EFFECTS OF NEUROTENSIN ON VISUAL NEURONS IN THE SUPERFICIAL LAMINAE OF THE HAMSTERS SUPERIOR COLLICULUS

Citation
Y. Zhang et al., EFFECTS OF NEUROTENSIN ON VISUAL NEURONS IN THE SUPERFICIAL LAMINAE OF THE HAMSTERS SUPERIOR COLLICULUS, Visual neuroscience, 13(2), 1996, pp. 237-246
Citations number
43
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
09525238
Volume
13
Issue
2
Year of publication
1996
Pages
237 - 246
Database
ISI
SICI code
0952-5238(1996)13:2<237:EONOVN>2.0.ZU;2-1
Abstract
Autoradiography with I-125-neurotensin in normal and enucleated hamste rs was used to define the distribution of receptors for this peptide i n the superficial layers of the superior colliculus (SC). Neurotensin binding sites were densely distributed in the stratum griseum superfic iale (SGS), and results from the enucleated animals indicated that the y were not located on retinal axons. The effects of neurotensin on ind ividual superficial layer cells were tested in single-unit recording e xperiments. Neurotensin was delivered via micropressure ejection durin g 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 neurot ensin 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 f our of these was greater than or equal to 30%). Neurotensin applicatio n also reduced responses to electrical stimulation of either OX or CTX , respectively, to 65.8 +/- 36.5% of control values (range of decremen t 2.6 to 97.4%; 12 neurons showed a weak increment less than or equal to 30%) and 68.0 +/- 38.5% (range of decrement 3.3 to 100%; five cells showed no effect or an increment, in one case greater than or equal t o 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 t he inhibitory effects of neurotensin were presynaptic or postsynaptic, Mg2+ ions were ejected iontophoretically to abolish synaptic response s, and the neurons (n = 16) were activated by iontophoresis of glutama te and then tested with neurotensin. Neurotensin reduced the glutamate -evoked responses to an average 59.3 +/- 37.9% of control values (rang e 2.3 to 92.5%; one cell showed an increment > 30%). This result sugge sts that the site of action of neurotensin is most likely postsynaptic .