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Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
PURPOSE: To investigate the mechanism of Periplaneta americana extract promoting intestinal mucosal repair of OXZ-induced colitis in rat. METHODS: All experiments used an equal number of male and female SD rats (n=48). We injected OXZ into the colon to induce UC rat model. To determine the optimal c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709898/ https://www.ncbi.nlm.nih.gov/pubmed/33237174 http://dx.doi.org/10.1590/s0102-865020200100000002 |
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author | Xue, Nan-nan He, Miao Li, Yue Wu, Jun-zhu Du, Wen-wen Wu, Xiu-mei Yang, Zi-zhong Zhang, Cheng-gui Li, Qi-yan Xiao, Huai |
author_facet | Xue, Nan-nan He, Miao Li, Yue Wu, Jun-zhu Du, Wen-wen Wu, Xiu-mei Yang, Zi-zhong Zhang, Cheng-gui Li, Qi-yan Xiao, Huai |
author_sort | Xue, Nan-nan |
collection | PubMed |
description | PURPOSE: To investigate the mechanism of Periplaneta americana extract promoting intestinal mucosal repair of OXZ-induced colitis in rat. METHODS: All experiments used an equal number of male and female SD rats (n=48). We injected OXZ into the colon to induce UC rat model. To determine the optimal concentration of P. Americana's extract (PA-40), it was classified into low (L), medium (M), and high (H) doses. After OXZ treatment, each drug was administered by enema for 7 consecutive days. Rats were divided into the following 6 groups: (1) Saline treatment group (NC), (2) OXZ treatment UC model group (MC), (3) OXZ + budesonide group (BUN), (4) OXZ + PA-40 L group, (5) OXZ + PA-40 M group, (6) OXZ + PA-40 H group. Disease activity index (DAI) scores, colon length, histopathological score, serum cytokine level (IL-4, IL-10, iNOS, tNOS), and amount of MPO, EGF, IL-13 in colonic mucosa were measured. RESULTS: PA treatment had a significant healing effect on the OXZ-colitis model and significantly reduced the lesioned area, especially in the PA-40H groups. PA treatment did not alter the expression of IL-10 and MPO level, but increased EGF (epidermal growth factor) and decrease IL-13 in the colonic tissue. PA inhibited the rise of NOSs (nitric oxide synthase) and decreased the serum IL-4 level. CONCLUSIONS: The data suggest that Periplaneta americana extract may be a potential compound for the treatment of colonic lesions. The mechanism may be related to inhibiting the secretion of IL-13 and promoting the formation of EGF. |
format | Online Article Text |
id | pubmed-7709898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-77098982020-12-07 Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat Xue, Nan-nan He, Miao Li, Yue Wu, Jun-zhu Du, Wen-wen Wu, Xiu-mei Yang, Zi-zhong Zhang, Cheng-gui Li, Qi-yan Xiao, Huai Acta Cir Bras Original Article PURPOSE: To investigate the mechanism of Periplaneta americana extract promoting intestinal mucosal repair of OXZ-induced colitis in rat. METHODS: All experiments used an equal number of male and female SD rats (n=48). We injected OXZ into the colon to induce UC rat model. To determine the optimal concentration of P. Americana's extract (PA-40), it was classified into low (L), medium (M), and high (H) doses. After OXZ treatment, each drug was administered by enema for 7 consecutive days. Rats were divided into the following 6 groups: (1) Saline treatment group (NC), (2) OXZ treatment UC model group (MC), (3) OXZ + budesonide group (BUN), (4) OXZ + PA-40 L group, (5) OXZ + PA-40 M group, (6) OXZ + PA-40 H group. Disease activity index (DAI) scores, colon length, histopathological score, serum cytokine level (IL-4, IL-10, iNOS, tNOS), and amount of MPO, EGF, IL-13 in colonic mucosa were measured. RESULTS: PA treatment had a significant healing effect on the OXZ-colitis model and significantly reduced the lesioned area, especially in the PA-40H groups. PA treatment did not alter the expression of IL-10 and MPO level, but increased EGF (epidermal growth factor) and decrease IL-13 in the colonic tissue. PA inhibited the rise of NOSs (nitric oxide synthase) and decreased the serum IL-4 level. CONCLUSIONS: The data suggest that Periplaneta americana extract may be a potential compound for the treatment of colonic lesions. The mechanism may be related to inhibiting the secretion of IL-13 and promoting the formation of EGF. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020-11-23 /pmc/articles/PMC7709898/ /pubmed/33237174 http://dx.doi.org/10.1590/s0102-865020200100000002 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Xue, Nan-nan He, Miao Li, Yue Wu, Jun-zhu Du, Wen-wen Wu, Xiu-mei Yang, Zi-zhong Zhang, Cheng-gui Li, Qi-yan Xiao, Huai Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat |
title |
Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
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title_full |
Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
|
title_fullStr |
Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
|
title_full_unstemmed |
Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
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title_short |
Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat
|
title_sort | periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709898/ https://www.ncbi.nlm.nih.gov/pubmed/33237174 http://dx.doi.org/10.1590/s0102-865020200100000002 |
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