Move to the rhythm: oscillations in the subthalamic nucleus-external globus pallidus network.

By M. Bevan, P. Magill, David H. Terman, J. Bolam, Charles J. Wilson. Trends in Neurosciences, 2002

633 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/dd4724d8f59ac90f583040187ebc3860b69eb33e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cellular and Molecular Neuroscience

In Neurology

Citations in the corpus

Information processing, dimensionality reduction and reinforcement learning in the basal ganglia. (2003, background): “In addition, the role of the reciprocal connections between the GPe and STN has been emphasized in recent physiological (Plenz and Kitai, 1999) and computational (Bevan et al., 2002; Terman et al., 2002) studies.”
The subthalamic nucleus in the context of movement disorders. (2004, background): “Multiple IPSPs not only reset the cycle but can also bring the potential of the membrane closer to the equilibrium potential of GABA, restoring rhythmic ®ring and promoting rebound spiking and bursting activity (Bevan et al., 2002b).”
Striatal plasticity and basal ganglia circuit function (2008, background): “In this scheme, synchronous firing of indirect-pathway projections to the GPe would be amplified by the recurrent GPe-STN circuit (Bevan et al., 2002), leading to abnormal oscillations that interfere with normal basal ganglia output, and that could also be associated with resting tremor in PD (Bevan”
Dynamic cross-frequency couplings of local field potential oscillations in rat striatum and hippocampus during performance of a T-maze task (2008, background): “Oscillatory activity in the striatal LFPs likely reflect rhythms in striatal inputs both from distant sources such as the thalamus and neocortex and from local sources, particularly the pallidum, itself part of a subthalamo–pallidal oscillatory circuit (34, 35).”
Parkinson disease: from pathology to molecular disease mechanisms. (2013, background): “The major contributor is the overactivity of the subthalamic nucleus (STN), which releases glutamate and which innervates the substantia nigra pars compacta and the internal segment of the globus pallidus [8,142].”
Beta oscillatory activity in the subthalamic nucleus and its relation to dopaminergic response in Parkinson's disease. (2006, background): “This implies that neuromodulators, such as dopamine, that influence the membrane potential of STN neurons will have a profound effect on the activity in the GPe–STN network (Bevan et al. 2002).”
Oscillations in the Basal Ganglia: The good, the bad, and the unexpected (2005, background): “The paucity of evidence for oscillatory activity in the BG of behaving animals stands in contrast to growing evidence that oscillatory activity is a property of subthalamo-pallidal circuit neurons, key modulators not only of the output of the BG to the thalamus, but also of other parts of the BG cir”
Hold your horses: A dynamic computational role for the subthalamic nucleus in decision making (2006, positive): “The current systems-level account is consistent with data showing that top-down cortical projections play a key role in the generation of STN bursts and associated oscillations (Bevan et al., 2002; Magill et al., 2001).”
Modulation of striatal projection systems by dopamine (2011, positive): “In diseases of the basal ganglia, like PD, the timing of activity, rather than the overall level of activity, appears to be the most important determinant of movement choice and initiation (Bevan et al., 2002).”