FGF-21通过Sirt-1途径对酒精诱导肝脏脂肪堆积改善作用的机制研究

批准号:
81500665
项目类别:
青年科学基金项目
资助金额:
17.0 万元
负责人:
郑明华
依托单位:
学科分类:
H0710.脂质代谢异常
结题年份:
2018
批准年份:
2015
项目状态:
已结题
项目参与者:
施可庆、王周光、万晓珊、陈瑞聪、王永林
国基评审专家1V1指导 中标率高出同行96.8%
结合最新热点,提供专业选题建议
深度指导申报书撰写,确保创新可行
指导项目中标800+,快速提高中标率
微信扫码咨询
中文摘要
成纤维细胞生长因子21(FGF-21)是新发现的调节糖脂代谢的细胞因子。研究表明:FGF-21对非酒精性脂肪肝具有明显的治疗作用,而酒精性脂肪肝和非酒精性脂肪肝具有相同的病理变化过程。我们的前期研究结果表明,给酒精性脂肪肝小鼠注射重组人FGF-21可以显著减轻肝脏的脂肪堆积,改善酒精对肝脏的损伤。因此,我们将在此基础上继续研究FGF-21对酒精性脂肪肝改善作用的分子生物学机制,探讨FGF-21逆转酒精性肝病发展过程的可能性。根据前期工作,我们假设FGF21通过调节Sirt-1-SREBP-1c/ PGC-1α发挥降低肝脏脂肪堆积的作用。我们将给酒精性脂肪肝小鼠注射FGF21研究FGF-21的调节作用,同时利用酒精处理肝细胞系H4IIE阐明Sirt-1途径在FGF21改善酒精诱导肝脏脂肪堆积中的机制。本研究的完成,将进一步阐明FGF-21的作用,同时为开发治疗酒精性肝病的药物提供理论基础。
英文摘要
Fibroblast growth factor (FGF)-21 is one of the cytokines recently discovered to regulate lipid and glycometabolism. Previous studies have demonstrated that FGF-21 may have therapeutic potential for the treatment of non-alcoholic fatty liver disease. Our preliminary findings show that injection of recombinant human FGF-21 in a rat model of alcoholic fatty liver disease can largely alleviate the accumulation of fat in the liver and reduce alcohol-induced liver injury. Given these promising findings, we propose to continue our research to further understand the molecular biological mechanisms for which FGF-21 may play a role in alcoholic fatty liver disease. We will explore the possible role of FGF-21 in the initiation and progression of alcohol-induced fatty liver. Earlier work has suggested that FGF-21 may play a role in alleviating fat accumulation in the liver via attenuation of the Sirt (sirtuin)-1-SREBP (sterol regulatory element binding protein)-1c/PGC (PPAR coactivator )-1a axis. Specifically we will a). confirm and extend our early findings by conducting a rigorous pharmacological investigation of a dose response of FGF-21 in the rodent model of alcoholic fatty liver disease b). investigate the biological activation and signaling of Sirt-1 and fat accumulation over a time course in hepatic cell H4IIE in vitro assays exposed to ethanol. The deliverables and results of this study will provide greater understanding of the role of FGF-21 and Sirt-1 in alcoholic fatty liver disease and may have important clinical and social significance by providing both a theoretical and tested concept as a basis for the development of new medicines aimed at curing alcoholic liver disease.
