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The effect of GABAergic blockade by picrotoxin on ganglion cells (GC) activity was investigated in perfused dark adapted eyecups of frog (Rana ridibunda). PT had diverse effects on the light responses of GC in contrast to its uniform potentiating effect on the amplitude of the ERG b- and d-wave. In some (n=32) of PT-sensitive ON-OFF GC the ON and OFF responses were changed in a similar manner (both responses were potentiated or both were inhibited), but in the other (n=10) the both responses were changed in a different manner. PT influenced differentially the activity of OFF GC (n=17) as well. It not only potentiated or inhibited their light responses, but changed also the temporal characteristics of the responses. Some tonic cells became phasic ones and in some phasic cells a late component appeared under the influence of PT. In some cases (n=4) the GABAergic blockade changed the apparent cell's type, because of appearance of a new type of response (ON or OFF) non-existing before the blockade. Our results indicate that the GABAergic interneurons are involved in different networks in the inner plexiform layer of frog retina.

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Perfusion of dark adapted frog eyecups with the ON pathway blocker 2-amino-4-phosphonobutyrate (APB) not only abolished the ganglion cells (GCs)' ON responses and the ERG b-wave, but it markedly potentiated the OFF responses of all ON-OFF and phasic OFF GCs and the d-wave amplitude of a simultaneously recorded ERG as well. The blockade of GABA(A) and GABA(C) receptors by picrotoxin eliminated this potentiating effect in 24 out of 41 GCs, although in the rest of the cells it did not produce any change in the APB effect. On the other hand, the d-wave potentiation was preserved during the GABAergic blockade in all experiments. Our results indicate that GABAergic transmission is involved in the inhibition exerted by the ON upon the OFF channel in part of the ON-OFF and phasic OFF GCs in the frog retina. The tonic OFF GCs probably do not receive an inhibitory input from the ON channel, because their light responses were not altered either by APB alone or by APB during blockade of GABA(A) and GABA(C) receptors.

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The expression of GABA receptors (GABARs) was studied in frog and turtle retinae. Using immunocytochemical methods, GABA(A)Rs and GABA(C)Rs were preferentially localized to the inner plexiform layer (IPL). Label in the IPL was punctate indicating a synaptic clustering of GABARs. Distinct, but weaker label was also present in the outer plexiform layer. GABA(A)R and GABA(C)R mediated effects were studied by recording electroretinograms (ERGs) and by the application of specific antagonists. Bicuculline, the GABA(A)R antagonist, produced a significant increase of the ERG. Picrotoxin, when co-applied with saturating doses of bicuculline, caused a further increase of the ERG due to blocking of GABA(C)Rs. The putative GABA(C)R antagonist Imidazole-4-acidic acid (I4AA) failed to antagonize GABA(C)R mediated inhibition and, in contrast, appeared rather as an agonist of GABARs.

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Perfusion with the ON channel blocker 2-amino-4-phosphonobutyrate (APB) of dark adapted frog eyecups not only abolished the ganglion cells' (GC) ON responses and the ERG b-wave, but markedly potentiated the OFF responses of ON-OFF and phasic OFF-GCs and the d-wave amplitude of simultaneously recorded local ERG. Glycinergic blockade by strychnine prevented this potentiating effect in 31 out of 69 GCs, but did not change it at all in the other cells. At the same time the d-wave potentiation was preserved during the glycinergic blockade in all eyecups. The results indicate that glycinergic transmission is involved in the inhibition exerted from ON upon OFF channel in some but not all frog retinal GCs.

