Aharon S, Parnas H, Parnas I
Department of Neurobiology, Hebrew University, Givat Ram, Jerusalem, Israel.
Bull Math Biol. 1994 Nov;56(6):1095-119. doi: 10.1007/BF02460288.
It is now widely accepted that localized high concentrations of Ca2+ (Ca2+ domains) play a major role in controlling the time course of neurotransmitter release. In the present work we calculate the magnitude and the time course of Ca2+ domains that evolve in the vicinity of a Ca2+ channel and an adjacent release site. In the calculations we consider a accurately dimensioned Ca2+ channel. Moreover, the Ca2+ current is continuously adjusted with regard to the accumulated intracellular Ca2+ and, in addition, endogenous buffers are considered. The calculations, carried out by the software FIDAP, based on finite element method, show that the Ca2+ concentrations achieved near the release sites are significantly lower than claimed by other investigators. Furthermore, we present arguments indicating that the Ca2+ domains, regardless of their magnitude, do not play a role in controlling the time course of release of neurotransmitter.
现在人们普遍认为,局部高浓度的Ca2+(Ca2+结构域)在控制神经递质释放的时间进程中起主要作用。在本研究中,我们计算了在Ca2+通道和相邻释放位点附近演变的Ca2+结构域的大小和时间进程。在计算中,我们考虑了一个精确尺寸的Ca2+通道。此外,Ca2+电流会根据细胞内积累的Ca2+不断进行调整,并且还考虑了内源性缓冲剂。由基于有限元方法的FIDAP软件进行的计算表明,在释放位点附近达到的Ca2+浓度明显低于其他研究者所声称的浓度。此外,我们提出的论据表明,Ca2+结构域无论其大小如何,在控制神经递质释放的时间进程中都不起作用。