Cross-correlated and oscillatory visual responses of superficial-layer and tecto-reticular neurones in cat superior colliculus

2000 ◽  
Vol 131 (1) ◽  
pp. 44-56 ◽  
Author(s):  
A. Chabli ◽  
D. Guitton ◽  
S. Fortin ◽  
S. Molotchnikoff
1993 ◽  
Vol 70 (2) ◽  
pp. 723-732 ◽  
Author(s):  
X. Huang ◽  
R. D. Mooney ◽  
R. W. Rhoades

1. Single-unit recording and iontophoretic techniques were used to test the effects of serotonin (5-HT) on the responses of neurons in the superficial layers (the stratum griseum superficiale and stratum opticum) of the hamster's superior colliculus (SC). 2. Iontophoresis of 5-HT produced a visual response suppression of 40% or greater in 78.1% (n = 50) of 64 neurons tested. 5-HT did not augment the visual responses of any of the cells tested. The average response suppression was 75.3 +/- 21.2% (mean +/- S.D.). 3. Iontophoresis of 5-HT had significantly different effects on activation of SC cells by optic chiasm (OX) and visual cortical (CTX) stimulation. Application of 5-HT suppressed the OX-evoked responses of 96.9% (n = 31) of the 32 SC cells tested by at least 40%, and the average response suppression for all 32 neurons tested was 87.1 +/- 22.5%. Application of 5-HT suppressed the responses of only 35.7% (n = 10) of the 28 cells tested with CTX stimulation by at least 40%. The average response suppression for all 28 cells was 35.3 +/- 38.8%. 4. The effects of 5-HT on the glutamate-evoked responses of SC cells that were synaptically "isolated" by concurrent application of Mg2+ were also evaluated. Application of 5-HT produced a response suppression > or = 40% in 29.7% (n = 19) of the 64 neurons tested under these conditions. The average response suppression for all of the cells tested was 28.4 +/- 35.7%. This effect of 5-HT was significantly weaker than that on visually evoked responses of these neurons. 5. The present results demonstrate that 5-HT markedly depresses the visual responses of most superficial layer SC neurons. They suggest further that much of this effect is mediated by presynaptic inhibition of retinotectal transmission.


1994 ◽  
Vol 11 (6) ◽  
pp. 1163-1173 ◽  
Author(s):  
Richard D. Mooney ◽  
Yi Zhang ◽  
Robert W. Rhoades

AbstractSuperficial layer superior colliculus (SC) neurons were recorded extracellularly with multibarreled recording/ejecting micropipettes. Angiotensin II was delivered via micropressure ejection during visual stimulation (n = 215 cells), or during electrical stimulation of either the optic chiasm (OX; n = 150 cells) or visual cortex (CTX; n = 42 cells). Application of angiotensin II decreased visual responses of SC cells to 43.8% ± 30.7% (mean ± S.D.) and reduced responses to electrical stimulation of the OX and CTX to 58.6% ± 34.1% and 43.8% ± 30.7% of control values, respectively. Angiotensin II enhanced responses by at least 30% in only 6 cells (1.5%). Of the 35 neurons tested with both OX and CTX stimulation, the correlation of evoked response suppression by angiotensin II was highly significant (r = 0.69; P < 0.001). This suggests that the suppressive effects of angiotensin II were common to both pathways. To test whether the inhibitory effects of angiotensin II were presynaptic or postsynaptic, Mg2+ ions were ejected iontophoretically to abolish synaptic responses, and the neurons were activated by iontophoresis of glutamate and then tested with angiotensin II. Angiotensin II reduced the glutamate-evoked responses to an average 29.1% ± 21.1% of control values (n = 9 cells). This suggests that the site of action of angiotensin II is most likely postsynaptic. To identify which receptors were involved in these effects, angiotensin II was ejected concurrently with the AT1 antagonist Losartan (DUP753) or with either of two AT2 antagonists, CGP42112A or PD123177. Losartan antagonized the action of angiotensin II in 65.6% of the cells tested (n = 99) and CGP42112A and PD123177 had antagonistic effects in 58% (n = 65) and 60% (n = 5), respectively. Both classes of antagonists were tested in 29 cells; and there was no significant correlation between their effectiveness. These results suggest that both AT1, and AT2 receptors may independently mediate the suppressive effects of angiotensin II, and that collicular neurons may have either or both receptor subtypes.


