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犬隐静脉神经外Q-甲基化系统的动力学特性及其抑制所引起的对儿茶酚胺的超敏反应。

The kinetic characteristics of the extraneuronal Q-methylating system of the dog saphenous vein and the supersensitivity to catecholamines caused by its inhibition.

作者信息

Paiva M Q, Guimarães S

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Aug;327(1):48-55. doi: 10.1007/BF00504991.

DOI:10.1007/BF00504991
PMID:6493350
Abstract

The "half-saturating outside concentration" and the Vmax of the extraneuronal O-methylating system of the dog saphenous vein were determined in vitro for 3 catecholamines: isoprenaline, adrenaline and noradrenaline. Strips pretreated with 1 mmol/l pargyline were exposed to 30 mumol/l cocaine for 30 min before and during the 30 min incubation with the amines. Two methods were used to reach our aims: a) the classical one in which the 3H-O-methylated metabolites formed from a mixture of unlabelled and labelled amine were determined by using final concentrations of the substrate ranging from 0.2 and 12.8 mumol/l and b) an indirect one in which 0.2 mumol/l 3H-(+/-)-isoprenaline was used to assess the extraneuronal O-methylation of the tracer amine, and then those concentrations of unlabelled amines were determined which reduce the O-methylation of 3H-(+/-)-isoprenaline by 50% (IC50). The "half-saturating outside concentrations" and the Vmax obtained by the first method were: 1.3, 2.5 and 3.4 mumol/l and 241, 317 and 294 pmol/g/min for 3H-(+/-)-isoprenaline, 3H-(+/-)-adrenaline and 3H-(-)-noradrenaline, respectively. The IC50s obtained by the second method used were: 1.1, 0.6, 0.7 and 1.4 mumol/l for (+/-)-isoprenaline, (-)-isoprenaline, (-)-adrenaline and (-)-noradrenaline, respectively. It was observed that the contraction of the strips caused by adrenaline and noradrenaline distorted IC50 values. In the presence of 1 mumol/l phentolamine the IC50 for adrenaline and noradrenaline was about 2.5 times higher than in its absence.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在体外测定了狗隐静脉神经外O -甲基化系统对3种儿茶酚胺(异丙肾上腺素、肾上腺素和去甲肾上腺素)的“半饱和外界浓度”和Vmax。用1 mmol/l优降宁预处理的血管条在与胺类孵育的30分钟之前及期间,先暴露于30 μmol/l可卡因30分钟。采用两种方法来达成我们的目标:a)经典方法,即通过使用终浓度范围为0.2至12.8 μmol/l的底物,测定由未标记和标记胺的混合物形成的3H - O -甲基化代谢物;b)间接方法,即使用0.2 μmol/l 3H-(±)-异丙肾上腺素来评估示踪胺的神经外O -甲基化,然后确定那些使3H-(±)-异丙肾上腺素的O -甲基化降低50%(IC50)的未标记胺的浓度。通过第一种方法获得的“半饱和外界浓度”和Vmax分别为:对于3H-(±)-异丙肾上腺素、3H-(±)-肾上腺素和3H - (-)-去甲肾上腺素,分别为1.3、2.5和3.4 μmol/l以及241、317和294 pmol/g/分钟。通过第二种方法获得的IC50分别为:对于(±)-异丙肾上腺素、(-)-异丙肾上腺素、(-)-肾上腺素和(-)-去甲肾上腺素,分别为1.1、0.6、0.7和1.4 μmol/l。观察到肾上腺素和去甲肾上腺素引起的血管条收缩会扭曲IC50值。在存在1 μmol/l酚妥拉明的情况下,肾上腺素和去甲肾上腺素的IC50比不存在时高约2.5倍。(摘要截短至250字)

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引用本文的文献

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本文引用的文献

1
The uptake of catechol amines at high perfusion concentrations in the rat isolated heart: A novel catechol amine uptake process.大鼠离体心脏在高灌注浓度下对儿茶酚胺的摄取:一种新的儿茶酚胺摄取过程。
Br J Pharmacol Chemother. 1965 Aug;25(1):18-33. doi: 10.1111/j.1476-5381.1965.tb01753.x.
2
THE FATE OF 3H-ISO-PROTERENOL IN THE RAT.大鼠体内3H-异丙肾上腺素的代谢情况
Biochem Pharmacol. 1964 Aug;13:1119-28. doi: 10.1016/0006-2952(64)90112-1.
3
Statistical estimations in enzyme kinetics.酶动力学中的统计估计
Naunyn Schmiedebergs Arch Pharmacol. 1986 Aug;333(4):368-76. doi: 10.1007/BF00500011.
4
The uptake and O-methylation of 3H-(+/-)-isoprenaline in rat cerebral cortex slices.
Naunyn Schmiedebergs Arch Pharmacol. 1988 Apr;337(4):397-405. doi: 10.1007/BF00169530.
5
The saturability of a site of loss and the degree of supersensitivity to agonists which are substrates of this site of loss.一个损失位点的饱和性以及对作为该损失位点底物的激动剂的超敏程度。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Mar;329(1):30-5. doi: 10.1007/BF00695188.
Biochem J. 1961 Aug;80(2):324-32. doi: 10.1042/bj0800324.
4
Uptake and O-methylation of isoprenaline in the rabbit ear artery.异丙肾上腺素在兔耳动脉中的摄取与O-甲基化作用。
Blood Vessels. 1980;17(5):229-45. doi: 10.1159/000158253.
5
A mathematical model representing the extraneuronal O-methylating system of the perfused rat heart.一种代表灌注大鼠心脏细胞外O-甲基化系统的数学模型。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Feb;311(1):17-32. doi: 10.1007/BF00500298.
6
The extraneuronal O-methylation of 3H-(+)isoprenaline by guinea-pig tracheal rings in vitro.豚鼠气管环对3H-(+)异丙肾上腺素的体外非神经元性O-甲基化作用。
Naunyn Schmiedebergs Arch Pharmacol. 1981 Dec;318(2):88-93. doi: 10.1007/BF00508831.
7
A kinetic analysis of the extraneuronal uptake and metabolism of catecholamines.儿茶酚胺的神经外摄取与代谢的动力学分析。
Rev Physiol Biochem Pharmacol. 1980;87:33-115. doi: 10.1007/BFb0030896.
8
The isotope effect of tritium in 3H-noradrenaline.3H-去甲肾上腺素中氚的同位素效应。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Jun;323(2):128-40. doi: 10.1007/BF00634260.
9
Kinetic constants for uptake and metabolism of 3H-(-)noradrenaline in rabbit aorta. Possible falsification of the constants by diffusion barriers within the vessel wall.兔主动脉中3H-(-)去甲肾上腺素摄取和代谢的动力学常数。血管壁内扩散屏障可能对这些常数造成的误判。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Jun;323(1):12-23. doi: 10.1007/BF00498822.
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A comparative study of the properties of the catechol-O-methyltransferase inhibitors, U-0521 and tropolone acetamide, in rat perfused heart.大鼠离体灌流心脏中儿茶酚-O-甲基转移酶抑制剂U-0521与托酚酮乙酰胺性质的比较研究
Naunyn Schmiedebergs Arch Pharmacol. 1983 Feb;322(1):6-19. doi: 10.1007/BF00649346.