Modulation of inducible nitric oxide synthase gene expression in RAW 264.7 murine macrophages by Pacific ciguatoxin

被引:22
|
作者
Kumar-Roine, Shilpa [2 ]
Matsui, Mariko [1 ,2 ]
Chinain, Mireille
Laurent, Dominique [2 ]
Pauillac, Serge [1 ]
机构
[1] Inst Pasteur Nouvelle Caledonie, Lab Biotoxines, Noumea 98845, New Caledonia
[2] Univ Toulouse 3, Lab Pharmacochim Subst Nat & Pharmacophores Redax, UMR IRD 152, Ctr IRD Noumea, Noumea 98848, New Caledonia
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2008年 / 19卷 / 01期
关键词
ciguatoxin; lipopolysaccharide; macrophage; inducible nitric oxide synthase; ciguatera; chronic fatigue syndrome;
D O I
10.1016/j.niox.2008.03.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate the possible involvement of the nitric oxide radical (NO) in ciguatera fish poisoning (CFP), the in vitro effects of the main Pacific ciguatoxin (P-CTX-1B) and bacterial lipopolysaccharide (LPS) were comparatively studied on neuroblastoma Neuro-2a and on macrophage RAW 264.7 cell lines. NO accumulation was quantified by measuring nitrite levels in cellular supernatant using Griess reagent while the up-regulation of inducible nitric oxide synthase (iNOS) at the mRNA level was quantified via Real-Time Reverse-Transcription Polymerase Chain Reaction (RT-PCR). P-CTX-1B caused a concentration-and time-dependent induction of iNOS in RAW 264.7 cells but not in Neuro-2a cells. NO production was evidenced by increased nitrite levels in the 10 mu M range after 48 h of RAW 264.7 cells exposure to LPS and P-CTX-1B (0.05 mu g/ml and 6 nM, respectively). The expression of MOS mRNA peaked at 8 h for LPS then gradually decreased to low level at 48 h. In contrast, a sustained level was recorded with P-CTX-1B in the 8-48 h time interval. The addition of N.-nitro-L-arginine methyl ester (L-NAME), a stereo-selective NOS inhibitor, strongly diminished NO formation but had no effect on iNOS mRNA synthesis. The implication of NO in CFP paves the way for new therapies for both western and traditional medicines. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 28
页数:8
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