Distal equivalent dendrite
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horizontal cell?
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Gaba
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The pharmacologically isolated, GABAergic synaptic currents in bipolar cells were long-lasting (compared with those in in ganglion cells, which are relatively brief). The GABAA receptor component of the bipolar cell response was relatively brief compared with the GABAC receptor component (Lukasiewicz PD and Shields CR, 19986 ). In retinal bipolar cells of bullfrog, both axon terminals and dendrites showed high GABA sensitivity mediated by both GABA(A) and GABA(C) receptors. GABA(A) and GABA(C) receptors may play different roles in the outer and inner retina and the differential complements of the two receptors on OFF and ON BCs may be closely related to physiological functions of these cells (Du JL and Yang XL, 20004 ). GABA(A) receptors mediate GABAergic inhibition on bipolar cell dendrites in the OPL, that GABA(A) and GABA(C) receptors mediate inhibition on axon terminals in the IPL, and that the GABA(C):GABA(A) on the terminals may tune the response characteristics of the bipolar cell (Shields CR et al, 20005 ). |
From photoreceptor
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Glutamate
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The balance between synaptic (glutamatergic) and non-synaptic conductance indicates that the synapse will not shunt the cell and the conductance ratio serves to maximize incremental gain at the photoreceptor to ON bipolar synapse.(Tian N and Slaughter MM, 19957 ). Three types of glutamate receptors for 1) cone-activated receptors of HCs; 2) cone-activated receptors of OFF-BPs; and 3) rod-activated receptors found in HCs and BPs (Kim HG and Miller RF, 19938 ). Response to glutamate in isolated bipolar cells(Attwell D et al, 19879 ). |
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Soma
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Glycine
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Response of isolated bipolar cells to glycine (Attwell D et al, 19879 ). |
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Gaba
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GABA and glycine conductances of isolated bipolar cells (Attwell D et al, 19879 ). |
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NMDA
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In Salamander (Matsui K et al, 199815 ). |
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I L high threshold
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(Straiker A et al, 199918 ). |
I Calcium
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Voltage-dependent Ca currents are seen in isolated bipolar cells (Lasater EM, 198826 ). In gold fish retinal bipolar cells, four currents are observed: Ca currents, voltage- and calcium-dependent K currents, and Ih current (Kaneko A and Tachibana M, 198527 ). In mouse retinal bipolar cells, T-type Ca currents were recorded in soma, while L-type currents were recorded from axonal terminal (Satoh H et al, 199819 ). |
I Potassium
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A slowly activating, outward rectifying potassium current is present in subpopulation of isolated bipolar cells (Lasater EM, 198826 ). In gold fish retinal bipolar cells, four currents are observed: Ca currents, voltage- and calcium-dependent K currents, and Ih current (Kaneko A and Tachibana M, 198527 ). |
I K,Ca
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Ca-dependent potassium currents are seen in dissociated cells (Lasater EM, 198826 ). In gold fish retinal bipolar cells, four currents are observed: Ca currents, voltage- and calcium-dependent K currents, and Ih current (Kaneko A and Tachibana M, 198527 ). |
I h
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In gold fish retinal bipolar cells, four currents are observed: Ca currents, voltage- and calcium-dependent K currents, and Ih current (Kaneko A and Tachibana M, 198527 ). |
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Axon terminal
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Gaba
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GABA(A) and GABA(C) receptor-mediated currents were observed in the isolated terminal (Pan ZH, 20011 ). Isolated rod-dominant on-center bipolar cells respond to GABA, the highest sensitivity of which being located at the axon terminal (Tachibana M and Kaneko A, 19872 ). Zn2+ modulates the inhibitory interaction between amacrine and bipolar cells, particularly that mediated by the GABA(C) receptor(Kaneda M et al, 20003 ). In retinal bipolar cells of bullfrog, both axon terminals and dendrites showed high GABA sensitivity mediated by both GABA(A) and GABA(C) receptors. GABA(A) and GABA(C) receptors may play different roles in the outer and inner retina and the differential complements of the two receptors on OFF and ON BCs may be closely related to physiological functions of these cells (Du JL and Yang XL, 20004 ). GABA(A) receptors mediate GABAergic inhibition on bipolar cell dendrites in the OPL, that GABA(A) and GABA(C) receptors mediate inhibition on axon terminals in the IPL, and that the GABA(C):GABA(A) on the terminals may tune the response characteristics of the bipolar cell (Shields CR et al, 20005 ). |
