Protective effect of turmeric extract on ethotrexate-induced intestinal damage and oxidative stress.
10.1016/S1875-5364(13)60087-4
- Author:
Adel Rezaei MOGHADAM
1
,
2
;
Daryoush MOHAJERI
3
;
Ali NAMVARAN-ABBAS-ABAD
4
;
Hamed MANAFI
5
;
Delavar SHAHI
5
;
Mohammad MAZANI
6
Author Information
1. Young Researchers Club, Ardabil Branch, Islamic Azad University, Ardabil, Iran
2. Faculty of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
3. Department of Pathobiology, Faculty of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
4. Young Researchers and Elite Club, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
5. Faculty of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran.
6. Department of Biochemistry, Ardabil University of Medical Science, Ardabil, Iran. Electronic address: m.mazani@arums.ac.ir.
- Publication Type:Journal Article
- Keywords:
Intestinal damage;
Methotrexate;
Oxidative stress;
Turmeric
- MeSH:
Animals;
Catalase;
metabolism;
Curcuma;
chemistry;
Glutathione Peroxidase;
metabolism;
Humans;
Intestinal Diseases;
chemically induced;
drug therapy;
enzymology;
metabolism;
Intestinal Mucosa;
metabolism;
Male;
Malondialdehyde;
metabolism;
Methotrexate;
adverse effects;
Oxidative Stress;
drug effects;
Plant Extracts;
administration & dosage;
Rats;
Rats, Wistar;
Superoxide Dismutase;
metabolism
- From:
Chinese Journal of Natural Medicines (English Ed.)
2013;11(5):477-483
- CountryChina
- Language:English
-
Abstract:
AIM:The most important side effect of methotrexate (MTX) is mucositis. The purpose of this study was to evaluate the effect of turmeric extract on intestinal damage and oxidative stress in rats receiving methotrexate.
METHODS:Experiments were performed on male Wistar albino rats divided into six groups. First group received normal saline orally, the second group received turmeric extract (100 mg·kg(-1)) orally for 30 days, the third group received turmeric extract (200 mg·kg(-1)) orally for 30 days, the fourth group received a single dose of methotrexate (20 mg·kg(-1)) i.p. at day 30, the fifth group received turmeric extract (100 mg·kg(-1)) orally for 30 days and a single dose of methotrexate (20 mg·kg(-1)) i.p. at day 30, and the sixth group received turmeric extract (200 mg·kg(-1)) orally for 30 days and single dose of methotrexate (20 mg·kg(-1)) i.p. at day 30. Four days after methotrexate injection, animals were anesthetized, blood samples were taken to determine total antioxidant status (TAS) and jejunum samples were taken for glutathione peroxidase (GPx), superoxidase dismutase (SOD), catalase (CAT), aldehyde malondialdehyde (MDA), and histopathological assessment.
RESULTS:Microscopic evaluation from intestinal tissues of the MTX treated group, showed severe villus shortening and blunting, inflammatory cell infiltration and hemorrhage in lamina propria, along with epithlial cell necrosis. Levels of SOD, GSH-Px and CAT decreased in the MTX received group, but increased significantly (P < 0.05) in the turmeric + MTX groups. MTX increased lipid peroxidation, however, turmeric decreased peroxidation significantly (P < 0.05).
CONCLUSION:These results suggest that turmeric extract may protect the small intestine of rats from methotrexate-induced damage. Turmeric effects could result from its antioxidant properties.
