PMID- 11884223 OWN - NLM STAT- MEDLINE DCOM- 20031125 LR - 20171116 IS - 1043-6618 (Print) IS - 1043-6618 (Linking) VI - 45 IP - 3 DP - 2002 Mar TI - A study on the relationship between homocysteine and diabetic nephropathy in rats. PG - 249-52 AB - Hyperhomocysteinemia is known to be associated with many of the occlusive vascular diseases including ischemic heart disease. Elevated plasma total homocysteine (t-Hcy) is also remarkably common among patients with moderate to severe renal failure. The purpose of this study was to investigate the role of homocysteine (Hcy) in the pathogenesis of diabetic nephropathy in the rat. Additionally, any effect of aminoguanidine (AG), an inhibitor of advanced glycation end product (AGE) formation, on the onset of nephropathic symptoms and on the concentrations of Hcy was searched for. Diabetes was induced in male Wistar albino rats (6 months old) by a single injection of 50 mg x kg (-1)streptozotocin (STZ) into the penile vein. Animals with blood glucose levels higher than 350 mg x dl (-1)72 h after STZ injection were included in the study. Age-matched rats receiving a single dose of citrate buffer served as controls. One half of the control and diabetic groups received AG via drinking water (1 g l (-1)). The experimental period lasted for ten weeks. Animals were killed by cardiac venipuncture after 24 hour urine samples were collected. Serum t-Hcy was quantified using HPLC, and urinary GAGs using the spectrophotometric 1,9-dimethyl methylene blue dye method. Serum glucose, protein, creatinine and total sulfydryl (t-SH) measurements, and urinary protein determinations were carried out spectrophotometrically. In diabetic rats, serum t-Hcy levels were significantly decreased (P< 0.001), and were negatively correlated with the urinary protein concentration (r= -0.67, P< 0.05). Urinary GAG levels were also increased in diabetic rats (P< 0.001). AG neither affected the t-Hcy levels, nor ameliorated the nephropathic symptoms. These results indicate that diabetic nephropathy is not linked to homocysteinemia in the rat. CI - Copyright 2002 Elsevier Science Ltd. FAU - Unlucerci, Yesim AU - Unlucerci Y AD - Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Capa 34390, Turkey. yesimunlucerci@hotmail.com FAU - Bekpinar, Selda AU - Bekpinar S FAU - Gurdol, Figen AU - Gurdol F FAU - Seferoglu, Gulay AU - Seferoglu G LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Netherlands TA - Pharmacol Res JT - Pharmacological research JID - 8907422 RN - 0 (Enzyme Inhibitors) RN - 0 (Glycation End Products, Advanced) RN - 0 (Glycosaminoglycans) RN - 0 (Guanidines) RN - 0LVT1QZ0BA (Homocysteine) RN - AYI8EX34EU (Creatinine) RN - SCQ4EZQ113 (pimagedine) SB - IM MH - Animals MH - Creatinine/blood/urine MH - Diabetic Nephropathies/*blood/urine MH - Enzyme Inhibitors/pharmacology MH - Glycation End Products, Advanced/blood/urine MH - Glycosaminoglycans/urine MH - Guanidines/pharmacology MH - Homocysteine/*blood MH - Male MH - Rats MH - Rats, Wistar EDAT- 2002/03/09 10:00 MHDA- 2003/12/03 05:00 CRDT- 2002/03/09 10:00 PHST- 2002/03/09 10:00 [pubmed] PHST- 2003/12/03 05:00 [medline] PHST- 2002/03/09 10:00 [entrez] AID - S1043661801909429 [pii] AID - 10.1006/phrs.2001.0942 [doi] PST - ppublish SO - Pharmacol Res. 2002 Mar;45(3):249-52. doi: 10.1006/phrs.2001.0942.