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AUTORADIOGRAPHIC DISTRIBUTION OF [H-3] L-N-G-NITRO-ARGININE BINDING IN RAT-BRAIN
被引:52
作者:
KIDD, EJ
MICHEL, AD
HUMPHREY, PPA
机构:
[1] Glaxo Institute of Applied Pharmacology, Department of Pharmacology, University of Cambridge, Cambridge, CB2 1QJ, Tennis Court Road
关键词:
NITRIC OXIDE SYNTHASE;
RAT CENTRAL NERVOUS SYSTEM;
H-3] L-N-G-NITRO-ARGININE;
AUTORADIOGRAPHY;
REGIONAL DISTRIBUTION;
QUANTIFICATION;
D O I:
10.1016/0028-3908(94)00132-C
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The distribution of nitric oxide synthase (NOS), the enzyme which produces nitric oxide, has previously been studied in the rat central nervous system (CNS) using the NADPH-diaphorase technique and anti-NOS antibodies. However, the former method may not always be selective for NOS while the latter is not quantitative. Therefore a selective, quantifiable method would be desirable. L-N-G-Nitro-arginine, an inhibitor of NOS, is available in a tritiated form which we have shown to bind to NOS. We have now examined the regional distribution of [H-3]L-N-G-nitro-arginine binding in the rat CNS using autoradiography. [H-3]L-N-G-nitro-arginine specific binding was seen in a number of brain regions with the highest levels in the accessory olfactory bulb, the amygdaloid complex, the islands of Calleja and the cerebellum. This regional distribution of [H-3]L-N-G-nitro-arginine binding sites in the rat CNS was, in general, similar to that seen with the NADPH-diaphorase method and anti-NOS antibodies, consistent with the view that all three methods identify NOS in the CNS. Thus, [H-3]L-N-G-nitro-arginine appears to be a useful radioligand for studying the distribution of NOS in the CNS as its binding is quantifiable and apparently selective for NOS.
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页码:63 / 73
页数:11
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