• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Effect of protriptyline on the formation of (3H)noradrenaline from (3H)dopa.

作者信息

Persson T, Waldeck B

出版信息

J Pharm Pharmacol. 1968 Dec;20(12):966-8. doi: 10.1111/j.2042-7158.1968.tb09688.x.

DOI:10.1111/j.2042-7158.1968.tb09688.x
PMID:4388345
Abstract
摘要

相似文献

1
Effect of protriptyline on the formation of (3H)noradrenaline from (3H)dopa.普罗替林对由(3H)多巴形成(3H)去甲肾上腺素的影响。
J Pharm Pharmacol. 1968 Dec;20(12):966-8. doi: 10.1111/j.2042-7158.1968.tb09688.x.
2
Central and peripheral catecholamine turnover studied by means of 3H-DOPA and 3H-tyrosine.采用3H-多巴和3H-酪氨酸研究中枢和外周儿茶酚胺的周转率。
Acta Pharmacol Toxicol (Copenh). 1969;27(6):397-409. doi: 10.1111/j.1600-0773.1969.tb00486.x.
3
The contents of DOPA and catecholamines in several rat tissues and nicotine-induced convulsions.
Jpn J Pharmacol. 1966 Sep;16(3):295-305. doi: 10.1254/jjp.16.295.
4
A source of error in catecholamine turnover studies with labelled DOPA: slow disappearance of the precursor.使用标记多巴进行儿茶酚胺周转研究时的一个误差来源:前体的缓慢消失。
Acta Pharmacol Toxicol (Copenh). 1970;28(6):466-76. doi: 10.1111/j.1600-0773.1970.tb00572.x.
5
Protriptyline induced inhibition of the in vivo 3H-noradrenaline synthesis from 3H-L-dopa in the rat brain.普罗替林抑制大鼠脑内由3H-L-多巴合成3H-去甲肾上腺素的体内过程。
Naunyn Schmiedebergs Arch Pharmacol. 1974;285(1):15-28. doi: 10.1007/BF00499525.
6
Formation of dopamine from 3-methoxytyrosine. Fact or artifact?
Naunyn Schmiedebergs Arch Pharmacol. 1972;272(4):441-6. doi: 10.1007/BF00501250.
7
3,4-Dihydroxyphenylalanine (dopa), dopamine and norepinephrine storage in the rat heart after L-dopa--further evidence for norepinephrine release.左旋多巴后大鼠心脏中3,4-二羟基苯丙氨酸(多巴)、多巴胺和去甲肾上腺素的储存——去甲肾上腺素释放的进一步证据
Biochem Pharmacol. 1973 Feb 1;22(3):417-25. doi: 10.1016/0006-2952(73)90422-x.
8
Changes in the formation of 3 H-catecholamines from 3 H-DOPA and 3 H-tyrosine induced by unlabelled DOPA.未标记的多巴诱导的由³H-多巴和³H-酪氨酸生成³H-儿茶酚胺的变化。
Acta Pharmacol Toxicol (Copenh). 1971;29(5):525-32. doi: 10.1111/j.1600-0773.1971.tb00626.x.
9
The effect of protriptyline on uptake and retention of dl-3H-noradrenaline in different tissues of the rat.普罗替林对大鼠不同组织中dl-3H-去甲肾上腺素摄取和潴留的影响。
Acta Physiol Scand. 1971 Jun;82(2):282-8. doi: 10.1111/j.1748-1716.1971.tb04969.x.
10
(S)-norepinephrine in the tissues of mice and rats given racemic erythro-3,4-dihydroxyphenylserine (DOPS).
Life Sci I. 1972 Aug 15;11(16):787-95. doi: 10.1016/0024-3205(72)90213-5.

引用本文的文献

1
Effect of desipramine on rat cortex slices incubated with 3H-dopamine.去甲丙咪嗪对用3H-多巴胺孵育的大鼠皮层切片的作用。
Psychopharmacologia. 1974;37(4):341-9. doi: 10.1007/BF00428920.
2
Pharmacological properties of centrally administered ouabain and their modification by other drugs.中枢给予哇巴因的药理特性及其被其他药物的修饰作用。
Br J Pharmacol. 1971 Jun;42(2):242-53. doi: 10.1111/j.1476-5381.1971.tb07105.x.
3
Protriptyline induced inhibition of the in vivo 3H-noradrenaline synthesis from 3H-L-dopa in the rat brain.普罗替林抑制大鼠脑内由3H-L-多巴合成3H-去甲肾上腺素的体内过程。
Naunyn Schmiedebergs Arch Pharmacol. 1974;285(1):15-28. doi: 10.1007/BF00499525.
4
An analysis of DOPA-induced locomotor stimulation in mice with inhibited extracerebral decarboxylase.
Psychopharmacologia. 1972;23(3):279-88. doi: 10.1007/BF00404133.
5
The effect of amitriptyline, desipramine and imipramine on the vivo brain synthesis of 3H-noradrenaline from 3H-L-dopa in the rat.阿米替林、去甲丙咪嗪和丙咪嗪对大鼠体内由3H-L-多巴合成3H-去甲肾上腺素的影响。
Psychopharmacologia. 1975;41(3):249-54. doi: 10.1007/BF00428932.
6
Effects of thymoleptics on behaviour associated with changes in brain dopamine. I. Potentiation of dopa-induced gnawing of mice.抗抑郁药对与脑多巴胺变化相关行为的影响。I. 增强多巴诱导的小鼠啃咬行为。
Psychopharmacologia. 1976 Feb 2;45(3):261-5. doi: 10.1007/BF00421137.