Perirenal Adipose Tissue Inflammation: Novel Insights Linking Metabolic Dysfunction to Renal Diseases

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Frontiers Media S.A.

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A healthy adipose tissue (AT) is indispensable to human wellbeing. Among other roles, it contributes to energy homeostasis and provides insulation for internal organs. Adipocytes were previously thought to be a passive store of excess calories, however this view evolved to include an endocrine role. Adipose tissue was shown to synthesize and secrete adipokines that are pertinent to glucose and lipid homeostasis, as well as inflammation. Importantly, the obesity-induced adipose tissue expansion stimulates a plethora of signals capable of triggering an inflammatory response. These inflammatory manifestations of obese AT have been linked to insulin resistance, metabolic syndrome, and type 2 diabetes, and proposed to evoke obesity-induced comorbidities including cardiovascular diseases (CVDs). A growing body of evidence suggests that metabolic disorders, characterized by AT inflammation and accumulation around organs may eventually induce organ dysfunction through a direct local mechanism. Interestingly, perirenal adipose tissue (PRAT), surrounding the kidney, influences renal function and metabolism. In this regard, PRAT emerged as an independent risk factor for chronic kidney disease (CKD) and is even correlated with CVD. Here, we review the available evidence on the impact of PRAT alteration in different metabolic states on the renal and cardiovascular function. We present a broad overview of novel insights linking cardiovascular derangements and CKD with a focus on metabolic disorders affecting PRAT. We also argue that the confluence among these pathways may open several perspectives for future pharmacological therapies against CKD and CVD possibly by modulating PRAT immunometabolism. © Copyright © 2021 Hammoud, AlZaim, Al-Dhaheri, Eid and El-Yazbi.

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Adipose tissue inflammation, Cardiovascular disease, Chronic kidney disease, Metabolic dysfunction, Perirenal adipose tissue, Adipocytokine, Angiotensin ii, Hypoxia inducible factor 1alpha, Immunoglobulin enhancer binding protein, Interleukin 1beta, Nitric oxide, Peroxisome proliferator activated receptor alpha, Plasminogen activator inhibitor 1, Reduced nicotinamide adenine dinucleotide phosphate oxidase 4, Transcription factor nrf2, Triacylglycerol, Tumor necrosis factor, Uncoupling protein 1, Adipogenesis, Cardiorenal syndrome, Cardiovascular function, Cardiovascular mortality, Cell infiltration, Chronic kidney failure, Dyslipidemia, Histology, Hypertension, Hypertriglyceridemia, Hypoxia, Inflammation, Jak-stat signaling, Kidney blood vessel, Kidney disease, Kidney function, Metabolic disorder, Natural killer cell, Pathogenesis, Perirenal fat, Renal cell carcinoma, Renin angiotensin aldosterone system, Review, Risk factor, Stem cell, Thermogenesis

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