Decreased prefrontal Myo-inositol in major depressive disorder

被引:140
作者
Coupland, NJ
Ogilvie, CJ
Hegadoren, KM
Seres, P
Hanstock, CC
Allen, PS
机构
[1] Univ Alberta, Psychopharmacol Res Unit, Dept Psychiat, Edmonton, AB T6G 2B7, Canada
[2] Univ Alberta, Dept Biomed Engn, Edmonton, AB T6G 2B7, Canada
基金
加拿大健康研究院;
关键词
major depressive disorder; glia; magnetic resonance spectroscopy; inositol; N-acetylaspartate; stress;
D O I
10.1016/j.biopsych.2005.02.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Postmortem studies have shown robust prefrontal cortex glial losses and more subtle neuronal changes in major depressive disorder (MDD). Earlier proton magnetic resonance spectroscopy (H-1-MRS) studies of the glial marker myo-inositol in MDD were subject to potential confounds. The primary hypothesis of this study was that MDD patients would show reduced prefrontal/anterior cingulate cortex levels of myo-inositol. Methods: Thirteen nonmedicated moderate-severe MDD patients and 13 matched control subjects were studied (six male, seven female per group). Proton magnetic resonance spectroscopy stimulated echo acquisition mode spectra (3.0 T, echo time = 168 msec: mixing time = 28 msec; repetition time = 3000 msec) were obtained from prefrontal anterior cingulate cortex. Metabolite data were adjusted for tissue composition. Results: Patients with MDD showed significantly lower myo-inositol creatine rations (.94 +/- .23) than control subjects (1.32 +/- .31) [F(1.23) = 6.9: p = .016]. Conclusions: These data suggest a reduction of myo-inositol in prefrontal anterior cingulate cortex in MDD, which could be a consequence of glial loss or altered glial metabolism. Additional in vivo studies of glial markers could add to the understanding of the pathophysiology of MDD.
引用
收藏
页码:1526 / 1534
页数:9
相关论文
共 80 条
[1]   Cerebrospinal fluid inositol monophosphatase: Elevated activity in depression and neuroleptic-treated schizophrenia [J].
Atack, JR ;
Levine, J ;
Belmaker, RH .
BIOLOGICAL PSYCHIATRY, 1998, 44 (06) :433-437
[2]   Reduced glutamate in the anterior cingulate cortex in depression:: An in vivo proton magnetic resonance spectroscopy study [J].
Auer, DP ;
Pütz, B ;
Kraft, E ;
Lipinski, B ;
Schill, J ;
Holsboer, F .
BIOLOGICAL PSYCHIATRY, 2000, 47 (04) :305-313
[3]   Glial cells and neurotransmission: An inclusive view of synaptic function [J].
Auld, DS ;
Robitaille, R .
NEURON, 2003, 40 (02) :389-400
[4]   N-acetylaspartate in the vertebrate brain:: Metabolism and function [J].
Baslow, MH .
NEUROCHEMICAL RESEARCH, 2003, 28 (06) :941-953
[5]   ANALYSIS OF MACROMOLECULE RESONANCES IN H-1-NMR SPECTRA OF HUMAN BRAIN [J].
BEHAR, KL ;
ROTHMAN, DL ;
SPENCER, DD ;
PETROFF, OAC .
MAGNETIC RESONANCE IN MEDICINE, 1994, 32 (03) :294-302
[6]  
BERRIDGE MJ, 1989, JAMA-J AM MED ASSOC, V262, P1834
[7]   Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brain [J].
Berry, GT ;
Buccafusca, R ;
Greer, JJ ;
Eccleston, E .
MOLECULAR GENETICS AND METABOLISM, 2004, 82 (01) :87-92
[8]  
Bitsch A, 1999, AM J NEURORADIOL, V20, P1619
[9]  
Bouras C, 2001, ACTA NEUROPATHOL, V102, P373
[10]   Low glial numbers in the amygdala in major depressive disorder [J].
Bowley, MP ;
Drevets, WC ;
Öngür, D ;
Price, JL .
BIOLOGICAL PSYCHIATRY, 2002, 52 (05) :404-412