On the Origin of Tremor in Parkinson’s Disease

• Published in: PloS one Vol. 7; no. 7; p. e41598
• Main Authors: Dovzhenok, Andrey, Rubchinsky, Leonid L.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 27.07.2012; Public Library of Science (PLoS)
• Subjects: Analysis; Anatomy & physiology; Antiparkinson agents; Basal ganglia; Basal Ganglia - metabolism; Basal Ganglia - pathology; Basal Ganglia - physiopathology; Biology; Calcium - metabolism; Central nervous system diseases; Cerebellar Cortex - metabolism; Cerebellar Cortex - pathology; Cerebellar Cortex - physiopathology; Conductance; Cortex; Dopamine; Dopamine receptors; Dopaminergic Neurons - pathology; Electrophysiological Phenomena; Feedback; Feedback, Physiological; Ganglia; Humans; Kinetics; Medicine; Models, Neurological; Movement disorders; Neurons; Oscillations; Parkinson disease; Parkinson Disease - complications; Parkinson Disease - physiopathology; Parkinson's disease; Physiology; Potassium - metabolism; Resistance; Rodents; Studies; Synapses - pathology; Thalamus - metabolism; Thalamus - pathology; Thalamus - physiopathology; Tremor; Tremor - etiology; Tremor - metabolism; Tremor - pathology; Tremor - physiopathology; Indiana; United States > US; Indianapolis Indiana
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0041598

The exact origin of tremor in Parkinson's disease remains unknown. We explain why the existing data converge on the basal ganglia-thalamo-cortical loop as a tremor generator and consider a conductance-based model of subthalamo-pallidal circuits embedded into a simplified representation of the basal ganglia-thalamo-cortical circuit to investigate the dynamics of this loop. We show how variation of the strength of dopamine-modulated connections in the basal ganglia-thalamo-cortical loop (representing the decreasing dopamine level in Parkinson's disease) leads to the occurrence of tremor-like burst firing. These tremor-like oscillations are suppressed when the connections are modulated back to represent a higher dopamine level (as it would be the case in dopaminergic therapy), as well as when the basal ganglia-thalamo-cortical loop is broken (as would be the case for ablative anti-parkinsonian surgeries). Thus, the proposed model provides an explanation for the basal ganglia-thalamo-cortical loop mechanism of tremor generation. The strengthening of the loop leads to tremor oscillations, while the weakening or disconnection of the loop suppresses them. The loop origin of parkinsonian tremor also suggests that new tremor-suppression therapies may have anatomical targets in different cortical and subcortical areas as long as they are within the basal ganglia-thalamo-cortical loop.