Parkinson patients have a presynaptic serotonergic deficit: A dynamic deep brain stimulation PET study

J Cereb Blood Flow Metab. 2021 Aug;41(8):1954-1963. doi: 10.1177/0271678X20982389. Epub 2021 Jan 18.

Abstract

Patients with Parkinson's disease (PD) often suffer from non-motor symptoms, which may be caused by serotonergic dysfunction. Apart from alleviating the motor symptoms, Deep Brain Stimulation (DBS) in the subthalamic nucleus (STN) may also influence non-motor symptoms. The aim of this study is to investigate how turning DBS off affects the serotonergic system. We here exploit a novel functional PET neuroimaging methodology to evaluate the preservation of serotonergic neurons and capacity to release serotonin. We measured cerebral 5-HT1BR binding in 13 DBS-STN treated PD patients, at baseline and after turning DBS off. Ten age-matched volunteers served as controls. Clinical measures of motor symptoms were assessed under the two conditions and correlated to the PET measures of the static and dynamic integrity of the serotonergic system. PD patients exhibited a significant loss of frontal and parietal 5-HT1BR, and the loss was significantly correlated to motor symptom severity. We saw a corresponding release of serotonin, but only in brain regions with preserved 5-HT1BR, suggesting the presence of a presynaptic serotonergic deficit. Our study demonstrates that DBS-STN dynamically regulates the serotonin system in PD, and that preservation of serotonergic functions may be predictive of DBS-STN effects.

Keywords: Deep brain stimulation; Parkinson’s disease; positron emission tomography; serotonin (5-HT); symptoms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Case-Control Studies
  • Deep Brain Stimulation*
  • Female
  • Frontal Lobe / diagnostic imaging
  • Frontal Lobe / physiology
  • Humans
  • Male
  • Middle Aged
  • Parkinson Disease / diagnostic imaging
  • Parkinson Disease / therapy*
  • Positron-Emission Tomography*
  • Receptor, Serotonin, 5-HT1B / metabolism
  • Serotonergic Neurons / metabolism
  • Serotonin / metabolism
  • Subthalamic Nucleus / physiopathology*

Substances

  • Receptor, Serotonin, 5-HT1B
  • Serotonin