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从离体肌性动脉释放内源性去甲肾上腺素。从离体肌性动脉释放内源性去甲肾上腺素。

Release of endogenous noradrenaline from an isolated muscular artery. Release of endogenous noradrenaline from an isolated muscular artery.

作者信息

Bell C, Vogt M

出版信息

J Physiol. 1971 Jun;215(2):509-20. doi: 10.1113/jphysiol.1971.sp009482.

Abstract
  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 x 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 x 10(5) varicosities. The mean tissue content of noradrenaline was found to be 9.6 mug/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 x 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 x 10(-4).
摘要
  1. 已在豚鼠子宫主动脉的离体标本中研究了通过对血管收缩神经进行场刺激来释放去甲肾上腺素的情况。

  2. 在未孕动物的标本中,以5次/秒和25次/秒的频率施加3000个方波脉冲串进行刺激,平均溢出量分别为0.56纳克/克·脉冲和1.53纳克/克·脉冲。

  3. 抑制单胺氧化酶和儿茶酚 - O - 甲基转移酶对任一刺激频率下的溢出均无一致影响。

  4. 去甲丙咪嗪(10⁻⁵摩尔/升)平均使以5次/秒刺激后的溢出量增加2.4倍,而苯氧苄胺(10⁻⁵摩尔/升)使溢出量增加3.8倍。这两种药物在以25次/秒刺激期间均未引起溢出的显著改变。

  5. 用去甲丙咪嗪加去甲变肾上腺素(4.5×10⁻⁴摩尔/升)处理组织,与单独用去甲丙咪嗪处理相比,溢出量增加不多。

  6. 得出结论:在该组织中,去甲肾上腺素在突触处的酶促代谢在功能上不太重要,而递质失活的最重要机制是通过神经再摄取。尽管苯氧苄胺在增加递质溢出方面比去甲丙咪嗪更有效,但未获得证据支持这种有效性部分归因于对“摄取2”的阻断这一观点。

  7. 有时从妊娠最后一周的动物获取的动脉中去甲肾上腺素溢出量非常低。在这些情况下,用苯氧苄胺处理组织后,以5次/秒刺激后的溢出量并未增加。

  8. 亚甲蓝和荧光显微镜技术表明,每条动脉中的终末肾上腺素能轴突约有8.74×10⁵个膨体。发现去甲肾上腺素的平均组织含量为9.6微克/克或29纳克/动脉。这些结果已与已知的形态学和电生理学数据相关联,得出传递过程中去甲肾上腺素的峰值节后浓度约为4×10⁻⁴摩尔/升。

  9. (在苯氧苄胺影响下)每个脉冲释放的动脉中去甲肾上腺素总含量的分数平均值为2.2×10⁻⁴。

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