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
相关论文
共 35 条
[11]   NITRIC-OXIDE IS NOT INVOLVED IN THE INITIATION OF INSULIN-SECRETION FROM RAT ISLETS OF LANGERHANS [J].
JONES, PM ;
PERSAUD, SJ ;
BJAALAND, T ;
PEARSON, JD ;
HOWELL, SL .
DIABETOLOGIA, 1992, 35 (11) :1020-1027
[12]  
KLATT P, 1994, J BIOL CHEM, V269, P1674
[13]   KINETIC CHARACTERISTICS OF NITRIC-OXIDE SYNTHASE FROM RAT-BRAIN [J].
KNOWLES, RG ;
PALACIOS, M ;
PALMER, RMJ ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1990, 269 (01) :207-210
[14]   Effects of the nitric oxide synthase inhibitor N-omega nitro-L-arginine methyl ester on electrical activity and ion channels of mouse pancreatic B cells [J].
KrippeitDrews, P ;
Welker, S ;
Drews, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 224 (01) :199-205
[15]  
Lajoix AD, 1999, DIABETOLOGIA, V42, pA142
[16]  
LAJOIX AD, 1999, DIABETOLOGIA S1, V42, P125
[17]  
MONCADA S, 1991, PHARMACOL REV, V43, P109
[18]   Citrulline-argininosuccinate-arginine cycle coupled to Ca2+-signaling in rat pancreatic beta-cells [J].
Nakata, M ;
Yada, T ;
Nakagawa, S ;
Kobayashi, K ;
Maruyama, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 235 (03) :619-624
[19]   NITRIC-OXIDE FROM L-ARGININE STIMULATES THE SOLUBLE GUANYLATE-CYCLASE IN ADRENAL-GLANDS [J].
PALACIOS, M ;
KNOWLES, RG ;
PALMER, RMJ ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (02) :802-809
[20]   L-ARGININE IS THE PHYSIOLOGICAL PRECURSOR FOR THE FORMATION OF NITRIC-OXIDE IN ENDOTHELIUM-DEPENDENT RELAXATION [J].
PALMER, RMJ ;
REES, DD ;
ASHTON, DS ;
MONCADA, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :1251-1256