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Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis

Natural compounds could be a complementary alternative to inflammatory bowel disease (IBD) management. This study determined the effects of an aqueous extract of Myrciaria jaboticaba peel (EJP) (50 g L(−1)) on 2,4,6-trinitrobenzenesulfonic acid-induced colitis. Wistar rats were randomized into five...

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Autores principales: da Silva-Maia, Juliana Kelly, Batista, Ângela Giovana, Cazarin, Cinthia Baú Betim, Soares, Edilene Siqueira, Bogusz Junior, Stanislau, Leal, Raquel Franco, da Cruz-Höfling, Maria Alice, Maróstica Junior, Mário Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893622/
https://www.ncbi.nlm.nih.gov/pubmed/31731626
http://dx.doi.org/10.3390/nu11112776
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author da Silva-Maia, Juliana Kelly
Batista, Ângela Giovana
Cazarin, Cinthia Baú Betim
Soares, Edilene Siqueira
Bogusz Junior, Stanislau
Leal, Raquel Franco
da Cruz-Höfling, Maria Alice
Maróstica Junior, Mário Roberto
author_facet da Silva-Maia, Juliana Kelly
Batista, Ângela Giovana
Cazarin, Cinthia Baú Betim
Soares, Edilene Siqueira
Bogusz Junior, Stanislau
Leal, Raquel Franco
da Cruz-Höfling, Maria Alice
Maróstica Junior, Mário Roberto
author_sort da Silva-Maia, Juliana Kelly
collection PubMed
description Natural compounds could be a complementary alternative to inflammatory bowel disease (IBD) management. This study determined the effects of an aqueous extract of Myrciaria jaboticaba peel (EJP) (50 g L(−1)) on 2,4,6-trinitrobenzenesulfonic acid-induced colitis. Wistar rats were randomized into five groups: HC—healthy control, CC—colitis control, DC—drug control, SJ—short-term treatment with EJP, and LJ—long-term treatment with EJP. The EJP treatments reduced body weight loss, stool consistency score, and spleen enlargement. Gut microbiota was modulated through increased Lactobacillus and Bifidobacterium counts after EJP treatment. Short-chain fatty acids were also higher in the EJP treatment groups. The antioxidant enzyme activities were greater than CC or DC controls. Myeloperoxidase activity (LJ), inducible nitric oxide synthase (LJ/SJ), and intercellular adhesion molecule (SJ) levels were lower than in the CC group. EJP decreased histological scoring, mucosal thickness, and preserved the crypts and histological structure. Therefore, EJP showed beneficial effects and could be potentially used as an adjuvant in IBD treatment.
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spelling pubmed-68936222019-12-23 Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis da Silva-Maia, Juliana Kelly Batista, Ângela Giovana Cazarin, Cinthia Baú Betim Soares, Edilene Siqueira Bogusz Junior, Stanislau Leal, Raquel Franco da Cruz-Höfling, Maria Alice Maróstica Junior, Mário Roberto Nutrients Article Natural compounds could be a complementary alternative to inflammatory bowel disease (IBD) management. This study determined the effects of an aqueous extract of Myrciaria jaboticaba peel (EJP) (50 g L(−1)) on 2,4,6-trinitrobenzenesulfonic acid-induced colitis. Wistar rats were randomized into five groups: HC—healthy control, CC—colitis control, DC—drug control, SJ—short-term treatment with EJP, and LJ—long-term treatment with EJP. The EJP treatments reduced body weight loss, stool consistency score, and spleen enlargement. Gut microbiota was modulated through increased Lactobacillus and Bifidobacterium counts after EJP treatment. Short-chain fatty acids were also higher in the EJP treatment groups. The antioxidant enzyme activities were greater than CC or DC controls. Myeloperoxidase activity (LJ), inducible nitric oxide synthase (LJ/SJ), and intercellular adhesion molecule (SJ) levels were lower than in the CC group. EJP decreased histological scoring, mucosal thickness, and preserved the crypts and histological structure. Therefore, EJP showed beneficial effects and could be potentially used as an adjuvant in IBD treatment. MDPI 2019-11-15 /pmc/articles/PMC6893622/ /pubmed/31731626 http://dx.doi.org/10.3390/nu11112776 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
da Silva-Maia, Juliana Kelly
Batista, Ângela Giovana
Cazarin, Cinthia Baú Betim
Soares, Edilene Siqueira
Bogusz Junior, Stanislau
Leal, Raquel Franco
da Cruz-Höfling, Maria Alice
Maróstica Junior, Mário Roberto
Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title_full Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title_fullStr Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title_full_unstemmed Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title_short Aqueous Extract of Brazilian Berry (Myrciaria jaboticaba) Peel Improves Inflammatory Parameters and Modulates Lactobacillus and Bifidobacterium in Rats with Induced-Colitis
title_sort aqueous extract of brazilian berry (myrciaria jaboticaba) peel improves inflammatory parameters and modulates lactobacillus and bifidobacterium in rats with induced-colitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893622/
https://www.ncbi.nlm.nih.gov/pubmed/31731626
http://dx.doi.org/10.3390/nu11112776
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