Coull B M, Owens D K, Cutler R W
Brain Res. 1981 Apr 6;210(1-2):301-9. doi: 10.1016/0006-8993(81)90903-3.
The vitreal space of the intact eye of albino rats was perfused in vivo. The concentration of several endogenous amino acids in the vitreal effluent was measured by the [3H]microdansylation procedure. GABA was never detected despite a sensitivity of the method of 0.5 pmol. In contrast to previous results obtained in pigmented rats, photic stimulation with flashing white light did not alter the release of glycine or any of the other amino acids. Potassium (60 mM) and ouabain (0.1 mM) evoked a specific release of glycine. The potassium-evoked release was blocked by magnesium suggesting a neuronal site of origin of glycine. Ouabain-evoked release was not blocked by magnesium. The results were contrasted with experiments on radiolabeled amino acid release from retinas preloaded and superfused in vitro, a condition in which glial localization of exogenous amino acids predominates.
对白化病大鼠完整眼睛的玻璃体腔进行体内灌注。通过[3H]微丹磺酰化法测量玻璃体流出液中几种内源性氨基酸的浓度。尽管该方法的灵敏度为0.5皮摩尔,但从未检测到γ-氨基丁酸(GABA)。与先前在有色大鼠中获得的结果相反,闪烁白光的光刺激并未改变甘氨酸或任何其他氨基酸的释放。钾(60 mM)和哇巴因(0.1 mM)引起甘氨酸的特异性释放。钾引起的释放被镁阻断,提示甘氨酸的神经元起源部位。哇巴因引起的释放未被镁阻断。将这些结果与体外预加载和灌注的视网膜中放射性标记氨基酸释放的实验进行对比,在这种情况下,外源性氨基酸主要定位于神经胶质细胞。