Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model

被引:8
作者
Sahreen, Sumaira [1 ]
Khan, Muhammad Rashid [2 ]
Khan, Rahmat Ali [2 ,3 ]
机构
[1] Pakistan Museum Nat Hist, Bot Sci Div, Garden Ave, Islamabad, Pakistan
[2] Quaid I Azam Univ, Fac Biol Sci, Dept Biochem, Islamabad, Pakistan
[3] Univ Sci & Technol, Fac Biol Sci, Dept Biotechnol, Bannu 28100, Kpk, Pakistan
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2017年 / 17卷
关键词
Rumex hastatus; leaves; Carbon tetrachloride; Hepatotoxicity; Oxidative stress; Fibrosis; TETRACHLORIDE-INDUCED HEPATOTOXICITY; CARBON-TETRACHLORIDE; OXIDATIVE STRESS; LIVER FIBROSIS; GLUTATHIONE; EXTRACT; CCL4; CARCINOGENESIS; ANTIOXIDANTS; PROTECTION;
D O I
10.1186/s12906-017-1943-5
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background: Rumex hastatus leaves have been widely used as food additive and for the treatment of various liver ailments. According to our previous studies, ethyle acetate (ERL) and methanolic (MRL) fractions of R. hastatus leaves are an accessible source of natural antioxidants. In the present research work we arranged to investigate the R. hastatus leaves as hepaptoprotective agent verse hepatic damages caused by CCl4. Methods: During this project we divided 48 rats into eight groups randomly. CCl4-induced damages were assessed through liver function markers viz.; alkaline phosphatase (ALP), alanine transaminase (ALT), aspartate transaminase (AST),gamma-glutamyltransferase (gamma-GT) and lactate dehydrogenase (LDH). Changes in lipid profile were checked by measuring serum total cholesterol (TC), triglycerides (Tg), high density lipoproteins (HDL) and low density lipoproteins (LDL). Antioxidant status was checked by the activities of antioxidant enzymes, DNA damages and cellular abnormalities at histo level. Results: Administration of CCl4 in rats caused significant increase in liver function and lipid profile indicating hepatic damages which were restored by co-administration of R. hastatus extracts. Cellular and DNA damages in hepatic tissues were caused by CCl4 which shown clear hepatic fibrosis in addition to disturb antioxidant enzyme level. Co-treatment with various fractions of R. hastatus leaves regulated these markers of oxidative dysfunctions. Conclusion: From the present report it was inferred that R. hastatus leaves have the ability to reverse CCl4 - induced hepatic damages.
引用
收藏
页数:8
相关论文
共 35 条
  • [1] Ahmad S., 2015, Pharmacol., V1, P13
  • [2] Antioxidant and anticholinesterase investigations of Rumex hastatus D. Don: potential effectiveness in oxidative stress and neurological disorders
    Ahmad, Sajjad
    Ullah, Farhat
    Ayaz, Muhammad
    Sadiq, Abdul
    Imran, Muhammad
    [J]. BIOLOGICAL RESEARCH, 2015, 48
  • [3] INCREASE OF NAD(P)H-QUINONE REDUCTASE BY DIETARY ANTIOXIDANTS - POSSIBLE ROLE IN PROTECTION AGAINST CARCINOGENESIS AND TOXICITY
    BENSON, AM
    HUNKELER, MJ
    TALALAY, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09): : 5216 - 5220
  • [4] Reversal of acetaminophen induced subchronic hepatorenal injury by propolis extract in rats
    Bhadauria, Monika
    Nirala, Satendra Kumar
    [J]. ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2009, 27 (01) : 17 - 25
  • [5] CARLBERG I, 1975, J BIOL CHEM, V250, P5475
  • [6] ASSAY OF CATALASES AND PEROXIDASES
    CHANCE, B
    MAEHLY, AC
    [J]. METHODS IN ENZYMOLOGY, 1955, 2 : 764 - 775
  • [7] Resveratrol prevents fibrosis, NF-κB activation and TGF-β increases induced by chronic CCl4 treatment in rats
    Chavez, Enrique
    Reyes-Gordillo, Karina
    Segovia, Jose
    Shibayama, Mineko
    Tsutsumi, Victor
    Vergara, Paula
    Moreno, Mario G.
    Muriel, Pablo
    [J]. JOURNAL OF APPLIED TOXICOLOGY, 2008, 28 (01) : 35 - 43
  • [8] Gorsi M.S., 2002, Asian J. Plant Sci., V1, P604
  • [9] HABIG WH, 1974, J BIOL CHEM, V249, P7130
  • [10] Effects of extract from Ginkgo biloba on carbon tetrachloride-induced liver injury in rats
    He, Shui-Xiang
    Luo, Jin-Yan
    Wang, Yue-Peng
    Wang, Yan-Li
    Fu, Han
    Xu, Jun-Li
    Zhao, Gang
    Liu, En-Qi
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (24) : 3924 - 3928