Aksentsev S L, Rakovich A A, Okoon I M, Konev S V, Orlov S N, Kravtsov G M
Pflugers Arch. 1983 Apr;397(2):135-40. doi: 10.1007/BF00582051.
Depolarization of synaptosomes with veratrine (0.1 mg/ml) or 50 mmol/l of KCl results in the release of radioactivity from 14C-choline loaded synaptosomes with partial dependence on external Ca2+. Like tetrodotoxin, tetracaine prevented veratrine but not KCl action, with a half-maximal effect at approximately 10(-5) mol/l of anesthetic. A similar half-maximal value was obtained for tetracaine blockade of veratrine-stimulated tetrodotoxin-sensitive 22Na influx into synaptosomes, complete blockage being achieved at 10(-4) mol/l. At this concentration tetracaine failed to modify Ca2+ channels measured by KCl-induced 45Ca uptake. Microviscosity of a lipid bilayer in synaptic membranes evaluated with 5- and 16-doxylstearate spin labels decreased at tetracaine concentrations exceeding 10(-3) mol/l. It is suggested that Na+ channels of synaptosomes are blocked by direct action of anesthetic or through changes in the channel annular lipids.
用藜芦碱(0.1毫克/毫升)或50毫摩尔/升氯化钾使突触体去极化,会导致14C-胆碱负载的突触体释放放射性,且部分依赖于细胞外钙离子。与河豚毒素一样,丁卡因可阻止藜芦碱的作用,但不能阻止氯化钾的作用,在约10^(-5)摩尔/升麻醉剂时达到半数最大效应。丁卡因对藜芦碱刺激的河豚毒素敏感的22Na流入突触体的阻断作用也得到类似的半数最大效应值,在10^(-4)摩尔/升时实现完全阻断。在此浓度下,丁卡因未能改变通过氯化钾诱导的45Ca摄取所测量的钙离子通道。用5-和16-二氧硬脂酸自旋标记评估的突触膜脂质双层的微粘度在丁卡因浓度超过10^(-3)摩尔/升时降低。提示突触体的钠离子通道被麻醉剂的直接作用或通过通道环形脂质的变化所阻断。