Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783265420522815488 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5608316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT huweisyun lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT rajendranperamaiyan lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT tzangborshow lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT yehyulan lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT shenchiayao lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT chenrayjade lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT hotsungjung lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT vijayapadmaviswanadha lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT chenyihsing lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice AT huangchihyang lactobacillusparacaseigmnl32exertsatherapeuticeffectoncardiacabnormalitiesinnzbwf1mice |