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用快速冷冻技术测量青蛙视网膜中光引发的环磷酸鸟苷水平变化。

Light-initiated changes of cyclic guanosine monophosphate levels in the frog retina measured with quick-freezing techniques.

作者信息

Kilbride P, Ebrey T G

出版信息

J Gen Physiol. 1979 Sep;74(3):415-26. doi: 10.1085/jgp.74.3.415.

Abstract

Although there is good agreement that light reduces the amount of cyclic GMP (cGMP) in the retina, the exact time-course of this decrease is not well established. Bullfrog retinal sections were isolated under infrared light and quick-frozen with liquid nitrogen-cooled, metal hammers after exposure to various intensities of continuous illumination. This quick-freezing should stop the degradation of cGMP within 50-100 ms. The frozen retinal sections were then slowly warmed up in the presence of perchloric acid to denature enzymes involved in cGmp metabolism. cGMP was determined by radioimmunoassay and comparison was made between light- and dark-adapted retinal sections from the same animal. The average cGMP concentration was 44.3 +/- 0.7 pmol cGMP/mg protein or 170.9 +/- 3.2 pmol cGMP/retina. After 1 s of illumination no significant change in cGMP concentration was found even with the brightest light used (approximately 7 x 10(7) rhodopsins bleached/second per rod. At this intensity the first significant decrease in cGMP from dark-adapted levels was detected 3-5 s after the initiation of illumination; cGMP decayed to 70-75% of the dark-adapted value after approximately 30 s. With lower intensity illumination the cGMP levels recovered to dark-adapted levels after the initial decrease even though the bleaching light remained on.

摘要

尽管人们普遍认为光会减少视网膜中环状鸟苷酸(cGMP)的含量,但这种减少的确切时间进程尚未完全明确。牛蛙视网膜切片在红外光下分离,并在暴露于不同强度的连续光照后,用液氮冷却的金属锤快速冷冻。这种快速冷冻应能在50 - 100毫秒内阻止cGMP的降解。然后将冷冻的视网膜切片在高氯酸存在下缓慢升温,以使参与cGMP代谢的酶变性。通过放射免疫测定法测定cGMP,并对来自同一动物的明适应和暗适应视网膜切片进行比较。cGMP的平均浓度为44.3±0.7皮摩尔cGMP/毫克蛋白质或170.9±3.2皮摩尔cGMP/视网膜。即使使用最亮的光(约7×10⁷个视紫红质每秒每根视杆细胞漂白)照射1秒后,cGMP浓度也未发现显著变化。在此强度下,在光照开始后3 - 5秒检测到cGMP从暗适应水平首次显著下降;约30秒后,cGMP降至暗适应值的70 - 75%。在较低强度光照下,即使漂白光仍亮着,cGMP水平在最初下降后也会恢复到暗适应水平。

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