Open AccessProtective effects ofTrifolium alexandrinumL. against lung injury induced by environmental toxin CCl4in experimental rats
Author(s) -
Rahmat Ali Khan,
Huda M. Alkreathy,
Abdus Saboorshah,
Mushtaq Ahmed,
Samiullah Khan
Publication year - 2016
Publication title -
food and nutrition research/food and nutrition research. supplement
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 37
eISSN - 1654-6628
pISSN - 1654-661X
DOI - 10.3402/fnr.v60.30433
Subject(s) - oxidative stress , carbon tetrachloride , catalase , glutathione , antioxidant , ccl4 , glutathione peroxidase , chemistry , thiobarbituric acid , tbars , pharmacology , biochemistry , lipid peroxidation , traditional medicine , biology , medicine , enzyme , organic chemistry
Background In Pakistan numerous medicinal floras has used in the treatment of various human ailments. Among them Trifolium alexandrinum L. is traditionally used in the curing of disease. Presently we designed to ascertain the protective role of Trifolium alexandrinum methanolic extracts (TAME) against carbon tetrachloride (CCl 4 )-induced lung injury and oxidative stress in rats. Methods Exposure to CCl 4 induces oxidative stress and causes tissue damage by the induction of CCl 4 free radicals. Twenty-four male albino rats were divided equally into four groups. Rats in group I had free access to drinking water and laboratory food. Group II was treated with 1 ml/kg body weight (b.w.) CCl 4 (30% in olive oil). Groups III and IV rats were fed (p.o.) 200 mg/kg b.w. TAME and 50 mg/kg b.w. silymarin after 24 h of CCl 4 treatment for 2 weeks. Results Administration of CCl 4 caused a significant ( p <0.01) decrease in the activities of antioxidant enzymes (catalase, peroxidase, glutathione peroxidase, glutathione- S -transferase), and glutathione contents were decreased; however, thiobarbituric acid-reactive substances were increased ( p <0.01). The alterations caused by CCl 4 were significantly ( p <0.01) reversed toward control levels by supplementation of TAME and silymarin. Conclusion These results suggest that in rats TAME and silymarin could protect the lungs against CCl 4 -induced oxidative damage.