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Review uncovers distinct vascular and immune alterations in mouse models, highlighting critical experimental differences between antibiotic depletion and germ-free systems.
Gut microbiota influence the host’s vascular physiology locally in the intestine, but also evoke remote effects that impact distant organ functions. Amongst others, the microbiota affect intestinal vascular remodeling, lymphatic development, cardiac output and vascular function, myelopoiesis, prothrombotic platelet function, and immunovigilance of the host. Experimentally, host-microbiota interactions are investigated by working with animals devoid of symbiotic bacteria, i.e. by the decimation of gut commensals by antibiotic administration, or by taking advantage of germ-free mouse technology. Remarkably, some of the vascular effects that were unraveled following antibiotic treatment were not observed in the germ-free animal models and vice versa. In this review, we will dissect the manifold influences that antibiotics have on the cardiovascular system and their effects on thromboinflammation.
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Bayer et al. (2019) studied this question.
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