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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。

Kinetic constants for uptake and metabolism of 3H-(-)noradrenaline in rabbit aorta. Possible falsification of the constants by diffusion barriers within the vessel wall.

作者信息

Henseling M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1983 Jun;323(1):12-23. doi: 10.1007/BF00498822.

DOI:10.1007/BF00498822
PMID:6877391
Abstract
  1. The neuronal uptake of 3H-(-)noradrenaline into aortic rings from reserpine-pretreated animals was a saturable process with a Km of 2.3 mumol X l-1 and a Vmax of 0.5 nmol X g-1 X min-1. Similar constants were obtained when the neuronal deamination of noradrenaline was taken as an index for neuronal uptake. When the tissue was incubated in the usual way, i.e., when the amine was allowed to enter the aortic rings via both the intimal and the adventitial surface, then there was no initial delay (tlag) for the neuronal uptake of noradrenaline (MAO and COMT inhibited). On the other hand, when the amine entry was restricted to the intimal surface, there was a tlag of 2 min, probably due to the slow equilibration of the extracellular space of the media with the incubation medium. Furthermore, for low amine concentrations the rate of uptake in the latter situation was about 10 times lower than that in the former one. Thus, the rate of uptake clearly depended on the way the amine entered the tissue. 2. The corticosterone-sensitive extraneural uptake of 3H-(-)noradrenaline determined in nerve-free aortic rings was characterised by a high Km (490 mumol X l-1) and Vmax (35 nmol X g-1 X min-1). For uptake2 a tlag of 1 min was observed. 3. The analysis of the extraneuronal O-methylating system in nerve-free aortic rings yielded a Km of 3.6 mumol X l-1 and a Vmax of 0.6 nmol X g-1 X min-1. The tlag for the O-methylation of noradrenaline was in the same order of magnitude as that for uptake2. At low amine concentrations the corticosterone-sensitive accumulation of noradrenaline was prevented by COMT, but not by MAO. The latter enzyme reduced the steady-state accumulation of noradrenaline by about 50%. When the amine entry was restricted to one surface only, the results indicated that the extraneuronal O-methylation of noradrenaline generated a steep concentration gradient of the parent amine within the extracellular space of the aorta. 4. All saturable processes fitted the Michaelis-Menten equation. However, kinetic constants determined in incubated organs may be falsified by poor diffusion of the substrate through the extracellular space.
摘要
  1. 用利血平预处理动物的主动脉环对3H-(-)去甲肾上腺素的神经元摄取是一个可饱和过程,其米氏常数(Km)为2.3 μmol·L-1,最大反应速度(Vmax)为0.5 nmol·g-1·min-1。以去甲肾上腺素的神经元脱氨作用为神经元摄取指标时,得到了相似的常数。当以常规方式孵育组织时,即当胺类物质通过内膜和外膜表面进入主动脉环时,去甲肾上腺素的神经元摄取没有初始延迟(tlag)(单胺氧化酶和儿茶酚-O-甲基转移酶被抑制)。另一方面,当胺类物质的进入仅限于内膜表面时,存在2分钟的tlag,这可能是由于培养基的细胞外空间与孵育培养基的平衡缓慢所致。此外,对于低胺浓度,后一种情况下的摄取速率比前一种情况低约10倍。因此,摄取速率明显取决于胺类物质进入组织的方式。2. 在无神经的主动脉环中测定的3H-(-)去甲肾上腺素的皮质酮敏感的非神经摄取,其特征为高Km(490 μmol·L-1)和Vmax(35 nmol·g-1·min-1)。对于摄取2,观察到1分钟的tlag。3. 对无神经的主动脉环中的非神经元O-甲基化系统的分析得出Km为3.6 μmol·L-1,Vmax为0.6 nmol·g-1·min-1。去甲肾上腺素O-甲基化的tlag与摄取2的tlag处于同一数量级。在低胺浓度下,儿茶酚-O-甲基转移酶可阻止皮质酮敏感的去甲肾上腺素积累,但单胺氧化酶不能。后一种酶使去甲肾上腺素的稳态积累降低约50%。当胺类物质的进入仅限于一个表面时,结果表明去甲肾上腺素的非神经元O-甲基化在主动脉的细胞外空间内产生了母体胺类物质的陡峭浓度梯度。4. 所有可饱和过程均符合米氏方程。然而,在孵育器官中测定的动力学常数可能会因底物在细胞外空间的扩散不良而被伪造。

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1
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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引用本文的文献

1
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.
2
Cyanine-related compounds: a novel class of potent inhibitors of extraneuronal noradrenaline transport.花青相关化合物:一类新型强效的非神经元去甲肾上腺素转运抑制剂。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Nov;348(5):458-65. doi: 10.1007/BF00173203.
3
Accumulation of 3H-(-)noradrenaline in the rabbit aorta not related to uptake1 and uptake2, but sensitive to 3,4-dihydroxy-2-methylpropiophenone (U-0521) and oxytetracycline.

