Goldman S S, Witkovsky P
Exp Eye Res. 1987 Jan;44(1):65-71. doi: 10.1016/s0014-4835(87)80026-x.
Evidence for the existence of a gluconeogenic pathway was provided in the amphibian retina. It was found that [3H]glutamate was converted to [3H]glucose derived from [3H]glutamate was incorporated into glycogen. The rate for this incorporation was found to be essentially the same in both light- and dark-adapted retinas: 0.147 vs. 0.142 nmol (mg protein X 2 hr)-1, respectively. However, the rate of incorporation was found to decline progressively with time. The rate for the incorporation of label derived from glutamate into glycogen was found to be considerably less than that for [3H]glucose: 10.2 nmol (mg protein X 2 hr)-1. The activity of a key gluconeogenic enzyme, fructose-1,6-bisphosphatase, also was demonstrated in retinal supernatants, approximately 1 nmol (mg X min)-1, and the activity of this enzyme was found to be inhibited both by adenosine monophosphate and by fructose-2,6-bisphosphate.
在两栖动物视网膜中发现了糖异生途径存在的证据。研究发现,[3H]谷氨酸被转化为[3H]葡萄糖,源自[3H]谷氨酸的葡萄糖被整合到糖原中。在明适应和暗适应的视网膜中,这种整合速率基本相同,分别为0.147和0.142 nmol(mg蛋白质×2小时)-1。然而,发现整合速率随时间逐渐下降。源自谷氨酸的标记物整合到糖原中的速率明显低于[3H]葡萄糖的速率:10.2 nmol(mg蛋白质×2小时)-1。关键的糖异生酶果糖-1,6-二磷酸酶的活性也在视网膜上清液中得到证实,约为1 nmol(mg×分钟)-1,并且发现该酶的活性受到单磷酸腺苷和果糖-2,6-二磷酸的抑制。