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Selective monoamine oxidase inhibitor drugs as aids in evaluating the role of type A and B enzymes.

作者信息

Fuentes J A, Neff N H

出版信息

Neuropharmacology. 1975 Nov;14(11):819-25. doi: 10.1016/0028-3908(75)90109-4.

DOI:10.1016/0028-3908(75)90109-4
PMID:1207877
Abstract
摘要

相似文献

1
Selective monoamine oxidase inhibitor drugs as aids in evaluating the role of type A and B enzymes.
Neuropharmacology. 1975 Nov;14(11):819-25. doi: 10.1016/0028-3908(75)90109-4.
2
The acetylenic monoamine oxidase inhibitors clorgyline, deprenyl, pargyline and J-508: their properties and applications.炔属单胺氧化酶抑制剂氯吉兰、司来吉兰、帕吉林和J-508：它们的性质与应用。
J Pharm Pharmacol. 1981 Jun;33(6):341-7. doi: 10.1111/j.2042-7158.1981.tb13800.x.
3
Inhibition of monoamine oxidase by N-phenacyl-cyclopropylamine.
Biochem Pharmacol. 1978;27(18):2255-61. doi: 10.1016/0006-2952(78)90085-0.
4
The nature of the inhibition of rat liver monoamine oxidase types A and B by the acetylenic inhibitors clorgyline, l-deprenyl and pargyline.炔丙型抑制剂氯吉兰、l-司来吉兰和帕吉林对大鼠肝脏A型和B型单胺氧化酶的抑制性质。
Biochem Pharmacol. 1982 Nov 15;31(22):3555-61. doi: 10.1016/0006-2952(82)90575-5.
5
Inhibition of monoamine oxidation in subfractions of crude mitochondria of rat brain by clorgyline and Lilly 51641.氯吉兰和礼来51641对大鼠脑粗线粒体亚组分中单胺氧化的抑制作用。
Biochem Pharmacol. 1978;27(20):2455-7. doi: 10.1016/0006-2952(78)90359-3.
6
SR 95191, a selective inhibitor of type A monoamine oxidase with dopaminergic properties. I. Psychopharmacological profile in rodents.SR 95191，一种具有多巴胺能特性的A型单胺氧化酶选择性抑制剂。I. 啮齿动物的精神药理学特征。
J Pharmacol Exp Ther. 1987 Jan;240(1):241-50.
7
Monoamine oxidase inhibition and the induction of ponto-geniculo-occipital wave activity by reserpine in the cat.
J Pharmacol Exp Ther. 1976 Jun;197(3):556-66.
8
Drug-induced changes in motor activity after selective MAO inhibition.选择性单胺氧化酶抑制后药物诱导的运动活动变化。
Pharmacol Biochem Behav. 1983 Aug;19(2):263-8. doi: 10.1016/0091-3057(83)90050-3.
9
Enhanced selectivity of pargyline as an inhibitor of type B monoamine oxidase in harmaline-treated rats.
Life Sci. 1978 Mar;22(12):1083-6. doi: 10.1016/0024-3205(78)90278-3.
10
Reciprocal changes in striatal dopamine and beta-phenylethylamine induced by reserpine in the presence of monoamine oxidase inhibitors.在单胺氧化酶抑制剂存在的情况下，利血平诱导纹状体多巴胺和β-苯乙胺的相互变化。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Dec;338(6):644-8. doi: 10.1007/BF00165628.

引用本文的文献

1
Effects of low oxygen on the release of dopamine from the rabbit carotid body in vitro.低氧对体外培养的兔颈动脉体多巴胺释放的影响。
J Physiol. 1982 Dec;333:93-110. doi: 10.1113/jphysiol.1982.sp014441.
2
alpha-Methyldopa, alpha-methyldopamine an alpha-methylnoradrenaline: substrates for the thermolabile form of human platelet phenol sulphotransferase.α-甲基多巴、α-甲基多巴胺和α-甲基去甲肾上腺素：人血小板酚磺基转移酶热不稳定形式的底物。
Br J Clin Pharmacol. 1982 Aug;14(2):231-9. doi: 10.1111/j.1365-2125.1982.tb01967.x.
3
Tyramine infusions and selective monoamine oxidase inhibitor treatment. II. Interrelationships among pressor sensitivity changes, platelet MAO inhibition, and plasma MHPG reduction.
酪胺输注与选择性单胺氧化酶抑制剂治疗。II. 升压敏感性变化、血小板单胺氧化酶抑制及血浆3-甲氧基-4-羟基苯乙二醇降低之间的相互关系。
Psychopharmacology (Berl). 1981;74(1):8-12. doi: 10.1007/BF00431748.
4
Tyramine infusions and selective monoamine oxidase inhibitor treatment. I. Changes in pressor sensitivity.酪胺输注与选择性单胺氧化酶抑制剂治疗。I. 升压敏感性的变化。
Psychopharmacology (Berl). 1981;74(1):4-7. doi: 10.1007/BF00431747.
5
Thermolabile and thermostable human platelet phenol sulfotransferase. Substrate specificity and physical separation.热不稳定和热稳定的人血小板酚磺基转移酶。底物特异性和物理分离。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Sep;324(2):140-7. doi: 10.1007/BF00497020.
6
Effects of tetrabenazine and phenylpiperidine analgesics during daily clorgyline treatment.在每日使用氯吉兰治疗期间丁苯那嗪和苯基哌啶类镇痛药的作用。
Psychopharmacology (Berl). 1981;74(3):221-5. doi: 10.1007/BF00427098.
7
Tyramine pressor sensitivity changes during deprenyl treatment.
Psychopharmacology (Berl). 1985;86(4):432-7. doi: 10.1007/BF00427904.
8
Selective inhibition of MAO-A, not MAO-B, results in antidepressant-like effects on DRL 72-s behavior.
Psychopharmacology (Berl). 1988;96(2):153-60. doi: 10.1007/BF00177554.
9
Potentiation by deprenyl of the autoreceptor-mediated inhibition of [3H]-5-hydroxytryptamine release by 5-methoxytryptamine.司来吉兰对5-甲氧基色胺通过自身受体介导抑制[3H]-5-羟色胺释放的增强作用。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Jul;333(3):330-3. doi: 10.1007/BF00512949.
10
Phenylethylamine-induced release of noradrenaline fails to stimulate alpha 1-adrenoceptors modulating [3H]-acetylcholine release in rat atria, but activates alpha 2-adrenoceptors modulating [3H]-serotonin release in the hippocampus.苯乙胺诱导的去甲肾上腺素释放未能刺激调节大鼠心房中[3H] - 乙酰胆碱释放的α1 - 肾上腺素能受体，但能激活调节海马体中[3H] - 5 - 羟色胺释放的α2 - 肾上腺素能受体。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Oct;334(2):149-55. doi: 10.1007/BF00505815.