Activation of the sigma receptor 1 modulates AMPA receptor-mediated light-evoked excitatory postsynaptic currents in rat retinal ganglion cells

Neuroscience ◽  
2016 ◽  
Vol 332 ◽  
pp. 53-60 ◽  
Author(s):  
Lei-Lei Liu ◽  
Qin-Qin Deng ◽  
Shi-Jun Weng ◽  
Xiong-Li Yang ◽  
Yong-Mei Zhong
2006 ◽  
Vol 56 (4) ◽  
pp. 427-434 ◽  
Author(s):  
Seong-Ah Jeong ◽  
Oh-Ju Kwon ◽  
Jea-Young Lee ◽  
Tae-Jin Kim ◽  
Chang-Jin Jeon

1998 ◽  
Vol 80 (4) ◽  
pp. 1752-1764 ◽  
Author(s):  
Fan Gao ◽  
Samuel M. Wu

Gao, Fan and Samuel M. Wu. Characterization of spontaneous inhibitory synaptic currents in salamander retinal ganglion cells. J. Neurophysiol. 80: 1752–1764, 1998. Spontaneous and light-evoked postsynaptic currents (sPSCs and lePSCs, respectively) in retinal ganglion cells of the larval tiger salamander were recorded under voltage-clamp conditions from living retinal slices. The focus of this study is to characterize the spontaneous inhibitory PSCs (sIPSCs) and their contribution to the light-evoked inhibitory PSCs (leIPSCs) in on-off ganglion cells. sIPSCs were isolated from spontaneous excitatory PSCs (sEPSCs) by application of 10 μM 6,7-dinitroquinoxaline-2,3-dione (DNQX) + 50 μM 2-amino-5-phosphonopentanoic acid (AP5). In ∼70% of on-off ganglion cells, bicuculline (or picrotoxin) completely blocks sIPSCs, suggesting all sIPSCs in these cells are mediated by GABAergic synaptic vesicles and γ-aminobutyric acid-A (GABAA) receptors (GABAergic sIPSCs, or GABAsIPSCs). In the remaining 30% of on-off ganglion cells, bicuculline (or picrotoxin) blocks 70–98% of the sIPSCs, and the remaining 2–30% are blocked by strychnine (glycinergic sIPSCs, or GLYsIPSCs). GABAsIPSCs occur randomly with an exponentially distributed interval probability density function, and they persist without noticeable rundown over time. The GABAsIPSC frequency is greatly reduced by cobalt, consistent with the idea that they are largely mediated by calcium-dependent vesicular release. GABAsIPSCs in DNQX + AP5 are tetrodotoxin (TTX) insensitive, suggesting that amacrine cells that release GABA under these conditions do not generate spontaneous action potentials. The average GABAsIPSCs exhibited linear current-voltage relation with a reversal potential near the chloride equilibrium potential, and an average peak conductance of 319.67 ± 252.83 (SD) pS. For GLYsIPSCs, the average peak conductance increase is 301.68 ± 94.34 pS. These parameters are of the same order of magnitude as those measured in inhibitory miniature postsynaptic currents (mIPSCs) associated with single synaptic vesicles in the CNS. The amplitude histograms of GABAsIPSCs did not exhibit multiple peaks, suggesting that the larger events are not discrete multiples of elementary events (or quanta). We propose that each GABAsIPSC or GLYsIPSC in retinal ganglion cells is mediated by a single or synchronized multiple of synaptic vesicles with variable neurotransmitter contents. In a sample of 16 on-off ganglion cells, the average peak leIPSC (held at 0 mV) at the light onset is 509.0 ± 233.85 pA and that at the light offset is 529.0 ± 339.88 pA. The approximate number of GABAsIPSCs and GLYsIPSCs required to generate the average light responses, calculated by the ratio of the charge (area under current traces) of the leIPSCs to that of the average single sIPSCs, is 118 ± 52 for the light onset, and 132 ± 76 for the light offset.


2015 ◽  
Vol 132 ◽  
pp. 136-150 ◽  
Author(s):  
Yong H. Park ◽  
Brett H. Mueller ◽  
Nolan R. McGrady ◽  
Hai-Ying Ma ◽  
Thomas Yorio

2007 ◽  
Vol 48 (10) ◽  
pp. 4785 ◽  
Author(s):  
Ying Dun ◽  
Muthusamy Thangaraju ◽  
Puttur Prasad ◽  
Vadivel Ganapathy ◽  
Sylvia B. Smith

2002 ◽  
Vol 107 (2) ◽  
pp. 97-107 ◽  
Author(s):  
M Shamsul Ola ◽  
Pamela Moore ◽  
Dennis Maddox ◽  
Amira El-Sherbeny ◽  
Wei Huang ◽  
...  

Neuroscience ◽  
2011 ◽  
Vol 177 ◽  
pp. 12-22 ◽  
Author(s):  
X.-J. Zhang ◽  
L.-L. Liu ◽  
S.-X. Jiang ◽  
Y.-M. Zhong ◽  
X.-L. Yang

2000 ◽  
Vol 83 (6) ◽  
pp. 3217-3229 ◽  
Author(s):  
Ethan D. Cohen

The excitatory amino acid receptor (EAAR) types involved in the generation of light-evoked excitatory postsynaptic currents (EPSCs) were examined in X-type retinal ganglion cells. Using isolated and sliced preparations of cat and ferret retina, the light-evoked EPSCs of X cells were isolated by adding picrotoxin and strychnine to the bath to remove synaptic inhibition. N-methyl-d-aspartate (NMDA) receptors contribute significantly to the light-evoked EPSCs of on- andoff-X cells at many different holding potentials. An NMDA receptor contribution to the EPSCs was observable when retinal synaptic inhibition was either normally present or pharmacologically blocked. NMDA receptors formed 80% of the peak light-evoked EPSC at a holding potential of −40 mV; however, even at −80 mV, 20% of the light-evoked EPSC was NMDA-mediated. An α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptor–mediated component to the light-evoked EPSCs predominated at a holding potential of −80 mV. The light-evoked EPSC was blocked by the AMPA receptor-selective antagonist GYKI52466 (50–100 μM). The AMPA receptor–mediated EPSC component had a linear current-voltage relation. AMPA receptors form the main non-NMDA EAAR current on bothon- and off- X ganglion cell dendrites. When synaptic transmission was blocked by the addition of Cd2+ to the Ringer, application of kainate directly to ganglion cells evoked excitatory currents that were strongly blocked by GYKI52466. Experiments using selective EAAR modulators showed the AMPA receptor–selective modulator cyclothiazide potentiated glutamate-evoked currents on X cells, while the kainate receptor–selective modulator concanavalin A (ConA) had no effect on kainate-evoked currents. Whereas the present study confirms the general notion that AMPA EAAR-mediated currents are transient and NMDA receptor–mediated currents are sustained, current-voltage relations of the light-evoked EPSC at different time points showed the contributions of these two receptor types significantly overlap. Both NMDA and AMPA EAARs can transmit transient and sustained visual signals in X ganglion cells, suggesting that much signal shaping occurs presynaptically in bipolar cells.


2006 ◽  
Vol 50 (3) ◽  
pp. 217-223 ◽  
Author(s):  
Atsuya Miki ◽  
Yasumasa Otori ◽  
Masaki Okada ◽  
Yasuo Tano

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