Rabl Katalin, Bryson Eric J, Thoreson Wallace B
Department of Ophthalmology, University of Nebraska Medical Center, Omaha 68198-5540, USA.
Vis Neurosci. 2003 Sep-Oct;20(5):557-66. doi: 10.1017/s0952523803205095.
We found that L-glutamate (L-Glu) inhibits L-type Ca2+ currents (ICa) in rod photoreceptors. This inhibition was studied in isolated rods or rods in retinal slices from tiger salamander using perforated patch whole cell recordings and Cl(-)-imaging techniques. Application of L-Glu inhibited ICa by approximately 20% at 0.1 mM and approximately 35% at 1 mM. L-Glu also produced an inward current that reversed around ECl. The metabotropic glutamate receptor (mGluR) agonists t-ADA (Group I), DCG-IV (Group II), and L-AP4 (Group III) had no effect on ICa. However, the glutamate transport inhibitor, TBOA (0.1 mM), prevented L-Glu from inhibiting ICa. D-aspartate (D-Asp), a glutamate transporter substrate, also inhibited ICa with significantly more inhibition at 1 mM than 0.1 mM. Using Cl imaging, L-Glu (0.1-1 mM) and D-Asp (0.1-1 mM) were found to stimulate a Cl- efflux from terminals of isolated rods whereas the ionotropic glutamate receptor agonists NMDA, AMPA, and kainate and the mGluR agonist, 1S,3R-ACPD, did not. Glutamate-evoked Cl- effluxes were blocked by the glutamate transport inhibitors TBOA and DHKA. Cl- efflux inhibits Ca2+ channel activity in rod terminals (Thoreson et al. (2000), Visual Neuroscience 17, 197). Consistent with the possibility that glutamate-evoked Cl- efflux may play a role in the inhibition, reducing intraterminal Cl- prevented L-Glu from inhibiting ICa. In summary, the results indicate that activation of glutamate transporters inhibits ICa in rods possibly as a consequence of Cl- efflux. The neurotransmitter L-Glu released from rod terminals might thus provide a negative feedback signal to inhibit further L-Glu release.
我们发现L-谷氨酸(L-Glu)可抑制视杆光感受器中的L型Ca2+电流(ICa)。利用穿孔膜片全细胞记录和Cl(-)成像技术,在分离的视杆细胞或虎螈视网膜切片中的视杆细胞中研究了这种抑制作用。施加0.1 mM的L-Glu可使ICa抑制约20%,施加1 mM时可抑制约35%。L-Glu还产生了一种在ECl附近反转的内向电流。代谢型谷氨酸受体(mGluR)激动剂t-ADA(I组)、DCG-IV(II组)和L-AP4(III组)对ICa无影响。然而,谷氨酸转运体抑制剂TBOA(0.1 mM)可阻止L-Glu抑制ICa。谷氨酸转运体底物D-天冬氨酸(D-Asp)也可抑制ICa,1 mM时的抑制作用明显强于0.1 mM。通过Cl成像发现,L-Glu(0.1 - 1 mM)和D-Asp(0.1 - 1 mM)可刺激分离视杆细胞终末的Cl-外流,而离子型谷氨酸受体激动剂NMDA、AMPA和海人酸以及mGluR激动剂1S,3R-ACPD则不能。谷氨酸诱发的Cl-外流被谷氨酸转运体抑制剂TBOA和DHKA阻断。Cl-外流抑制视杆细胞终末的Ca2+通道活性(Thoreson等人,(2000年),《视觉神经科学》17,197)。与谷氨酸诱发的Cl-外流可能在抑制中起作用的可能性一致,降低终末内的Cl-可阻止L-Glu抑制ICa。总之,结果表明谷氨酸转运体的激活可能通过Cl-外流抑制视杆细胞中的ICa。因此,从视杆细胞终末释放的神经递质L-Glu可能提供一个负反馈信号来抑制进一步的L-Glu释放。