Anti-inflammatory and hepatoprotective effects of total flavonoid C-glycosides from Abrus mollis extracts.
10.1016/S1875-5364(14)60090-X
- Author:
Mi CHEN
1
;
Tao WANG
1
;
Zhen-Zhou JIANG
2
,
3
;
Chun SHAN
1
;
Hao WANG
4
;
Mei-Juan WU
1
;
Shuang ZHANG
1
;
Yun ZHANG
5
;
Lu-Yong ZHANG
2
,
6
Author Information
1. Jiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, China.
2. Jiangsu Center for Drug Screening, China Pharmaceutical University, Nanjing 210009, China
3. Jiangsu Center for Pharmacodynamics Research and Evaluation, China Pharmaceutical University, Nanjing 210009, China.
4. Department of Natural Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China.
5. Biology Institute of Shandong Academy of Sciences, Jinan 250014, China.
6. Key Laboratory of Drug Quality Control and Pharmacovigilance (China Pharmaceutical University), Ministry of Education, Nanjing 210009, China. Electronic address: lyzhang@cpu.edu.cn.
- Publication Type:Journal Article
- Keywords:
Abrus mollis;
Flavonoid C-glycosides;
Inflammation;
Liver injury
- MeSH:
Abrus;
chemistry;
Animals;
Anti-Inflammatory Agents;
pharmacology;
therapeutic use;
Biomarkers;
blood;
Carbon Tetrachloride;
Carrageenan;
Chemical and Drug Induced Liver Injury;
drug therapy;
metabolism;
pathology;
Edema;
chemically induced;
drug therapy;
Female;
Flavonoids;
pharmacology;
therapeutic use;
Galactosamine;
Glycosides;
pharmacology;
therapeutic use;
Inflammation;
chemically induced;
drug therapy;
pathology;
Liver;
drug effects;
metabolism;
pathology;
Liver Cirrhosis;
drug therapy;
Male;
Mice, Inbred ICR;
Monosaccharides;
Phytotherapy;
Plant Extracts;
pharmacology;
therapeutic use;
Protective Agents;
pharmacology;
therapeutic use;
Rats, Sprague-Dawley;
Xylenes
- From:
Chinese Journal of Natural Medicines (English Ed.)
2014;12(8):590-598
- CountryChina
- Language:English
-
Abstract:
The aim of this study was to evaluate the anti-inflammatory and hepatoprotective effects of the total flavonoid C-glycosides isolated from Abrus mollis extracts (AME). In the anti-inflammatory tests, xylene-induced ear edema model in mice and carrageenan-induced paw edema model in rats were applied. The hepatoprotective effects of AME were evaluated with various in vivo models of acute and chronic liver injury, including carbon tetrachloride (CCl4)-induced hepatitis in mice, D-galactosamine (D-GalN)-induced hepatitis in rats, as well as CCl4-induced hepatic fibrosis in rats. In the acute inflammation experiment, AME significantly suppressed xylene-induced ear edema and carrageenan-induced paw edema, respectively. In the acute hepatitis tests, AME significantly attenuated the excessive release of ALT and AST induced by CCl4 and D-GalN. In CCl4-induced hepatic fibrosis model, AME alleviated liver injury induced by CCl4 shown by histopathological sections of livers and improved liver function as indicated by decreased liver index, serum ALT, AST, TBIL, and ALP levels and hydroxyproline contents in liver tissues, and increased serum ALB and GLU levels. These results indicated that AME possesses potent anti-inflammatory activity in acute inflammation models and hepatoprotective activity in both acute and chronic liver injury models. In conclusion, AME is a potential anti-inflammatory and hepatoprotective agent and a viable candidate for treating inflammation, hepatitis, and hepatic fibrosis.
