Okada Shinichi, Saito Motoaki, Kazuyama Emi, Hanada Takuya, Kawaba Yasuo, Hayashi Atsushi, Satoh Keisuke, Kanzaki Susumu
Division of Pediatrics and Perinatology, Tottori University, 36-1 Nishi-machi, Yonago, Tottori, Japan.
Mol Cell Biochem. 2008 Aug;315(1-2):169-77. doi: 10.1007/s11010-008-9804-7. Epub 2008 Jun 5.
We attempted to clarify the effects of cyclohexenonic long-chain fatty alcohol (N-hexacosanol) on nitric oxide synthase (NOS) in streptozotocin-induced diabetic nephropathy. After induction of experimental diabetes with streptozotocin, rats were maintained for 8 weeks with or without treatment by N-hexacosanol (8 mg/kg i.p. every day). Urinary albumin excretion, blood chemistry, immunoblot analysis, and real-time polymerase chain reactions (real-time PCR) of endothelial nitric oxide synthase (eNOS), inducible NOS (iNOS), and neuronal NOS (nNOS) were investigated. Although N-hexacosanol had no effects on serum glucose or insulin level, it normalized serum creatinine and urinary albumin excretion. N-hexacosanol was found to improve the diabetes-induced alterations in the eNOS, iNOS, and nNOS protein and their mRNA levels. Histologically, N-hexacosanol inhibited the progression to glomerular sclerosis. Our data suggest that N-hexacosanol improves diabetes-induced NOS alterations in the kidney, resulting in the amelioration of diabetic nephropathy.
我们试图阐明环己烯基长链脂肪醇(N-二十六醇)对链脲佐菌素诱导的糖尿病肾病中一氧化氮合酶(NOS)的影响。用链脲佐菌素诱导实验性糖尿病后,将大鼠分为两组,一组每天腹腔注射N-二十六醇(8毫克/千克),另一组不进行该处理,持续8周。检测尿白蛋白排泄、血液生化指标,并通过免疫印迹分析和实时聚合酶链反应(real-time PCR)研究内皮型一氧化氮合酶(eNOS)、诱导型一氧化氮合酶(iNOS)和神经元型一氧化氮合酶(nNOS)。虽然N-二十六醇对血糖或胰岛素水平无影响,但它使血清肌酐和尿白蛋白排泄恢复正常。发现N-二十六醇可改善糖尿病引起的eNOS、iNOS和nNOS蛋白及其mRNA水平的改变。组织学检查显示,N-二十六醇可抑制肾小球硬化的进展。我们的数据表明,N-二十六醇可改善糖尿病引起的肾脏中NOS的改变,从而改善糖尿病肾病。