去甲肾上腺素与钠离子在神经元摄取过程中相互作用的动力学分析：共转运的动力学证据。 - Suppr

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超能文献

Kinetic analysis of the interaction between noradrenaline and Na+ in neuronal uptake: kinetic evidence for CO-transport.

作者信息

Sammet S, Graefe K H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):99-107. doi: 10.1007/BF00501216.

DOI:10.1007/BF00501216

PMID:522908

Abstract

摘要

相似文献

Kinetic analysis of the interaction between noradrenaline and Na+ in neuronal uptake: kinetic evidence for CO-transport.去甲肾上腺素与钠离子在神经元摄取过程中相互作用的动力学分析：共转运的动力学证据。

Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):99-107. doi: 10.1007/BF00501216.

Nature of neuronal uptake and noradrenaline--adrenaline effects in the isolated rat vas deferens.离体大鼠输精管中去甲肾上腺素和肾上腺素作用的神经元摄取性质

Eur J Pharmacol. 1975 Apr;31(2):363-6. doi: 10.1016/0014-2999(75)90061-8.

The inhibitory effect of some monovalent cations on the stimulation by Na+ of the neuronal uptake of noradrenaline.某些单价阳离子对钠离子刺激去甲肾上腺素神经元摄取的抑制作用。

Naunyn Schmiedebergs Arch Pharmacol. 1979 Nov;309(2):89-97. doi: 10.1007/BF00501215.

Sodium-dependence of the potency of inhibitors of the neuronal noradrenaline carrier in the rat vas deferens.大鼠输精管中神经元去甲肾上腺素载体抑制剂效力的钠依赖性。

Naunyn Schmiedebergs Arch Pharmacol. 1986 Dec;334(4):397-402. doi: 10.1007/BF00569377.

Effects of phenoxybenzamine on the uptake and metabolism of noradrenaline in the rat heart and vas deferens.酚苄明对大鼠心脏和输精管中去甲肾上腺素摄取及代谢的影响。

Br J Pharmacol. 1969 Nov;37(3):627-37. doi: 10.1111/j.1476-5381.1969.tb08501.x.

Failure of K+ to affect the potency of inhibitors of the neuronal noradrenaline carrier in the rat vas deferens.钾离子未能影响大鼠输精管中神经元去甲肾上腺素载体抑制剂的效力。

Naunyn Schmiedebergs Arch Pharmacol. 1987 Mar;335(3):250-4. doi: 10.1007/BF00172792.

Naunyn Schmiedebergs Arch Pharmacol. 1990 Apr;341(4):295-300. doi: 10.1007/BF00180654.

Stereoselectivity in the metabolism of 3H-noradrenaline during uptake into and efflux from the isolated rat vas deferens.3H-去甲肾上腺素在离体大鼠输精管摄取和流出过程中代谢的立体选择性。

Naunyn Schmiedebergs Arch Pharmacol. 1977 Oct;299(3):225-38. doi: 10.1007/BF00500315.

Evaluation of mechanisms controlling the release and inactivation of the adrenergic transmitter in the rabbit portal vein and vas deferens.家兔门静脉和输精管中肾上腺素能递质释放及失活调控机制的评估

Br J Pharmacol. 1972 Mar;44(3):472-91. doi: 10.1111/j.1476-5381.1972.tb07285.x.

Chloride-dependence of the potency of inhibitors of the neuronal noradrenaline carrier in the rat vas deferens.大鼠输精管中神经元去甲肾上腺素载体抑制剂效力的氯离子依赖性

Naunyn Schmiedebergs Arch Pharmacol. 1989 Jan-Feb;339(1-2):65-70. doi: 10.1007/BF00165128.

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Naunyn Schmiedebergs Arch Pharmacol. 1996 Jun;354(1):7-16. doi: 10.1007/BF00168700.

Evidence for uptake1-mediated efflux of catecholamines from pulmonary endothelial cells of perfused lungs of rats.摄取1介导的儿茶酚胺从大鼠灌注肺的肺内皮细胞中流出的证据。

Naunyn Schmiedebergs Arch Pharmacol. 1996 Apr;353(5):528-35. doi: 10.1007/BF00169172.

