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利血平处理后酪氨酸对大鼠心房变时作用的恢复。

Restoration of the chronotropic effect of tyramine on rat atria after reserpine.

作者信息

Murnaghan M F

出版信息

Br J Pharmacol. 1968 Sep;34(1):88-98. doi: 10.1111/j.1476-5381.1968.tb07953.x.

Abstract
  1. The restoration by various sympathomimetic amines of the chronotropic response to tyramine was studied on the isolated atria of rats pretreated with reserpine. The atria were exposed to the "restorative" sympathomimetic amine for 10 min, washed over a period of 1 hr and then tested with 10 muM tyramine. The effect of noradrenaline, dopamine and norphenylephrine before and after inhibition of monoamine oxidase by 0.5 mM iproniazid were compared with their alpha-methyl and N-alkyl analogues in their ability to restore the chronotropic response to tyramine.2. Noradrenaline and adrenaline restored the chronotropic response to tyramine, the degree of restoration depending on the concentration of the restorative amine used. Noradrenaline after iproniazid and alpha-methylnoradrenaline were equipotent and were about 1,000 times more active than noradrenaline where monoamine oxidase was not inhibited. Dopamine, epinine, norphenylephrine, phenylephrine, octopamine, synephrine and isoprenaline in the absence of monoamine oxidase inhibition had no effect. Dopamine after iproniazid and alpha-methyldopamine were equipotent and were about 1/10 as active as alpha-methylnoradrenaline. Norphenylephrine after iproniazid and metaraminol were equipotent and were about 1/500 as active as alpha-methylnoradrenaline. Octopamine after iproniazid was even less active. The N-methylated analogues were about 1/10 as active as their nor-compounds but the N-isopropyl analogue, isoprenaline, was devoid of activity.3. Dopamine after iproniazid and alpha-methyldopamine were inactive if a dopamine-beta-hydroxylase inhibitor, disulphiram or sodium diethyldithiocarbamate, was present.4. It is concluded that, in atria of reserpinized rats, (a) protection from monoamine oxidase increases; (b) N-substitution decreases; and (c) hydroxyl groups at the beta-carbon and ring positions 3 and 4 increase the capabilities of a sympathomimetic amine to restore the chronotropic response to tyramine.
摘要
  1. 研究了多种拟交感胺对利血平预处理大鼠离体心房对酪胺变时反应的恢复作用。将心房暴露于“恢复性”拟交感胺10分钟,冲洗1小时,然后用10μM酪胺进行测试。比较了去甲肾上腺素、多巴胺和去氧肾上腺素在被0.5mM异烟肼抑制单胺氧化酶前后,与其α-甲基和N-烷基类似物恢复对酪胺变时反应的能力。

  2. 去甲肾上腺素和肾上腺素恢复了对酪胺的变时反应,恢复程度取决于所用恢复性胺的浓度。异烟肼处理后的去甲肾上腺素和α-甲基去甲肾上腺素等效,且比未抑制单胺氧化酶时的去甲肾上腺素活性高约1000倍。在未抑制单胺氧化酶时,多巴胺、去甲变肾上腺素、去氧肾上腺素、苯肾上腺素、章鱼胺、辛弗林和异丙肾上腺素无作用。异烟肼处理后的多巴胺和α-甲基多巴胺等效,活性约为α-甲基去甲肾上腺素的1/10。异烟肼处理后的去氧肾上腺素和间羟胺等效,活性约为α-甲基去甲肾上腺素的1/500。异烟肼处理后的章鱼胺活性更低。N-甲基化类似物的活性约为其去甲化合物的1/10,但N-异丙基类似物异丙肾上腺素无活性。

  3. 如果存在多巴胺-β-羟化酶抑制剂双硫仑或二乙基二硫代氨基甲酸钠,异烟肼处理后的多巴胺和α-甲基多巴胺无活性。

  4. 得出结论,在利血平化大鼠的心房中,(a) 对单胺氧化酶的保护作用增强;(b) N-取代作用减弱;(c) β-碳以及3和4位环上的羟基增强了拟交感胺恢复对酪胺变时反应的能力。

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本文引用的文献

1
The oxidation of adrenaline and other amines.肾上腺素及其他胺类的氧化。
Biochem J. 1937 Dec;31(12):2187-96. doi: 10.1042/bj0312187.
6
8
BETA-HYDROXYLATION OF TYRAMINE IN VIVO.体内酪胺的β-羟基化作用
Acta Pharmacol Toxicol (Copenh). 1963;20:371-4. doi: 10.1111/j.1600-0773.1964.tb01759.x.
9
THE UPTAKE OF NORADRENALINE BY THE ISOLATED PERFUSED RAT HEART.去甲肾上腺素在离体灌注大鼠心脏中的摄取
Br J Pharmacol Chemother. 1963 Dec;21(3):523-37. doi: 10.1111/j.1476-5381.1963.tb02020.x.

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