Aging and cholinergic modulation of the transient magnetic 40-Hz auditory response

被引:14
作者
Ahveninen, J
Jääskeläinen, IP
Kaakkola, S
Tiitinen, H
Pekkonen, E
机构
[1] Univ Helsinki, Dept Psychol, Cognit Brain Res Unit, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Psychol, Appercept & Cort Dynam Res Team, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Dept Neurol, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Cent Hosp, Med Engn Ctr, Biomag Lab, Helsinki, Finland
[5] Harvard Univ, Sch Med, Massachusetts Gen Hosp, NMR Ctr, Charlestown, MA USA
基金
芬兰科学院;
关键词
40-Hz response; acetylcholine; aging; Alzheimer's disease; auditory event-related potentials; electroencephalography; magnetoencephalography; memory; muscarinic receptors; scopolamine;
D O I
10.1006/nimg.2001.0956
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cholinergic blockade by scopolamine, a central muscarinic receptor antagonist, may produce transient memory impairment in healthy subjects, and it has been used as a neurochemical model of cognitive degeneration in aged individuals. To observe the muscarinic modulation of memory and cortical auditory processing, nine cognitively intact elderly subjects (59-80 years) were studied using neuropsychological tests and 122-channel magnetoencephalography (MEG) after an administration of scopolamine hydrobromide (0.3 mg, iv) or glycopyrrolate (0.2 mg, iv), a peripheral muscarinic antagonist. A double-blind randomized crossover design was used in two sessions separated by at least 1 week. Scopolamine, but not glycopyrrolate, produced a transient impairment of verbal memory performance in the elderly subjects. MEG indicated that tire auditory-evoked 40-Hz magnetic response was significantly larger after scopolamine than after glycopyrrolate administration. Furthermore, reanalysis of our earlier results in younger subjects (20-31 years), basically supporting the present MEG findings, tentatively suggests that the scopolamine effects on the 40-Hz response may be slightly pronounced with aging. In sum, the transient magnetic 40-Hz auditory response may be useful in studies on brain cholinergic deficits in elderly subjects. (C) 2002 Elsevier Science.
引用
收藏
页码:153 / 158
页数:6
相关论文
共 29 条
[11]   Muscarinic signaling in the central nervous system - Recent developments and anesthetic implications [J].
Durieux, ME .
ANESTHESIOLOGY, 1996, 84 (01) :173-189
[12]   TEMPORAL CODING IN THE VISUAL-CORTEX - NEW VISTAS ON INTEGRATION IN THE NERVOUS-SYSTEM [J].
ENGEL, AK ;
KONIG, P ;
KREITER, AK ;
SCHILLEN, TB ;
SINGER, W .
TRENDS IN NEUROSCIENCES, 1992, 15 (06) :218-226
[13]   HYPERSENSITIVITY TO SCOPOLAMINE IN THE ELDERLY [J].
FLICKER, C ;
FERRIS, SH ;
SERBY, M .
PSYCHOPHARMACOLOGY, 1992, 107 (2-3) :437-441
[14]   CHOLINERGIC MODULATION OF HUMAN P3 EVENT-RELATED POTENTIALS [J].
HAMMOND, EJ ;
MEADOR, KJ ;
AUNGDIN, R ;
WILDER, BJ .
NEUROLOGY, 1987, 37 (02) :346-350
[15]   Scopolamine enhances middle-latency auditory evoked magnetic fields [J].
Jääskeläinen, IP ;
Hirvonen, J ;
Huttunen, J ;
Kaakkola, S ;
Pekkonen, E .
NEUROSCIENCE LETTERS, 1999, 259 (01) :41-44
[16]   HUMAN OSCILLATORY BRAIN ACTIVITY NEAR 40 HZ COEXISTS WITH COGNITIVE TEMPORAL BINDING [J].
JOLIOT, M ;
RIBARY, U ;
LLINAS, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11748-11751
[17]   LONG-TERM STIMULATION ATTENUATES THE TRANSIENT 40-HZ RESPONSE [J].
MAY, P ;
TIITINEN, H ;
SINKKONEN, J ;
NAATANEN, R .
NEUROREPORT, 1994, 5 (15) :1918-1920
[18]   CHOLINERGIC AND SEROTONERGIC EFFECTS ON THE P3 POTENTIAL AND RECENT MEMORY [J].
MEADOR, KJ ;
LORING, DW ;
DAVIS, HC ;
SETHI, KD ;
PATEL, BR ;
ADAMS, RJ ;
HAMMOND, EJ .
JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY, 1989, 11 (02) :252-260
[19]   NUCLEUS BASALIS STIMULATION FACILITATES THALAMOCORTICAL SYNAPTIC TRANSMISSION IN THE RAT AUDITORY-CORTEX [J].
METHERATE, R ;
ASHE, JH .
SYNAPSE, 1993, 14 (02) :132-143
[20]   RELATIONSHIP OF TRANSIENT AND STEADY-STATE AUDITORY-EVOKED FIELDS [J].
PANTEV, C ;
ELBERT, T ;
MAKEIG, S ;
HAMPSON, S ;
EULITZ, C ;
HOKE, M .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1993, 88 (05) :389-396