Sela Rotem, Segel Lee, Parnas Itzchak, Parnas Hanna
Department of Neurobiology, Hebrew University, Jerusalem, 91904, Israel.
J Comput Neurosci. 2005 Aug;19(1):5-20. doi: 10.1007/s10827-005-0187-4.
The primacy of Ca2+ in controlling the amount of released neurotransmitter is well established. However, it is not yet clear what controls the time-course (initiation and termination) of release. Various experiments indicated that the time-course is controlled by membrane potential per se. Consequently the phenomenological Ca-Voltage-Hypothesis (CVH) was formulated. The CVH was later embodied in a molecular level mathematical model, whose key predictions were affirmed experimentally. Nonetheless, the single most important basis for the CVH, namely that depolarization per se is needed to induce physiological phasic release, was challenged by two major experimental findings. (i) Release was induced by Ca2+ alone by means of Ca2+-uncaging. (ii) There was at most a small additional effect when depolarization was applied after release was induced by Ca2+-uncaging. Point (i) was dealt with previously, but additional conclusions are drawn here. Here we concentrate on (ii) and show that the experimental results can be fully accounted for by the molecular level CVH model, with essentially the same parameters.
钙离子在控制神经递质释放量方面的首要地位已得到充分确立。然而,目前尚不清楚是什么控制着释放的时间进程(起始和终止)。各种实验表明,时间进程由膜电位本身控制。因此,提出了现象学的钙 - 电压假说(CVH)。CVH后来体现在一个分子水平的数学模型中,其关键预测得到了实验证实。尽管如此,CVH的最重要依据,即去极化本身是诱导生理性相位释放所必需的,受到了两项主要实验结果的挑战。(i)通过钙离子解笼技术单独用钙离子诱导释放。(ii)在通过钙离子解笼技术诱导释放后施加去极化时,至多只有很小的额外效应。(i)点之前已作处理,但这里得出了额外的结论。这里我们关注(ii)点,并表明实验结果可以用分子水平的CVH模型完全解释,且参数基本相同。