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 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.
3
Electron microscopy of the normal rabbit aorta.正常兔主动脉的电子显微镜检查。
3H-(-)去甲肾上腺素在兔主动脉中的蓄积与摄取1和摄取2无关,但对3,4-二羟基-2-甲基苯丙酮(U-0521)和土霉素敏感。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Jun;323(2):121-7. doi: 10.1007/BF00634259.
4
The role of neuronal and extraneuronal uptake in the inactivation of 3H-(--)noradrenaline in the rabbit aorta determined by a method relating with amine diffusion in the tissue.通过一种与胺在组织中扩散相关的方法所确定的,神经元和非神经元摄取在兔主动脉中3H-(-)去甲肾上腺素失活过程中的作用。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Nov;324(3):163-8. doi: 10.1007/BF00503889.
5
The influence of uptake2 on the inhibition by unlabelled noradrenaline of the stimulation-evoked overflow of 3H-noradrenaline in rabbit aorta with regard to surface of amine entry.就胺进入的表面而言,摄取2对未标记去甲肾上腺素抑制兔主动脉中刺激诱发的3H-去甲肾上腺素溢出的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1983 Sep;324(2):99-107. doi: 10.1007/BF00497014.
6
Stereoselectivity of extraneuronal uptake of catecholamines in rabbit aorta.兔主动脉中儿茶酚胺的非神经元摄取的立体选择性
Naunyn Schmiedebergs Arch Pharmacol. 1984 Dec;328(2):219-20. doi: 10.1007/BF00512077.
7
Kinetics of the O-methylating system for isoprenaline in the trachea and aorta of rabbit.兔气管和主动脉中异丙肾上腺素O-甲基化系统的动力学
Naunyn Schmiedebergs Arch Pharmacol. 1984 Nov;328(1):56-61. doi: 10.1007/BF00496107.
8
The influence of inhibition of catechol-O-methyl transferase or of monoamine oxidase on the extraneuronal metabolism of 3H-(-)-noradrenaline in the rat heart.儿茶酚-O-甲基转移酶抑制或单胺氧化酶抑制对大鼠心脏中3H-(-)-去甲肾上腺素细胞外代谢的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Oct;327(4):285-92. doi: 10.1007/BF00506238.
9
The contribution of diffusion to the entry of catecholamines into guinea-pig trachealis smooth muscle cells.扩散对儿茶酚胺进入豚鼠气管平滑肌细胞的作用。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Sep;327(2):133-8. doi: 10.1007/BF00500907.
10
The kinetic characteristics of the extraneuronal Q-methylating system of the dog saphenous vein and the supersensitivity to catecholamines caused by its inhibition.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。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Aug;327(1):48-55. doi: 10.1007/BF00504991.
Acta Pathol Microbiol Scand. 1963;57:154-68. doi: 10.1111/j.1699-0463.1963.tb03440.x.
4
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.
5
The fate of isoprenaline after inhibition of O-methylation and of extraneuronal uptake.在抑制O-甲基化和非神经元摄取后异丙肾上腺素的命运。
Eur J Pharmacol. 1980 Oct 17;67(2-3):247-53. doi: 10.1016/0014-2999(80)90505-1.
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Comparison of 3H-norepinephrine and 3H-metaraminol accumulation as indices of adrenergic nerve density in rabbit blood vessels.比较3H-去甲肾上腺素和3H-间羟胺蓄积作为兔血管肾上腺素能神经密度指标的情况。
Eur J Pharmacol. 1980 Oct 31;67(4):355-61. doi: 10.1016/0014-2999(80)90176-4.
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Functional activity of the noradrenergic innervation of large cerebral arteries.大脑大动脉去甲肾上腺素能神经支配的功能活动。
Br J Pharmacol. 1980 Jun;69(2):193-9. doi: 10.1111/j.1476-5381.1980.tb07890.x.
8
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.
9
Affinities of catecholamines for extraneuronal uptake in smooth muscle cells in trachealis muscle of guinea-pig.儿茶酚胺对豚鼠气管平滑肌细胞非神经元摄取的亲和力。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Mar;311(2):139-46. doi: 10.1007/BF00510252.
10
False labelling of commercially available 3H-catecholamines?市售3H-儿茶酚胺存在错误标签的情况?
Naunyn Schmiedebergs Arch Pharmacol. 1980 Mar;311(2):109-12. doi: 10.1007/BF00510248.