Chrysin protects against cisplatin-induced colon. toxicity via amelioration of oxidative stress and apoptosis: Probable role of p38MAPK and p53
Description
Cisplatin, an antineoplastic drug, is widely used as a foremost therapy against numerous forms of cancer but it has pronounced adverse effects viz., nephrotoxicity, ototoxicity etc. CDDP-induced emesis and diarrhea are also marked toxicities that may be due to intestinal injury. Chrysin (5,7-dihydroxyflavone), a natural flavone commonly found in many plants possesses multiple biological activities, such as antioxidant, anti-inflammatory and anti-cancer effects. In the present study, we investigated the protective effect of chrysin against CDDP-induced colon toxicity. The plausible mechanism of CDDP-induced colon toxicity and damage includes oxidative stress, activation of p38MAPK and p53, and colonic epithelial cell apoptosis via upregulating the expression of Bak and cleaved caspase-3. Chrysin was administered to Wistar rats once daily for 14 consecutive days at the doses of 25 and 50 mg/kg body weight orally in corn oil. On day 14, a single intraperitoneal injection of cisplatin was given at the dose of 7.5 mg/kg body weight and animals were euthanized after 24 h of cisplatin injection. Chrysin ameliorated CDDP-induced lipid peroxidation, xanthine oxidase activity, glutathione depletion, decrease in antioxidant (catalase, glutathione reductase, glutathione peroxidase and glucose-6 phosphate dehydrogenase) and phase-II detoxifying (glutathione-S-transferase and quinone reductase) enzyme activities. Chrysin also attenuated goblet cell disintegration, expression of phospho-p38MAPK and p53, and apoptotic tissue damage which were induced by CDDP. Histological findings further supported the protective effects of chrysin against CDDP-induced colonic damage. The results of the present study suggest that the protective effect of chrysin against CDDP-induced colon toxicity was related with attenuation of oxidative stress, activation of p38MAPK and p53, and apoptotic tissue damage. Highlights: ► Cisplatin-induced colon toxicity is associated with oxidative stress and apoptosis. ► Chrysin abrogates cisplatin-induced phospho-p38MAPK, p53, Bak and caspase-3 expression. ► Chrysin abrogates cisplatin-induced goblet cell damage and histological alterations. ► Chrysin protects against cisplatin-induced apoptotic damages and oxidative stress.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2011.11.013Additional details
Identifiers
- DOI
- 10.1016/j.taap.2011.11.013;
- PII
- S0041-008X(11)00449-2;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 258
- Journal Issue
- 3
- Journal Page Range
- p. 315-329
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45036188
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANIMAL TISSUES; ANTINEOPLASTIC DRUGS; APOPTOSIS; BENZOQUINONES; BIOLOGICAL STRESS; CATALASE; CORN OIL; DAMAGE; GLUCOSE; GLUTATHIONE; INTRAPERITONEAL INJECTION; LARGE INTESTINE; NEOPLASMS; OXIDASES; OXIDATION; RATS; THERAPY; TOXICITY
- Descriptors DEC
- ALDEHYDES; ANIMALS; AROMATICS; BODY; CARBOHYDRATES; CHEMICAL REACTIONS; DIGESTIVE SYSTEM; DISEASES; DRUGS; ENZYMES; ESTERS; GASTROINTESTINAL TRACT; HEXOSES; INJECTION; INTAKE; INTESTINES; LIPIDS; MAMMALS; MEDICINE; MONOSACCHARIDES; OILS; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANS; OTHER ORGANIC COMPOUNDS; OXIDOREDUCTASES; PEPTIDES; PEROXIDASES; POLYPEPTIDES; PROTEINS; QUINONES; RADIOPROTECTIVE SUBSTANCES; RESPONSE MODIFYING FACTORS; RODENTS; SACCHARIDES; TRIGLYCERIDES; VEGETABLE OILS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.