Highstein Stephen M, Rabbitt Richard D, Holstein Gay R, Boyle Richard D
Washington University School of Medicine, Department of Otolaryngology, St. Louis, MO 63110, USA.
J Neurophysiol. 2005 May;93(5):2359-70. doi: 10.1152/jn.00533.2004.
The vestibular semicircular canals are internal sensors that signal the magnitude, direction, and temporal properties of angular head motion. Fluid mechanics within the 3-canal labyrinth code the direction of movement and integrate angular acceleration stimuli over time. Directional coding is accomplished by decomposition of complex angular accelerations into 3 biomechanical components-one component exciting each of the 3 ampullary organs and associated afferent nerve bundles separately. For low-frequency angular motion stimuli, fluid displacement within each canal is proportional to angular acceleration. At higher frequencies, above the lower corner frequency, real-time integration is accomplished by viscous forces arising from the movement of fluid within the slender lumen of each canal. This results in angular velocity sensitive fluid displacements. Reflecting this, a subset of afferent fibers indeed report angular acceleration to the brain for low frequencies of head movement and report angular velocity for higher frequencies. However, a substantial number of afferent fibers also report angular acceleration, or a signal between acceleration and velocity, even at frequencies where the endolymph displacement is known to follow angular head velocity. These non-velocity-sensitive afferent signals cannot be attributed to canal biomechanics alone. The responses of non-velocity-sensitive cells include a mathematical differentiation (first-order or fractional) imparted by hair-cell and/or afferent complexes. This mathematical differentiation from velocity to acceleration cannot be attributed to hair cell ionic currents, but occurs as a result of the dynamics of synaptic transmission between hair cells and their primary afferent fibers. The evidence for this conclusion is reviewed below.
前庭半规管是内部传感器,可对头角运动的大小、方向和时间特性发出信号。三管迷路内的流体力学对运动方向进行编码,并随时间整合角加速度刺激。方向编码是通过将复杂的角加速度分解为3个生物力学分量来完成的——一个分量分别刺激3个壶腹器官和相关传入神经束中的每一个。对于低频角运动刺激,每个半规管内的流体位移与角加速度成正比。在更高频率,即高于下角频率时,实时积分是由每个半规管细长管腔内流体运动产生的粘性力完成的。这导致了对角速度敏感的流体位移。反映这一点的是,一部分传入纤维确实在头部运动低频时向大脑报告角加速度,而在高频时报告角速度。然而,即使在内淋巴位移已知跟随头角速度的频率下,也有相当数量的传入纤维报告角加速度,或加速度与速度之间的信号。这些非速度敏感的传入信号不能仅归因于半规管生物力学。非速度敏感细胞的反应包括毛细胞和/或传入复合体赋予的数学微分(一阶或分数阶)。这种从速度到加速度的数学微分不能归因于毛细胞离子电流,而是由于毛细胞与其初级传入纤维之间突触传递的动力学而发生的。下面将回顾这一结论的证据。