Manigandan Krishnan, Richard L. Jayaraj, Jayasekar Megala, Namasivayam Elangovan
{"title":"Antioxidant mediated antiulcer effect of Eupatorium triplinerve Vahl against acetic acid induced ulcerative colitis in mice","authors":"Manigandan Krishnan, Richard L. Jayaraj, Jayasekar Megala, Namasivayam Elangovan","doi":"10.1016/j.biomag.2013.12.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p><span>Ulcerative colitis<span> (UC) is associated with tainted neutrophil infiltration<span>, deregulated pro-inflammatory mediators, characterized by severe oxidative stress of the intestine. In the present study, an effort was made to evaluate the effect of methanolic fractions of </span></span></span><span><em>Eupatorium</em><em> triplinerve</em></span> (<em>E.</em> <em>triplinerve</em>) (ET) on acetic acid induced ulcerative colitis in male adult mice.</p></div><div><h3>Methods</h3><p><span>Colitis in mice was induced with 3.0% acetic acid (v/v) in saline via rectal route. Pre-intervention with </span><em>E.</em> <em>triplinerve</em> extract (100<!--> <!-->mg and 200<!--> <!-->mg<!--> <!-->kg<sup>−1</sup><span> body weight, oral) and reference drug<span> ranitidine (50</span></span> <!-->mg<!--> <!-->kg<sup>−1</sup> body weight used as reference, oral) 4<!--> <!-->days before induction of colitis and was extended up to 8<!--> <!-->days.</p></div><div><h3>Results</h3><p>The phase of inflammation before <em>E.</em> <em>triplinerve</em><span><span> extract pre-treatment significantly showed attenuated macroscopic damage, argyrophilic nuclear organization regions (AgNORs) count and histological changes. Similarly, extract also effectively detracts the activity of both Myeloperoxidase (MPO) and </span>Malondialdehyde<span><span> (MDA) levels by enhancing the cellular antioxidant enzyme levels (Glutathione-s-transferase [GST], </span>Glutathione<span><span> peroxidise [GPx] and Catalase [CAT]) at the site of </span>ulceration.</span></span></span></p></div><div><h3>Conclusions</h3><p>The <em>E.</em> <em>triplinerve</em><span> based therapy resolved that some constituents in extract have an antiulcer effect against UC at colon specific area through its inviolable radical scavenging activity.</span></p></div>","PeriodicalId":100181,"journal":{"name":"Biomedicine & Aging Pathology","volume":"4 2","pages":"Pages 153-160"},"PeriodicalIF":0.0000,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.biomag.2013.12.002","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Aging Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210522013000610","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15
Abstract
Purpose
Ulcerative colitis (UC) is associated with tainted neutrophil infiltration, deregulated pro-inflammatory mediators, characterized by severe oxidative stress of the intestine. In the present study, an effort was made to evaluate the effect of methanolic fractions of Eupatorium triplinerve (E.triplinerve) (ET) on acetic acid induced ulcerative colitis in male adult mice.
Methods
Colitis in mice was induced with 3.0% acetic acid (v/v) in saline via rectal route. Pre-intervention with E.triplinerve extract (100 mg and 200 mg kg−1 body weight, oral) and reference drug ranitidine (50 mg kg−1 body weight used as reference, oral) 4 days before induction of colitis and was extended up to 8 days.
Results
The phase of inflammation before E.triplinerve extract pre-treatment significantly showed attenuated macroscopic damage, argyrophilic nuclear organization regions (AgNORs) count and histological changes. Similarly, extract also effectively detracts the activity of both Myeloperoxidase (MPO) and Malondialdehyde (MDA) levels by enhancing the cellular antioxidant enzyme levels (Glutathione-s-transferase [GST], Glutathione peroxidise [GPx] and Catalase [CAT]) at the site of ulceration.
Conclusions
The E.triplinerve based therapy resolved that some constituents in extract have an antiulcer effect against UC at colon specific area through its inviolable radical scavenging activity.