Phosphorus Supplementation Mitigates Perivascular Adipose Inflammation– Induced Cardiovascular Consequences in Early Metabolic Impairment
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American Heart Association Inc.
Abstract
BACKGROUND: The complexity of the interaction between metabolic dysfunction and cardiovascular complications has long been recognized to extend beyond simple perturbations of blood glucose levels. Yet, structured interventions targeting the root pathologies are not forthcoming. Growing evidence implicates the inflammatory changes occurring in perivascular adipose tissue (PVAT) as early instigators of cardiovascular deterioration. METHODS AND RESULTS: We used a nonobese prediabetic rat model with localized PVAT inflammation induced by hypercaloric diet feeding, which dilutes inorganic phosphorus (Pi) to energy ratio by 50%, to investigate whether Pi supplementation ameliorates the early metabolic impairment. A 12-week Pi supplementation at concentrations equivalent to and twice as much as that in the control diet was performed. The localized PVAT inflammation was reversed in a dose-dependent manner. The increased expression of UCP1 (uncoupling protein1), HIF-1α (hypoxia inducible factor-1α), and IL-1β (interleukin-1β), representing the hallmark of PVAT inflammation in this rat model, were reversed, with normalization of PVAT macrophage polarization. Pi supplementation restored the metabolic efficiency consistent with its putative role as an UCP1 inhibitor. Alongside, parasympathetic autonomic and cerebrovascular dysfunction function observed in the prediabetic model was reversed, together with the mitigation of multiple molecular and histological cardiovascular damage markers. Significantly, a Pi-deficient control diet neither induced PVAT inflammation nor cardiovascular dysfunction, whereas Pi reinstatement in the diet after a 10-week exposure to a hypercaloric low-Pi diet ameliorated the dysfunction. CONCLUSIONS: Our present results propose Pi supplementation as a simple intervention to reverse PVAT inflammation and its early cardiovascular consequences, possibly through the interference with hypercaloric-induced increase in UCP1 expression/ activity. © 2021 The Authors.
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Inorganic phosphorous, Perivascular adipose inflammation, Prediabetes, Uncoupling protein 1, Adipose tissue, Animals, Cardiovascular diseases, Dietary supplements, Inflammation, Metabolic diseases, Phosphorus, Prediabetic state, Rats, Hypoxia inducible factor 1alpha, Interleukin 1beta, Adipose tissue inflammation, Adult, Animal experiment, Animal model, Animal tissue, Article, Autonomic neuropathy, Brain stem, Cardiovascular disease, Controlled study, Diet supplementation, High calorie diet, Human, Human cell, Impaired glucose tolerance, Macrophage, Male, Metabolic disorder, Nonhuman, Perivascular adipose tissue, Phenotype, Protein expression, Protein function, Rat, Animal, Complication, Dietary supplement, Metabolism, Pathology