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一种在清醒动物中研究大脑产生3-甲氧基-4-羟基苯乙二醇(MHPG)的直接方法。

A direct method for studying 3-methoxy-4-hydroxyphenethyleneglycol (MHPG) production by brain in awake animals.

作者信息

Maas J W, Hattox S E, Landis D H, Roth R H

出版信息

Eur J Pharmacol. 1977 Dec 1;46(3):221-8. doi: 10.1016/0014-2999(77)90337-5.

DOI:10.1016/0014-2999(77)90337-5
PMID:412681
Abstract

A direct method for measuring the rate of production of neurotransmitter metabolites by the brain of awake monkeys is described. The method utilizes a coupling of a measure of cerebral blood flow with the determination of the difference in concentration of the metabolite under study in arterial and internal jugular bulb blood. A consistent veno-arterial difference for 3-methoxy-4-hydroxyphenethylenglycol (MHPG) has been found. The concentration of MHPG in blood obtained from the right and left venous outflows from brain were not significantly different indicating that blood from either the right or left internal jugular bulb may be used with this method. The rate of production of MHPG by the brain of thw awake monkey is estimated to be 24.1 ng/100 g brain/min. The rate of MHPG production by brain is increased by the administration of piperoxan and decreased by clonidine. Using the experimentally determined rate of production of MHPG by brain and extrapolating to the human it is suggested that a substantial fraction of the total body production of MHPG in man occurs in brain.

摘要

本文描述了一种直接测量清醒猴子大脑中神经递质代谢产物生成速率的方法。该方法将脑血流量测量与所研究代谢产物在动脉血和颈内静脉球部血中浓度差异的测定相结合。已发现3-甲氧基-4-羟基苯乙二醇(MHPG)存在一致的静脉-动脉差异。从大脑右侧和左侧静脉流出的血液中MHPG的浓度无显著差异,这表明使用该方法时,右侧或左侧颈内静脉球部的血液均可使用。清醒猴子大脑中MHPG的生成速率估计为24.1纳克/100克脑/分钟。给予哌罗克生可使大脑中MHPG的生成速率增加,而可乐定则使其降低。利用实验确定的大脑中MHPG的生成速率并外推至人类,提示人类全身MHPG生成总量的很大一部分发生在大脑中。

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1
A direct method for studying 3-methoxy-4-hydroxyphenethyleneglycol (MHPG) production by brain in awake animals.一种在清醒动物中研究大脑产生3-甲氧基-4-羟基苯乙二醇(MHPG)的直接方法。
Eur J Pharmacol. 1977 Dec 1;46(3):221-8. doi: 10.1016/0014-2999(77)90337-5.
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Plasma and cerebrospinal fluid 3-methoxy-4-hydroxyphenylethylene glycol (MHPG) as indices of brain norepinephrine metabolism in primates.血浆和脑脊液中3-甲氧基-4-羟基苯乙二醇(MHPG)作为灵长类动物脑去甲肾上腺素代谢指标
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The determination of a brain arteriovenous difference for 3-methoxy-4-hydroxyphenethyleneglycol (MHPG).3-甲氧基-4-羟基苯乙二醇(MHPG)脑动静脉差的测定
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Relative importance of 3-methoxy-4-hydroxyphenylglycol and 3,4-dihydroxyphenylglycol as norepinephrine metabolites in rat, monkey, and humans.3-甲氧基-4-羟基苯乙二醇和3,4-二羟基苯乙二醇作为大鼠、猴子和人类去甲肾上腺素代谢产物的相对重要性。
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Interaction of antidepressants with clonidine on rat brain total 3-methoxy-4-hydroxyphenylglycol.抗抑郁药与可乐定对大鼠脑总3-甲氧基-4-羟基苯乙二醇的相互作用。
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The effect of clonidine withdrawal on total 3-methoxy-4-hydroxyphenylglycol in the rat brain.
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Regional distribution and production rate of 3-methoxy-4-hydroxyphenylethyleneglycol sulphate (MHPG-SO4) in rat brain.大鼠脑中3-甲氧基-4-羟基苯乙二醇硫酸盐(MHPG-SO4)的区域分布及生成速率
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3-Methoxy-4-hydroxyphenylethyleneglycol (mhpg) transport from the spinal cord during spinal subarachnoid perfusion.
Brain Res. 1976 Jan 30;102(1):131-41. doi: 10.1016/0006-8993(76)90579-5.

引用本文的文献

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Central nervous system norepinephrine metabolism in hypertension.高血压患者中枢神经系统去甲肾上腺素的代谢
Curr Hypertens Rep. 2000 Jun;2(3):302-10. doi: 10.1007/s11906-000-0014-2.
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Assessment of central dopaminergic function using plasma-free homovanillic acid after debrisoquin administration.使用去甲丙咪嗪给药后血浆游离高香草酸评估中枢多巴胺能功能。
J Neural Transm. 1986;67(1-2):31-43. doi: 10.1007/BF01243357.
3
The effect of clonidine on plasma MHPG: evidence against tonic alpha 2-adrenoceptor control of noradrenergic function.
可乐定对血浆3-甲氧基-4-羟基苯乙二醇的影响:反对去甲肾上腺素能功能的紧张性α2-肾上腺素能受体控制的证据。
Psychopharmacology (Berl). 1986;90(4):509-12. doi: 10.1007/BF00174070.
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Raised plasma concentrations of 3-methoxy-4-hydroxyphenylethyleneglycol in cirrhotic patients with or without hepatic encephalopathy.伴有或不伴有肝性脑病的肝硬化患者血浆中3-甲氧基-4-羟基苯乙二醇浓度升高。
Gut. 1989 May;30(5):656-64. doi: 10.1136/gut.30.5.656.
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3-Methoxy-4-hydroxyphenylglycol excretion in acutely schizophrenic patients during a controlled clinical trial of the isomers of flupenthixol.在氟哌噻吨异构体的一项对照临床试验期间,急性精神分裂症患者的3-甲氧基-4-羟基苯乙二醇排泄情况。
Psychopharmacology (Berl). 1979 Jun 28;64(1):35-40. doi: 10.1007/BF00427342.