scholarly journals On the excitatory post-synaptic potential evoked by stimulation of the optic tract in the rat lateral geniculate nucleus.

1987 ◽  
Vol 384 (1) ◽  
pp. 603-618 ◽  
Author(s):  
V Crunelli ◽  
J S Kelly ◽  
N Leresche ◽  
M Pirchio
2003 ◽  
Vol 90 (2) ◽  
pp. 1063-1070 ◽  
Author(s):  
Jokūbas Ziburkus ◽  
Fu-Sun Lo ◽  
William Guido

Using intracellular recordings in an isolated (in vitro) brain stem preparation, we examined the inhibitory postsynaptic responses of developing neurons in the dorsal lateral geniculate nucleus (LGN) of the rat. As early as postnatal day (P) 1–2, 31% of all excitatory postsynaptic (EPSP) activity evoked by electrical stimulation of the optic tract was followed by inhibitory postsynaptic potentials (IPSPs). By P5, 98% of all retinally evoked EPSPs were followed by IPSP activity. During the first postnatal week, IPSPs were mediated largely by GABAA receptors. Additional GABAB-mediated IPSPs emerged at P3–4 but were not prevalent until after the first postnatal week. Experiments involving the separate stimulation of each optic nerve indicated that developing LGN cells were binocularly innervated. At P11–14, it was common to evoke EPSP/IPSP pairs by stimulating either the contralateral or ipsilateral optic nerve. During the third postnatal week, binocular excitatory responses were encountered far less frequently. However, a number of cells still maintained a binocular inhibitory response. These results provide insight about the ontogeny and nature of postsynaptic inhibitory activity in the LGN during the period of retinogeniculate axon segregation.


2020 ◽  
Vol 124 (2) ◽  
pp. 404-417 ◽  
Author(s):  
Peter W. Campbell ◽  
Gubbi Govindaiah ◽  
Sean P. Masterson ◽  
Martha E. Bickford ◽  
William Guido

The thalamic reticular nucleus (TRN) modulates thalamocortical transmission through inhibition. In mouse, TRN terminals in the dorsal lateral geniculate nucleus (dLGN) form synapses with relay neurons but not interneurons. Stimulation of TRN terminals in dLGN leads to a frequency-dependent form of inhibition, with higher rates of stimulation leading to a greater suppression of spike firing. Thus, TRN inhibition appears more dynamic than previously recognized, having a graded rather than an all-or-none impact on thalamocortical transmission.


2017 ◽  
Vol 34 ◽  
Author(s):  
CHARLES L. COX ◽  
JOSEPH A. BEATTY

AbstractIntrinsic interneurons within the dorsal lateral geniculate nucleus (dLGN) provide a feed-forward inhibitory pathway for afferent visual information originating from the retina. These interneurons are unique because in addition to traditional axodendritic output onto thalamocortical neurons, these interneurons have presynaptic dendrites that form dendrodendritic synapses onto thalamocortical neurons as well. These presynaptic dendrites, termed F2 terminals, are tightly coupled to the retinogeniculate afferents that synapse onto thalamocortical relay neurons. Retinogeniculate stimulation of F2 terminals can occur through the activation of ionotropic and/or metabotropic glutamate receptors. The stimulation of ionotropic glutamate receptors can occur with single stimuli and produces a short-lasting inhibition of the thalamocortical neuron. By contrast, activation of metabotropic glutamate receptors requires tetanic activation and results in longer-lasting inhibition in the thalamocortical neuron. The F2 terminals are predominantly localized to the distal dendrites of interneurons, and the excitation and output of F2 terminals can occur independent of somatic activity within the interneuron thereby allowing these F2 terminals to serve as independent processors, giving rise to focal inhibition. By contrast, strong transient depolarizations at the soma can initiate a backpropagating calcium-mediated potential that invades the dendritic arbor activating F2 terminals and leading to a global form of inhibition. These distinct types of output, focal versus global, could play an important role in the temporal and spatial roles of inhibition that in turn impacts thalamocortical information processing.


1987 ◽  
Vol 35 (2) ◽  
pp. 115 ◽  
Author(s):  
AM Harman ◽  
DP Crewther ◽  
JE Nelson ◽  
SG Crewther

