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4-氨基吡啶对神经刺激引起的灌注猫脾脏去甲肾上腺素释放的影响。

Effect of 4-aminopyridine on release of noradrenaline from the perfused cat spleen by nerve stimulation.

作者信息

Kirpekar M, Kirpekar S M, Prat J C

出版信息

J Physiol. 1977 Nov;272(3):517-28. doi: 10.1113/jphysiol.1977.sp012057.

Abstract
  1. 4-aminopyridine (4-AP, 1 mM) increased noradrenaline (NA) output from the perfused cat spleen at 5 Hz by about fivefold. Enhancement of NA release by 4-AP was reversible. Output of NA induced by potassium was not affected. 2. NA output was doubled at low concentrations (0.1--0.3 mM) of 4-AP, but maximal effect was obtained at 1--3 mM. At 10 mM, it induced spontaneous release of NA which was insensitive to calcium. 3. Insignificant outputs obtained at 5 Hz in 0.1 and 0.3 mM calcium-Krebs solution were markedly enhanced by 4-AP. 4-AP enhanced release at all calcium concentrations up to 5 mM, but maximum output was obtained at 2.5 mM. 4. 4-AP at pH 8.5 was more effective in enhancing NA release than at pH 7.4. 5. 4-AP increased the recovery of intra-arterially infused NA from the control 26 to 47%. 6. 4-AP did not affect release of catecholamines (CA) from the perfused cat adrenal gland by acetylcholine (ACh). 7. It is suggested that 4-AP inactivates potassium current in sympathetic nerves and prolongs the duration of the action potential, thereby allowing a greater influx of calcium ions into the neurone to enhance release of NA.
摘要
  1. 4-氨基吡啶(4-AP,1毫摩尔)使灌注猫脾脏在5赫兹频率下的去甲肾上腺素(NA)输出量增加了约五倍。4-AP对NA释放的增强作用是可逆的。钾诱导的NA输出不受影响。2. 在低浓度(0.1 - 0.3毫摩尔)的4-AP作用下,NA输出量翻倍,但在1 - 3毫摩尔时达到最大效应。在10毫摩尔时,它诱导NA的自发释放,且这种释放对钙不敏感。3. 在0.1和0.3毫摩尔钙 - 克雷布斯溶液中,5赫兹频率下获得的微不足道的输出量被4-AP显著增强。在高达5毫摩尔的所有钙浓度下,4-AP都增强了释放,但在2.5毫摩尔时获得最大输出量。4. pH 8.5的4-AP在增强NA释放方面比pH 7.4时更有效。5. 4-AP使动脉内注入的NA的回收率从对照的26%提高到47%。6. 4-AP不影响乙酰胆碱(ACh)从灌注猫肾上腺释放儿茶酚胺(CA)。7. 有人提出,4-AP使交感神经中的钾电流失活并延长动作电位的持续时间,从而使更多钙离子流入神经元以增强NA的释放。

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