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齐墩果酸二氟甲酯的合成及其抗肝纤维化作用

王娟 郑兴 张思 王冠 戴玲 于樱姿 姚旭 郑自通

药学研究2025,Vol.44Issue(6):543-546,4.
药学研究2025,Vol.44Issue(6):543-546,4.DOI:10.13506/j.cnki.jpr.2025.06.004

齐墩果酸二氟甲酯的合成及其抗肝纤维化作用

Synthesis of gem-difluoromethylenated oleanolic acid and its anti-hepatic fibrosis effect

王娟 1郑兴 2张思 3王冠 4戴玲 3于樱姿 4姚旭 4郑自通5

作者信息

  • 1. 长沙市第三医院<湖南大学附属长沙医院>药学部,湖南长沙 410000
  • 2. 南华大学衡阳医学院药学院药物药理研究所,湖南衡阳 421001||湖南科技职业学院药学院,湖南长沙 410000
  • 3. 湖南科技职业学院药学院,湖南长沙 410000
  • 4. 南华大学衡阳医学院药学院药物药理研究所,湖南衡阳 421001
  • 5. 南华大学附属第二医院药学部,湖南衡阳 421001
  • 折叠

摘要

Abstract

Objective To assess the protective efficacy of the novel compound difluoromethylenated oleanolic acid(DFOA)against liver fibrosis injury in mice,induced by carbon tetrachloride(CCl4).Methods To prepare DFOA and confirm its structure,84 mice were divided into normal control,liver fibrosis model,and low,medium,and high-dose DFOA groups,as well as a positive control group.Liver fibrosis was induced using CCl4,and the mice were administered drugs by gavage for 4 weeks.Serum liver function indicators(ALT,AST,ALB)were tested,and histopathological analysis of liver tis-sue was performed.Results Treatment with DFOA led to a statistically significant decrease in ALT and AST levels in mice with liver fibrosis,accompanied by a notable increase in ALB levels.Compared to the model group,DFOA-treated mice ex-hibited marked improvements in liver injury and a reduced extent of fibrosis.Conclusion DFOA emerges as a promising a-gent with a notable protective effect against CCl4-induced liver fibrosis,highlighting its potential applications in hepatopro-tection,transaminase reduction,and fibrosis antagonism.

关键词

齐墩果酸/小鼠/齐墩果酸二氟甲酯/肝纤维化

Key words

Oleanolic acid/Mice/Gem-difluoromethylenated oleanolic acid/Hepatic fibrosis

分类

医药卫生

引用本文复制引用

王娟,郑兴,张思,王冠,戴玲,于樱姿,姚旭,郑自通..齐墩果酸二氟甲酯的合成及其抗肝纤维化作用[J].药学研究,2025,44(6):543-546,4.

基金项目

中国科学院有机氟化学重点实验室项目(No.2018-10) (No.2018-10)

湖南省自然科学基金项目(No.2020JJ6052、2021JJ80015) (No.2020JJ6052、2021JJ80015)

湖南省科技厅重点项目(No.2016DK2001) (No.2016DK2001)

大学生创新创业训练计划项目(No.S202310555311) (No.S202310555311)

药学研究

2095-5375

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