presynaptic receptors
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mGluR
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Group III mGluRs mediate a direct suppression of bipolar cell transmitter release, through a mechanism of presynaptic autoreceptors (Awatramani GB and Slaughter MM, 200110 ). |
amacrine
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Glycine
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Depolarization induced transient outward currents that resembled IPSCs and were blocked by GABA and glycine receptor antagonists, suggesting that they arise from activation of amacrine feedback synapses (Protti DA and Llano I, 199811 ). The OFF cone bipolar cells seem dominated by glycinergic input and the ON cone bipolar and rod bipolar cells by GABAergic input (Grünert U, 200012 ). |
amacrine
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Gaba
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The rod-dominant ON-type bipolar cells and some bipolar cells with a small axon terminal receive negative feedback inputs from GABAergic amacrine cells (Tachibana M and Kaneko A, 198813 ). Depolarization induced transient outward currents that resembled IPSCs and were blocked by GABA and glycine receptor antagonists, suggesting that they arise from activation of amacrine feedback synapses (Protti DA and Llano I, 199811 ). The OFF cone bipolar cells seem dominated by glycinergic input and the ON cone bipolar and rod bipolar cells by GABAergic input (Grünert U, 200012 ). The responses of most retinal ganglion cells are transient because bipolar-to-ganglion cell transmission is truncated after 150 msec by a feedback inhibition to bipolar cell terminals from GABAergic amacrine cells; the feedback inhibition itself must be delayed by approximately 150 msec to allow the initial bipolar-ganglion cell transmission. One source of the delay appears to be glycinergic amacrine cells to GABAergic amacrine cells to bipolar cell terminals. Results suggest that, after a light flash, a population of glycinergic amacrine cells responds first, inhibiting a population of GABAergic amacrine cells for approximately 150 msec. The GABAergic amacrine cells feed back to bipolar terminals, only after the 150 msec delay, thus allowing the bipolar terminals to excite ganglion cells for the first 150 msec. (Roska B et al, 199814 ). |
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I T low threshold
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Low-voltage-activated (LVA) and high-voltage-activated (HVA) Ca2+ currents were observed in the isolated rod bipolar cell terminal recordings(Pan ZH, 20011 ). T-type calcium current recorded in bipolar cells in slice in mouse (de la Villa P et al, 199816 ). (Hartveit E, 199917 ). |
I L high threshold
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High-voltage-activated (HVA) and low-voltage-activated (LVA) Ca2+ currents were observed in the isolated rod bipolar cell terminal recordings(Pan ZH, 20011 ). Whole-cell patch-clamp recording of ICa from presynaptic boutons are comparable to that obtained from somatic recordings, but elevation of intracellular Ca is restricted to the presynaptic terminals, with no somatic or axonal changes observed (Protti DA and Llano I, 199811 ). L-type ICa was found only in cells that retained axon terminals ramifying in the inner plexiform layer(de la Villa P et al, 199816 ). (Hartveit E, 199917 ). |
I Calcium
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Activation of the Ca2+ current by depolarization as short as 15 ms in a single bipolar cell evokes the glutamatergic postsynaptic currents, of both both NMDA and non-NMDA types, in the Ganglion cells (Matsui K et al, 199815 ). In mouse retinal bipolar cells, T-type Ca currents were recorded in soma, while L-type currents were recorded from axonal terminal (Satoh H et al, 199819 ). |
I K,Ca
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Ca2+ -activated K+ current at presynaptic terminals of goldfish retinal bipolar cells (Sakaba T et al, 199720 ). |
I Cl,Ca
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Ca -dependent Chloride current at the presynaptic terminals of goldfish retinal bipolar cells (Okada T et al, 199521 ). |
I CNG
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(Shiells RA and Falk G, 199022 ). (Nawy S and Jahr CE, 199023 ). (Nawy S and Jahr CE, 199124 ). (Shiells RA and Falk G, 199225 ). |
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Glutamate
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activate both NMDA and nonNMDA receptors of ganglion cells
| Activation of the Ca2+ current by depolarization as short as 15 ms in a single bipolar cell evokes the glutamatergic postsynaptic currents, of both both NMDA and non-NMDA types, in the Ganglion cells (Matsui K et al, 199815 ). (Hartveit E, 199917 ). |
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