JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 73: 2470-2485, 1995;
0022-3077/95 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ando, N.
Right arrow Articles by Shinoda, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ando, N.
Right arrow Articles by Shinoda, Y.

Journal of Neurophysiology, Vol 73, Issue 6 2470-2485, Copyright © 1995 by APS


ARTICLES

Relative contributions of thalamic reticular nucleus neurons and intrinsic interneurons to inhibition of thalamic neurons projecting to the motor cortex

N. Ando, Y. Izawa and Y. Shinoda
Department of Physiology, School of Medicine, Tokyo Medical and Dental University, Japan.

1. Intracellular responses to stimulation of the cerebral cortex (Cx) and cerebellum were analyzed in thalamocortical neurons (TCNs) in the ventroanterior-ventrolateral (VA-VL) complex of the thalamus and neurons in the thalamic reticular nuclei (RNs) of anesthetized cats, and the contribution of reticular nucleus neurons (RNNs) and thalamic interneurons (TINs) to cerebral and cerebellar inhibition of TCNs was determined. 2. Single TCNs projecting to area 4 or 6 received convergent monosynaptic excitatory and disynaptic inhibitory inputs from both the dentate nucleus (DN) and the interpositus nucleus (IN). These TCNs also received monosynaptic excitatory postsynaptic potentials (EPSPs) and disynaptic inhibitory postsynaptic potentials (IPSPs) from the pericruciate cortex (areas 4 and 6). Each TCN received the strongest excitatory and inhibitory inputs from the cortical area to which that TCN projected, and weaker inhibitory inputs from adjacent cortical areas. 3. RNNs were identified morphologically by intracellular injection of horseradish peroxidase (HRP). Stimulation of the brachium conjunctivum (BC) evoked disynaptic EPSPs with a long decay phase in RNNs in the anterior ventrolateral part of the RN. Single RNNs received convergent disynaptic excitatory inputs from both the DNA and the IN. Stimulation of the Cx produced monosynaptic long-lasting EPSPs with two different latencies in these RNNs: early EPSPs with latencies of 0.9-2.1 ms and late EPSPs with latencies of 1.8-3.5 ms. Collision experiments with BC- and Cx-evoked EPSPs in RNNs indicated that BC-evoked disynaptic EPSPs and Cx-evoked early EPSPs were produced by axon collaterals of TCNs to RNNs. The latencies of the Cx-evoked late EPSPs in RNNs were almost identical to those of Cx-evoked monosynaptic EPSPs in TCNs, indicating that corticothalamic neurons (CTNs) exert monosynaptic excitatory effects on RNNs and TCNs. 4. Stimulation of the Cx produced IPSPs in TCNs with short latencies of 1.8-2.7 ms and longer latencies of > or = 2.8 ms. The Cx-evoked early IPSPs with latencies of 1.8-2.7 ms were mediated by RNNs. The origin of Cx-evoked late IPSPs with latencies of > or = 2.8 ms in TCNs was twofold, Cx-induced early IPSPs in TCNs were facilitated by conditioning cortical stimulation that induced late IPSPs in the TCNs. The same conditioning cortical stimulation also facilitated BC-evoked disynaptic IPSPs. The time course of this facilitatation indicated that CTNs produce long-lasting excitation in TINs. These results indicated that Cx-evoked IPSPs with latencies of > 2.7 ms were mediated at least in part by RNNs and inhibitory TINs in the VA-VL complex.(ABSTRACT TRUNCATED AT 400 WORDS)


This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
S. K. Esser, S. L. Hill, and G. Tononi
Modeling the Effects of Transcranial Magnetic Stimulation on Cortical Circuits
J Neurophysiol, July 1, 2005; 94(1): 622 - 639.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
Z. J. Daskalakis, G. O. Paradiso, B. K. Christensen, P. B. Fitzgerald, C. Gunraj, and R. Chen
Exploring the connectivity between the cerebellum and motor cortex in humans
J. Physiol., June 1, 2004; 557(2): 689 - 700.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
L. Zhang and E. G. Jones
Corticothalamic Inhibition in the Thalamic Reticular Nucleus
J Neurophysiol, February 1, 2004; 91(2): 759 - 766.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
A. O. Ceballos-Baumann, H. Boecker, W. Fogel, F. Alesch, P. Bartenstein, B. Conrad, N. Diederich, I. von Falkenhayn, J. R. Moringlane, M. Schwaiger, et al.
Thalamic stimulation for essential tremor activates motor and deactivates vestibular cortex
Neurology, May 22, 2001; 56(10): 1347 - 1354.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
R. N. Holdefer, L. E. Miller, L. L. Chen, and J. C. Houk
Functional Connectivity Between Cerebellum and Primary Motor Cortex in the Awake Monkey
J Neurophysiol, July 1, 2000; 84(1): 585 - 590.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online