|
|
||||||||
Department of Neurophysiology, University of Oslo, N-0317 Oslo, Norway
Hartveit, Espen. Functional organization of cone bipolar cells in the rat retina. J. Neurophysiol. 77: 1716-1730, 1997. The responses of cone bipolar cells in slices of rat retina to ionotropic glutamate receptor agonists were recorded with the whole cell voltage-clamp technique in the presence of 5 mM Co2+ and nominally 0 mM Ca2+ extracellularly. Application of the non-N-methyl-D-aspartate (non-NMDA) receptor agonists kainate and (S)-
-amino-3-hydroxy-5-methyl-4-isoxazolepropionate had a series of effects on cone bipolar cells (types 1-9), and the different cell types could be classified as ON- or OFF-type cells according to which type(s) of responses they displayed. First, direct responses were observed in cell types 1-4 as short-latency inward currents at
70 mV with reversal potentials (Erevs) close to 0 mV, characteristic of nonselective cation channels. Second, some cells, among types 5-9, did not display short-latency inward currents to kainate at
70 mV. Other type 5-8 cells displayed short-latency kainate responses, but the currents could not be reversed (Erev of +40 mV or greater). I suggest that these responses are conveyed to the cone bipolar cells through gap junctions, most likely with AII amacrine cells. The lack of reversal is likely due to a substantial voltage drop across the gap junctions resulting in an inadequate voltage control of AII amacrine cells when the recording pipette is on the cone bipolar cell. Kainate responses recorded directly from AII amacrine cells had Erev ~ 0 mV. Third, long-latency indirect responses selective for chloride ions (Erev ~ chloride equilibrium potential) were observed in many cone bipolar cells during longer-lasting application of kainate. The long-latency response component was suppressed by coapplication of the
-aminobutyric acid-A (GABAA) receptor antagonist picrotoxin and the GABAC receptor antagonist 3-aminopropyl(methyl)phosphinic acid. This long-latency component was absent in axotomized bipolar cells, suggesting that it was due to external Ca2+-independent release of GABA onto the axon terminals of the cone bipolar cells. All kainate-evoked response components were blocked by the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione. Application of NMDA evoked no response in cone bipolar cells. These results suggest that cone bipolar cells types 1-4 are OFF cone bipolar cells, whereas cone bipolar cells types 5-9 are ON cone bipolar cells.
This article has been cited by other articles:
![]() |
M. L. Veruki and E. Hartveit Meclofenamic Acid Blocks Electrical Synapses of Retinal AII Amacrine and ON-Cone Bipolar Cells J Neurophysiol, May 1, 2009; 101(5): 2339 - 2347. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Wassle, C. Puller, F. Muller, and S. Haverkamp Cone Contacts, Mosaics, and Territories of Bipolar Cells in the Mouse Retina J. Neurosci., January 7, 2009; 29(1): 106 - 117. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Oltedal, S. H. Morkve, M. L. Veruki, and E. Hartveit Patch-Clamp Investigations and Compartmental Modeling of Rod Bipolar Axon Terminals in an In Vitro Thin-Slice Preparation of the Mammalian Retina J Neurophysiol, February 1, 2007; 97(2): 1171 - 1187. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-J. Pang, F. Gao, and S. M. Wu Light-evoked current responses in rod bipolar cells, cone depolarizing bipolar cells and AII amacrine cells in dark-adapted mouse retina J. Physiol., August 1, 2004; 558(3): 897 - 912. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-J. Pang, F. Gao, and S. M. Wu Stratum-by-stratum projection of light response attributes by retinal bipolar cells of Ambystoma J. Physiol., July 1, 2004; 558(1): 249 - 262. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. H. Singer and J. S. Diamond Sustained Ca2+ Entry Elicits Transient Postsynaptic Currents at a Retinal Ribbon Synapse J. Neurosci., November 26, 2003; 23(34): 10923 - 10933. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y.-P. Ma, J. Cui, H.-J. Hu, and Z.-H. Pan Mammalian Retinal Bipolar Cells Express Inwardly Rectifying K+ Currents (IKir) With a Different Distribution Than That of Ih J Neurophysiol, November 1, 2003; 90(5): 3479 - 3489. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. L. Veruki and E. Hartveit Electrical Synapses Mediate Signal Transmission in the Rod Pathway of the Mammalian Retina J. Neurosci., December 15, 2002; 22(24): 10558 - 10566. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Billups and D. Attwell Control of intracellular chloride concentration and GABA response polarity in rat retinal ON bipolar cells J. Physiol., November 15, 2002; 545(1): 183 - 198. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z.-H. Pan and H.-J. Hu Voltage-Dependent Na+ Currents in Mammalian Retinal Cone Bipolar Cells J Neurophysiol, November 1, 2000; 84(5): 2564 - 2571. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Gründer, K. Kohler, and E. Guenther Distribution and Developmental Regulation of AMPA Receptor Subunit Proteins in Rat Retina Invest. Ophthalmol. Vis. Sci., October 1, 2000; 41(11): 3600 - 3606. [Abstract] [Full Text] |
||||
![]() |
A. Berntson and W R. Taylor Response characteristics and receptive field widths of on-bipolar cells in the mouse retina J. Physiol., May 1, 2000; 524(3): 879 - 889. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Euler and R. H. Masland Light-Evoked Responses of Bipolar Cells in a Mammalian Retina J Neurophysiol, April 1, 2000; 83(4): 1817 - 1829. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Baier and D. Copenhagen Combining physiology and genetics in the zebrafish retina J. Physiol., April 1, 2000; 524(1): 1 - 1. [Full Text] [PDF] |
||||
![]() |
Z.-H. Pan Differential Expression of High- and Two Types of Low-Voltage-Activated Calcium Currents in Rod and Cone Bipolar Cells of the Rat Retina J Neurophysiol, January 1, 2000; 83(1): 513 - 527. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Johansson, A. Bruun, J. deVente, and B. Ehinger Immunohistochemical Analysis of the Developing Inner Plexiform Layer in Postnatal Rat Retina Invest. Ophthalmol. Vis. Sci., January 1, 2000; 41(1): 305 - 313. [Abstract] [Full Text] |
||||
![]() |
E. Hartveit Reciprocal Synaptic Interactions Between Rod Bipolar Cells and Amacrine Cells in the Rat Retina J Neurophysiol, June 1, 1999; 81(6): 2923 - 2936. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. J. Calkins, Y. Tsukamoto, and P. Sterling Microcircuitry and Mosaic of a Blue-Yellow Ganglion Cell in the Primate Retina J. Neurosci., May 1, 1998; 18(9): 3373 - 3385. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Euler and H. Wassle Different Contributions of GABAA and GABAC Receptors to Rod and Cone Bipolar Cells in a Rat Retinal Slice Preparation J Neurophysiol, March 1, 1998; 79(3): 1384 - 1395. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |