Oral administration of the flavonoid myricitrin prevents dextran sulfate sodium‐induced experimental colitis in mice through modulation of PI3K/Akt signaling pathway. Issue 11 (17th July 2013)

• Record Type: Journal Article
• Authors: Schwanke, Raquel Cristina; Marcon, Rodrigo; Meotti, Flavia Carla; Bento, Allisson Freire; Dutra, Rafael Cypriano; Pizzollatti, Moacir Geraldo; Calixto, João B.
• Is Part Of: Molecular nutrition & food research. Volume 57:Issue 11(2013:Nov.)
• Page Start: 1938
• Page End: 1949
• Publication Date: 2013-07-17
• Subjects: Food -- Biotechnology -- Periodicals; Food -- Microbiology -- Periodicals; Nutrition -- Periodicals; Food -- Toxicology -- Periodicals; Nutrition -- Periodicals; Food Microbiology -- Periodicals; Food Technology -- Periodicals; Molecular Biology -- Periodicals; 664.0705
• DOI: 10.1002/mnfr.201300134
• Languages: English
• ISSNs: 1613-4125

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr2021-sec-0010" sec-type="section"> <title>Scope</title> <p>We investigated the protective effect of the flavonoid myricitrin in dextran sulfate sodium (DSS) induced colitis as promising candidate for the treatment of ulcerative colitis which is considered an important worldwide public health problem.</p> </sec> <sec id="mnfr2021-sec-0020" sec-type="section"> <title>Methods and results</title> <p>Male CD1 mice were provided with a solution of filtered water containing 3% w/v DSS ad libitum over a 5‐day period followed by 2 days with normal drinking water. Myricitrin was administered orally, once a day, at the doses 1, 3, and 10 mg/kg of body weight. At the end of day 7th, the animals were euthanized and the colonic tissue was collected to be analyzed by RT‐PCR, immunohistochemistry and Western blot. Our results showed that oral treatment with myricitrin exerts consistent anti‐inflammatory action in DSS‐induced acute colitis in mice by the inhibition of the Akt/phosphatidylinositol‐3 kinase‐dependent phosphorylation. Consequently, the phosphorylation of mitogen‐activated protein kinases (MAPK) p38, extracellular signal‐regulated protein kinase (ERK1/2), and c‐Jun <italic>N</italic>‐terminal kinase and of the nuclear factor B (NF‐κB) was reduced and prevented an increase in the cytokines/chemokines levels.</p> </sec> <sec id="mnfr2021-sec-0030" sec-type="section"> <title>Conclusion</title> <p>Together, these data reveal that the anti‐inflammatory effect of myricitrin in DSS‐induced colitis in mice is likely associated with its ability to prevent the activation of upstream kinases, such as phosphatidylinositol‐3 kinase‐dependent Akt, NF‐κB, and mitogen‐activated protein kinase.</p> </sec> </abstract>