoneal injection of 40 mg/kg MK-4 solution,and after 1 hour,the mice in this group and the CCl4 model group(6-hour,12-hour,and 24-hour)were given intraperitoneal injection of 0.3 mL/kg CCl4 solution,with samples collected at 6,12,and 24 hours.HE staining was used to observe the pathological changes of mouse liver;Prussian blue staining was used to observe iron accumulation in liver tissue;a biochemical analyzer was used to measure the serum levels of aspartate aminotransferase(AST)and alanine aminotransferase(ALT);related kits were used to measure the levels of tissue iron content and the oxidative stress indices malondialdehyde(MDA)and glutathione(GSH)in liver homogenate;RT-PCR was used to measure the expression levels of ferroptosis marker genes(acyl-CoA synthetase long-chain family member 4[ACSL4],prostaglandin-endoperoxide synthase 2[PTGS2],and glutathione peroxidase 4[GPX4])and iron metabolism-related genes(hemojuvelin[HJV],transferrin receptor 1[TFR1],and ferroportin[FPN]),and Western blot was used to measure the protein expression level of GPX4.A one-way analysis of variance was used for comparison of continuous data between multiple groups,and the least significant difference t-test was used for further comparison between two groups.Results In the aging study,compared with the Control group,the CCl4 model group(6-hour,12-hour,and 24-hour)had significant increases in liver weight coefficient and the serum levels of ALT and AST(all P<0.05),and HE staining also showed that liver injury gradually aggravated over time.Meanwhile,compared with the CCl4 model group(6-hour,12-hour,and 24-hour),the MK-4+CCl4(12-hour)group had significant reductions in liver weight coefficient and the serum levels of ALT and AST(all P<0.05),with a reduction in the necrotic area of liver tissue,and therefore,12-hour mouse tissue samples were used for detection in the following study.Compared with the Control group,the CCl4 group had a significant increase in MDA and a significant reduction in GSH(both P<0.05),and compared with the CCl4 group,the MK-4+CCl4 group had a significant reduction in MDA and a significant increase in GSH(both P<0.05).Compared with the Control group,the CCl4 group had significant increases in the key ferroptosis indices ASCL4 and PTGS2 and a significant reduction in GPX4(all P<0.05);compared with the CCl4 group,the MK-4+CCl4 group had significant reductions in the mRNA expression levels of ASCL4 and PTGS2 and a significant increase in the mRNA expression level of GPX4(all P<0.05).Western blotting showed that compared with the Control group,the CCl4 group had a significant reduction in the protein expression level of GPX4(P<0.05),and compared with the CCl4 group,the MK-4+CCl4 group had a significant increase in the protein expression level of GPX4(P<0.05).Prussian blue staining showed that compared with the Control group,the CCl4 group had a significant increase in iron accumulation;after MK-4 intervention,compared with the CCl4 group,the MK-4+CCl4 group had a significant reduction in iron accumulation.As for the measurement of iron metabolism genes in mouse liver,compared with the Control group,the CCl4 group had a significant increase in iron content,significant reductions in the mRNA expression levels of FPN and HJV,and a significant increase in the mRNA expression level of TFR1(all P<0.05);after protection with MK-4,there was a significant reduction in iron content,significant increases in the mRNA expression levels of FPN and HJV,and a significant reduction in the mRNA expression level of TFR1(all P<0.05).Conclusion MK-4 intervention in advance can alleviate CCl4-induced ALI in mice,possibly by inhibiting ferroptosis and improving the expression of iron metabolism-related genes in mouse liver.关键词
肝功能衰竭,急性/铁死亡/甲萘醌4/小鼠,近交ICRKey words
Liver Failure,Acute/Ferroptosis/Menaquinone-4/Mice,Inbred ICR引用本文复制引用
叶露,赵凡,黄倩倩,张佳怡,王建青..四烯甲萘醌(MK-4)对CCl4诱导的急性肝损伤小鼠模型的保护作用分析[J].临床肝胆病杂志,2024,40(1):121-128,8.基金项目
国家自然科学基金(82073566) （82073566）
安徽省高校优秀青年人才支持计划资助项目(gxyq2019014) （gxyq2019014）
临床药学与药理学共建项目(2020) （2020）
安徽省公共卫生临床中心安徽医科大学第一附属医院北区科研培育基金资助项目(2023YKJ14,2023YKJ06,2023YKJ11) National Natural Science Foundation of China(82073566) （2023YKJ14,2023YKJ06,2023YKJ11）
The Program of Excellent Young Talents in Universities of Anhui Province(gxyq2019014) （gxyq2019014）
Clinical Pharmacy and Pharmacology(2020) （2020）
Anhui Public Health Clinical Center,Supported by North District Scientific Research and Cultivation Foundation of the First Affiliated Hospital of Anhui Medical University(2023YKJ14,2023YKJ06,2023YKJ11) （2023YKJ14,2023YKJ06,2023YKJ11）
