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Release of endogenous noradrenaline from an isolated muscular artery

机译:从孤立的肌肉动脉释放内源性去甲肾上腺素

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摘要

1. The release of noradrenaline by field stimulation of vasoconstrictor nerves has been studied in isolated preparations of the main uterine artery of the guinea-pig.2. In preparations from virgin animals stimulation with trains of 3000 square pulses at 5 and 25 pulses/sec resulted in mean overflows of 0·56 ng/g.pulse and 1·53 ng/g.pulse respectively.3. Inhibition of monoamine oxidase and catechol-O-methyltransferase had no consistent effect on overflow at either stimulation frequency.4. Desmethylimipramine (10-5 M) caused, on the average, a 2·4-fold increase in overflow following stimulation at 5 pulses/sec while phenoxybenzamine (10-5 M) caused a 3·8-fold increase. Neither of these drugs caused a significant alteration of the overflow during stimulation at 25 pulses/sec.5. Treatment of the tissues with desmethylimipramine plus normetanephrine (4·5 × 10-4 M) caused no more increase in overflow than treatment with desmethylimipramine alone.6. It is concluded that enzymatic metabolism of noradrenaline at the synapse is of little functional importance in this tissue, and that the most important mechanism of transmitter inactivation is by nervous re-uptake. Although phenoxybenzamine was more effective than desmethylimipramine in increasing transmitter overflow, no evidence was obtained to support the view that this effectiveness was due partly to blockade of `Uptake 2'.7. There was sometimes very low overflow of noradrenaline from arteries taken from animals in the last week of pregnancy. In these instances overflow following stimulation at 5 pulses/sec was not increased by phenoxybenzamine treatment of the tissue.8. Methylene blue and fluorescence microscopic techniques indicated that the terminal adrenergic axons in each artery possess approximately 8·74 × 105 varicosities. The mean tissue content of noradrenaline was found to be 9·6 μg/g or 29 ng/artery. These results have been correlated with known morphological and electrophysiological data to derive a peak post-junctional concentration of noradrenaline during transmission of about 4 × 10-4 M.9. The fraction of total noradrenaline content of the artery released per pulse (under the influence of phenoxybenzamine) had a mean value of 2·2 × 10-4.
机译:1.在豚鼠主要子宫动脉的分离制剂中,研究了通过血管收缩神经的野外刺激释放去甲肾上腺素的作用。在处女动物的制剂中,以5和25脉冲/秒的速度训练3000平方脉冲,分别导致平均溢出量为0·56 ng / g.pulse和1·53 ng / g.pulse。单胺氧化酶和儿茶酚-O-甲基转移酶的抑制在任一刺激频率下对溢流都没有一致的影响。4。去甲丙咪嗪(10 -5 M)引起的平均增速是5脉冲/秒刺激后溢出的2·4倍,而苯氧基苯甲胺(10 -5 M )引起了3·8倍的增长。这些药物都没有以25脉冲/秒的速度引起刺激过程中溢出的显着改变5。用去甲基米帕明加去甲肾上腺素(4·5×10 -4 M)处理组织不会导致溢流增加,而仅使用去甲基米帕明即可。6。结论是,去甲肾上腺素在突触中的酶促代谢在该组织中的功能重要性不高,并且递质失活的最重要机制是通过神经的再摄取。尽管苯氧苯甲胺比去甲丙咪嗪在增加递质溢流方面更有效,但没有证据支持这种有效性部分归因于对“摄取2” .7的阻滞。在怀孕的最后一周,从动物抽取的动脉有时会出现少量去甲肾上腺素溢出。在这些情况下,苯氧苯扎明对组织的刺激在以5个脉冲/秒的速度刺激后不会溢出。8。亚甲基蓝和荧光显微镜技术表明,每条动脉的终末肾上腺素能轴突具有大约8·74×10 5 的曲张度。去甲肾上腺素的平均组织含量为9·6μg/ g或29 ng /动脉。这些结果已与已知的形态学和电生理数据相关,得出了在传输过程中去甲肾上腺素的结后峰值浓度约为4×10 -4 M.9。每个脉冲释放的总去甲肾上腺素含量的分数(在苯氧基苯扎明的影响下)的平均值为2·2×10 -4

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