1978 ◽  
Vol 41 (1) ◽  
pp. 55-64 ◽  
Author(s):  
B. E. Stein

1. The effects of cortical cooling on the responses of cells to visual, somatic, and acoustic stimuli were studied in the cat superior colliculus (SC). When the visual cortex was cooled, the responses of many visual cells of the SC were depressed or eliminated, but the activity of nonvisual cells remained unchanged. This response depression was found in visual cells located in both superficial and deep laminae and was most pronounced in neurons which were binocular and directionally selective. 2. Cooling somatic and/or auditory cortex had no effect on visual SC cells and, with few exceptions, did not alter the activity of somatic or acoustic cells either. 3. The specificity of visual cortex influences on visual responding in the SC was most apparent in multimodal cells. In trimodal cells, the simultaneous cooling of visual, somatic, and auditory cortex eliminated responses to visual stimuli, but did not affect responses to somatic or acoustic stimuli. Visual responses were returned to the precooling level in both unimodal and multimodal cells by cortical rewarming. 4. The present experiments indicate that despite the organizational parallels among visual, somatic, and acoustic cells of the cat SC, the influences they receive from cortex are non-equivalent. Cortical influences appear to play a more critical role in the responses of visual cells than in the responses of somatic and acoustic cells. These observations raise questions about the functional significance of nonvisual corticotectal systems.


1996 ◽  
Vol 13 (2) ◽  
pp. 237-246 ◽  
Author(s):  
Yi Zhang ◽  
Richard D. ◽  
Carol A. Bennett-Clarke ◽  
Robert W. Rhoades

AbstractAutoradiography with 125I-neurotensin in normal and enucleated hamsters was used to define the distribution of receptors for this peptide in the superficial layers of the superior colliculus (SC). Neurotensin binding sites were densely distributed in the stratum griseum superficiale (SGS), and results from the enucleated animals indicated that they were not located on retinal axons. The effects of neurotensin on individual superficial layer cells were tested in single-unit recording experiments. Neurotensin was delivered via micropressure ejection during visual stimulation (n = 75 cells), or during electrical stimulation of either the optic chiasm (OX; n = 47 cells) or visual cortex (CTX; n = 29 cells). In comparison with control values, application of neurotensin decreased visual responses of all SC cells tested to 54.1 ± 34.9% (mean ± standard deviation; range of decrement 7.5 to 100%; nine cells showed no effect or an increase in visual activity, which for four of these was ≥30%). Neurotensin application also reduced responses to electrical stimulation of either OX or CTX, respectively, to 65.8 ± 36.5% of control values (range of decrement 2.6 to 97.4%; 12 neurons showed a weak increment ≤ 30%) and 68.0 ± 38.5% (range of decrement 3.3 to 100%; five cells showed no effect or an increment, in one case ≥ 30%). Of the 25 neurons tested with both OX and CTX stimulation, the correlation of evoked response suppression by neurotensin was highly significant (r = 0.70; P < 0.001). This suggests that the suppressive effects of neurotensin were common to both pathways. To test whether the inhibitory effects of neurotensin were presynaptic or postsynaptic, Mg2+ ions were ejected iontophoretically to abolish synaptic responses, and the neurons (n = 16) were activated by iontophoresis of glutamate and then tested with neurotensin. Neurotensin reduced the glutamate-evoked responses to an average 59.3 ± 37.9% of control values (range 2.3 to 92.5%; one cell showed an increment >30%). This result suggests that the site of action of neurotensin is most likely postsynaptic.


Author(s):  
Caroline A. Miller ◽  
Laura L. Bruce

The first visual cortical axons arrive in the cat superior colliculus by the time of birth. Adultlike receptive fields develop slowly over several weeks following birth. The developing cortical axons go through a sequence of changes before acquiring their adultlike morphology and function. To determine how these axons interact with neurons in the colliculus, cortico-collicular axons were labeled with biocytin (an anterograde neuronal tracer) and studied with electron microscopy.Deeply anesthetized animals received 200-500 nl injections of biocytin (Sigma; 5% in phosphate buffer) in the lateral suprasylvian visual cortical area. After a 24 hr survival time, the animals were deeply anesthetized and perfused with 0.9% phosphate buffered saline followed by fixation with a solution of 1.25% glutaraldehyde and 1.0% paraformaldehyde in 0.1M phosphate buffer. The brain was sectioned transversely on a vibratome at 50 μm. The tissue was processed immediately to visualize the biocytin.


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