In Alzheimer's disease (AD), transcranial magnetic stimulation (TMS) studies have shown abnormalities of motor cortical excitability, such as a decreased intra-cortical inhibition (ICI) and changes in resting motor threshold (rMT). We studied the effects of L-dopa on rMT and ICI in a cohort of moderate AD patients after paired-pulse TMS. Results were compared with a control group of healthy subjects. As expected, AD patients showed a significant reduction in ICI and a lower rMT. L-dopa administration (soluble form, melevodopa 200 mg) promptly reversed the ICI impairment up to normalization. This effect was specific, since it was not mimicked in control subjects. These results indicate a possible role of dopamine in modulating AD cortical excitability, thus suggesting an interaction between dopaminergic ascending pathways and endogenous intracortical transmitters. In addition, considering that L-dopa showed a pharmacological profile similar to the one of cholinomimetics, L-dopa might represent a reliable tool to study new therapeutic perspective and strategies for AD.

Martorana, A., Stefani, A., Palmieri, M., Esposito, Z., Bernardi, G., Sancesario, G., et al. (2008). L-dopa modulates motor cortex excitability in Alzheimer's disease patients. JOURNAL OF NEURAL TRANSMISSION, 115(9), 1313-1319 [10.1007/s00702-008-0082-z].

L-dopa modulates motor cortex excitability in Alzheimer's disease patients

MARTORANA, ALESSANDRO;STEFANI, ALESSANDRO;BERNARDI, GIORGIO;SANCESARIO, GIUSEPPE;PIERANTOZZI, MARIANGELA
2008-09-01

Abstract

In Alzheimer's disease (AD), transcranial magnetic stimulation (TMS) studies have shown abnormalities of motor cortical excitability, such as a decreased intra-cortical inhibition (ICI) and changes in resting motor threshold (rMT). We studied the effects of L-dopa on rMT and ICI in a cohort of moderate AD patients after paired-pulse TMS. Results were compared with a control group of healthy subjects. As expected, AD patients showed a significant reduction in ICI and a lower rMT. L-dopa administration (soluble form, melevodopa 200 mg) promptly reversed the ICI impairment up to normalization. This effect was specific, since it was not mimicked in control subjects. These results indicate a possible role of dopamine in modulating AD cortical excitability, thus suggesting an interaction between dopaminergic ascending pathways and endogenous intracortical transmitters. In addition, considering that L-dopa showed a pharmacological profile similar to the one of cholinomimetics, L-dopa might represent a reliable tool to study new therapeutic perspective and strategies for AD.
set-2008
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/26 - NEUROLOGIA
English
Con Impact Factor ISI
acetylcholine; domperidone; levodopa methyl ester; placebo; aged; Alzheimer disease; article; blood pressure variability; clinical article; controlled study; drug effect; electromyography; evoked muscle response; female; heart rate variability; human; inhibition kinetics; male; motor activity; motor cortex; nausea; nerve excitability; neuromodulation; neurotransmission; outcome assessment; priority journal; side effect; tachypnea; transcranial magnetic stimulation; Acetylcholine; Afferent Pathways; Aged; Aged, 80 and over; Alzheimer Disease; Cholinergic Agents; Dopamine; Dopamine Agents; Evoked Potentials, Motor; Female; Humans; Levodopa; Male; Middle Aged; Motor Cortex; Neural Inhibition; Neural Pathways; Nootropic Agents; Reaction Time; Synaptic Transmission; Time Factors; Transcranial Magnetic Stimulation
Martorana, A., Stefani, A., Palmieri, M., Esposito, Z., Bernardi, G., Sancesario, G., et al. (2008). L-dopa modulates motor cortex excitability in Alzheimer's disease patients. JOURNAL OF NEURAL TRANSMISSION, 115(9), 1313-1319 [10.1007/s00702-008-0082-z].
Martorana, A; Stefani, A; Palmieri, M; Esposito, Z; Bernardi, G; Sancesario, G; Pierantozzi, M
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
martoranaJNT.pdf

solo utenti autorizzati

Licenza: Non specificato
Dimensione 281.02 kB
Formato Adobe PDF
281.02 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/40633
Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 40
  • ???jsp.display-item.citation.isi??? 37
social impact