Gallic acid prevents 1, 2-Dimethylhydrazine induced colon inflammation, toxicity, mucin depletion, and goblet cell disintegration.


Journal

Environmental toxicology
ISSN: 1522-7278
Titre abrégé: Environ Toxicol
Pays: United States
ID NLM: 100885357

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 19 10 2019
revised: 30 11 2019
accepted: 27 12 2019
pubmed: 12 1 2020
medline: 17 6 2020
entrez: 12 1 2020
Statut: ppublish

Résumé

1,2-Dimethylhydrazine (DMH), an environmental toxicant specifically targets the colon. The present study was aimed to evaluate the efficacy of gallic acid (GA) against colon toxicity induced by DMH in Wistar rats. GA, a phenolic acid has numerous beneficial properties, which include antiviral, antifungal and antioxidant properties which help cells to overcome oxidative stress and balance the redox homeostasis. GA was administered orally at two doses (25 and 50 mg/kg body weight) once daily for 14 days and a single dose (40 mg/kg body weight) of DMH was administered subcutaneously on 14th day. Animals were sacrificed on the 15th day and we could find that GA at both the doses significantly ameliorates DMH-induced increased toxicity markers and also substantially increases the glutathione content level and activities of detoxifying enzymes. It also ameliorates the expression of proliferation, inflammation, apoptosis, goblet cell disintegration, and mucin depletion in the colon that was elevated upon administration of DMH. Histological alterations provide further confirmation of the protective role of GA against DMH-induced colon toxicity. The results of this study clearly indicate supplementation of GA is beneficial in ameliorating DMH-induced oxidative stress, inflammation, proliferation, apoptosis, mucin depletion, and goblet cell disintegration in colon of Wistar rats.

Identifiants

pubmed: 31925992
doi: 10.1002/tox.22900
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Antioxidants 0
Mucins 0
Gallic Acid 632XD903SP
Glutathione GAN16C9B8O
1,2-Dimethylhydrazine IX068S9745

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

652-664

Informations de copyright

© 2020 Wiley Periodicals, Inc.

