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去甲丙咪嗪、三氟拉嗪及其他钙调蛋白抑制剂对肾上腺髓质及唾液腺节后交感神经儿茶酚胺分泌的影响。

Effects of desipramine, trifluoperazine and other inhibitors of calmodulin on the secretion of catecholamines from the adrenal medulla and postganglionic sympathetic nerves of the salivary gland.

作者信息

Wakade A R, Wakade T D

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Apr;325(4):320-7. doi: 10.1007/BF00504376.

Abstract

The effects of various drugs, known to be inhibitors of calmodulin, were tested on the secretion of catecholamines (CA) from the adrenal medulla and sympathetic nerves of the salivary gland of the rat. Secretion of CA from the perfused adrenal gland was evoked by injection of acetylcholine (ACh, 50 micrograms), excess K (700 micrograms), or transmural stimulation of splanchnic nerves (300 pulses at 10 Hz). Release of 3H-noradrenaline in the perfused salivary gland was evoked by transmural stimulation at 3 Hz for 30 s. CA secretion was reduced in a dose-dependent manner by 0.3 microM to 10 microM desipramine or imipramine. The effect of low doses (0.3 microM) was more pronounced on the secretion evoked by ACh and splanchnic nerve stimulation than that by excess K. The inhibition was independent of the frequency of nerve stimulation. Trifluoperazine (10-100 microM) and chlorpromazine (10-100 microM) reduced CA secretion evoked by all of the three procedures. The inhibitory effects of desipramine, trifluoperazine and chlorpromazine were completely reversed within 1 h after their washout. Secretion of CA obtained after reintroduction of Ca to the adrenal gland previously perfused with Ca-free medium was not blocked by desipramine or trifluoperazine. In fact, these agents markedly enhanced the secretory response. None of the drugs enhanced spontaneous secretion of CA from the adrenal gland during the nonstimulation period. Adrenal medullary cells accumulated significant amounts of Ca45 (0.88 pg/mg) after stimulation with ACh.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已知多种药物为钙调蛋白抑制剂,本研究测试了它们对大鼠肾上腺髓质和唾液腺交感神经中儿茶酚胺(CA)分泌的影响。通过注射乙酰胆碱(ACh,50微克)、过量钾(700微克)或经壁刺激内脏神经(10赫兹,300个脉冲)来诱发灌注肾上腺中CA的分泌。通过3赫兹经壁刺激30秒来诱发灌注唾液腺中3H-去甲肾上腺素的释放。0.3微摩尔至10微摩尔的地昔帕明或丙咪嗪可使CA分泌呈剂量依赖性减少。低剂量(0.3微摩尔)对ACh和内脏神经刺激诱发的分泌的影响比对过量钾诱发的分泌更明显。这种抑制与神经刺激频率无关。三氟拉嗪(10 - 100微摩尔)和氯丙嗪(10 - 100微摩尔)可减少所有这三种程序诱发的CA分泌。地昔帕明、三氟拉嗪和氯丙嗪的抑制作用在洗脱后1小时内完全逆转。向先前用无钙培养基灌注的肾上腺重新添加钙后获得的CA分泌不受地昔帕明或三氟拉嗪的阻断。事实上,这些药物显著增强了分泌反应。在非刺激期,没有一种药物增强肾上腺CA的自发分泌。用ACh刺激后,肾上腺髓质细胞积累了大量的Ca45(0.88皮克/毫克)。(摘要截短于250字)

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