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灌注大鼠心脏中3H-(-)-去甲肾上腺素的神经元和非神经元摄取及代谢

The neuronal and extraneuronal uptake and metabolism of 3H-(-)-noradrenaline in the perfused rat heart.

作者信息

Fiebig E R, Trendelenburg U

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 May;303(1):21-35. doi: 10.1007/BF00496182.

Abstract
  1. Hearts were obtained from reserpine-pretreated rats and perfused with 0.95 micron 3H(-)-noradrenaline. The rate of removal of 3H-noradrenaline from the perfusion fluid was measured (from the arterio-venous difference) as well as the rate at which the 3H-metabolites appeared in the venous effluent. 2. When either 30micron corticosterone was added under steady-state conditions during perfusion with 3H-noradrenaline (to inhibit neuronal and extraneuronal uptake, respectively), each inhibitor reduced the removal of noradrenaline by about 50%; in the presence of both inhibitors removal was abolished. 3. Dihydroxymandelic acid (DOMA) was of neuronal, normetanephrine (NMN) of extraneuronal origin; dihydroxyphenylglycol (DOPEG) and the OMDA fraction (containing methoxyhydroxyphenylglycol-MOPEG-and methoxyhydroxymandelic acid-VMA) were formed both neuronally and extra-neuronally. 4. The extraneuronal metabolism of 3H-noradrenaline was in quick equilibrium with the 3H-noradrenaline in the perfusion fluid; most of the total formation of DOPEG, MOPEG and NMN was recovered from the venous effluent. 5. Extraneuronally formed DOPEG, MOPEG and NMN distributed in the tissue with half times corresponding to their half time for efflux. 6. Inhibition of monoamine oxidase (MAO) by pargyline increased the extraneuronal formation of NMN; MAO and catechol-O-methyl transferase (COMT) appear to be contained in the same extraneuronal compartment. 7. The extraneuronal accumulation of 3H-noradrenaline required 30 min or more to reach a steady state; inhibition of one or both enzymes slowed this process. Inhibition of MAO increased the extra-neuronal accumulation of 3H-noradrenaline; inhibition of COMT failed to do so, since the enzyme inhibitor (U-0521) was a weak inhibitor of extra-neuronal uptake. 8. The rate constants for the efflux of the metabolites of noradrenaline decreased in the order of MOPEG greater than DOPEG greater than NMN greater than DOMA greater than VMA.
摘要
  1. 从经利血平预处理的大鼠获取心脏,并用0.95微米的3H(-)-去甲肾上腺素进行灌注。测定了灌注液中3H-去甲肾上腺素的清除率(根据动静脉差异)以及3H-代谢产物在静脉流出液中出现的速率。2. 当在3H-去甲肾上腺素灌注的稳态条件下加入30微米的皮质酮(分别抑制神经元和非神经元摄取)时,每种抑制剂使去甲肾上腺素的清除率降低约50%;在两种抑制剂同时存在时,清除被消除。3. 二羟扁桃酸(DOMA)源于神经元,去甲变肾上腺素(NMN)源于非神经元;二羟苯乙二醇(DOPEG)和OMDA部分(包含甲氧基羟苯乙二醇-MOPEG-和甲氧基羟扁桃酸-VMA)在神经元和非神经元中均有形成。4. 3H-去甲肾上腺素的非神经元代谢与灌注液中的3H-去甲肾上腺素处于快速平衡状态;DOPEG、MOPEG和NMN的总生成量大部分从静脉流出液中回收。5. 非神经元形成的DOPEG、MOPEG和NMN在组织中的分布半衰期与其流出半衰期相对应。6. 优降宁抑制单胺氧化酶(MAO)增加了NMN的非神经元生成;MAO和儿茶酚-O-甲基转移酶(COMT)似乎存在于同一非神经元区室中。7. 3H-去甲肾上腺素的非神经元蓄积需要30分钟或更长时间才能达到稳态;抑制一种或两种酶会减缓这一过程。抑制MAO增加了3H-去甲肾上腺素的非神经元蓄积;抑制COMT则未达到此效果,因为酶抑制剂(U-0521)是一种较弱的非神经元摄取抑制剂。8. 去甲肾上腺素代谢产物流出的速率常数按MOPEG>DOPEG>NMN>DOMA>VMA的顺序降低。

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