Références

Schulz MD, Atay Ç, Heringer J, et al. High-fat-diet-mediated dysbiosis promotes intestinal carcinogenesis independently of obesity. Nature. 2014;514(7523):508.
Reddy BS. Diet and colon cancer: evidence from human and animal model studies. Diet, Nutrition and Cancer: A Critical Evaluation. Abingdon, UK: CRC Press: Taylor and Francis; 2018:47-66.
Adams JM, Cory S. The Bcl-2 protein family: arbiters of cell survival. Science. 1998;281(5381):1322-1326.
Mols F, Beijers T, Lemmens V, van den Hurk CJ, Vreugdenhil G, van de Poll-Franse LV. Chemotherapy-induced neuropathy and its association with quality of life among 2-to 11-year colorectal cancer survivors: results from the population-based PROFILES registry. J Clin Oncol. 2013;31(21):2699-2707.
Jadon A, Bhadauria M, Shukla S. Protective effect of Terminalia belerica Roxb. And gallic acid against carbon tetrachloride induced damage in albino rats. J Ethnopharmacol. 2007;109(2):214-218.
Otles S, Nakilcioglu E. Determination of phenolic compounds (Gallic, Caffeic, Ferulic, and p-Coumaric acids). Flow Injection Analysis of Food Additives. Florida, USA: CRC Press: Taylor and Francis; Vol 1; 2015:393.
Kumar M, Kumar S, Kaur S. Role of ROS and COX-2/iNOS inhibition in cancer chemoprevention: a review. Phytochem Rev. 2012;11(2-3):309-337.
Bv K, Van den Berg A, Van Ufford HQ, Van Dijk H, Labadie R. Anti-inflammatory activity of gallic acid. Planta Med. 1992;58(6):499-504.
Gichner T, Pospíšil F, Velemínský J, Volkeova V, Volke J. Two types of antimutagenic effects of gallic and tannic acids towards N-nitroso-compounds-induced mutagenicity in the amesSalmonella assay. Folia Microbiol. 1987;32(1):55-62.
Niho N, Shibutani M, Tamura T, et al. Subchronic toxicity study of gallic acid by oral administration in F344 rats. Food Chem Toxicol. 2001;39(11):1063-1070.
Hazra B, Sarkar R, Biswas S, Mandal N. The antioxidant, iron chelating and DNA protective properties of 70% methanolic extract of “Katha” (heartwood extract of Acacia catechu). J Complement Integr Med. 2010;7(1):374-384.
Kim B, ParK J-S, Choi H-Y, Kwak J-H, Kim W-G. Differential effects of alkyl gallates on quorum sensing in Pseudomonas aeruginosa. Sci Rep. 2019;9(1):7741.
Maruszewska A, Tarasiuk J. Antitumour effects of selected plant polyphenols, gallic acid and ellagic acid, on sensitive and multidrug-resistant leukaemia HL60 cells. Phytother Res. 2019;33(4):1208-1221.
Frazier DE, Tarr MJ, Olsen RG. The in Vltro and in vivo effects of 1.1-Dimethylhydrazine (Udmh) on murine lymphocyte subsets and Ia antigen expression. Immunopharmacol Immunotoxicol. 1991;13(1-2):25-46.
Toth B, Gannett P. Carcinogenesis study in mice by 3-methylbutanal methylformylhydrazone of Gyromitra esculenta. In Vivo. 1990;4(5):283-288.
Arutiunian A, Prokopenko V, Burmistrov S, et al. Free-radical processes in blood serum, liver and large bowel during 1, 2-dimethylhydrazine-induced carcinogenesis in rats. Vopr Onkologii. 1997;43(6):618-622.
Buttke TM, Sandstrom PA. Oxidative stress as a mediator of apoptosis. Immunol Today. 1994;15(1):7-10.
Fiala ES. Investigations into the metabolism and mode of action of the colon carcinogens 1, 2-dimethylhydrazine and azoxymethane. Cancer. 1977;40(S5):2436-2445.
Fiala ES, Sohn OS, Hamilton SR. Effects of chronic dietary ethanol on in vivo and in vitro metabolism of methylazoxymethanol and on methylazoxymethanol-induced DNA methylation in rat colon and liver. Cancer Res. 1987;47(22):5939-5943.
Hsu C-L, Yen G-C. Effect of gallic acid on high fat diet-induced dyslipidaemia, hepatosteatosis and oxidative stress in rats. Br J Nutr. 2007;98(4):727-735.
Raina K, Rajamanickam S, Deep G, Singh M, Agarwal R, Agarwal C. Chemopreventive effects of oral gallic acid feeding on tumor growth and progression in TRAMP mice. Mol Cancer Ther. 2008;7(5):1258-1267.
Hamiza OO, Rehman MU, Tahir M, et al. Amelioration of 1, 2 Dimethylhydrazine (DMH) induced colon oxidative stress, inflammation and tumor promotion response by tannic acid in Wistar rats. Asian Pac J Cancer Prev. 2012;13(9):4393-4402.
