Acetylcholinesterase inhibitors may improve myelin integrity

被引:31
作者
Bartzokis, George
机构
[1] Univ Calif Los Angeles, Rush Alzheimers Dis Ctr, Div Brain Mapping,Dept Neurol, Lab Neuroimaging, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Brain Res Inst, Los Angeles, CA 90095 USA
[3] Greater Los Angeles Vet Affairs Healthcare Syst, Los Angeles, CA USA
关键词
AAMI; acetylcholinesterase; ADHD; Alzheimer; cholinergic; cognition; MCI; oligodendrocyte; schizophrenia; white matter;
D O I
10.1016/j.biopsych.2006.08.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent clinical trials have revealed that cholinergic treatments are efficacious in a wide spectrum of neuropsychiatric disorders that span the entire human lifespan and include disorders without cholinergic deficits. Furthermore, some clinical and epidemiological data suggest that cholinergic treatments have disease modifying/preventive effects. It is proposed that these observations can be usefully understood in a myelin-centered model of the human brain. The model proposes that the human brain's extensive myelination is the central evolutionary change that defines our uniqueness as a species and our unique vulnerability to highly prevalent neuropsychiatric disorders. Within the framework of this model the clinical, biochemical, and epidemiologic data can be reinterpreted to suggest that nonsynaptic effects of cholinergic treatments on the process of myelination and myelin repair contributes to their mechanism of action and especially to their disease modifying/preventive effects. The ability to test the model in human populations with safe and noninvasive imaging technologies makes it possible to undertake novel clinical trial efforts directed at primary prevention of some of the most prevalent and devastating of human disorders.
引用
收藏
页码:294 / 301
页数:8
相关论文
共 125 条
[81]  
Perry DC, 1999, J PHARMACOL EXP THER, V289, P1545
[82]   Neurochemistry of consciousness: cholinergic pathologies in the human brain [J].
Perry, EK ;
Perry, RH .
ACETYLCHOLINE IN THE CEREBRAL CORTEX, 2004, 145 :287-299
[83]   Cholinergic activity in autism: Abnormalities in the cerebral cortex and basal forebrain [J].
Perry, EK ;
Lee, MLW ;
Martin-Ruiz, CM ;
Court, JA ;
Volsen, SG ;
Merrit, J ;
Folly, E ;
Iversen, PE ;
Bauman, ML ;
Perry, RH ;
Wenk, GL .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (07) :1058-1066
[84]   Oligodendrocytes, their progenitors and other neuroglial cells in the aging primate cerebral cortex [J].
Peters, A ;
Sethares, C .
CEREBRAL CORTEX, 2004, 14 (09) :995-1007
[85]   EFFECTS OF AGING ON THE NEUROGLIAL CELLS AND PERICYTES WITHIN AREA 17 OF THE RHESUS-MONKEY CEREBRAL-CORTEX [J].
PETERS, A ;
JOSEPHSON, K ;
VINCENT, SL .
ANATOMICAL RECORD, 1991, 229 (03) :384-398
[86]   Vitamin E and donepezil for the treatment of mild cognitive impairment [J].
Petersen, RC ;
Thomas, RG ;
Grundman, M ;
Bennett, D ;
Doody, R ;
Ferris, S ;
Galasko, D ;
Jin, S ;
Kaye, J ;
Levey, A ;
Pfeiffer, E ;
Sano, M ;
van Dyck, CH ;
Thal, LJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (23) :2379-2388
[87]   Nicotinic receptors in aging and dementia [J].
Picciotto, MR ;
Zoli, M .
JOURNAL OF NEUROBIOLOGY, 2002, 53 (04) :641-655
[88]   Nicotinic acetylcholine receptor distribution in Alzheimer's disease, dementia with lewy bodies, Parkinson's disease, and vascular dementia:: In vitro binding study using 5-[125I]-A-85380 [J].
Pimlott, SL ;
Piggott, M ;
Owens, J ;
Greally, E ;
Court, JA ;
Jaros, E ;
Perry, RH ;
Perry, EK ;
Wyper, D .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (01) :108-116
[89]   Effects of acute nicotine administration on behavioral inhibition in adolescents with attention-deficit/hyperactivity disorder [J].
Potter, AS ;
Newhouse, PA .
PSYCHOPHARMACOLOGY, 2004, 176 (02) :182-194
[90]   ApoE genotype accounts for the vast majority of AD risk and AD pathology [J].
Raber, J ;
Huang, YD ;
Ashford, JW .
NEUROBIOLOGY OF AGING, 2004, 25 (05) :641-650