JN Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 87: 1993-2008, 2002;
0022-3077/02 $5.00
This Article
Right arrow Full Text
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 Web of Science
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 Web of Science (19)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lang, E. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lang, E. J.

The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 1993-2008
Copyright ©2002 by the American Physiological Society

GABAergic and Glutamatergic Modulation of Spontaneous and Motor-Cortex-Evoked Complex Spike Activity

Eric J. Lang

Department of Physiology and Neuroscience, New York University School of Medicine, New York, New York 10016

Lang, Eric J. GABAergic and Glutamatergic Modulation of Spontaneous and Motor-Cortex-Evoked Complex Spike Activity. J. Neurophysiol. 87: 1993-2008, 2002. Olivocerebellar activity is organized such that synchronous complex spikes occur primarily among Purkinje cells located within the same parasagittally oriented strip of cortex. Previous findings have shown that this synchrony distribution is modulated by the release of GABA and glutamate within the inferior olive, which probably act by controlling the efficacy of the electrotonic coupling between olivary neurons. The relative strengths of these two neurotransmitters in modulating the patterns of synchrony were compared by obtaining multiple electrode recordings of spontaneous crus 2a complex spike activity during intraolivary injection of solutions containing a GABAA (picrotoxin) and/or AMPA [1,2,3,4-tetrahydro-6-nitro-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide disodium (NBQX)] receptor antagonist. Injection of either antagonist led to increased synchrony between cells located within the same parasagittally oriented approx 250-µm-wide cortical strip. Picrotoxin also increased complex spike synchrony among cells located in different cortical strips, leading to a less prominent banding pattern, whereas injections of NBQX tended to decrease complex spike synchrony among such cells, enhancing the banding pattern. The relative strength of these two classes of olivary afferents was assessed by first injecting one of the antagonists alone and then in combination with the other. The enhanced banding pattern of complex spike synchrony following injection of NBQX alone remained during the subsequent combined injection of both antagonists. Furthermore, the widespread synchronization of complex spike activity following injection of picrotoxin alone was partially or completely reversed by combined injection of picrotoxin and NBQX. Changes in the climbing fiber reflex induced by the intraolivary injections paralleled the changes observed for spontaneous complex spike activity, indicating that the effects of picrotoxin and NBQX on the synchrony distribution reflect changes in the pattern of effective coupling of inferior olivary neurons and demonstrating that synchronous complex spike activity does not require simultaneous excitatory input to olivary cells. Finally the pattern of synchrony during motor cortical stimulation was examined. It was found that the patterns of synchrony for motor-cortex-evoked complex spike activity were similar to those of spontaneous activity, indicating an important role for electrotonic coupling in determining the response of the olivocerebellar system to afferent input. Moreover, intraolivary injections of picrotoxin increased the spatial distribution of the evoked response. In sum, the results provide evidence for the hypothesis that electrotonic coupling of inferior olivary neurons via gap junctions is the mechanism underlying complex spike synchrony and that this coupling plays an important role in determining the responses of the olivocerebellar system to synaptic input.




This article has been cited by other articles:


Home page
J. Neurosci.Home page
I. Ozden, M. R. Sullivan, H. M. Lee, and S. S.-H. Wang
Reliable Coding Emerges from Coactivation of Climbing Fibers in Microbands of Cerebellar Purkinje Neurons
J. Neurosci., August 26, 2009; 29(34): 10463 - 10473.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
G. A. Jacobson, I. Lev, Y. Yarom, and D. Cohen
Invariant phase structure of olivo-cerebellar oscillations and its putative role in temporal pattern generation
PNAS, March 3, 2009; 106(9): 3579 - 3584.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
N. Wada, Y. Kishimoto, D. Watanabe, M. Kano, T. Hirano, K. Funabiki, and S. Nakanishi
Conditioned eyeblink learning is formed and stored without cerebellar granule cell transmission
PNAS, October 16, 2007; 104(42): 16690 - 16695.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. Khosrovani, R. S. Van Der Giessen, C. I. De Zeeuw, and M. T. G. De Jeu
In vivo mouse inferior olive neurons exhibit heterogeneous subthreshold oscillations and spiking patterns
PNAS, October 2, 2007; 104(40): 15911 - 15916.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
E. Chorev, Y. Yarom, and I. Lampl
Rhythmic Episodes of Subthreshold Membrane Potential Oscillations in the Rat Inferior Olive Nuclei In Vivo
J. Neurosci., May 9, 2007; 27(19): 5043 - 5052.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. M. Ackert, S. H. Wu, J. C. Lee, J. Abrams, E. H. Hu, I. Perlman, and S. A. Bloomfield
Light-induced changes in spike synchronization between coupled ON direction selective ganglion cells in the mammalian retina.
J. Neurosci., April 19, 2006; 26(16): 4206 - 4215.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
E. J. Lang, I. Sugihara, and R. Llinas
Olivocerebellar modulation of motor cortex ability to generate vibrissal movements in rat
J. Physiol., February 15, 2006; 571(1): 101 - 120.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. A. Blenkinsop and E. J. Lang
Block of Inferior Olive Gap Junctional Coupling Decreases Purkinje Cell Complex Spike Synchrony and Rhythmicity
J. Neurosci., February 8, 2006; 26(6): 1739 - 1748.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. Leznik and R. Llinas
Role of Gap Junctions in Synchronized Neuronal Oscillations in the Inferior Olive
J Neurophysiol, October 1, 2005; 94(4): 2447 - 2456.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
A. Hewitt, R. Barrie, M. Graham, K. Bogus, J. C. Leiter, and J. S. Erlichman
Ventilatory effects of gap junction blockade in the RTN in awake rats
Am J Physiol Regulatory Integrative Comp Physiol, December 1, 2004; 287(6): R1407 - R1418.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
E. J. Lang and J. Rosenbluth
Role of Myelination in the Development of a Uniform Olivocerebellar Conduction Time
J Neurophysiol, April 1, 2003; 89(4): 2259 - 2270.
[Abstract] [Full Text] [PDF]




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