TY - JOUR
T1 - Alterations in event-related potentials (ERPs) of MPTP-treated monkeys
AU - Glover, Andrew
AU - Ghilardi, M. Felice
AU - Bodis-Wollner, Ivan
AU - Onofrj, Marco
N1 - Funding Information:
We would like to thank Pauline Sobelman for assistance in the manuscript preparation. This study was supported by N1H Grants EY01708, EY07014, and NS-11631. We also thank Sigma Tau (Pomezia, Italy) for partial support.
PY - 1988
Y1 - 1988
N2 - Using an auditory 'oddball' paradigm and classical conditioning, we have studied auditory evoked potentials (AEPs) and P300-like potentials in monkeys pre- and post-MPTP treatment. Free-field acoustic stimuli were 500 Hz and 4000 Hz tones, which were designated as the 'frequent' and 'rare' conditions, respectively. The 4000 Hz stimuli were reinforced with mild somatosensory electrical stimulation. During the first few weeks following 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP) administration, all monkeys gradually developed a parkinsonian syndrome, which partially, but not completely improved within 30-40 days in 2 animals. The amplitudes of the AEP were initially significantly decreased, but progressively returned to pretreatment magnitudes in the 2 monkeys which partially recovered. P300-like potentials were initially abolished in all animals; however, 30-40 days later P300 spontaneously re-emerged in the same 2 monkeys. Latencies of both of these signals were unaffected by MPTP. Acute administration of dopamine precursor during the first phase of neurotoxicity partially and temporarily improved depressed AEP amplitudes, but did not restore absent P300-like potentials. The relevance of these results for Parkinson's disease is discussed.
AB - Using an auditory 'oddball' paradigm and classical conditioning, we have studied auditory evoked potentials (AEPs) and P300-like potentials in monkeys pre- and post-MPTP treatment. Free-field acoustic stimuli were 500 Hz and 4000 Hz tones, which were designated as the 'frequent' and 'rare' conditions, respectively. The 4000 Hz stimuli were reinforced with mild somatosensory electrical stimulation. During the first few weeks following 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine (MPTP) administration, all monkeys gradually developed a parkinsonian syndrome, which partially, but not completely improved within 30-40 days in 2 animals. The amplitudes of the AEP were initially significantly decreased, but progressively returned to pretreatment magnitudes in the 2 monkeys which partially recovered. P300-like potentials were initially abolished in all animals; however, 30-40 days later P300 spontaneously re-emerged in the same 2 monkeys. Latencies of both of these signals were unaffected by MPTP. Acute administration of dopamine precursor during the first phase of neurotoxicity partially and temporarily improved depressed AEP amplitudes, but did not restore absent P300-like potentials. The relevance of these results for Parkinson's disease is discussed.
KW - 1-Methyl-3-phenyl-1,2,5,6-tetrahydropyridine
KW - AEP
KW - Dopamine
KW - Monkey
KW - P300
KW - Parkinson's disease
UR - http://www.scopus.com/inward/record.url?scp=0023737505&partnerID=8YFLogxK
U2 - 10.1016/0168-5597(88)90050-0
DO - 10.1016/0168-5597(88)90050-0
M3 - Article
C2 - 2460327
AN - SCOPUS:0023737505
SN - 0168-5597
VL - 71
SP - 461
EP - 468
JO - Electroencephalography and Clinical Neurophysiology/ Evoked Potentials
JF - Electroencephalography and Clinical Neurophysiology/ Evoked Potentials
IS - 6
ER -