High glucose inhibits expression of inducible and constitutive nitric oxide synthase in bovine aortic endothelial cells

被引:0
作者
Guo, X [1 ]
Chen, LW [1 ]
Liu, WL [1 ]
Guo, ZG [1 ]
机构
[1] Hunan Med Univ, Mol Pharmacol Lab, Changsha 410078, Peoples R China
来源
ACTA PHARMACOLOGICA SINICA | 2000年 / 21卷 / 04期
关键词
nitric-oxide synthase; glucose; lipopolysaccharides; Western blotting; vascular endothelium; cultured cells;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
AIM: To investigate the effects of high glucose on the expression of nitric-oxide synthase (NOS) in cultured bovine aortic endothelial cells (BAEC). METHODS: BAEC were cultured and passaged in normal glucose (NG) 5.5 mmol.L-1, high glucose (HG) 25 mmol.L-1, or high osmolarity (glucose 5.5 mmol.L-1 + mannitol 19.5 mmol.L-1, Mann-BAEC), lipopolysaccharides (LPS)-induced nitric oxide (NO) production was assessed by Griess reaction. The expression of inducible NOS (iNOS) and constitutive NOS (ecNOS) was determined by Western blot. RESULTS: At a concentration range from 0.5 to 2 mg.L-1, LPS stimulated NO production in NG-BAEC in a concentration-dependent manner. NO production reached the peak level at LPS 1 mg.L-1. HG inhibited NO production, when compared with NG- and Mann-BAEC (nitrite mu mol.L-1: HG-BAEC 43 +/- 8, vs NG-BAEC 71 +/- 11, Mann-BAEC 70 +/- 9, n = 4 experiments, P < 0.01). iNOS expression was decreased by 39.9 % and 39.3 %, and ecNOS by 28 % and 24 % respectively in HG-BAEC, when compared with NG- or Mann-BAEC. However, no marked difference was observed in the LPS-induced NO production and the expression of iNOS and ecNOS between NG- and Mann-BAEC. CONCLUSIONS: Inhibition of BAEC NO production by HG was mainly due to a decreased expression of NOS protein.
引用
收藏
页码:325 / 328
页数:4
相关论文
共 15 条
[1]   The L-arginine-nitric oxide pathway: Role in atherosclerosis and therapeutic implications [J].
Boger, RH ;
BodeBoger, SM ;
Frolich, JC .
ATHEROSCLEROSIS, 1996, 127 (01) :1-11
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P218
[3]  
Buttery LDK, 1996, LAB INVEST, V75, P77
[4]   Constitutive nitric oxide synthase expression in retinal vascular endothelial cells is suppressed by high glucose and advanced glycation end products [J].
Chakravarthy, U ;
Hayes, RG ;
Stitt, AW ;
McAuley, E ;
Archer, DB .
DIABETES, 1998, 47 (06) :945-952
[5]  
Cosentino F, 1998, J CARDIOVASC PHARM, V32, pS54
[6]  
Cosentino F, 1997, CIRCULATION, V96, P25
[7]   Oxidative stress and diabetic vascular complications [J].
Giugliano, D ;
Ceriello, A ;
Paolisso, G .
DIABETES CARE, 1996, 19 (03) :257-267
[8]   INDUCTION OF NITRIC-OXIDE SYNTHASE GENE BY INTERLEUKIN IN VASCULAR SMOOTH-MUSCLE CELLS [J].
KANNO, K ;
HIRATA, Y ;
IMAI, T ;
MARUMO, F .
HYPERTENSION, 1993, 22 (01) :34-39
[9]   INHIBITORY EFFECT OF BISBENZYLISOQUINOLINE ALKALOIDS ON NITRIC-OXIDE PRODUCTION IN ACTIVATED MACROPHAGES [J].
KONDO, Y ;
TAKANO, F ;
HOJO, H .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (11) :1887-1892
[10]   Calcium and protein kinase C mediate high-glucose-induced inhibition of inducible nitric oxide synthase in vascular smooth muscle cells [J].
Muniyappa, R ;
Srinivas, PR ;
Ram, JL ;
Walsh, MF ;
Sowers, JR .
HYPERTENSION, 1998, 31 (01) :289-295