安非他命对猫颈上神经节3h -去甲肾上腺素体外释放的影响。

Acta physiologica latino americana Pub Date : 1981-01-01
E J Filinger, F J Stefano
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引用次数: 0

摘要

研究了d-安非他明产生的3h -去甲肾上腺素(3H-NA)在猫颈上神经节(细胞体)和烟幕膜(神经末梢)中的释放和代谢。将烟化膜暴露于10微米的d-安非他明中,导致释放总放射性的5.1%。主要以3h -去甲肾上腺素(3H-NMN)和3H-NA的形式收集;3h -3,4-二羟基苯基乙二醇(3H-DOPEG)不参与药物诱导的放射性外流。相比之下,神经节细胞体暴露于10 μ m d-安非他明10 min仅释放1.74%的组织总放射性,3H-DOPEG是释放放射性的最重要部分。当神经节暴露于30 μ m d-安非他明时,放射性释放量为5.2%;3H-NA和3H-NMN的比例增加,3H-DOPEG减少。结果表明:a) d-安非他明从预标记的细胞体和神经末梢释放3H-NA;B) d-安非他明在神经末梢的效力高于在细胞体中的效力,c)在低浓度d-安非他明下,肾上腺素能神经元两部分释放的神经递质代谢不同。
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In vitro release of 3H-noradrenaline by amphetamine from the superior cervical ganglion of the cat.

The release and metabolism of 3H-noradrenaline (3H-NA) produced by d-amphetamine was studied in the superior cervical ganglion of the cat (cell bodies) and in the nictitating membrane (nerve endings). Exposure of the nictitating membrane to 10 microM d-amphetamine, resulted in the release of 5.1% of the total radioactivity. This was mainly collected as 3H-normetanephrine (3H-NMN) and as 3H-NA; 3H-3,4-dihydroxyphenylglycol (3H-DOPEG) did not contribute to the drug-induced outflow of radioactivity. In contrast, exposure of ganglionic cell bodies to 10 microM d-amphetamine for 10 min released only 1.74% of the total tissue radioactivity and 3H-DOPEG represented the most important fraction of the released radioactivity. When ganglia were exposed to 30 microM d-amphetamine, the radioactivity released was 5.2%; the proportion of 3H-NA and 3H-NMN increased and 3H-DOPEG was reduced. These results show that: a) d-amphetamine releases 3H-NA from prelabeled cell bodies and nerve endings; b) the potency of d-amphetamine was higher in nerve terminals than in cell bodies, and c) at low concentrations of d-amphetamine, the metabolism of the released neurotransmitter differed between both parts of the adrenergic neuron.

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