Interactions between Advanced Glycation End-products (AGE) and their receptors in the development and progression of diabetic nephropathy - Are these receptors valid therapeutic targets

Current Drug Targets

Volumn 10, Issue 1, 2009, Pages 42-50

  Sourris, Karly C ^a   Forbes, Josephine M ^a,b  

^a BAKER IDI HEART AND DIABETES INSTITUTE   (Australia)

^b MONASH UNIVERSITY   (Australia)

Author keywords

Advanced glycation end products (AGEs); AGE R1; Diabetic nephropathy; Modulation of AGE receptors; RAGE; Soluble RAGE

Indexed keywords

2 (2 AMINO 3 METHOXYPHENYL)CHROMONE; 2 ISOPROPYLIDENEHYDRAZONO 4 OXO 5 THIAZOLIDINYLACETANILIDE; 6 N CARBOXYMETHYLLYSINE; ADVANCED GLYCATION END PRODUCT; ADVANCED GLYCATION END PRODUCT RECEPTOR; ALAGEBRIUM; AMINOGUANIDINE; AMYLOID A PROTEIN; AMYLOID BETA PROTEIN; ANTIDIABETIC AGENT; ANTIHYPERTENSIVE AGENT; BENFOTIAMINE; CD36 ANTIGEN; CREATININE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FLUINDOSTATIN; GLITAZONE DERIVATIVE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; LOW MOLECULAR WEIGHT HEPARIN; LR 90; METFORMIN; MITHRAMYCIN; PARTHENOLIDE; PENTOSIDINE; PERINDOPRIL; PROTEIN S 100; PYRIDOXAMINE; SIMVASTATIN; TELMISARTAN; UNCLASSIFIED DRUG; UNINDEXED DRUG; ADVANCED GLYCOSYLATION END PRODUCT RECEPTOR; ADVANCED GLYCOSYLATION END-PRODUCT RECEPTOR; IMMUNOGLOBULIN RECEPTOR; LIGAND; MONOCLONAL ANTIBODY;

CLINICAL TRIAL; CREATININE CLEARANCE; DIABETES MELLITUS; DIABETIC NEPHROPATHY; DISEASE COURSE; DRUG EFFICACY; DRUG POTENCY; DRUG TARGETING; EXTRACELLULAR MATRIX; HUMAN; NONHUMAN; OXIDATIVE STRESS; PATHOGENESIS; PROTEIN CARBOHYDRATE INTERACTION; PROTEIN EXPRESSION; RENAL PROTECTION; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; REVIEW; ANIMAL; BIOSYNTHESIS; CHRONIC KIDNEY FAILURE; DRUG ANTAGONISM; METABOLISM; PHYSIOLOGY; PROTEIN BINDING;

ANIMALS; ANTIBODIES, MONOCLONAL; DIABETIC NEPHROPATHIES; DISEASE PROGRESSION; GLYCOSYLATION END PRODUCTS, ADVANCED; HUMANS; KIDNEY FAILURE, CHRONIC; LIGANDS; PROTEIN BINDING; RECEPTORS, IMMUNOLOGIC;

EID: 63049117088     PISSN: 13894501     EISSN: None     Source Type: Journal    
DOI: 10.2174/138945009787122905     Document Type: Review

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