Raiteri M, Marchi M, Bonanno G, Melchiorri P, Erspamer V
Istituto di Farmacologia e Farmacognosia, Università degli Studi di Genova, Italy.
Eur J Pharmacol. 1989 Aug 15;172(3):223-9. doi: 10.1016/0922-4106(89)90052-7.
A partly purified extract of the skin of the Australian frog Pseudophryne coriacea (PsC) evoked the release of [3H]acetylcholine [( 3H]ACh) and of [3H]5-hydroxytryptamine [( 3H]5-HT) from superfused rat cerebral cortex synaptosomes prelabeled with [3H]choline or [3H]5-HT, respectively. The PsC-evoked release of both transmitters was sensitive to tetrodotoxin and was strictly Ca2+-dependent. The release of [3H]5-HT caused by PsC was unaffected by the 5-HT uptake inhibitor citalopram. Activation of muscarinic autoreceptors by ACh or of serotonin autoreceptors by 5-HT depressed the PsC-evoked release of [3H]ACh or of [3H]5-HT, respectively. It is concluded that PsC elicits a Ca2+-dependent exocytotic-like transmitter release, possibly by opening Na+ channels in the presynaptic membrane.
澳大利亚蛙(Pseudophryne coriacea,简称PsC)皮肤的部分纯化提取物,分别从预先用[3H]胆碱或[3H]5-羟色胺([3H]5-HT)标记的大鼠大脑皮层突触体中,诱发了[3H]乙酰胆碱([3H]ACh)和[3H]5-羟色胺([3H]5-HT)的释放。PsC诱发的这两种递质的释放对河豚毒素敏感,且严格依赖Ca2+。PsC引起的[3H]5-HT释放不受5-HT摄取抑制剂西酞普兰的影响。乙酰胆碱对毒蕈碱自身受体的激活或5-HT对5-羟色胺自身受体的激活,分别抑制了PsC诱发的[3H]ACh或[3H]5-HT的释放。结论是,PsC可能通过打开突触前膜中的Na+通道,引发一种依赖Ca2+的、类似胞吐作用的递质释放。