Prophylactic Supplementation with Lactobacillus Reuteri or Its Metabolite GABA Protects Against Acute Ischemic Cardiac Injury

Author:

Wang Jiawan1234ORCID,Zhang Hao1235ORCID,Yuan Hailong1236ORCID,Chen Siqi1235ORCID,Yu Ying57,Zhang Xuan7,Gao Zeyu123,Du Heng1235ORCID,Li Weitao8,Wang Yaohui6,Xia Pengyan8,Wang Jun57ORCID,Song Moshi1235ORCID

Affiliation:

1. State Key Laboratory of Membrane Biology Institute of Zoology Chinese Academy of Sciences Beijing 100101 China

2. Beijing Institute for Stem Cell and Regenerative Medicine Beijing 100101 China

3. Key Laboratory of Organ Regeneration and Reconstruction Chinese Academy of Sciences Beijing 100101 China

4. Beijing Chao‐Yang Hospital Department of Anesthesiology Beijing 100020 China

5. University of Chinese Academy of Sciences Beijing 100049 China

6. Joint National Laboratory for Antibody Drug Engineering Henan University Kaifeng 475004 China

7. CAS Key Laboratory of Pathogenic Microbiology and Immunology Chinese Academy of Sciences Beijing 100101 China

8. Department of Immunology School of Basic Medical Sciences Peking University Beijing 100191 China

Abstract

AbstractThe gut microbiome has emerged as a potential target for the treatment of cardiovascular disease. Ischemia/reperfusion (I/R) after myocardial infarction is a serious complication and whether certain gut bacteria can serve as a treatment option remains unclear. Lactobacillus reuteri (L. reuteri) is a well‐studied probiotic that can colonize mammals including humans with known cholesterol‐lowering properties and anti‐inflammatory effects. Here, the prophylactic cardioprotective effects of L. reuteri or its metabolite γ‐aminobutyric acid (GABA) against acute ischemic cardiac injury caused by I/R surgery are demonstrated. The prophylactic gavage of L. reuteri or GABA confers cardioprotection mainly by suppressing cardiac inflammation upon I/R. Mechanistically, GABA gavage results in a decreased number of proinflammatory macrophages in I/R hearts and GABA gavage no longer confers any cardioprotection in I/R hearts upon the clearance of macrophages. In vitro studies with LPS‐stimulated bone marrow‐derived macrophages (BMDM) further reveal that GABA inhibits the polarization of macrophages toward the proinflammatory M1 phenotype by inhibiting lysosomal leakage and NLRP3 inflammasome activation. Together, this study demonstrates that the prophylactic oral administration of L. reuteri or its metabolite GABA attenuates macrophage‐mediated cardiac inflammation and therefore alleviates cardiac dysfunction after I/R, thus providing a new prophylactic strategy to mitigate acute ischemic cardiac injury.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

State Key Laboratory of Membrane Biology

Publisher

Wiley

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