Flatman J A, Lambert J D, Engberg I
Acta Physiol Scand. 1985 Jul;124(3):421-7. doi: 10.1111/j.1748-1716.1985.tb07678.x.
Intracellular recordings were made from lumbosacral motoneurones of barbiturate-anaesthetized cats. DL-homocysteate (DLH) and L-glutamate were iontophoresed extracellularly over a range of distances from the impaled motoneurone. Movement of the iontophoretic electrode unit was controlled by a micromanipulator which was advanced independently of that moving the intracellular electrode. Depolarizations to DLH were first detected at a greater distance from the impaled motoneurones (mean, 383 micron) than depolarizations to L-glutamate (mean, 165 micron). As the point of application approached the soma of the motoneurone, depolarizations developed more rapidly, were larger and the latent period of the L-glutamate depolarization became shorter. Dendritic 'hot-spots' of the depolarizing action of L-glutamate were not detected.
在巴比妥麻醉的猫的腰骶运动神经元上进行细胞内记录。将DL-高半胱氨酸(DLH)和L-谷氨酸在离刺入的运动神经元不同距离处进行细胞外离子电泳。离子电泳电极单元的移动由一个微操纵器控制,该微操纵器独立于移动细胞内电极的操纵器向前推进。与对L-谷氨酸的去极化(平均165微米)相比,对DLH的去极化首先在离刺入的运动神经元更远的距离(平均383微米)处被检测到。随着施加点接近运动神经元的胞体,去极化发展得更快、幅度更大,并且L-谷氨酸去极化的潜伏期变得更短。未检测到L-谷氨酸去极化作用的树突“热点”。