Cargando…

Protective Effects of Guava Pulp on Cholestatic Liver Injury

Background. Cholestatic liver injury is a leading cause of chronic liver diseases involved with oxidative stress changes and inflammation; thus, antioxidant and anti-inflammation compound-rich guava may play a pivotal role in protecting against the cholestatic liver damages. Our aims for this study...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Jian, Yue, Chunyan, Qiu, Kai, Chen, Jie, Aller, Maria-Angeles, Ko, Kwang Suk, Yang, Heping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890915/
https://www.ncbi.nlm.nih.gov/pubmed/27335829
http://dx.doi.org/10.1155/2013/601071
_version_ 1782435183543189504
author Peng, Jian
Yue, Chunyan
Qiu, Kai
Chen, Jie
Aller, Maria-Angeles
Ko, Kwang Suk
Yang, Heping
author_facet Peng, Jian
Yue, Chunyan
Qiu, Kai
Chen, Jie
Aller, Maria-Angeles
Ko, Kwang Suk
Yang, Heping
author_sort Peng, Jian
collection PubMed
description Background. Cholestatic liver injury is a leading cause of chronic liver diseases involved with oxidative stress changes and inflammation; thus, antioxidant and anti-inflammation compound-rich guava may play a pivotal role in protecting against the cholestatic liver damages. Our aims for this study are to determine whether guava pulp (GP) has protective effects on cholestatic liver injury-induced mouse model and on interleukin-6 (IL-6) mediated proliferation of QBC939 cholangiocarcinoma cell line. Methods. Mice were induced to cholestatic liver damage by left and median bile duct ligation (LMBDL) surgery and then treated with GP. Plasma and liver samples were collected for biochemical and pathological assays. 5-Bromo-2′-deoxyuridine (BrdU) assay and Western blots were used to detect proliferation and gene expression in QBC939 cells, respectively. Results. Compared with LMBDL only group, in GP-treated mice, the levels of alanine aminotransferase (ALT) and bilirubin decreased, biliary epithelial cell proliferation and liver fibrogenesis were suppressed, Src/MEK/ERK1/2/c-Myc pathway and expressions of transforming growth factor β1(TGF-β1), tissue inhibitor of metalloproteinases TIMP), and procollagen 1α1(COL1α1) were downregulated significantly. Moreover, the GP extract reduced IL-6-enhanced QBC939 cell proliferation, p-ERK, and c-Myc expression as well. Conclusions. GP may provide a new perspective for the treatment of cholestatic liver injury.
format Online
Article
Text
id pubmed-4890915
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-48909152016-06-22 Protective Effects of Guava Pulp on Cholestatic Liver Injury Peng, Jian Yue, Chunyan Qiu, Kai Chen, Jie Aller, Maria-Angeles Ko, Kwang Suk Yang, Heping ISRN Hepatol Research Article Background. Cholestatic liver injury is a leading cause of chronic liver diseases involved with oxidative stress changes and inflammation; thus, antioxidant and anti-inflammation compound-rich guava may play a pivotal role in protecting against the cholestatic liver damages. Our aims for this study are to determine whether guava pulp (GP) has protective effects on cholestatic liver injury-induced mouse model and on interleukin-6 (IL-6) mediated proliferation of QBC939 cholangiocarcinoma cell line. Methods. Mice were induced to cholestatic liver damage by left and median bile duct ligation (LMBDL) surgery and then treated with GP. Plasma and liver samples were collected for biochemical and pathological assays. 5-Bromo-2′-deoxyuridine (BrdU) assay and Western blots were used to detect proliferation and gene expression in QBC939 cells, respectively. Results. Compared with LMBDL only group, in GP-treated mice, the levels of alanine aminotransferase (ALT) and bilirubin decreased, biliary epithelial cell proliferation and liver fibrogenesis were suppressed, Src/MEK/ERK1/2/c-Myc pathway and expressions of transforming growth factor β1(TGF-β1), tissue inhibitor of metalloproteinases TIMP), and procollagen 1α1(COL1α1) were downregulated significantly. Moreover, the GP extract reduced IL-6-enhanced QBC939 cell proliferation, p-ERK, and c-Myc expression as well. Conclusions. GP may provide a new perspective for the treatment of cholestatic liver injury. Hindawi Publishing Corporation 2013-11-17 /pmc/articles/PMC4890915/ /pubmed/27335829 http://dx.doi.org/10.1155/2013/601071 Text en Copyright © 2013 Jian Peng et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Peng, Jian
Yue, Chunyan
Qiu, Kai
Chen, Jie
Aller, Maria-Angeles
Ko, Kwang Suk
Yang, Heping
Protective Effects of Guava Pulp on Cholestatic Liver Injury
title Protective Effects of Guava Pulp on Cholestatic Liver Injury
title_full Protective Effects of Guava Pulp on Cholestatic Liver Injury
title_fullStr Protective Effects of Guava Pulp on Cholestatic Liver Injury
title_full_unstemmed Protective Effects of Guava Pulp on Cholestatic Liver Injury
title_short Protective Effects of Guava Pulp on Cholestatic Liver Injury
title_sort protective effects of guava pulp on cholestatic liver injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4890915/
https://www.ncbi.nlm.nih.gov/pubmed/27335829
http://dx.doi.org/10.1155/2013/601071
work_keys_str_mv AT pengjian protectiveeffectsofguavapulponcholestaticliverinjury
AT yuechunyan protectiveeffectsofguavapulponcholestaticliverinjury
AT qiukai protectiveeffectsofguavapulponcholestaticliverinjury
AT chenjie protectiveeffectsofguavapulponcholestaticliverinjury
AT allermariaangeles protectiveeffectsofguavapulponcholestaticliverinjury
AT kokwangsuk protectiveeffectsofguavapulponcholestaticliverinjury
AT yangheping protectiveeffectsofguavapulponcholestaticliverinjury