Effects of aldehyde/aldose reductase inhibition on neuronal metabolism of norepinephrine

被引:21
作者
Kawamura, M
Kopin, IJ
Kador, PF
Sato, S
Tjurmina, O
Eisenhofer, G
机构
[1] NINCDS,CLIN NEUROSCI BRANCH,NIH,BETHESDA,MD 20892
[2] NEI,LAB OCULAR THERAPUT,NIH,BETHESDA,MD 20892
来源
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM | 1997年 / 66卷 / 03期
关键词
aldehyde reductase; 3,4-dihydroxymandelic acid; 3,4-dihydroxyphenylglycol; norepinephrine; sympathetic nervous system; monoamine oxidase;
D O I
10.1016/S0165-1838(97)00086-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
After norepinephrine (NE) is deaminated by monoamine oxidase (MAO), the aldehyde formed is either metabolized to 3,4-dihydroxymandelic acid (DHMA) by aldehyde dehydrogenase or is converted to 3,4-dihydroxyphenylglycol (DHPG) by aldehyde or aldose reductase. The present study examined the effects of inhibition of aldehyde and aldose reductase on production of DHPG and DHMA in rats. Mean (+/-S.E.) baseline plasma concentrations of DHPG (4.73 +/- 0.21 pmol/ml) were 60-fold higher than those of DHMA (0.08 +/- 0.01 pmol/ml). Inhibition of aldose and aldehyde reductase reduced plasma DHPG concentrations to 1.88 +/- 0.14 pmol/ml and increased plasma DHMA to 4.43 +/- 0.29 pmol/ml; additional inhibition of MAO reduced plasma DHPG to 0.16 +/- 0.06 pmol/ml and DHMA to 0.19 +/- 0.02 pmol/ml. Inhibition of aldehyde and aldose reductase also increased brain tissue levels of DHMA from 8 +/- 2 to 384 +/- 47 pmol/g and decreased levels of DHPG from 70 +/- 9 to 44 +/- 5 pmol/g. The results show that DHMA is normally a minor metabolite of NE, but becomes a major metabolite after aldehyde/aldose reductase inhibition. Published by Elsevier Science B.V.
引用
收藏
页码:145 / 148
页数:4
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