Bifidobacterium animalis subsp. lactis 420 mitigates the pathological impact of myocardial infarction in the mouse

C. A. Danilo, E. Constantopoulos, L. A. McKee, H. Chen, J. A. Regan, Y. Lipovka, S. Lahtinen, L. K. Stenman, T. V.V. Nguyen, Kristian Doyle, Marvin J Slepian, Zain I Khalpey, John Konhilas

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

There is a growing appreciation that our microbial environment in the gut plays a critical role in the maintenance of health and the pathogenesis of disease. Probiotic, beneficial gut microbes, administration can directly attenuate cardiac injury and post-myocardial infarction (MI) remodelling, yet the mechanisms of cardioprotection are unknown. We hypothesised that administration of Bifidobacterium animalis subsp. lactis 420 (B420), a probiotic with known anti-inflammatory properties, to mice will mitigate the pathological impact of MI, and that anti-inflammatory T regulatory (Treg) immune cells are necessary to impart protection against MI as a result of B420 administration. Wild-type male mice were administered B420, saline or Lactobacillus salivarius 33 (Ls-33) by gavage daily for 14 or 35 days, and underwent ischemia/reperfusion (I/R). Pretreatment with B420 for 10 or 28 days attenuated cardiac injury from I/R and reduced levels of inflammatory markers. Depletion of Treg cells by administration of anti-CD25 monoclonal antibodies eliminated B420-mediated cardio-protection. Further cytokine analysis revealed a shift from a pro-inflammatory to an anti-inflammatory environment in the probiotic treated post-MI hearts compared to controls. To summarise, B420 administration mitigates the pathological impact of MI. Next, we show that Treg immune cells are necessary to mediate B420-mediated protection against MI. Finally, we identify putative cellular, epigenetic and/or post-translational mechanisms of B420-mediated protection against MI.

Original languageEnglish (US)
Pages (from-to)257-269
Number of pages13
JournalBeneficial microbes
Volume8
Issue number2
DOIs
StatePublished - 2017

Fingerprint

Myocardial Infarction
Probiotics
Anti-Inflammatory Agents
Regulatory T-Lymphocytes
Bifidobacterium animalis
Reperfusion Injury
Epigenomics
Reperfusion
Ischemia
Monoclonal Antibodies
Cytokines
Health
Wounds and Injuries

Keywords

  • B. animalis ssp. lactis
  • Cardiovascular disease
  • Inflammation
  • Probiotics
  • Regulatory T cells

ASJC Scopus subject areas

  • Microbiology
  • Microbiology (medical)

Cite this

Bifidobacterium animalis subsp. lactis 420 mitigates the pathological impact of myocardial infarction in the mouse. / Danilo, C. A.; Constantopoulos, E.; McKee, L. A.; Chen, H.; Regan, J. A.; Lipovka, Y.; Lahtinen, S.; Stenman, L. K.; Nguyen, T. V.V.; Doyle, Kristian; Slepian, Marvin J; Khalpey, Zain I; Konhilas, John.

In: Beneficial microbes, Vol. 8, No. 2, 2017, p. 257-269.

Research output: Contribution to journalArticle

Danilo, CA, Constantopoulos, E, McKee, LA, Chen, H, Regan, JA, Lipovka, Y, Lahtinen, S, Stenman, LK, Nguyen, TVV, Doyle, K, Slepian, MJ, Khalpey, ZI & Konhilas, J 2017, 'Bifidobacterium animalis subsp. lactis 420 mitigates the pathological impact of myocardial infarction in the mouse', Beneficial microbes, vol. 8, no. 2, pp. 257-269. https://doi.org/10.3920/BM2016.0119
Danilo, C. A. ; Constantopoulos, E. ; McKee, L. A. ; Chen, H. ; Regan, J. A. ; Lipovka, Y. ; Lahtinen, S. ; Stenman, L. K. ; Nguyen, T. V.V. ; Doyle, Kristian ; Slepian, Marvin J ; Khalpey, Zain I ; Konhilas, John. / Bifidobacterium animalis subsp. lactis 420 mitigates the pathological impact of myocardial infarction in the mouse. In: Beneficial microbes. 2017 ; Vol. 8, No. 2. pp. 257-269.
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AU - Constantopoulos, E.

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AU - Chen, H.

AU - Regan, J. A.

AU - Lipovka, Y.

AU - Lahtinen, S.

AU - Stenman, L. K.

AU - Nguyen, T. V.V.

AU - Doyle, Kristian

AU - Slepian, Marvin J

AU - Khalpey, Zain I

AU - Konhilas, John

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