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龙虾神经肌肉突触处不同易化形式的潜在机制。

Mechnisms underlying different facilitation forms at the lobster neuromuscular synapse.

作者信息

Bykhovskaia Maria, Polagaeva Elena, Hackett John T

机构信息

Department of Biological Sciences, Lehigh University, 111 Research Dr., Bethlehem, PA 18015, USA.

出版信息

Brain Res. 2004 Sep 3;1019(1-2):10-21. doi: 10.1016/j.brainres.2004.05.037.

Abstract

At the crustacean neuromuscular junction, facilitation elicited by a repetitive stimulation reaches a plateau level that is proportional to the stimulation frequency. In the present study we demonstrated that plateau facilitation (F(plateau)) does not depend on Ca(2+) manipulations. We manipulated Ca(2+) concentration in the following ways: (1) applying cell permeable chelators BAPTA-AM or EGTA-AM; (2) decreasing Ca(2+) concentration in the extracellular media; (3) enhancing Ca(2+) influx by 4-aminipyridin. We found that neither F(plateau) is decreased by lowering Ca(2+) nor it is increased by enhancing Ca(2+) influx. In contrast, facilitation elicited by a short train of stimuli (F(growth)) was altered by Ca(2+) manipulations. These results suggested that F(plateau) does not result from accumulation of free intracellular Ca(2+). We hypothesized that F(plateau) results from the accumulation of synaptic vesicles properly activated for transmitter release, the readily releasable pool (RRP). To test this hypothesis, we measured the increase in RRP employing local applications of hypertonic solutions (HS). We found that the size of RRP was significantly increased after F(plateau) was induced. Our results suggest that facilitation is mediated by two mechanisms: the increase in the residual Ca(2+) and the increase in RRP. Frequency facilitation during continuous stimulation, F(plateau), is primarily controlled by the increase in RRP.

摘要

在甲壳类动物的神经肌肉接头处,重复刺激引发的易化作用会达到一个与刺激频率成正比的平台水平。在本研究中,我们证明平台期易化作用(F(plateau))并不依赖于Ca(2+)的调控。我们通过以下方式调控Ca(2+)浓度:(1)应用细胞可渗透螯合剂BAPTA-AM或EGTA-AM;(2)降低细胞外介质中的Ca(2+)浓度;(3)通过4-氨基吡啶增强Ca(2+)内流。我们发现,降低Ca(2+)浓度并不会使F(plateau)降低,增强Ca(2+)内流也不会使其升高。相反,短串刺激引发的易化作用(F(growth))会因Ca(2+)的调控而改变。这些结果表明,F(plateau)并非由细胞内游离Ca(2+)的积累所致。我们推测F(plateau)是由为递质释放而被适当激活的突触小泡(即可释放池,RRP)积累引起的。为验证这一假设,我们通过局部应用高渗溶液(HS)来测量RRP的增加。我们发现,诱导出F(plateau)后,RRP的大小显著增加。我们的结果表明,易化作用由两种机制介导:残余Ca(2+)的增加和RRP的增加。持续刺激期间的频率易化作用F(plateau)主要由RRP的增加所控制。

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