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Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid

Reactive oxygen and nitrogen species (ROS/RNS) play a crucial role in inflammatory bowel disease (IBD) exacerbating the chronic inflammatory process. Endogenous and diet antioxidants can neutralize these compounds. The apple is widely consumed, with several antioxidant activity compounds. The presen...

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Autores principales: Pastrelo, Maurício Mercaldi, Dias Ribeiro, Carla Caroline, Duarte, Joselmo Willamys, Bioago Gollücke, Andréa Pitelli, Artigiani-Neto, Ricardo, Ribeiro, Daniel Araki, Miszputen, Sender Jankiel, Fujiyama Oshima, Celina Tizuko, Ribeiro Paiotti, Ana Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Babol University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568191/
https://www.ncbi.nlm.nih.gov/pubmed/28868268
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author Pastrelo, Maurício Mercaldi
Dias Ribeiro, Carla Caroline
Duarte, Joselmo Willamys
Bioago Gollücke, Andréa Pitelli
Artigiani-Neto, Ricardo
Ribeiro, Daniel Araki
Miszputen, Sender Jankiel
Fujiyama Oshima, Celina Tizuko
Ribeiro Paiotti, Ana Paula
author_facet Pastrelo, Maurício Mercaldi
Dias Ribeiro, Carla Caroline
Duarte, Joselmo Willamys
Bioago Gollücke, Andréa Pitelli
Artigiani-Neto, Ricardo
Ribeiro, Daniel Araki
Miszputen, Sender Jankiel
Fujiyama Oshima, Celina Tizuko
Ribeiro Paiotti, Ana Paula
author_sort Pastrelo, Maurício Mercaldi
collection PubMed
description Reactive oxygen and nitrogen species (ROS/RNS) play a crucial role in inflammatory bowel disease (IBD) exacerbating the chronic inflammatory process. Endogenous and diet antioxidants can neutralize these compounds. The apple is widely consumed, with several antioxidant activity compounds. The present study evaluated the effects of concentrated apple extract (CAE) in acetic acid induced colitis. 29 Wistar male rats were randomized into 5 groups. G1–Sham/saline solution, G2–CAE/control, G3–acetic acid/control, G4–curative- CAE treatment and G5–preventive-CAE treatment. Eight days later, the animals were euthanized and the colonic segment resected for macroscopic and histological analysis. Gene expression was evaluated for inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), catalase and copper and zinc superoxide dismutase (CuZnSOD) by quantitative real time PCR, while protein expression was assessed for iNOS, COX-2 and 8-hydroxy-20-deoxyguanosine (8-OHdG) via immunohistochemistry. The groups G3, G4 and G5 had weight loss, while G5 had weight increase at the end of the experiment. The treatment with CAE reduced the macroscopic and microscopic injury, decreased iNOS mRNA expression and increased CuZnSOD mRNA expression in animals with induced acetic acid-colitis. The findings of the present study suggest that CAE treatment exerts an antioxidant role by downregulating iNOS and upregulating CuZnSOD.
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spelling pubmed-55681912017-09-01 Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid Pastrelo, Maurício Mercaldi Dias Ribeiro, Carla Caroline Duarte, Joselmo Willamys Bioago Gollücke, Andréa Pitelli Artigiani-Neto, Ricardo Ribeiro, Daniel Araki Miszputen, Sender Jankiel Fujiyama Oshima, Celina Tizuko Ribeiro Paiotti, Ana Paula Int J Mol Cell Med Original Article Reactive oxygen and nitrogen species (ROS/RNS) play a crucial role in inflammatory bowel disease (IBD) exacerbating the chronic inflammatory process. Endogenous and diet antioxidants can neutralize these compounds. The apple is widely consumed, with several antioxidant activity compounds. The present study evaluated the effects of concentrated apple extract (CAE) in acetic acid induced colitis. 29 Wistar male rats were randomized into 5 groups. G1–Sham/saline solution, G2–CAE/control, G3–acetic acid/control, G4–curative- CAE treatment and G5–preventive-CAE treatment. Eight days later, the animals were euthanized and the colonic segment resected for macroscopic and histological analysis. Gene expression was evaluated for inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), catalase and copper and zinc superoxide dismutase (CuZnSOD) by quantitative real time PCR, while protein expression was assessed for iNOS, COX-2 and 8-hydroxy-20-deoxyguanosine (8-OHdG) via immunohistochemistry. The groups G3, G4 and G5 had weight loss, while G5 had weight increase at the end of the experiment. The treatment with CAE reduced the macroscopic and microscopic injury, decreased iNOS mRNA expression and increased CuZnSOD mRNA expression in animals with induced acetic acid-colitis. The findings of the present study suggest that CAE treatment exerts an antioxidant role by downregulating iNOS and upregulating CuZnSOD. Babol University of Medical Sciences 2017 2017-02-13 /pmc/articles/PMC5568191/ /pubmed/28868268 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Pastrelo, Maurício Mercaldi
Dias Ribeiro, Carla Caroline
Duarte, Joselmo Willamys
Bioago Gollücke, Andréa Pitelli
Artigiani-Neto, Ricardo
Ribeiro, Daniel Araki
Miszputen, Sender Jankiel
Fujiyama Oshima, Celina Tizuko
Ribeiro Paiotti, Ana Paula
Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title_full Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title_fullStr Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title_full_unstemmed Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title_short Effect of Concentrated Apple Extract on Experimental Colitis Induced by Acetic Acid
title_sort effect of concentrated apple extract on experimental colitis induced by acetic acid
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568191/
https://www.ncbi.nlm.nih.gov/pubmed/28868268
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