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Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice

Systemic lupus erythematosus (SLE) is a disease that mostly affects women. Accelerated atherosclerosis is a high-risk factor associated with SLE patients. SLE associated with cardiovascular disease is one of the most important causes of death. In this study, we demonstrated that Lactobacillus paraca...

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Autores principales: Hu, Wei-Syun, Rajendran, Peramaiyan, Tzang, Bor-Show, Yeh, Yu-Lan, Shen, Chia-Yao, Chen, Ray-Jade, Ho, Tsung-Jung, Vijaya Padma, Viswanadha, Chen, Yi-Hsing, Huang, Chih-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608316/
https://www.ncbi.nlm.nih.gov/pubmed/28934296
http://dx.doi.org/10.1371/journal.pone.0185098
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author Hu, Wei-Syun
Rajendran, Peramaiyan
Tzang, Bor-Show
Yeh, Yu-Lan
Shen, Chia-Yao
Chen, Ray-Jade
Ho, Tsung-Jung
Vijaya Padma, Viswanadha
Chen, Yi-Hsing
Huang, Chih-Yang
author_facet Hu, Wei-Syun
Rajendran, Peramaiyan
Tzang, Bor-Show
Yeh, Yu-Lan
Shen, Chia-Yao
Chen, Ray-Jade
Ho, Tsung-Jung
Vijaya Padma, Viswanadha
Chen, Yi-Hsing
Huang, Chih-Yang
author_sort Hu, Wei-Syun
collection PubMed
description Systemic lupus erythematosus (SLE) is a disease that mostly affects women. Accelerated atherosclerosis is a high-risk factor associated with SLE patients. SLE associated with cardiovascular disease is one of the most important causes of death. In this study, we demonstrated that Lactobacillus paracasei GMNL-32 (GMNL-32), a probiotic species, exhibits anti-fibrosis and anti-apoptotic effects on the cardiac tissue of NZB/WF1 mice. Female NZB/W F1 mice, a well-known and commonly used lupus-prone mouse strain, were treated with or without GMNL-32 administration for 12 weeks. Oral administration of GMNL-32 to NZB/WF1 mice significantly increased the ventricular thickness when compared to that of NZB/WF1 mice. Administration of GMNL-32 significantly attenuated the cardiac cell apoptosis that was observed in exacerbate levels in the control NZB/WF1 mice. Further, the cellular morphology that was slightly distorted in the NZB/WF1 was effectively alleviated in the treatment group mice. In addition, GMNL-32 reduced the level of Fas death receptor-related pathway of apoptosis signaling and enhanced anti-apoptotic proteins. These results indicate that GMNL-32 exhibit an effective protective effect on cardiac cells of SLE mice. Thus, GMNL-32 may be a potential therapeutic strategy against SLE associated arthrosclerosis.
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spelling pubmed-56083162017-10-09 Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice Hu, Wei-Syun Rajendran, Peramaiyan Tzang, Bor-Show Yeh, Yu-Lan Shen, Chia-Yao Chen, Ray-Jade Ho, Tsung-Jung Vijaya Padma, Viswanadha Chen, Yi-Hsing Huang, Chih-Yang PLoS One Research Article Systemic lupus erythematosus (SLE) is a disease that mostly affects women. Accelerated atherosclerosis is a high-risk factor associated with SLE patients. SLE associated with cardiovascular disease is one of the most important causes of death. In this study, we demonstrated that Lactobacillus paracasei GMNL-32 (GMNL-32), a probiotic species, exhibits anti-fibrosis and anti-apoptotic effects on the cardiac tissue of NZB/WF1 mice. Female NZB/W F1 mice, a well-known and commonly used lupus-prone mouse strain, were treated with or without GMNL-32 administration for 12 weeks. Oral administration of GMNL-32 to NZB/WF1 mice significantly increased the ventricular thickness when compared to that of NZB/WF1 mice. Administration of GMNL-32 significantly attenuated the cardiac cell apoptosis that was observed in exacerbate levels in the control NZB/WF1 mice. Further, the cellular morphology that was slightly distorted in the NZB/WF1 was effectively alleviated in the treatment group mice. In addition, GMNL-32 reduced the level of Fas death receptor-related pathway of apoptosis signaling and enhanced anti-apoptotic proteins. These results indicate that GMNL-32 exhibit an effective protective effect on cardiac cells of SLE mice. Thus, GMNL-32 may be a potential therapeutic strategy against SLE associated arthrosclerosis. Public Library of Science 2017-09-21 /pmc/articles/PMC5608316/ /pubmed/28934296 http://dx.doi.org/10.1371/journal.pone.0185098 Text en © 2017 Hu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hu, Wei-Syun
Rajendran, Peramaiyan
Tzang, Bor-Show
Yeh, Yu-Lan
Shen, Chia-Yao
Chen, Ray-Jade
Ho, Tsung-Jung
Vijaya Padma, Viswanadha
Chen, Yi-Hsing
Huang, Chih-Yang
Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title_full Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title_fullStr Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title_full_unstemmed Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title_short Lactobacillus paracasei GMNL-32 exerts a therapeutic effect on cardiac abnormalities in NZB/W F1 mice
title_sort lactobacillus paracasei gmnl-32 exerts a therapeutic effect on cardiac abnormalities in nzb/w f1 mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608316/
https://www.ncbi.nlm.nih.gov/pubmed/28934296
http://dx.doi.org/10.1371/journal.pone.0185098
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