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β-卤代烷基胺和麻黄碱对猫完整脾脏去甲肾上腺素释放的影响。

Effect of beta-haloalkylamines and ephedrine on noradrenaline release from the intact spleen of the cat.

作者信息

Kirpekar S M, Wakade A R

出版信息

Br J Pharmacol. 1970 Jul;39(3):533-41. doi: 10.1111/j.1476-5381.1970.tb10361.x.

Abstract
  1. The effects of beta-haloalkylamines, phenoxybenzamine (PBZ), N-alpha-naphthyl-methyl-N-ethyl-beta-bromoethylamine (SY28), N-cyclohexyl-methyl-N-ethyl-beta-chloroethylamine (GD131) and ephedrine on noradrenaline (NA) output following nerve stimulation were studied in the intact spleen of the cat. Postganglionic sympathetic nerves were stimulated at frequencies of 10 and 30 Hz for a total of 210 stimuli.2. PBZ and SY28 (10 mg/kg) increased the transmitter output at 10 Hz by nearly 5-10 times.3. Administration of GD131 (10 mg/kg) had no effect on output at either frequency. Phentolamine (3 mg/kg) given after GD131 increased NA output at 10 Hz.4. Ephedrine (0.5 mg/kg) caused no changes in catecholamine output, while higher doses of ephedrine (10-20 mg/kg) increased the amount released at 10 Hz.5. Perfusion of the spleen with Krebs-bicarbonate solution containing either SY28, GD131 or ephedrine (10 mug/ml) increased the recovery of infused NA by 80-90%.6. It is concluded that presynaptic as well as postsynaptic events determine the overflow of NA following stimulation of sympathetic nerves of the spleen.
摘要
  1. 在猫的完整脾脏中,研究了β-卤代烷基胺、酚苄明(PBZ)、N-α-萘基甲基-N-乙基-β-溴乙胺(SY28)、N-环己基甲基-N-乙基-β-氯乙胺(GD131)和麻黄碱对神经刺激后去甲肾上腺素(NA)释放量的影响。节后交感神经以10赫兹和30赫兹的频率刺激,共刺激210次。

  2. PBZ和SY28(10毫克/千克)使10赫兹时递质释放量增加近5至10倍。

  3. 给予GD131(10毫克/千克)对任一频率的释放量均无影响。在GD131之后给予酚妥拉明(3毫克/千克)可增加10赫兹时的NA释放量。

  4. 麻黄碱(0.5毫克/千克)对儿茶酚胺释放量无影响,而较高剂量的麻黄碱(10至20毫克/千克)可增加10赫兹时的释放量。

  5. 用含有SY28、GD131或麻黄碱(10微克/毫升)的 Krebs-碳酸氢盐溶液灌注脾脏,可使注入的NA回收率提高80%至90%。

  6. 得出结论:突触前和突触后事件均决定了刺激脾脏交感神经后NA的溢出。

相似文献

本文引用的文献

1
The action of ephedrine.麻黄碱的作用。
J Physiol. 1938 Oct 14;94(1):87-100. doi: 10.1113/jphysiol.1938.sp003664.
8
The output of sympathetic transmitter from the spleen of the cat.猫脾脏交感递质的释放
J Physiol. 1957 Aug 29;138(1):81-102. doi: 10.1113/jphysiol.1957.sp005839.

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