L-arginine uptake, the citrulline-NO cycle and arginase II in the rat brain: an in situ hybridization study

被引:102
作者
Braissant, O [1 ]
Gotoh, T
Loup, M
Mori, M
Bachmann, C
机构
[1] Univ Lausanne Hosp, Cent Lab Clin Chem, CH-1011 Lausanne, Switzerland
[2] Kumamoto Univ, Sch Med, Dept Mol Genet, Kumamoto 8600811, Japan
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 70卷 / 02期
关键词
brain; arginine; nitric oxide; system y(+); arginase; argininosuccinate; in situ hybridization;
D O I
10.1016/S0169-328X(99)00151-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nitric oxide (NO) is synthesized from a unique precursor, arginine, by nitric oxide synthase (NOS). In brain cells, arginine is supplied by protein breakdown or extracted from the blood through cationic amino acid transporters (CATs). Arginine can also be recycled from the citrulline produced by NOS activity, through argininosuccinate synthetase (AS) and argininosuccinate lyase (AL) activities, and metabolized by arginase. NOS, AS and AL constitute the so-called citrulline-NO cycle. In order to better understand arginine transport, recycling and degradation, we studied the regional distribution of cells expressing CAT1, CAT3, AS, AL, neuronal NOS (nNOS) and arginase II (AII) in the adult rat brain by non-radioisotopic in situ hybridization (ISH). CAT1, AL and All presented an ubiquitous neuronal and glial expression, whereas CAT3 and AS were confined to neurons. nNOS was restricted to scattered neurons and a few brain nuclei and layers. We demonstrate by this study that cells expressing nNOS all appear to express the entire citrulline-NO cycle, whereas numerous cells expressing AL do not express AS. The differential expression of these genes within the same anatomical structure could indicate that intercellular exchanges of citrulline-NO cycle metabolites are relevant. Thus vicinal interactions should be taken into account to study their regulatory mechanisms. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:231 / 241
页数:11
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