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The ERG ON- (b-wave) and OFF-response (d-wave) to differently coloured stimuli was studied using a wide range of stimulus intensities in dark adapted turtle retina. The intensity-response curve of the b-wave showed saturation but that of the d-wave, decline in the high-intensity stimulus range. The curves of the relative spectral sensitivity of the ERG ON- and OFF-response were similar and showed a maximum in the longwave part of the spectrum. GABAergic blockade by 50 mumol L-1 picrotoxin caused an increase of the sensitivity, contrast sensitivity and the amplitude range of both ON- and OFF-responses without narrowing of the response dynamic range. In the range of lower stimulus intensities the ON-responses to blue stimuli and the OFF-responses to red stimuli were affected to a greater extent. An increased ERG b- and d-wave sensitivity was also observed during glycinergic blockade by 50 mumol L-1 strychnine. In the low intensity stimulus range the effect was maximal on the ON-response to blue stimuli and on the OFF-responses to 570 nm stimuli. It was concluded that the GABA- and glycinergic systems in the retina equalize rather than make different the relative spectral sensitivities of the ON- and OFF-responses.

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The aim of the present work was to investigate the role of GABA and glycine, the two main inhibitory neurotransmitters in the retina, in the spectral sensitivity coding under conditions of light adaptation. To study this question, spectral sensitivity curves, based on the turtle ERG responses to stimuli of different wavelengths, were constructed. The spectral sensitivity curves. obtained before and during treatment with picrotoxin (PT), a GABAA antagonist, or with strychnine (ST), a glycine antagonist, were compared. Both PT and ST increased the b- and d-wave absolute sensitivity in a wavelength-dependent manner. PT significantly changed the shape of the b- and d-wave spectral sensitivity curves and the latter lost their peaks. It is concluded that, under conditions of light adaptation, GABA and glycine took part in the formation of the b- and d-wave spectral sensitivity curves, that both of them exerted an effect on the gain and that furthermore,GABA had a well pronounced effect on the tuning of the spectral sensitivity curves.

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The intensity-response (V/log I) function of ERG OFF response (d-wave) in dark and light adapted superfused frog eyecups was investigated before and after blockade of the retinal ON channel by 2-amino-4-phosphonobutyrate (APB). The V/log I function of the dark adapted d-wave had two distinct components, each of them consisting of an ascendent and descendent part. In eyes adapted to mesopic or photopic background the V/log I function had only one component. It was shifted to the right along the intensity axis, had a steeper slope and a higher maximal response amplitude compared with the two components of the dark-adapted V/log I curve. Perfusion with 200 mumol APB markedly increased the d-wave amplitude at all stimulus intensities except for the threshold ones in both dark and light adapted eyes. The position of the V/log I curve was shifted slightly to the left along the intensity axis in dark adapted eyes, but was not changed in light adapted eyes. Thus the adaptational mechanism responsible for changes in the decremental sensitivity with increased background illumination was not altered by APB. The effect of APB was studied also in chromatically adapted eyes, in which the responses were predominantly mediated by one photoreceptor type. The results showed that the potentiating effect of APB on d-wave did not depend on photoreceptor input.

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Superfusion with 200 microM 2-amino-4-phosphonobutyrate (APB) of dark and chromatically adapted frog eyecups caused marked potentiation of the ERG OFF-response (d-wave). Blockade of the glycinergic synapses by strychnine did not change this effect at all. Blockade of the GABAergic synapses by picrotoxin slightly diminished the effect of APB in chromatically-adapted eyes with isolated cones' activity, and did not change it in dark-adapted eyes. The results indicate that the action of APB on ERG OFF-response does not depend significantly on GABAergic and glycinergic neurotransmission in frog retina.

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1. Electroretinogram (ERG) and responses of single ganglion cells to 75 microseconds light flashes, applied at two different backgrounds, were studied. Additionally, a stimulation with long-lasting stimuli (ordinarily 5 sec ON-, 5 sec OFF-) was used. Both white and coloured light stimuli were presented. 2. 150 microM 2-amino-4-phosphonobutyrate (APB) was used to separate OFF- from ON- channels. 3. Before APB application, one or two components in the impulse activity in response to a flash were observed, depending on the type of ganglion cell (ON-, OFF- or ON-OFF). the latency of the first component was 60 msec and the latency of the second one was from 160 to 430 msec on average, at different background conditions. APB abolished the first component and enhanced the second one. 4. By means of APB, two components were shown to exist in the main positive wave of the flash ERG. APB abolished the first component and did not influence or enhance the second one. 5. The data obtained show that both ON- and OFF- channels take part in the generation of the frog retinal responses to brief stimuli.

