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2
Uptake kinetics and metabolism of 7-3H-dopamine in the isolated perfused rat heart.7-³H-多巴胺在离体灌注大鼠心脏中的摄取动力学与代谢
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3
Effect of 6-hydroxydopamine on [3H]-adenine nucleotide and [3H]-noradrenaline release from the guinea-pig taenia caecum evoked by electrical field stimulation, nicotine and perivascular nerve stimulation.6-羟基多巴胺对电场刺激、尼古丁及血管周围神经刺激诱发的豚鼠盲肠带[³H]-腺嘌呤核苷酸和[³H]-去甲肾上腺素释放的影响。
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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.
2
ACTION OF 2, 4, 5-TRIHYDROXYPHENYLETHYLAMINE ON THE STORAGE AND RELEASE OF NORADRENALINE.2,4,5-三羟基苯乙胺对去甲肾上腺素储存与释放的作用
Br J Pharmacol Chemother. 1965 Apr;24(2):549-60. doi: 10.1111/j.1476-5381.1965.tb01745.x.
3
SYNTHESIS, BINDING, RELEASE, AND METABOLISM OF NOREPINEPHRINE IN NORMAL AND TRANSPLANTED DOG HEARTS.去甲肾上腺素在正常及移植犬心脏中的合成、结合、释放及代谢
Circ Res. 1965 May;16:468-81. doi: 10.1161/01.res.16.5.468.
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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.
5
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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PROPERTIES OF NOREPINEPHRINE STORAGE PARTICLES OF THE RAT HEART.大鼠心脏去甲肾上腺素储存颗粒的特性
J Pharmacol Exp Ther. 1963 Dec;142:299-305.
7
Effect of 6-hydroxydopamine and some other compounds on the concentration of norepinephrine in the hearts of mice.6-羟基多巴胺及其他一些化合物对小鼠心脏中去甲肾上腺素浓度的影响。
J Pharmacol Exp Ther. 1963 Jun;140:308-16.
8
The physiological disposition of H3-epinephrine and its metabolite metanephrine.H3-肾上腺素及其代谢产物间甲肾上腺素的生理处置
J Pharmacol Exp Ther. 1959 Dec;127:251-6.
9
The fate of H3-norepinephrine in animals.动物体内H3-去甲肾上腺素的命运
J Pharmacol Exp Ther. 1961 May;132:193-201.
10
The metabolic fate of H3-epinephrine and C14-metanephrine in the rat.大鼠体内H3-肾上腺素和C14-间甲肾上腺素的代谢归宿
J Biol Chem. 1961 Jul;236:2109-13.

6-羟基多巴胺预处理对离体灌注大鼠心脏儿茶酚胺摄取和代谢的影响。

Effect of pretreatment with 6-hydroxydopamine on the uptake and metabolism of catecholamines by the isolated perfused rat heart.

作者信息

Hellmann G, Hertting G, Peskar B

出版信息

Br J Pharmacol. 1971 Feb;41(2):270-7. doi: 10.1111/j.1476-5381.1971.tb08027.x.

DOI:10.1111/j.1476-5381.1971.tb08027.x
PMID:5572277
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1703281/
Abstract
  1. Isolated rat hearts from control and 6-hydroxydopamine pretreated animals were perfused with (3)H-noradrenaline or (3)H-dopamine, either at a low perfusion concentration (1.50 x 10(-10) mol/ml (3)H-dopamine; 1.18 x 10(-10) mol/ml (3)H-noradrenaline) or a high perfusion concentration (296.69 x 10(-10) mol/ml (3)H-noradrenaline, 327.45 x 10(-10) mol/ml (3)H-dopamine) for 8 minutes.2. At the low perfusion concentration, the total activity, the radioactivity in the alumina eluates (sum of (3)H-dopamine, (3)H-noradrenaline and deaminated catechol metabolites) and the concentration of (3)H-dopamine. (3)H-noradrenaline and the deaminated catechol metabolites were decreased in the hearts of the pretreated rats as compared with the controls. The O-methylated amine metabolites were increased. The deaminated O-methylated metabolites were increased in the experiments with (3)H-noradrenaline and decreased in the (3)H-dopamine experiments.3. Uptake of (3)H-dopamine and (3)H-noradrenaline by the hearts of 6-hydroxydopamine pretreated rats was decreased to a much smaller extent when perfused with the high concentration than with the low concentration.4. At the high perfusion concentration there was a significant difference between control and pretreated animals with regard to the total radioactivity and the radioactivity in the alumina eluates only. The absolute and relative amounts of metabolites were not significantly changed by pretreatment with the exception of the deaminated catechol metabolites in the (3)H-dopamine experiments.5. It is concluded that neuronal Uptake 1 is greatly impaired in the hearts from rats pretreated with 6-hydroxydopamine, but extraneuronal Uptake 2 remains intact.
摘要
  1. 从对照组和经6-羟基多巴胺预处理的动物中分离出大鼠心脏,用(3)H-去甲肾上腺素或(3)H-多巴胺进行灌注,灌注浓度分为低浓度(1.50×10⁻¹⁰mol/ml(3)H-多巴胺;1.18×10⁻¹⁰mol/ml(3)H-去甲肾上腺素)或高浓度(296.69×10⁻¹⁰mol/ml(3)H-去甲肾上腺素,327.45×10⁻¹⁰mol/ml(3)H-多巴胺),持续8分钟。

  2. 在低灌注浓度下,与对照组相比,预处理大鼠心脏中的总活性、氧化铝洗脱液中的放射性((3)H-多巴胺、(3)H-去甲肾上腺素和脱氨基儿茶酚代谢物的总和)以及(3)H-多巴胺、(3)H-去甲肾上腺素和脱氨基儿茶酚代谢物的浓度均降低。O-甲基化胺代谢物增加。在(3)H-去甲肾上腺素实验中,脱氨基O-甲基化代谢物增加,而在(3)H-多巴胺实验中则减少。

  3. 当用高浓度灌注时,6-羟基多巴胺预处理大鼠心脏对(3)H-多巴胺和(3)H-去甲肾上腺素的摄取减少程度比用低浓度灌注时小得多。

  4. 在高灌注浓度下,对照组和预处理动物之间仅在总放射性和氧化铝洗脱液中的放射性方面存在显著差异。除了(3)H-多巴胺实验中的脱氨基儿茶酚代谢物外,预处理对代谢物的绝对量和相对量没有显著影响。

  5. 得出的结论是,在用6-羟基多巴胺预处理的大鼠心脏中,神经元摄取1受到极大损害,但非神经元摄取2保持完整。