Department of Anesthesiology, Far Eastern Memorial Hospital, Pan-Chiao, Taipei, Taiwan 220.
Synapse. 2010 May;64(5):390-6. doi: 10.1002/syn.20738.
Osthole and imperatorin, two active compounds of Cnidium monnieri (L.) Cusson, have previously been shown to facilitate depolarization-evoked glutamate release from rat hippocampal nerve terminals by increasing voltage-dependent Ca(2+) entry. In this study, we further investigated whether osthole and imperatorin possess an action at the exocytotic machinery itself, downstream of a Ca(2+) influx. Our data showed that ionomycin-induced glutamate release and KCl-evoked FM1-43 release were facilitated by osthole and imperatorin, suggesting that some steps after Ca(2+) entry are regulated by these two compounds. Consistent with this, osthole or imperatorin-mediated facilitation of ionomycin-induced glutamate release was occluded by cytochalasin D that inhibits actin polymerization, implying that the disassembly of cytoskeleton is involved. In addition, the facilitatory action of osthole or imperatorin on ionomycin-induced glutamate release was attenuated by the Ca(2+)/calmodulin-dependent kinase II (CaMKII) inhibitor KN62. Furthermore, Western blotting analysis further showed that osthole or imperatorin significantly increased ionomycin-induced phosphorylation of CaMKII and synapsin I, the main presynaptic target of CaMKII. These results suggest, therefore, that osthole or imperatorin-mediated facilitation of glutamate release involves modulation of downstream events controlling synaptic vesicle recruitment and exocytosis, possibly through an increase of CaMKII activation and synapsin I phosphorylation, thereby increasing synaptic vesicle availability for exocytosis.
蛇床子素和欧前胡素是蛇床子(Cnidium monnieri(L.)Cusson)中的两种活性化合物,先前已被证明可通过增加电压依赖性 Ca(2+) 内流促进大鼠海马神经末梢去极化诱导的谷氨酸释放。在这项研究中,我们进一步研究了蛇床子素和欧前胡素是否在 Ca(2+) 内流的下游作用于胞吐机制本身。我们的数据表明,离子霉素诱导的谷氨酸释放和 KCl 诱导的 FM1-43 释放均被蛇床子素和欧前胡素促进,表明 Ca(2+) 内流后某些步骤受到这两种化合物的调节。与此一致,蛇床子素或欧前胡素介导的离子霉素诱导的谷氨酸释放的促进作用被细胞松弛素 D 阻断,细胞松弛素 D 抑制肌动蛋白聚合,表明细胞骨架的解聚参与其中。此外,Ca(2+)/钙调蛋白依赖性激酶 II(CaMKII)抑制剂 KN62 减弱了蛇床子素或欧前胡素对离子霉素诱导的谷氨酸释放的促进作用。此外,Western 印迹分析进一步表明,蛇床子素或欧前胡素显著增加了离子霉素诱导的 CaMKII 和突触素 I 的磷酸化,突触素 I 是 CaMKII 的主要突触前靶标。因此,这些结果表明,蛇床子素或欧前胡素介导的谷氨酸释放的促进作用涉及调节控制突触囊泡募集和胞吐的下游事件,可能通过增加 CaMKII 的激活和突触素 I 的磷酸化,从而增加突触囊泡用于胞吐的可用性。