Effect of low concentrations of K+ and Cl- on the Na(+)-dependent neuronal uptake of [3H] dopamine.低浓度钾离子和氯离子对钠离子依赖的神经元摄取[3H]多巴胺的影响。

Naunyn Schmiedebergs Arch Pharmacol. 1996 May;353(6):610-5. doi: 10.1007/BF00167179.

Norepinephrine transporters have channel modes of conduction.去甲肾上腺素转运体具有通道传导模式。

Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8671-6. doi: 10.1073/pnas.93.16.8671.

High-affinity uptake of noradrenaline in postsynaptic neurones.去甲肾上腺素在突触后神经元中的高亲和力摄取。

Br J Pharmacol. 1993 Jun;109(2):299-307. doi: 10.1111/j.1476-5381.1993.tb13570.x.

Glial alpha 2-receptors probably inhibit the high-affinity uptake of noradrenaline into astrocytes in the rat brain in vivo.神经胶质α2受体可能在体内抑制去甲肾上腺素向大鼠脑内星形胶质细胞的高亲和力摄取。

Neurochem Res. 1995 Mar;20(3):291-7. doi: 10.1007/BF00969545.

Contrasting effects of the imidazol(in)e alpha 2-adrenoceptor agonists, medetomidine, clonidine and UK 14,304 on extraneuronal levels of noradrenaline in the rat frontal cortex: evaluation using in vivo microdialysis and synaptosomal uptake studies.咪唑啉α2 -肾上腺素能受体激动剂美托咪定、可乐定和UK 14,304对大鼠额叶皮质去甲肾上腺素细胞外水平的不同影响：采用体内微透析和突触体摄取研究进行评估

Br J Pharmacol. 1995 Apr;114(8):1717-23. doi: 10.1111/j.1476-5381.1995.tb14962.x.

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.

本文引用的文献

A Note on the Kinetics of Enzyme Action.关于酶作用动力学的注释

Biochem J. 1925;19(2):338-9. doi: 10.1042/bj0190338.

[ON THE EVALUATION OF TEST RESULTS: THE TEST, WHETHER CURVES ARE DIFFERENT IN COURSE].关于测试结果的评估：测试，曲线在过程中是否不同。

Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1965 Mar 9;250:383-96. doi: 10.1007/BF00258530.

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.

The kinetics of enzyme-catalyzed reactions with two or more substrates or products. I. Nomenclature and rate equations.具有两种或更多种底物或产物的酶催化反应动力学。I. 命名法和速率方程。

Biochim Biophys Acta. 1963 Jan 8;67:104-37. doi: 10.1016/0006-3002(63)91800-6.

Statistical estimations in enzyme kinetics.酶动力学中的统计估计

Biochem J. 1961 Aug;80(2):324-32. doi: 10.1042/bj0800324.

Graphical determination of the dissociation constants for two-substrate enzyme systems.双底物酶系统解离常数的图形测定法。

Biochim Biophys Acta. 1957 Sep;25(3):575-8. doi: 10.1016/0006-3002(57)90529-2.

Cation dependence of sympathetic transmitter retention by slices of rat ventricle.大鼠心室切片对交感神经递质保留的阳离子依赖性

Br J Pharmacol Chemother. 1967 Mar;29(3):309-18. doi: 10.1111/j.1476-5381.1967.tb01962.x.

A comparison of certain properties of catechol-O-methyl transferase to those of adrenergic beta receptors.儿茶酚-O-甲基转移酶某些特性与肾上腺素能β受体特性的比较。

J Pharmacol Exp Ther. 1967 May;156(2):201-6.

Discrimination of single transport systems. The Na plus-sensitive transport of neutral amino acids in the Ehrlich cell.单一转运系统的鉴别。艾氏腹水癌细胞中对钠离子敏感的中性氨基酸转运

J Gen Physiol. 1966 Sep;50(1):203-24. doi: 10.1085/jgp.50.1.203.

Role of sodium and potassium ions in storage of norepinephrine by sympathetic nerve endings.钠和钾离子在交感神经末梢储存去甲肾上腺素中的作用。

Life Sci. 1966 Sep;5(17):1563-9. doi: 10.1016/0024-3205(66)91025-3.

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