Tabti N, Bourret C, Mallart A
Unité de Physiologie Neuromusculaire, Laboratoire de Neurobiologie Cellulaire et Moléculaire, C.N.R.S., Gif sur Yvette, France.
Pflugers Arch. 1989 Feb;413(4):395-400. doi: 10.1007/BF00584489.
A study of the K conductance of the presynaptic membrane has been performed in the triangularis sterni muscle of the mouse. External currents generated in the presynaptic terminals upon invasion by action potentials have been recorded using microelectrodes inserted into the perineurium of preterminal nerve bundles. The voltage-dependent K current could be pharmacologically dissected into fast (IKf) and slow (IKs) components. While both are sensitive to 3,4-diaminopyridine (3,4-DAP), only IKf is sensitive to tetraethylammonium (TEA). Uranyl (100-200 microM) and guanidine (5-10 mM) produced a near complete block of IKf and IKs, which can explain their facilitatory effect upon transmitter release. The third K current of presynaptic terminals is Ca2+-dependent, but was activated also by Sr2+. This current could be suppressed by nanomolar doses of charybdotoxin; it is also sensitive to TEA but not to 3,4-DAP, uranyl or guanidine.
在小鼠的胸骨三角肌中对突触前膜的钾离子电导进行了一项研究。使用插入终末前神经束神经外膜的微电极记录了动作电位侵入时突触前终末产生的外向电流。电压依赖性钾电流在药理学上可分为快速成分(IKf)和慢速成分(IKs)。虽然两者都对3,4 - 二氨基吡啶(3,4 - DAP)敏感,但只有IKf对四乙铵(TEA)敏感。铀酰(100 - 200微摩尔)和胍(5 - 10毫摩尔)几乎完全阻断了IKf和IKs,这可以解释它们对递质释放的促进作用。突触前终末的第三种钾电流依赖于钙离子,但也可被锶离子激活。该电流可被纳摩尔剂量的蝎毒素抑制;它也对TEA敏感,但对3,4 - DAP、铀酰或胍不敏感。