成纤维细胞生长因子21(FGF-21)是新发现的调节糖脂代谢的细胞因子。最新研究表明:FGF-21对非酒精性脂肪肝具有明显的治疗作用,而酒精性脂肪肝和非酒精性脂肪肝具有相同的病理变化过程。我们的研究结果表明,给酒精性肝病小鼠注射重组人FGF-21可以逆转慢性酒精饲喂引起的肝脏脂肪变性和炎症损伤。我们还发现FGF21对慢性-急性酒精性肝损伤的保护作用。同时,我们也体外培养H4ⅡE细胞,研究FGF-21发挥作用的分子调控机制。发现酒精显著诱导肝H4IIE细胞脂肪堆积,当我们同时给予5ug/ml的重组FGF21处理时,酒精诱导的脂肪堆积显著降低。此外,我们也探讨了FGF21在慢性酒精诱导脂肪肝小鼠中的作用以及作用机理。将雄性FGF21敲除(FGF21KO)和对照(WT)小鼠分别喂含有5%酒精的Lieber DeCarli饮食和等热量(对照)饮食处理4周,评估肝脂肪变性和炎症损害程度。同时,分析肝脏中参与脂肪生成和脂肪酸β-氧化的蛋白和基因水平。喂饲酒精显著增加循环和肝脏中FGF21的表达。FGF21缺失加剧了酒精诱导的肝脂肪变性和肝损伤,与参与SREBP1c介导的脂肪生成的基因的活化增强有关,同时降低了由PGC1α介导的脂肪酸β-氧化的基因的表达。这些结果表明酒精诱导的FGF21表达是脂质失调时肝脏的适应性反应。靶向FGF21信号的干预可能是酒精性脂肪性肝炎的新型治疗方法。本研究结果进一步阐明了FGF-21的生物学功能,为开发治疗酒精性肝病的药物提供理论和前期基础,具有重要的临床意义和社会价值。
期刊论文列表
专著列表
科研奖励列表
会议论文列表
专利列表
The NAFL Risk Score: A simple scoring model to predict 4-y risk for non-alcoholic fatty liver
NAFL 风险评分:预测非酒精性脂肪肝 4 年风险的简单评分模型
DOI:10.1016/j.cca.2017.01.021
发表时间:2017-05-01
期刊:CLINICA CHIMICA ACTA
影响因子:5
作者:Zhou, Yu-Jie;Zheng, Ji-Na;Zheng, Ming-Hua
通讯作者:Zheng, Ming-Hua
Elevation of plateletcrit increasing the risk of non-alcoholic fatty liver disease development in female adults: A large population-based study
血小板压积升高会增加成年女性患非酒精性脂肪肝的风险:一项基于大规模人群的研究
DOI:10.1016/j.cca.2017.08.031
发表时间:2017
期刊:Clinica Chimica Acta
影响因子:5
作者:Wang Li-Ren;Zhou Yi-Fan;Zhou Yu-Jie;Zhang Shu-Hao;Liu Wen-Yue;Wu Sheng-Jie;Van Poucke Sven;Zheng Ming-Hua
通讯作者:Zheng Ming-Hua
NAFL screening score: A basic score identifying ultrasound-diagnosed nonalcoholic fatty liver
NAFL 筛查评分:识别超声诊断非酒精性脂肪肝的基本评分
DOI:10.1016/j.cca.2017.09.020
发表时间:2017-12-01
期刊:CLINICA CHIMICA ACTA
影响因子:5
作者:Zhou, Yu-Jie;Zhou, Yi-Fan;Zheng, Ming-Hua
通讯作者:Zheng, Ming-Hua
Association between oxytocin and receptor genetic polymorphisms and aggression in a northern Chinese Han population with alcohol dependence
中国北方汉族酒精依赖人群催产素与受体基因多态性与攻击行为的关系
DOI:10.1016/j.neulet.2016.10.066
发表时间:2017
期刊:Neuroscience Letters
影响因子:2.5
作者:Yang Ling;Wang Fan;Wang Meiling;Han Mei;Hu Lufeng;Zheng Minghua;Ma Ji;Kang Yimin;Wang Pengxiang;Sun Hongqiang;Zuo Wei;Xie Longteng;Wang Aiju;Yu Dongsheng;Liu Yanlong
通讯作者:Liu Yanlong
DOI:S0304-3940(16)30808-4 [pii]
发表时间:2017
期刊:Neurosci Lett
影响因子:--
作者:L. Yang;F. Wang;M. Wang;M. Han;L. Hu;M. Zheng;J. Ma;Y. Kang;P. Wang;H. Sun;W. Zuo;L. Xie;A. Wang;D. Yu;Y. Liu
通讯作者:Y. Liu
SEMA7A基因突变促进非酒精性脂肪性肝病进展的机制研究
- 批准号:82370577
- 项目类别:面上项目
- 资助金额:48万元
- 批准年份:2023
- 负责人:郑明华
- 依托单位:
S100家族A11在非酒精性脂肪性肝炎的作用及机制研究
- 批准号:82070588
- 项目类别:面上项目
- 资助金额:55万元
- 批准年份:2020
- 负责人:郑明华
- 依托单位:
国内基金
海外基金
