Wolburg H
Z Naturforsch C Biosci. 1976 Nov-Dec;31(11-12):683-6. doi: 10.1515/znc-1976-11-1210.
[3H]Proline and [3H]uridine were injected into both eyes of the goldfish. 1 h before and after this injection 3X10)-6)M ouabain was administrated unilaterally to the retina. 8 h and 24 h after tracer injection the radioactivity in the retina, optic nerve and tectum was measured. It is suggested that the inhibition of the neuronal Na+-K+-ATPase inside the retina is responsible for the reduction of the labelled material transported into the optic nerve.
将[3H]脯氨酸和[3H]尿苷注入金鱼的双眼。在注射前1小时和注射后,将3×10⁻⁶M哇巴因单侧施用于视网膜。在注射示踪剂后8小时和24小时,测量视网膜、视神经和视叶中的放射性。研究表明,视网膜内神经元钠钾ATP酶的抑制作用是导致转运至视神经中的标记物质减少的原因。