Prophylactic Supplementation with Lactobacillus Reuteri or Its Metabolite GABA Protects Against Acute Ischemic Cardiac Injury.
Jia-Wan WangHao ZhangHailong YuanSiqi ChenYing YuXuan ZhangZeyu GaoHeng DuWeitao LiYaohui WangPengyan XiaJun WangMoshi SongPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
The 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.
Keyphrases
- left ventricular
- cardiovascular disease
- liver failure
- oxidative stress
- respiratory failure
- type diabetes
- adipose tissue
- drug induced
- ischemia reperfusion injury
- heart failure
- intensive care unit
- inflammatory response
- coronary artery disease
- signaling pathway
- mesenchymal stem cells
- minimally invasive
- blood brain barrier
- atrial fibrillation
- bone marrow
- combination therapy
- brain injury
- dna methylation
- cerebral ischemia
- acute respiratory distress syndrome
- percutaneous coronary intervention
- metabolic syndrome
- surgical site infection