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1. Electroretinogram (ERG) and responses of single ganglion cells to 75 microseconds light flashes, presented on two different backgrounds, were studied. Additionally, stimulation with long lasting stimuli (ordinarily 5 sec ON-, 15 sec OFF-) was used. 2. 2-amino-4-phosphonobutyrate (APB) at a concentration of 450 microM on average was used to separate OFF- from ON- channels. It is known, that in other species APB selectively blocks the activity of ON- channel only. 3. The existence of APB- sensitive membrane receptors was demonstrated in the turtle retina. As in other species, APB abolished the ERG b-wave and enhanced the d-wave, when long lasting stimulation was used. 4. By means of APB, two components were shown to exist in the ERG positive wave in response to a flash. APB abolished the first component and did not influence or enhanced the second one. 5. By means of APB, one or two components in the impulse activity in response to flash were demonstrated, depending on the type of ganglion cell (ON-, OFF- or ON-OFF). The latency of the first component was 70 msec and the latency of the second one 210 msec on average. APB abolished the first component, and enhanced the second one. 6. The data obtained show that both ON- and OFF- channels take part in the generation of the turtle retinal responses to brief stimuli. 7. Based on the results obtained, some peculiarities of the network organization of the ganglion cells' receptive fields are discussed.

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A comparative study was made of the ERG b- and d-wave intensity-response functions before and after GABAergic blockade by means of 0.4 mmol l-1 picrotoxin. A wide range of background intensities, including part of the high photopic range, were used. The intensity-response functions of both the ERG waves fitted well to the Michaelis-Menten equation (V/Vmax = In/(In + sigma n). A sigma-value decrease and a Vmax and n increase were observed after picrotoxin treatment. The analysis of the intensity-response functions shows that, under a wide range of backgrounds, the GABAergic neurons influence the ON- and OFF-response in the distal retina in a similar way. They decrease the gain and the contrast gain of the b- and d-wave generating neuronal mechanisms and widen the intensity span of their responses under given background illumination. The GABAergic system is involved also in response 'scaling' in the ON- and OFF-channels in the distal retina. A very important effect in this respect seems to be the equalization of the range of the responses to increment stimuli under different backgrounds.

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The effect of background intensity on the spatial summation of rectangular stimuli of varying length and width was studied in human psychophysical experiments and compared with the known effects of light adaptation on the spatial summation of circular stimuli. Both the detection threshold and the threshold of orientation identification were measured. In agreement with previous data, summation was more efficient along the line stimulus than across it. This asymmetry was found to exist at all adaptation levels studied (1-1000 trolands). The adaptation level affected both length and width summation; the change in the length of summation was twice as great as the change in the diameter of summation with circular stimuli. Orientation selectivity was reduced for short lines presented on a dim background. The results suggest the existence of mechanisms of light adaptation at the level of cortical orientation-selective units.

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The responses of visual cells in the 17th cortical area to stimulation with bright strips of various width were studied in immobilized cats. The impulse activity was counted in successive time intervals from the beginning of the stimulation and plotted as a function of the stimulus area. Significant differences in time course of the inhibitory process were found between the cortical and geniculate levels. The lag of inhibition behind excitation was much smaller in the cortex than in the geniculate body. Similar data were obtained from cortical response elicited by simultaneous or successive application of two bright strips, one in the excitatory centre and the second in the inhibitory zone of the receptive field. If both strips were placed in the excitatory zone of the field, inhibition depended on the order of illumination of the strips. When this order coincided with the direction in which a moving stimulus had a maximal effect, a large facilitation of the response to the second stimulus was obtained. When the order of presentation was reversed, a strong inhibition appeared. This selectivity of the inhibitory mechanism was attenuated at the periphery of the field where any succession of the stimuli elicited an inhibitory effect.

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