Khan R, Sultana S. Farnesol attenuates 1, 2-dimethylhydrazine induced oxidative stress, inflammation and apoptotic responses in the colon of Wistar rats. Chem Biol Interact. 2011;192(3):193-200.
Mohandas J, Marshall JJ, Duggin GG, Horvath JS, Tiller DJ. Differential distribution of glutathione and glutathione-related enzymes in rabbit kidney: possible implications in analgesic nephropathy. Biochem Pharmacol. 1984;33(11):1801-1807.
Carlberg I, Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem. 1975;250(14):5475-5480.
Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases the first enzymatic step in mercapturic acid formation. J Biol Chem. 1974;249(22):7130-7139.
Claiborne A. Catalase activity. CRC Handbook of Methods for Oxygen Radical Research. Florida, USA: CRC Press: Taylor and Francis; 1986.
Jollow D, Mitchell J, Zampaglione N, Gillette J. Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology. 1974;11(3):151-169.
Wright J, Colby H, Miles P. Cytosolic factors which affect microsomal lipid peroxidation in lung and liver. Arch Biochem Biophys. 1981;206(2):296-304.
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265-275.
Hasan SK, Islam J, Vafa A, et al. Colono-protective potentiality of Methanolic bark extract of Acacia catechu: a medicinal plant against 1, 2-Dimethylhydrazine-induced toxicity in Wistar rats. J Environ Pathol Toxicol Oncol. 2018;37(4):273-289.
Khan R, Khan AQ, Lateef A, et al. Glycyrrhizic acid suppresses the development of precancerous lesions via regulating the hyperproliferation, inflammation, angiogenesis and apoptosis in the colon of Wistar rats. PLoS One. 2013;8(2):e56020.
Rayaprolu SJ, Hettiarachchy NS, Chen P, Kannan A, Mauromostakos A. Peptides derived from high oleic acid soybean meals inhibit colon, liver and lung cancer cell growth. Food Res Int. 2013;50(1):282-288.
Bickers DR, Athar M. Oxidative stress in the pathogenesis of skin disease. J Invest Dermatol. 2006;126(12):2565-2575.
Visconti R, Grieco D. New insights on oxidative stress in cancer. Curr Opin Drug Discov Devel. 2009;12(2):240-245.
Ravi T, Mahima B, Deepti P, Kanchan K, Reena N, Khanna H. Oxidative stress induced lipid peroxidation and DNA adduct formation in the pathogenesis of multiple myeloma and lymphoma. J Stress Physiol Biochem. 2013;9(1):106-112.
Shahid A, Ali R, Ali N, et al. Attenuation of genotoxicity, oxidative stress, apoptosis and inflammation by rutin in benzo (a) pyrene exposed lungs of mice: plausible role of NF-κB, TNF-α and Bcl-2. J Comp Integr Med. 2016;13(1):17-29.
Sharma S, Sultana S. Modulatory effect of soy isoflavones on biochemical alterations mediated by TPA in mouse skin model. Food Chem Toxicol. 2004;42(10):1669-1675.
Ortega-Muñoz M, Rodríguez-Serrano F, De los Reyes-Berbel E, et al. Biological evaluation and docking studies of synthetic Oleanane-type triterpenoids. ACS Omega. 2018;3(9):11455-11468.
Takasaki Y, Deng J-S, Tan EM. A nuclear antigen associated with cell proliferation and blast transformation. J Exp Med. 1981;154(6):1899-1909.
Kannan K, Jain SK. Oxidative stress and apoptosis. Pathophysiology. 2000;7(3):153-163.
Carthy CM, Yanagawa B, Luo H, et al. Bcl-2 and Bcl-xL overexpression inhibits cytochrome c release, activation of multiple caspases, and virus release following coxsackievirus B3 infection. Virology. 2003;313(1):147-157.
Tanaka T. Colorectal carcinogenesis: review of human and experimental animal studies. J Carcinog. 2009;8: http://doi.org/10.4103/1477-3163.49014.

Auteurs

Alpa Shree (A)

Department of Medical Elementology and Toxicology, Jamia Hamdard, New Delhi, India.

Johirul Islam (J)

Department of Medical Elementology and Toxicology, Jamia Hamdard, New Delhi, India.

Abul Vafa (A)

Department of Medical Elementology and Toxicology, Jamia Hamdard, New Delhi, India.

Sheikh Mohammad Afzal (S)

Department of Medical Elementology and Toxicology, Jamia Hamdard, New Delhi, India.

Sarwat Sultana (S)

Department of Medical Elementology and Toxicology, Jamia Hamdard, New Delhi, India.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH