Cargando…

Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity

BACKGROUND: The cortex of Magnolia officinalis has long been used as an element of traditional Chinese medicine for the treatment of anxiety, chronic bronchitis, and gastrointestinal dysfunction. This study aimed to elucidate the underlying mechanism of its functional ingredients (magnolol and honok...

Descripción completa

Detalles Bibliográficos
Autores principales: Deng, Yanli, Han, Xuefeng, Tang, Shaoxun, Li, Chengjian, Xiao, Wenjun, Tan, Zhiliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990993/
https://www.ncbi.nlm.nih.gov/pubmed/29782483
http://dx.doi.org/10.12659/MSM.910350
_version_ 1783329713599545344
author Deng, Yanli
Han, Xuefeng
Tang, Shaoxun
Li, Chengjian
Xiao, Wenjun
Tan, Zhiliang
author_facet Deng, Yanli
Han, Xuefeng
Tang, Shaoxun
Li, Chengjian
Xiao, Wenjun
Tan, Zhiliang
author_sort Deng, Yanli
collection PubMed
description BACKGROUND: The cortex of Magnolia officinalis has long been used as an element of traditional Chinese medicine for the treatment of anxiety, chronic bronchitis, and gastrointestinal dysfunction. This study aimed to elucidate the underlying mechanism of its functional ingredients (magnolol and honokiol) in modifying the secretion and absorption homeostasis and protecting mucosal integrity in an Enterotoxigenic Escherichia coli (ETEC)-induced diarrhea mouse model. MATERIAL/METHODS: This study established a diarrhea mouse model infected by ETEC at a dosage of 0.02 ml/g live body weight (BW) in vivo. Magnolol or honokiol was followed by an intraperitoneal administration at dosages of 100, 300, and 500 mg/kg BW according to a 3×3 factorial arrangement. The useful biomarkers for evaluating the integrity of intestinal tract and histologic injury were analyzed and morphological development (including villus height, crypt depth, and ratio of villus height to crypt depth) and the expressions of inflammatory cytokines were determined by real-time PCR. RESULTS: The results showed that magnolol and honokiol (500 mg/kg BW) reduced the concentrations of NO, DAO, and DLA, and iNOS activity, and the mRNA expressions of the interferon gamma (IFN-γ) and interleukin 10 (IL-10), and inhibited intestinal epithelial cell apoptosis. Magnolol and honokiol (300 mg/kg BW) elongated the villus height and crypt depth and decreased the number of goblet cells and the ratio of villus height to crypt depth. CONCLUSIONS: The current results indicate that magnolol and honokiol enhance the intestinal anti-inflammatory capacities, elongate the villus height and crypt depth, and reduce goblet cell numbers to inhibit the intestinal epithelium apoptosis and effectively protect the intestinal mucosa. These results show that magnolol and honokiol protect the intestinal mucosal integrity and regulate gastrointestinal dysfunction.
format Online
Article
Text
id pubmed-5990993
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-59909932018-06-07 Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity Deng, Yanli Han, Xuefeng Tang, Shaoxun Li, Chengjian Xiao, Wenjun Tan, Zhiliang Med Sci Monit Lab/In Vitro Research BACKGROUND: The cortex of Magnolia officinalis has long been used as an element of traditional Chinese medicine for the treatment of anxiety, chronic bronchitis, and gastrointestinal dysfunction. This study aimed to elucidate the underlying mechanism of its functional ingredients (magnolol and honokiol) in modifying the secretion and absorption homeostasis and protecting mucosal integrity in an Enterotoxigenic Escherichia coli (ETEC)-induced diarrhea mouse model. MATERIAL/METHODS: This study established a diarrhea mouse model infected by ETEC at a dosage of 0.02 ml/g live body weight (BW) in vivo. Magnolol or honokiol was followed by an intraperitoneal administration at dosages of 100, 300, and 500 mg/kg BW according to a 3×3 factorial arrangement. The useful biomarkers for evaluating the integrity of intestinal tract and histologic injury were analyzed and morphological development (including villus height, crypt depth, and ratio of villus height to crypt depth) and the expressions of inflammatory cytokines were determined by real-time PCR. RESULTS: The results showed that magnolol and honokiol (500 mg/kg BW) reduced the concentrations of NO, DAO, and DLA, and iNOS activity, and the mRNA expressions of the interferon gamma (IFN-γ) and interleukin 10 (IL-10), and inhibited intestinal epithelial cell apoptosis. Magnolol and honokiol (300 mg/kg BW) elongated the villus height and crypt depth and decreased the number of goblet cells and the ratio of villus height to crypt depth. CONCLUSIONS: The current results indicate that magnolol and honokiol enhance the intestinal anti-inflammatory capacities, elongate the villus height and crypt depth, and reduce goblet cell numbers to inhibit the intestinal epithelium apoptosis and effectively protect the intestinal mucosa. These results show that magnolol and honokiol protect the intestinal mucosal integrity and regulate gastrointestinal dysfunction. International Scientific Literature, Inc. 2018-05-21 /pmc/articles/PMC5990993/ /pubmed/29782483 http://dx.doi.org/10.12659/MSM.910350 Text en © Med Sci Monit, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Deng, Yanli
Han, Xuefeng
Tang, Shaoxun
Li, Chengjian
Xiao, Wenjun
Tan, Zhiliang
Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title_full Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title_fullStr Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title_full_unstemmed Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title_short Magnolol and Honokiol Attenuate Apoptosis of Enterotoxigenic Escherichia Coli-Induced Intestinal Epithelium by Maintaining Secretion and Absorption Homeostasis and Protecting Mucosal Integrity
title_sort magnolol and honokiol attenuate apoptosis of enterotoxigenic escherichia coli-induced intestinal epithelium by maintaining secretion and absorption homeostasis and protecting mucosal integrity
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990993/
https://www.ncbi.nlm.nih.gov/pubmed/29782483
http://dx.doi.org/10.12659/MSM.910350
work_keys_str_mv AT dengyanli magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity
AT hanxuefeng magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity
AT tangshaoxun magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity
AT lichengjian magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity
AT xiaowenjun magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity
AT tanzhiliang magnololandhonokiolattenuateapoptosisofenterotoxigenicescherichiacoliinducedintestinalepitheliumbymaintainingsecretionandabsorptionhomeostasisandprotectingmucosalintegrity