A constitutive nitric oxide synthase modulates insulin secretion in the INS-1 cell line

被引:17
作者
Beffy, P
Lajoix, AD
Masiello, P
Dietz, S
Péraldi-Roux, S
Chardés, T
Ribes, G
Gross, R
机构
[1] CNR, Ist Mutagenesi & Differenziamento, Pisa, Italy
[2] Univ Montpellier 1, CNRS, UMR 5094, Montpellier, France
[3] Univ Pisa, Dipartimento Patol Sperimentale, Pisa, Italy
[4] INRA, UMR 5087, St Christol Les Ales, France
[5] CNRS, Lab Pathol Comparee, St Christol Les Ales, France
关键词
INS-1; cells; insulin secretion; neuronal nitric oxide synthase;
D O I
10.1016/S0303-7207(01)00610-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We provide immunocytochemical evidence that the neuronal isoform of constitutive NO synthase (cNOS) is expressed in the rat insulinoma cell line INS-1. Furthermore, using N omega -nitro-L-arginine methyl ester (L-NAME), a pharmacological inhibitor of cNOS activity, we show that this enzyme is implicated in the modulation of insulin secretion in INS-1 cells. Indeed, in the presence of 2.8 MM glucose, L-NAME induced a specific and dose-dependent increase in insulin release, suggesting that cNOS exerts an inhibitory tone on basal insulin secretion. Moreover, L-arginine, the physiological substrate of cNOS, significantly reduced the marked enhancing effect Of L-NAME on insulin release and to a lesser extent, at low concentrations, that of 10 mM KC1. L-NAME also potentiated the insulin secretion stimulated by 5.5 and 8.3 mM glucose, but in this case, its effect was not reduced by L-arginine. In conclusion, our data show that the neuronal isoform of cNOS exerts a negative modulation on insulin secretion in INS-1 cells, confirming the previous results obtained in the isolated perfused rat pancreas or pancreatic islets. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
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