Thoreson W B, Miller R F
Department of Ophthalmology, Gifford Laboratory of Ophthalmology, University of Nebraska Medical Center, Omaha 68198, USA.
J Gen Physiol. 1996 May;107(5):631-42. doi: 10.1085/jgp.107.5.631.
Removal of extracellular Cl- has been shown to suppress light-evoked voltage responses of ON bipolar and horizontal cells, but not photoreceptors or OFF bipolar cells, in the amphibian retina. A substantial amount of experimental evidence has demonstrated that the photoreceptor transmitter, L-glutamate, activates cation, not Cl-, channels in these cells. The mechanism for Cl-free effects was therefore reexamined in a superfused retinal slice preparation from the mudpuppy (Necturus maculosus) using whole-cell voltage and current clamp techniques. In a Cl-free medium, light-evoked currents were maintained in rod and cone photoreceptors but suppressed in horizontal, ON bipolar, and OFF bipolar cells. Changes in input resistance and dark current in bipolar and horizontal cells were consistent with the hypothesis that removal of Cl- suppresses tonic glutamate release from photoreceptors. The persistence of light-evoked voltage responses in OFF bipolar cells, despite the suppression of light-evoked currents, is due to a compensatory increase in input resistance. Focal application of hyperosmotic sucrose to photoreceptor terminals produced currents in bipolar and horizontal cells arising from two sources: (a) evoked glutamate release and (b) direct actions of the hyperosmotic solution on postsynaptic neurons. The inward currents resulting from osmotically evoked release of glutamate in OFF bipolar and horizontal cells were suppressed in a Cl-free medium. For ON bipolar cells, both the direct and evoked components of the hyperosmotic response resulted in outward currents and were thus difficult to separate. However, in some cells, removal of extracellular Cl- suppressed the outward current consistent with a suppression of presynaptic glutamate release. The results of this study suggest that removal of extracellular Cl- suppresses glutamate release from photoreceptor terminals. Thus, it is possible that control of [Cl-] in and around photoreceptors may regulate glutamate release from these cells.
在两栖动物视网膜中,去除细胞外氯离子已被证明可抑制视锥双极细胞和水平细胞的光诱发电压反应,但对光感受器或视锥双极细胞无此作用。大量实验证据表明,光感受器递质L-谷氨酸激活这些细胞中的阳离子通道而非氯离子通道。因此,利用全细胞电压钳和电流钳技术,在泥螈(Necturus maculosus)的视网膜切片灌流标本中重新研究了无氯离子效应的机制。在无氯离子培养基中,光诱发电流在视杆和视锥光感受器中得以维持,但在水平细胞、视锥双极细胞和视锥双极细胞中受到抑制。双极细胞和水平细胞输入电阻和暗电流的变化与去除氯离子抑制光感受器持续性谷氨酸释放的假设一致。尽管光诱发电流受到抑制,但视锥双极细胞中光诱发电压反应的持续存在是由于输入电阻的代偿性增加。向光感受器终末局部施加高渗蔗糖会在双极细胞和水平细胞中产生两种来源的电流:(a)诱发谷氨酸释放,(b)高渗溶液对突触后神经元的直接作用。在无氯离子培养基中,视锥双极细胞和水平细胞中因渗透压诱发的谷氨酸释放所产生的内向电流受到抑制。对于视锥双极细胞,高渗反应的直接成分和诱发成分均导致外向电流,因此难以区分。然而,在一些细胞中,去除细胞外氯离子会抑制外向电流,这与突触前谷氨酸释放受到抑制一致。本研究结果表明,去除细胞外氯离子会抑制光感受器终末的谷氨酸释放。因此,光感受器内外氯离子浓度的控制可能调节这些细胞的谷氨酸释放。