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胍对猫灌注脾脏中去甲肾上腺素释放的影响。

Effect of guanidine on release of noradrenaline from the perfused spleen of the cat.

作者信息

Hirsch J, Kirpekar S M, Prat J C

出版信息

Br J Pharmacol. 1979 Aug;66(4):537-46. doi: 10.1111/j.1476-5381.1979.tb13692.x.

Abstract

1 Guanidine increased noradrenaline (NA) output at 5 Hz by 3 to 6 fold, and doubled it at 30 Hz. Onset of maximum activity was slow, and reversal was also slow. Output of NA induced by potassium, sodium deprivation, or tyramine was not affected. 2 NA output was doubled at low concentrations (1 to 2 mM) of guanidine, but maximal effect was obtained at 4 mM. At 10 mM, spontaneous release was occasionally observed. 3 The effect of guanidine on NA release was related to the external calcium concentration. Outputs which previously have been shown to be insignificant at 5 Hz in 0.25 and 0.75 mM calcium-Krebs solution were markedly enhanced by guanidine. Guanidine enhanced release at all calcium concentrations up to 7.5 mM, but maximum output was obtained at 2.5 mM. 4 Guanidine had no effect on the recovery of intra-arterially infused NA. 5 The effects of guanidine and tetraethyl-ammonium (TEA) on NA release at 5 Hz were additive. 6 Guanidine reversed the inhibition of NA release by guanethidine during nerve stimulation at 5 and 10 Hz, and the NA output increased nearly 2.5 fold after repeated stimulation of the nerves. Guanidine was less effective in reversing the inhibitory effects of guanethidine on NA release at 30 Hz. 7 Guanidine did not affect release of catecholamines (CA) from the perfused cat adrenal gland by splanchnic nerve stimulation. 8 It is suggested that guanidine enhances NA release partly by increasing the influx of calcium into the neurone during an action potential, and also by interfering with intracellular binding of calcium.

摘要
  1. 胍使5赫兹时去甲肾上腺素(NA)的释放量增加3至6倍,30赫兹时则使其加倍。最大活性的起效缓慢,恢复也缓慢。钾、钠缺乏或酪胺诱导的NA释放不受影响。2. 低浓度(1至2毫摩尔)的胍使NA释放量加倍,但在4毫摩尔时获得最大效应。在10毫摩尔时,偶尔会观察到自发释放。3. 胍对NA释放的作用与细胞外钙浓度有关。在0.25和0.75毫摩尔钙 - 克雷布斯溶液中,先前已证明在5赫兹时无显著作用的释放量,因胍而显著增强。胍在高达7.5毫摩尔的所有钙浓度下均增强释放,但在2.5毫摩尔时获得最大释放量。4. 胍对动脉内注入的NA的恢复没有影响。5. 胍和四乙铵(TEA)对5赫兹时NA释放的作用是相加的。6. 在5赫兹和10赫兹的神经刺激期间,胍逆转了胍乙啶对NA释放的抑制作用,并且在神经反复刺激后,NA释放量增加了近2.5倍。胍在逆转胍乙啶对30赫兹时NA释放的抑制作用方面效果较差。7. 胍不影响内脏神经刺激对灌注猫肾上腺中儿茶酚胺(CA)的释放。8. 有人认为,胍部分通过增加动作电位期间钙流入神经元以及通过干扰钙的细胞内结合来增强NA释放。

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