Serotonergic central tone in Parkinson’s disease with fatigue: Evidence from the loudness dependence of auditory evoked potentials (LDAEP)

• Published in: Neuroscience letters 2021-11, Vol.764, p.136242-136242, Article 136242
• Main Authors: Pauletti, Caterina, Mannarelli, Daniela, Locuratolo, Nicoletta, Maffucci, Andrea, Currà, Antonio, Marinelli, Lucio, Fattapposta, Francesco
• Format: Article
• Language: English
• Subjects: Aged; Auditory evoked potentials; Case-Control Studies; Electroencephalography; Evoked Potentials, Auditory - physiology; Fatigue; Fatigue - etiology; Fatigue - metabolism; Fatigue - physiopathology; Female; Frontal Lobe - metabolism; Frontal Lobe - physiopathology; Humans; LDAEP; Loudness Perception - physiology; Male; Middle Aged; Motivation - physiology; Neostriatum - metabolism; Neostriatum - physiopathology; Parkinson Disease - complications; Parkinson Disease - metabolism; Parkinson Disease - physiopathology; Parkinson’s disease; Quality of Life; Serotonin; Serotonin - metabolism; Synaptic Transmission
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2021.136242

•LDAEP is a neurophysiological tool that measures serotonergic central tone in vivo.•Serotonergic central tone is significantly lower in PD patients than controls.•Serotonergic central tone is comparable in PD patients with and without fatigue.•Fatigue is likely related to serotonin/dopamine imbalance. Central fatigue in Parkinson’s disease (PD) is a common and disabling symptom that further worsens the patients’ quality of life. A deficit in the serotonergic system may be implicated in the occurrence of fatigue in patients with PD as well as in those with other chronic conditions characterized by fatigue. The loudness dependence of auditory evoked potentials (LDAEP) is a neurophysiological tool that has proved to be effective in measuring the serotonergic central function in vivo. The aim of the present study was to assess central serotonergic activity in PD patients and to explore its possible association with the presence of fatigue. LDAEP was recorded in 38 PD patients (26 without fatigue – PDnF and 12 with fatigue – PDF) and 34 healthy controls. A significant difference between parkinsonian patients and controls emerged, with patients displaying stronger LDAEP values (which reflect a lower serotonergic central tone) than controls. By contrast, no differences in LDAEP emerged between PDF and PDnF. Our electrophysiological data confirmed the presence of a deficit in serotonergic central transmission in PD. An association between this deficit and fatigue was not demonstrated. It is likely that an altered dopamine/serotonin balance, rather than a serotonin deficit alone, is involved in the genesis of central fatigue. This complex and multifaceted symptom is related above all to a dysfunction in the striato-thalamo-cortical loop that connects the neostriatum to the frontal lobe and is strongly affected by motivation.