scholarly journals Synchronous Unit Activity and Local Field Potentials Evoked in the Subthalamic Nucleus by Cortical Stimulation

2004 ◽  
Vol 92 (2) ◽  
pp. 700-714 ◽  
Author(s):  
Peter J. Magill ◽  
Andrew Sharott ◽  
Mark D. Bevan ◽  
Peter Brown ◽  
J. Paul Bolam

The responses of single subthalamic nucleus (STN) neurons to cortical activation are complex and depend on the relative activation of several neuronal circuits, making theoretical extrapolation of single neuron responses to the population level difficult. To understand better the degree of synchrony imposed on STN neurons and associated neuronal networks by cortical activation, we recorded the responses of single units, pairs of neighboring neurons, and local field potentials (LFPs) in STN to discrete electrical stimulation of the cortex in anesthetized rats. Stimulation of ipsilateral frontal cortex, but not temporal cortex, generated synchronized “multiphasic” responses in neighboring units in rostral STN, usually consisting of a brief, short-latency excitation, a brief inhibition, a second excitation, and a long-duration inhibition. Evoked LFPs in STN consistently mirrored unit responses; brief, negative deflections in the LFP coincided with excitations and brief, positive deflections with inhibitions. This characteristic LFP was dissimilar to potentials evoked in cortex and structures surrounding STN and was resistant to fluctuations in forebrain activity. The short-latency excitation and associated LFP deflection exhibited the highest fidelity to low-intensity cortical stimuli. Unit response failures, which mostly occurred in caudal STN, were not associated with LFPs typical of rostral STN. These data suggest that local populations of STN neurons can be synchronized by both direct and indirect cortical inputs. Synchronized ensemble activity is dependent on topography and input intensity. Finally, the stereotypical, multiphasic profile of the evoked LFP indicates that it might be useful for locating the STN in clinical as well as nonclinical settings.

Neuron ◽  
2006 ◽  
Vol 49 (3) ◽  
pp. 433-445 ◽  
Author(s):  
Gabriel Kreiman ◽  
Chou P. Hung ◽  
Alexander Kraskov ◽  
Rodrigo Quian Quiroga ◽  
Tomaso Poggio ◽  
...  

2017 ◽  
Vol 20 (5) ◽  
pp. 471-477 ◽  
Author(s):  
Arun Chockalingam ◽  
Abigail Belasen ◽  
Nita Chen ◽  
Adolfo Ramirez-Zamora ◽  
Youngwon Youn ◽  
...  

2008 ◽  
Vol 100 (1) ◽  
pp. 385-396 ◽  
Author(s):  
Cyril Dejean ◽  
Christian E. Gross ◽  
Bernard Bioulac ◽  
Thomas Boraud

It is well established that parkinsonian syndrome is associated with alterations in the temporal pattern of neuronal activity and local field potentials in the basal ganglia (BG). An increase in synchronized oscillations has been observed in different BG nuclei in parkinsonian patients and animal models of this disease. However, the mechanisms underlying this phenomenon remain unclear. This study investigates the functional connectivity in the cortex-BG network of a rodent model of Parkinson's disease. Single neurons and local field potentials were simultaneously recorded in the motor cortex, the striatum, and the substantia nigra pars reticulata (SNr) of freely moving rats, and high-voltage spindles (HVSs) were used to compare signal transmission before and after dopaminergic depletion. It is shown that dopaminergic lesion results in a significant enhancement of oscillatory synchronization in the BG: the coherence between pairs of structures increased significantly and the percentage of oscillatory auto- and cross-correlograms. HVS episodes were also more numerous and longer. These changes were associated with a shortening of the latency of SNr response to cortical activation, from 40.5 ± 4.8 to 10.2 ± 1.07 ms. This result suggests that, in normal conditions, SNr neurons are likely to be driven by late inputs from the indirect pathway; however, after the lesion, their shorter latency also indicates an overactivation of the hyperdirect pathway. This study confirms that neuronal signal transmission is altered in the BG after dopamine depletion but also provides qualitative evidence for these changes at the cellular level.


NeuroImage ◽  
2019 ◽  
Vol 197 ◽  
pp. 232-242
Author(s):  
Joan Duprez ◽  
Jean-François Houvenaghel ◽  
Thibaut Dondaine ◽  
Julie Péron ◽  
Claire Haegelen ◽  
...  

2002 ◽  
Vol 177 (2) ◽  
pp. 581-585 ◽  
Author(s):  
Peter Brown ◽  
Andreas Kupsch ◽  
Peter J. Magill ◽  
Andrew Sharott ◽  
Daniel Harnack ◽  
...  

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