Cooper R L, Harrington C C, Marin L, Atwood H L
Department of Physiology, MRC Neural Group, University of Toronto, Ontario, Canada.
J Comp Neurol. 1996 Nov 25;375(4):583-600. doi: 10.1002/(SICI)1096-9861(19961125)375:4<583::AID-CNE3>3.0.CO;2-Y.
Synaptic transmission was measured at visualized terminal varicosities of the motor axon providing the sole excitatory innervation of the "opener" muscle in walking legs of crayfish (Procambarus clarkii Girard). Two questions were addressed: 1) How uniform is quantal emission at different locations along terminals innervating a single muscle fiber, and 2) can differences in quantal emission account for the different excitatory postsynaptic potential (EPSP) amplitudes generated by terminals localized in defined regions of the muscle? Extracellular "macropatch" electrodes were placed over individual varicosities, viewed after brief exposure to a fluorescent dye, and synaptic currents were recorded to determine quantal content of transmission. Along terminals supplying a single muscle fiber, nonuniform release was found: Varicosities closer to the point of origin of the terminal branch released more transmitter than those located more distally. Quantal content was higher for varicosities of the muscle's proximal region (where large EPSPs occur) than for varicosities of the central region (where small EPSPs occur). The probability of transmitter release per synapse is estimated to be greater for the proximal varicosities. At low frequencies of stimulation, quantal content per muscle fiber is two to four times larger in the proximal region. Taken in conjunction with a twofold higher mean input resistance for the proximal muscle fibers, the difference in quantal content can account for a four- to eightfold difference in EPSP amplitude. The observed mean EPSP amplitude is at least eight times larger in the proximal region. We discuss factors contributing to differences in EPSP amplitudes.
在小龙虾(克氏原螯虾,Girard)步足中,对为“开肌”提供唯一兴奋性神经支配的运动轴突的可视化终末膨体进行了突触传递测量。研究了两个问题:1)沿着支配单个肌纤维的终末不同位置,量子释放的均匀性如何?2)量子释放的差异能否解释位于肌肉特定区域的终末所产生的不同兴奋性突触后电位(EPSP)幅度?在短暂暴露于荧光染料后可见的单个膨体上方放置细胞外“大斑片”电极,并记录突触电流以确定传递的量子含量。沿着供应单个肌纤维的终末,发现释放不均匀:终末分支起源点附近的膨体比更远端的膨体释放更多的递质。肌肉近端区域(产生大EPSP的地方)膨体的量子含量高于中央区域(产生小EPSP的地方)膨体的量子含量。估计近端膨体每个突触释放递质的概率更大。在低频刺激下,近端区域每个肌纤维中的量子含量比中央区域大两到四倍。结合近端肌纤维平均输入电阻高两倍的情况,量子含量的差异可以解释EPSP幅度四到八倍的差异。观察到近端区域的平均EPSP幅度至少大八倍。我们讨论了导致EPSP幅度差异的因素。