Supplementation with the Postbiotic BPL1™-HT (Heat-Inactivated Bifidobacterium animalis subsp. Lactis) Attenuates the Cardiovascular Alterations Induced by Angiotensin II Infusion in Mice.

2025-02-08
Antioxidants (Basel, Switzerland) 14(2)

PubMed: 40002381
DOI: 10.3390/antiox14020193

Study Design

Population: C57BL/6J male mice
Methods: Three groups of C57BL/6J male mice were used: mice infused with saline (control); mice infused with AngII for 4 weeks (AngII); and mice supplemented with BPL1™ HT in the drinking water (1010 cells/animal/day) for 8 weeks and infused with AngII for the last 4 weeks (AngII + BPL1™ HT).

Hypertension is associated with alterations in the composition and diversity of the intestinal microbiota. Indeed, supplementation with probiotics and prebiotics has shown promising results in modulating the gut microbiota and improving cardiovascular health. However, there are no studies regarding the possible beneficial effects of postbiotics on cardiovascular function and particularly on hypertension-induced cardiovascular alterations. Thus, the aim of this study was to analyze the effect of supplementation with the heat-treated Bifidobacterium animalis subsp. lactis CECT 8145 strain (BPL1™ HT), a postbiotic developed by the company ADM-Biopolis, on cardiovascular alterations induced by angiotensin II (AngII) infusion in mice. For this purpose, three groups of C57BL/6J male mice were used: (i) mice infused with saline (control); (ii) mice infused with AngII for 4 weeks (AngII); and (iii) mice supplemented with BPL1™ HT in the drinking water (1010 cells/animal/day) for 8 weeks and infused with AngII for the last 4 weeks (AngII + BPL1™ HT). AngII infusion was associated with heart hypertrophy, hypertension, endothelial dysfunction, and overexpression of proinflammatory cytokines in aortic tissue. BPL1™ HT supplementation reduced systolic blood pressure and attenuated AngII-induced endothelial dysfunction in aortic segments. Moreover, mice supplemented with BPL1™ HT showed a decreased gene expression of the proinflammatory cytokine interleukin 6 (Il-6) and the prooxidant enzymes NADPH oxidases 1 (Nox-1) and 4 (Nox-4), as well as an overexpression of AngII receptor 2 (At2r) and interleukin 10 (Il-10) in arterial tissue. In the heart, BPL1™ HT supplementation increased myocardial contractility and prevented ischemia-reperfusion-induced cardiomyocyte apoptosis. In conclusion, supplementation with the postbiotic BPL1™ HT prevents endothelial dysfunction, lowers blood pressure, and has cardioprotective effects in an experimental model of hypertension induced by AngII infusion in mice.

Research Insights

Supplement	Dose	Health Outcome	Effect Type	Effect Size	Source
Bifidobacterium animalis subsp. lactis BPL1	—	Improved Cardiac Function	Beneficial	Moderate	View source In the heart, BPL1™ HT supplementation increased myocardial contractility and prevented ischemia-reperfusion-induced cardiomyocyte apoptosis
Bifidobacterium animalis subsp. lactis BPL1	—	Improved Vascular Endothelial Function	Beneficial	Moderate	View source attenuated AngII-induced endothelial dysfunction in aortic segments
Bifidobacterium animalis subsp. lactis BPL1	—	Reduced Blood Pressure	Beneficial	Moderate	View source BPL1™ HT supplementation reduced systolic blood pressure
Bifidobacterium animalis subsp. lactis BPL1	—	Reduced Inflammation	Beneficial	Moderate	View source decreased gene expression of the proinflammatory cytokine interleukin 6 (Il-6) ... as well as an overexpression of ... interleukin 10 (Il-10)
Bifidobacterium animalis subsp. lactis BPL1	—	Reduced Oxidative Stress	Beneficial	Moderate	View source decreased gene expression of the prooxidant enzymes NADPH oxidases 1 (Nox-1) and 4 (Nox-4)