The retinal projections of the northern native cat, Dasyurus hallucatus, were studied by the anterograde transport of tritiated proline and by autoradiography. Seven regions in the brain were found to receive direct retinal projections: (1) the suprachiasmatic nucleus; (2) the dorsal lateral geniculate nucleus; (3) the ventral lateral geniculate nucleus; (4) the lateral posterior nucleus; (5) the nuclei of the accessory optic tract; (6) the pretectal nuclei; (7) the superior colliculus. All nuclei studied received a bilateral retinal projection except the medial terminal nucleus of the accessory optic system, in which only a contralateral input was found. The contralateral eye had a greater input in all cases. As with the related species, Dasyurus viverrinus, there is extensive binocular overlap in the dorsal lateral geniculate nucleus (LGNd). In the LGNd contralateral to the injected eye, the autoradiographs show four contralateral terminal bands occupying most of the nucleus. The axonal terminations in the ipsilateral LGNd are more diffuse but show a faint lamination pattern of four bands. The ventral portion of the LGNd receives only contralateral retinal input, and therefore probably represents the monocular visual field. The other principal termination of the optic nerve, the superior colliculus, has a predominantly contralateral input to both sublayers of the stratum griseum superficiale. However, the ipsilateral fibres terminate only in patches in the more inferior sublayer.


1986 ◽  
Vol 56 (5) ◽  
pp. 1297-1309 ◽  
Author(s):  
Y. Kayama ◽  
M. Takagi ◽  
T. Ogawa

The effect of stimulation of the laterodorsal tegmental nucleus (LDT) on the activity of single neurons in the dorsal lateral geniculate nucleus was studied in rats anesthetized with urethan. The LDT is the largest aggregation of cholinergic neurons in the brain stem that project to the thalamus, and in the rat is sufficiently compact to permit its localized stimulation. Position of stimulating electrodes was confirmed on histological sections processed with NADPH-diaphorase histochemistry, which in the rat brain stem selectively stains cholinergic neurons. Repetitive stimulation of the LDT at 200 Hz increased the firing rate of substantially all geniculate relay neurons and weakly depressed the activity of intrinsic interneurons. These effects usually occurred within several hundred milliseconds after the onset of stimulation and began to fade within a few seconds, despite continuing stimulation. The excitatory effects on relay neurons were blocked by scopolamine applied ionophoretically or intravenously, but not by noradrenergic antagonists, suggesting the cholinergic nature of LDT-induced excitation. During LDT stimulation the number of spikes evoked by photic stimulation of the receptive field of relay neurons usually increased, but it remained unchanged in a few cases. The increase was due to simple enhancement of photic responses or due to conversion of phasic type responses to tonic ones. As to the balance of background activity and photic responses, the effects of LDT stimulation varied from neuron to neuron. Even in a given neuron, the effects varied depending on its excitability level or the nature of the photic stimulation. These results show that the cholinergic projection from the LDT may be involved in the ascending reticular activating system, although the functional significance of the activating system in visual information processing in the geniculate nucleus remains to be clarified.


2009 ◽  
Vol 101 (4) ◽  
pp. 1761-1773 ◽  
Author(s):  
G. Govindaiah ◽  
Charles L. Cox

The ventral lateral geniculate nucleus (vLGN) has been implicated in numerous functions including circadian rhythms, brightness discrimination, pupillary light reflex, and other visuomotor functions. The contribution of inhibitory mechanisms in the regulation of vLGN neuron excitability remains unexplored. We examined the actions of metabotropic glutamate receptor (mGluR) activation on the intrinsic excitability and inhibitory synaptic transmission in different lamina of vLGN. Activation of mGluRs exerts distinct pre- and postsynaptic actions in vLGN neurons. In the lateral magnocellular subdivision of vLGN (vLGNl), the general mGluR agonist (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (ACPD) enhanced the frequency of GABAA receptor-mediated spontaneous inhibitory postsynaptic currents (sIPSC) that persisted in the presence of sodium channel blocker tetrodotoxin (TTX) in a subpopulation of neurons (TTX insensitive). This increase is attributed to the increased output of dendritic GABA release from vLGN interneurons. In contrast, in the medial subdivision of vLGN (vLGNm), the mGluR agonist-mediated increase in sIPSC frequency was completely blocked by TTX. The selective Group I mGluR agonist ( RS)-3,5-dihydroxyphenylglycine (DHPG) increased sIPSC frequency, whereas the selective Group II mGluR agonist (2 R, 4 R)-4-aminopyrrolidine-2,4-dicarboxylate (APDC) significantly decreased sIPSC frequency in vLGNl neurons. Optic tract stimulation also produced an mGluR-dependent increase in sIPSC frequency in vLGNl neurons. In contrast, we were unable to synaptically evoke alterations in sIPSC activity in vLGNm neurons. In addition to these presynaptic actions, DHPG depolarized both vLGNl and vLGNm neurons. In vLGN interneurons, mGluR activation produced opposing actions: APDC hyperpolarized the membrane potential, whereas DHPG produced a membrane depolarization. The present findings demonstrate diverse actions of mGluRs on vLGN neurons localized within different vLGN lamina. Considering these different lamina are coupled with distinct functional roles, thus these diverse actions may be involved in distinctive forms of visual and visuomotor information processing.


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