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大鼠脑中的前甲基咪唑乙酸:其区域分布及与组胺代谢途径的关系。

pros-methylimidazoleacetic acid in rat brain: its regional distribution and relationship to metabolic pathways of histamine.

作者信息

Prell G D, Khandelwal J K, Hough L B, Green J P

机构信息

Department of Pharmacology, Mount Sinai School of Medicine, City University of New York, New York.

出版信息

J Neurochem. 1989 Feb;52(2):561-7. doi: 10.1111/j.1471-4159.1989.tb09156.x.

DOI:10.1111/j.1471-4159.1989.tb09156.x
PMID:2911030
Abstract

pros-Methylimidazoleacetic acid (p-MIAA; 1-methylimidazole-5-acetic acid), an isomer of the histamine metabolite, tele-methylimidazoleacetic acid (t-MIAA), is present in brain and CSF. Its relationship to histamine synthesis and catabolism was assessed in brains of rats. p-MIAA distribution in brain regions was heterogeneous although the concentrations in regions with the highest (hypothalamus) and the lowest (medulla-pons) levels differed less than four-fold. There was no significant correlation between the regional distributions of p-MIAA with those of histamine or its metabolites. pros-Methylhistidine (1 g/kg, i.p.) produced a 20-fold increase in mean levels of p-MIAA and up to a 50-fold increase in levels of pros-methylhistamine (p-MH), a putative intermediate; levels of histamine and its metabolites were unaltered. L-Histidine (1 g/kg, i.p.) or alpha-fluoromethylhistidine (100 mg/kg, i.p.), the irreversible inhibitor of histamine synthesis, did not alter the levels of p-MIAA in brain. Like the levels of t-MIAA, the levels of p-MIAA were unaltered after probenecid administration. Contrary to its effects in lowering t-MIAA levels, pargyline (75 mg/kg, i.p.) produced a slight rise in levels of p-MIAA in all regions. These findings suggest that, in brain, the metabolic pathways of histamine are independent of pathways that generate p-MIAA. Further, since brain is capable of p-MH formation, its use as an internal standard in analytical methods merits caution.

摘要

前甲基咪唑乙酸(p-MIAA;1-甲基咪唑-5-乙酸)是组胺代谢产物远甲基咪唑乙酸(t-MIAA)的异构体,存在于脑和脑脊液中。在大鼠脑中评估了它与组胺合成及分解代谢的关系。p-MIAA在脑区的分布是不均匀的,尽管最高(下丘脑)和最低(延髓-脑桥)水平区域的浓度差异不到四倍。p-MIAA的区域分布与组胺或其代谢产物的区域分布之间没有显著相关性。前甲基组氨酸(1 g/kg,腹腔注射)使p-MIAA的平均水平增加了20倍,使假定中间体前甲基组胺(p-MH)的水平增加了多达50倍;组胺及其代谢产物的水平未改变。L-组氨酸(1 g/kg,腹腔注射)或组胺合成的不可逆抑制剂α-氟甲基组氨酸(100 mg/kg,腹腔注射)未改变脑中p-MIAA的水平。与t-MIAA水平一样,丙磺舒给药后p-MIAA的水平未改变。与它降低t-MIAA水平的作用相反,优降宁(75 mg/kg,腹腔注射)使所有区域的p-MIAA水平略有升高。这些发现表明,在脑中,组胺的代谢途径独立于产生p-MIAA的途径。此外,由于脑能够形成p-MH,因此在分析方法中将其用作内标时应谨慎。

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