Suppr超能文献

挥发性麻醉剂对牛肾上腺嗜铬细胞刺激-分泌偶联的作用。

The action of volatile anaesthetics on stimulus-secretion coupling in bovine adrenal chromaffin cells.

作者信息

Pocock G, Richards C D

机构信息

Department of Physiology, Royal Free Hospital School of Medicine, London.

出版信息

Br J Pharmacol. 1988 Sep;95(1):209-17. doi: 10.1111/j.1476-5381.1988.tb16566.x.

Abstract
  1. The action of four volatile anaesthetics, ethrane, halothane, isoflurane and methoxyflurane on stimulus-secretion coupling has been studied in isolated bovine adrenal medullary cells. All four agents inhibited the secretion of adrenaline and noradrenaline evoked by 500 microM carbachol at concentrations within the anaesthetic range. Total catecholamine secretion induced by stimulation with 77 mM potassium was also inhibited but at higher concentrations. All four agents inhibited the 45Ca influx evoked by stimulation with 500 microM carbachol and the 45Ca influx in response to K+-depolarization. 2. When total catecholamine secretion in response to potassium or carbachol was modulated by varying extracellular calcium or by adding halothane or methoxyflurane to the incubation medium, the amount of catecholamine secretion for a given Ca2+ entry was the same. 3. The action of methoxyflurane on the relationship between intracellular free Ca and exocytosis was examined using electropermeabilised cells, which were suspended in solutions containing a range of concentrations of ionised calcium between 10(-8) and 10(-4)M. The anaesthetic had no effect on the activation of exocytosis by intracellular free calcium. 4. Halothane and methoxyflurane inhibited the carbachol-induced secretion of catecholamines in a non-competitive manner. 5. Halothane and methoxyflurane inhibited the increase in 22Na influx evoked by carbachol. For halothane and methoxyflurane this inhibition of Na influx appears to be sufficient to account for the inhibition of the evoked catecholamine secretion. 6. We conclude that the volatile anaesthetics ethrane, halothane, isoflurane and methoxyflurane inhibit the secretion of adrenaline and noradrenaline induced by carbachol at concentrations that lie within the range encountered during general anaesthesia. In addition all four also inhibit the secretion of catecholamines induced by depolarization with 77 mM K+ but at much higher concentrations. The decrease in Ca influx caused by methoxyflurane accounts fully for the decrease in secretion in response to depolarization with potassium. Similar actions at synapses within the CNS may underlie the general anaesthetic effects of these agents.
摘要
  1. 已在分离的牛肾上腺髓质细胞中研究了四种挥发性麻醉剂,即恩氟烷、氟烷、异氟烷和甲氧氟烷对刺激 - 分泌偶联的作用。在麻醉浓度范围内,所有这四种药物均抑制了由500微摩尔卡巴胆碱诱发的肾上腺素和去甲肾上腺素的分泌。用77毫摩尔钾刺激诱导的总儿茶酚胺分泌也受到抑制,但所需浓度更高。所有这四种药物均抑制了由500微摩尔卡巴胆碱刺激诱发的45钙内流以及对钾去极化的45钙内流。2. 当通过改变细胞外钙或向孵育培养基中添加氟烷或甲氧氟烷来调节对钾或卡巴胆碱的总儿茶酚胺分泌时,对于给定的钙内流,儿茶酚胺分泌量是相同的。3. 使用电通透细胞研究了甲氧氟烷对细胞内游离钙与胞吐作用之间关系的影响,这些细胞悬浮于含有10⁻⁸至10⁻⁴摩尔/升一系列浓度的离子钙的溶液中。该麻醉剂对细胞内游离钙激活胞吐作用没有影响。4. 氟烷和甲氧氟烷以非竞争性方式抑制卡巴胆碱诱导的儿茶酚胺分泌。5. 氟烷和甲氧氟烷抑制了卡巴胆碱诱发的22钠内流增加。对于氟烷和甲氧氟烷而言,这种对钠内流的抑制似乎足以解释对诱发的儿茶酚胺分泌的抑制。6. 我们得出结论,挥发性麻醉剂恩氟烷、氟烷、异氟烷和甲氧氟烷在全身麻醉期间遇到的浓度范围内抑制卡巴胆碱诱导的肾上腺素和去甲肾上腺素分泌。此外,所有这四种药物也抑制由77毫摩尔钾去极化诱导的儿茶酚胺分泌,但所需浓度要高得多。甲氧氟烷引起的钙内流减少完全解释了对钾去极化反应中分泌的减少。这些药物在中枢神经系统内突触处的类似作用可能是这些药物全身麻醉作用的基础。

相似文献

引用本文的文献

5
Isoflurane inhibits the neurotransmitter release machinery.异氟烷抑制神经递质释放机制。
J Neurophysiol. 2009 Aug;102(2):1265-73. doi: 10.1152/jn.00252.2009. Epub 2009 Jun 10.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验