Manigandan Krishnan, Richard L. Jayaraj, Jayasekar Megala, Namasivayam Elangovan
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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":"{\"title\":\"Antioxidant mediated antiulcer effect of Eupatorium triplinerve Vahl against acetic acid induced ulcerative colitis in mice\",\"authors\":\"Manigandan Krishnan, Richard L. 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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. 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引用次数: 15
摘要
目的溃疡性结肠炎(UC)与中性粒细胞浸润污染、促炎介质失调有关,其特征是肠道严重氧化应激。本研究探讨了紫茎泽兰(E. triplinerve) (ET)甲醇组分对醋酸诱导的成年雄性小鼠溃疡性结肠炎的影响。方法用3.0%醋酸(v/v)灌胃盐水经直肠诱导小鼠结肠炎。在结肠炎诱导前4天给予三叶麻提取物(100 mg和200 mg kg - 1体重,口服)和参比药物雷尼替丁(50 mg kg - 1体重,口服)进行干预,并延长至8天。结果三叶麻提取物预处理前炎症期宏观损伤、亲银核组织区(AgNORs)计数及组织学改变明显减轻。同样,提取物还通过提高溃疡部位的细胞抗氧化酶(谷胱甘肽-s转移酶[GST]、谷胱甘肽过氧化物酶[GPx]和过氧化氢酶[CAT])水平,有效降低髓过氧化物酶(MPO)和丙二醛(MDA)水平的活性。结论三叶藤提取物中部分成分通过其不可侵犯的自由基清除活性,在结肠特定区域对UC具有抗溃疡作用。
Antioxidant mediated antiulcer effect of Eupatorium triplinerve Vahl against acetic acid induced ulcerative colitis in mice
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.