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血流阻断对正常脾脏以及用可卡因、酚妥拉明或酚苄明处理过的脾脏中去甲肾上腺素释放的影响。

Effect of flow-stop on noradrenaline release from normal spleens and spleens treated with cocaine, phentolamine or phenoxybenzamine.

作者信息

Kirpekar S M, Puig M

出版信息

Br J Pharmacol. 1971 Oct;43(2):359-69.

Abstract
  1. Cat spleens were perfused with Krebs-bicarbonate solution, using a constant-flow pump at a rate of about 7 ml/min at 33-35 degrees C. Noradrenaline (NA) overflow by nerve stimulation at 10 Hz for 20 s was determined with or without flow-stop before and after treatment with cocaine, phentolamine or phenoxybenzamine. In order to determine the effect of flow-stop on overflow, the arterial and the venous flows were occluded by clamping the inflow and outflow tubes during the period of stimulation plus 30, 60 or 120 seconds.2. Without flow-stop, NA output was 0.93+/-0.25 ng/stimulus, which was significantly increased after cocaine (123+/-6.6%), phentolamine (415+/-93%) and phenoxybenzamine (578+/-107%). Phentolamine and phenoxybenzamine were much more effective than cocaine in enhancing overflow.3. Before treatment with drugs, flow-stops of 30, 60 and 120 s reduced NA outputs to 70+/-6.6, 27.5+/-2 and 7%, respectively, of the control outputs without flow-stop. None of the drugs significantly influenced the percentage reductions in NA outputs during a 30 s flow-stop. However, the percentage outputs after cocaine or phenoxybenzamine treatment during a 60 s flow-stop significantly increased to 45+/-2.5% and 57+/-6%, respectively, as compared to the percentage output of 27.5+/-2% from untreated spleens during a corresponding flow-stop period. During flow-stop, there was no appreciable metabolism of the released transmitter.4. Diffusion of the released transmitter from the site of liberation plays only a minor role in the removal of the released NA.5. It is suggested that the NA released by nerve stimulation acts on the presynaptic alpha sites to inhibit its own release by a negative feedback mechanism. Adrenoceptor blocking agents enhance the NA overflow from spleen because they remove this autoinhibition by blocking the presynaptic alpha sites.
摘要
  1. 将猫的脾脏用 Krebs - 碳酸氢盐溶液灌注,在33 - 35摄氏度下使用恒流泵,流速约为7毫升/分钟。在用可卡因、酚妥拉明或酚苄明处理前后,通过在10赫兹频率下神经刺激20秒来测定去甲肾上腺素(NA)的溢出量,刺激前后分别测定有无停流情况下的溢出量。为了确定停流对溢出量的影响,在刺激期间加上30、60或120秒时,通过夹闭流入管和流出管来阻断动脉和静脉血流。

  2. 在不停流的情况下,NA输出量为0.93±0.25纳克/刺激,在用可卡因(增加123±6.6%)、酚妥拉明(增加至415±93%)和酚苄明(增加至578±107%)处理后显著增加。酚妥拉明和酚苄明在增强溢出方面比可卡因有效得多。

  3. 在药物处理前,30、60和120秒的停流分别将NA输出量降低至不停流时对照输出量的70±6.6%、27.5±2%和7%。在30秒停流期间,没有一种药物对NA输出量的降低百分比有显著影响。然而,在60秒停流期间,可卡因或酚苄明处理后的输出百分比分别显著增加至45±2.5%和57±6%,相比之下,在相应停流期间未处理脾脏的输出百分比为27.5±2%。在停流期间,释放的递质没有明显的代谢。

  4. 释放的递质从释放部位的扩散在去除释放的NA中仅起次要作用。

  5. 提示神经刺激释放的NA作用于突触前α位点,通过负反馈机制抑制其自身释放。肾上腺素能受体阻断剂增强脾脏的NA溢出,因为它们通过阻断突触前α位点消除了这种自身抑制。

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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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