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Peroxisome proliferator-activated receptors (PPARs): Novel therapeutic targets in renal disease

期刊

KIDNEY INTERNATIONAL
卷 60, 期 1, 页码 14-30

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ELSEVIER SCIENCE INC
DOI: 10.1046/j.1523-1755.2001.00766.x

关键词

fibrate; thiazolidinedione; lipid metabolism; adipogenesis; atherosclerosis; diabetes; hypertension; kidney disease

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Peroxisome proliferator-activated receptors (PPARs): Novel therapeutic targets in renal disease. Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear hormone receptor superfamily of ligand-dependent transcription Factors. PPARs play an important role in the general transcriptional control of numerous cellular processes, including lipid metabolism. glucose homeostasis, cell cycle progression, cell differentiation, inflammation and extracellular matrix remodeling. Three PPAR isoforms, designated PPAR alpha. PPAR beta and PPAR I, have been cloned and are differentially expressed in several tissues including the kidney. PPARa primary regulates lipid metabolism and modulates inflammation. PPAR alpha is the molecular target of the hypolipidemic fibrates including bezafibrate and clofibrate. PPAR beta participates in embryonic development, implantation and bone formation. PPAR gamma is a key factor in adipogenesis and also plays an important role in insulin sensitivity cell cycle regulation and cell differentiation. Antidiabetic thiazolidinediones (TZDs) such as troglitazone and rosiglitazone are specific ligands of PPAR gamma, and this interaction is responsible for the insulin-sensitizing and hypoglycemic effect of these drugs. The kidney has been shown to differentially express all PPAR isoforms. PPAR alpha is predominantly expressed in proximal tubules and medullary thick ascending limbs, while PPAR alpha is expressed in medullary collecting ducts. pelvic urothelium and glomerular mesangial cells. PPAR beta is ubiquitously expressed at low levels in all segments of nephron. Accumulating data has begun to emerge suggesting physiological and pathophysiological roles of PPARs in several tissues including the kidney. The availability of PPAR-selective agonists and antagonists may provide a new approach to modulate the renal response to diseases including glomerulonephritis. glomerulosclerosis and diabetic nephropathy.

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