Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation

Abstract Recent trials demonstrate that systemic anti-inflammatory therapy reduces cardiovascular events in coronary artery disease (CAD) patients. We recently demonstrated Lactobacillus plantarum 299v (Lp299v) supplementation improved vascular endothelial function in men with stable CAD. Whether th...

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Autores principales: Benjamin C. Hofeld, Venkata K. Puppala, Sudhi Tyagi, Kwang Woo Ahn, Amberly Anger, Shuang Jia, Nita H. Salzman, Martin J. Hessner, Michael E. Widlansky
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:d7166fea3e3149f68f5acd9747714a2b2021-12-02T12:11:45ZLactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation10.1038/s41598-021-83252-72045-2322https://doaj.org/article/d7166fea3e3149f68f5acd9747714a2b2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-83252-7https://doaj.org/toc/2045-2322Abstract Recent trials demonstrate that systemic anti-inflammatory therapy reduces cardiovascular events in coronary artery disease (CAD) patients. We recently demonstrated Lactobacillus plantarum 299v (Lp299v) supplementation improved vascular endothelial function in men with stable CAD. Whether this favorable effect is in part due to anti-inflammatory action remains unknown. Testing this hypothesis, we exposed plasma obtained before and after Lp299v supplementation from these subjects to a healthy donor’s PBMCs and measured differences in the PBMC transciptome, performed gene ontological analyses, and compared Lp299v-induced transcriptome changes with changes in vascular function. Daily alcohol users (DAUs) (n = 4) had a significantly different response to Lp299v and were separated from the main analyses. Non-DAUs- (n = 15) showed improved brachial flow-mediated dilation (FMD) and reduced circulating IL-8, IL-12, and leptin. 997 genes were significantly changed. I.I.com decreased (1.01 ± 0.74 vs. 0.22 ± 0.51; P < 0.0001), indicating strong anti-inflammatory effects. Pathway analyses revealed downregulation of IL-1β, interferon-stimulated pathways, and toll-like receptor signaling, and an increase in regulator T-cell (Treg) activity. Reductions in GBP1, JAK2, and TRAIL expression correlated with improved FMD. In non-DAU men with stable CAD, post-Lp299v supplementation plasma induced anti-inflammatory transcriptome changes in human PBMCs that could benefit CAD patients. Future studies should delineate changes in circulating metabolites responsible for these effects.Benjamin C. HofeldVenkata K. PuppalaSudhi TyagiKwang Woo AhnAmberly AngerShuang JiaNita H. SalzmanMartin J. HessnerMichael E. WidlanskyNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Benjamin C. Hofeld
Venkata K. Puppala
Sudhi Tyagi
Kwang Woo Ahn
Amberly Anger
Shuang Jia
Nita H. Salzman
Martin J. Hessner
Michael E. Widlansky
Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
description Abstract Recent trials demonstrate that systemic anti-inflammatory therapy reduces cardiovascular events in coronary artery disease (CAD) patients. We recently demonstrated Lactobacillus plantarum 299v (Lp299v) supplementation improved vascular endothelial function in men with stable CAD. Whether this favorable effect is in part due to anti-inflammatory action remains unknown. Testing this hypothesis, we exposed plasma obtained before and after Lp299v supplementation from these subjects to a healthy donor’s PBMCs and measured differences in the PBMC transciptome, performed gene ontological analyses, and compared Lp299v-induced transcriptome changes with changes in vascular function. Daily alcohol users (DAUs) (n = 4) had a significantly different response to Lp299v and were separated from the main analyses. Non-DAUs- (n = 15) showed improved brachial flow-mediated dilation (FMD) and reduced circulating IL-8, IL-12, and leptin. 997 genes were significantly changed. I.I.com decreased (1.01 ± 0.74 vs. 0.22 ± 0.51; P < 0.0001), indicating strong anti-inflammatory effects. Pathway analyses revealed downregulation of IL-1β, interferon-stimulated pathways, and toll-like receptor signaling, and an increase in regulator T-cell (Treg) activity. Reductions in GBP1, JAK2, and TRAIL expression correlated with improved FMD. In non-DAU men with stable CAD, post-Lp299v supplementation plasma induced anti-inflammatory transcriptome changes in human PBMCs that could benefit CAD patients. Future studies should delineate changes in circulating metabolites responsible for these effects.
format article
author Benjamin C. Hofeld
Venkata K. Puppala
Sudhi Tyagi
Kwang Woo Ahn
Amberly Anger
Shuang Jia
Nita H. Salzman
Martin J. Hessner
Michael E. Widlansky
author_facet Benjamin C. Hofeld
Venkata K. Puppala
Sudhi Tyagi
Kwang Woo Ahn
Amberly Anger
Shuang Jia
Nita H. Salzman
Martin J. Hessner
Michael E. Widlansky
author_sort Benjamin C. Hofeld
title Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
title_short Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
title_full Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
title_fullStr Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
title_full_unstemmed Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
title_sort lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/d7166fea3e3149f68f5acd9747714a2b
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