Jensen R J
Department of Biomedical Sciences, Southern College of Optometry, Memphis, TN 38104, USA.
Vis Neurosci. 1999 Mar-Apr;16(2):205-19. doi: 10.1017/s0952523899162023.
Previous studies in the rabbit retina have shown that drugs which block AMPA glutamate receptors abolish directional selectivity in ON-OFF directionally selective (DS) ganglion cells. The effects of activation of AMPA receptors on the directionally selective responses of these ganglion cells had not been studied. In the present study, extracellular recordings of the responses of ON-OFF DS ganglion cells to a moving bar of light were made in an in vitro rabbit retinal preparation. In control solution, bath application of AMPA (7-10 microM) abolished the light responses of most ON-OFF DS ganglion cells. On washout of AMPA, the light responses rapidly returned; however, the cells temporarily lost the ability to discriminate the direction of the moving bar of light. That is, the cells responded equally to movement in the preferred and null directions. Pretreatment of retinas with the glycine receptor antagonist strychnine (1-2 microM) did not alter the effects of AMPA. On the other hand, in retinas pretreated with the GABA(A) receptor antagonist SR95531 (0.2-0.25 microM), AMPA did not abolish the light responses of ON-OFF DS ganglion cells but instead abolished directional selectivity in these cells by bringing out a response to movement in the null direction. This finding suggests that an AMPA-induced GABA efflux from cells in the retina was responsible for the suppression of the light responses by AMPA. In control solution, application of the selective AMPA receptor agonist (S)-5-fluorowillardiine (2-3 microM) only temporarily abolished the light responses of ON-OFF DS ganglion cells. As the light responses returned, it was clear that directional selectivity had been abolished by (S)-5-fluorowillardiine. In control solution, blocking AMPA receptor desensitization with cyclothiazide (80-100 microM) greatly reduced the light responses of ON-OFF DS ganglion cells. As the light responses slowly returned on washout of cyclothiazide, directional selectivity was clearly reduced although not abolished. In retinas pretreated with SR95531, application of cyclothiazide abolished directional selectivity. Diazoxide (700-1000 microM), another blocker of AMPA receptor desensitization, abolished directional selectivity in ON-OFF DS ganglion cells without the need of adding SR95531 to the bathing solution. It is concluded that, in the rabbit retina, AMPA receptors play an important role in generating directional selectivity in ON-OFF DS ganglion cells. Moreover, excessive activation of AMPA receptors greatly compromises the mechanism for directional selectivity in ON-OFF DS ganglion cells.
先前在兔视网膜上进行的研究表明,阻断AMPA型谷氨酸受体的药物会消除开-关方向选择性(DS)神经节细胞的方向选择性。而AMPA受体激活对这些神经节细胞方向选择性反应的影响尚未得到研究。在本研究中,在体外兔视网膜标本上对开-关DS神经节细胞对移动光条的反应进行了细胞外记录。在对照溶液中,浴加AMPA(7 - 10微摩尔)可消除大多数开-关DS神经节细胞的光反应。洗脱AMPA后,光反应迅速恢复;然而,这些细胞暂时失去了辨别移动光条方向的能力。也就是说,这些细胞对在偏好方向和无效方向上的移动反应相同。用甘氨酸受体拮抗剂士的宁(1 - 2微摩尔)预处理视网膜并不会改变AMPA的作用。另一方面,在用GABA(A)受体拮抗剂SR95531(0.2 - 0.25微摩尔)预处理的视网膜中,AMPA并没有消除开-关DS神经节细胞的光反应,而是通过引发对无效方向上移动的反应消除了这些细胞的方向选择性。这一发现表明,视网膜细胞中AMPA诱导的GABA外流是AMPA抑制光反应的原因。在对照溶液中,应用选择性AMPA受体激动剂(S)-5-氟威拉地丁(2 - 3微摩尔)仅暂时消除了开-关DS神经节细胞的光反应。随着光反应恢复,很明显(S)-5-氟威拉地丁消除了方向选择性。在对照溶液中,用环噻嗪(80 - 100微摩尔)阻断AMPA受体脱敏可大大降低开-关DS神经节细胞的光反应。随着环噻嗪洗脱后光反应缓慢恢复,方向选择性明显降低,尽管并未消除。在用SR95531预处理的视网膜中,应用环噻嗪消除了方向选择性。二氮嗪(700 - 1000微摩尔),另一种AMPA受体脱敏阻滞剂,无需在浴液中添加SR95531即可消除开-关DS神经节细胞的方向选择性。得出的结论是,在兔视网膜中,AMPA受体在开-关DS神经节细胞产生方向选择性方面发挥重要作用。此外,AMPA受体的过度激活极大地损害了开-关DS神经节细胞的方向选择性机制。