Lithium and valproic acid treatment effects on brain chemistry in bipolar disorder

被引:117
作者
Friedman, SD
Dager, SR
Parow, A
Hirashima, F
Demopulos, C
Stoll, AL
Lyoo, IK
Dunner, DL
Renshaw, PF
机构
[1] Univ Washington, Sch Med, Dept Radiol, Seattle, WA 98105 USA
[2] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98105 USA
[3] Univ Washington, Dept Bioengn, Seattle, WA 98105 USA
[4] Seoul Natl Univ, Dept Psychiat, Seoul, South Korea
[5] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA
关键词
bipolar disorder; glutamate; glutamine; lithium; valproic acid; spectroscopy;
D O I
10.1016/j.biopsych.2004.06.012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Prior work? reported elevated gray matter (Gill) lactate and Glx (glutamate + glutamine + GABA) concentrations in unmedicated patients with bipolar disorder (BP) compared with healthy controls (HC), This stud)) examined whether lithium (Li) and valproic acid (VPA) treatment modulated these chemicals. Methods. A subset of previously reported BP patients were treated with Li (n = 12, 3.6 +/- 1.9 months) or VPA (n = 9, 1.4 +/- 1.7 months) and compared untreated HC sujects (n = 12, 2.9 - +/- 2.4 months) using proton echo-planar spectroscopic imaging. Regression analyses (voxel gray/white composition by chemistry) were preformed at each time point, and change scores computed. Metabolite relaxation and regions of interest (ROI) were also examined. Results: Across treatment, Li-treated BP subjects demonstrated GM Glx decreases (Li-HC, p =.08; Li-VPA p =.04) and GM myo-inositol increases (Li-HCp =.07; Li-VPAp = .12). Other measures were not significant. Serum Li levels were positively correlated with Glx decreases at the trend level. Conclusions: Li treatment of BP was associated with specific GM Glx decreases and myo-inositol increases. Findings are discussed in the context of cellular mechanisms postulated to underlie Li and VPA therapeutic efficacy.
引用
收藏
页码:340 / 348
页数:9
相关论文
共 85 条
[1]   EFFECTS OF LITHIUM ON MYOINOSITOL LEVELS IN LAYERS OF FRONTAL CEREBRAL-CORTEX, IN CEREBELLUM, AND IN CORPUS-CALLOSUM OF THE RAT [J].
ALLISON, JH ;
BOSHANS, RL ;
HALLCHER, LM ;
PACKMAN, PM ;
SHERMAN, WR .
JOURNAL OF NEUROCHEMISTRY, 1980, 34 (02) :456-458
[2]  
[Anonymous], DIAGN STAT MAN DIS
[3]  
Antonelli T, 2000, SYNAPSE, V38, P355, DOI 10.1002/1098-2396(20001201)38:3<355::AID-SYN15>3.0.CO
[4]  
2-E
[5]  
Baldessarini RJ, 2003, J CLIN PSYCHIAT, V64, P44
[6]   LITHIUM - EFFECT ON [H-3] SPIPERONE BINDING, IONIC CONTENT, AND AMINO-ACID LEVELS IN THE BRAIN OF RATS [J].
BANAYSCHWARTZ, M ;
WAJDA, IJ ;
MANIGAULT, I ;
DEGUZMAN, T ;
LAJTHA, A .
NEUROCHEMICAL RESEARCH, 1982, 7 (02) :179-189
[7]   TOWARD A CRYSTAL-CLEAR VIEW OF LITHIUMS SITE OF ACTION [J].
BARABAN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (13) :5738-5739
[8]   N-acetylaspartate in the vertebrate brain:: Metabolism and function [J].
Baslow, MH .
NEUROCHEMICAL RESEARCH, 2003, 28 (06) :941-953
[9]   Functions of N-acetyl-L-aspartate and N-acetyl-L-aspartylglutamate in the vertebrate brain:: Role in glial cell-specific signaling [J].
Baslow, MH .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (02) :453-459
[10]   Evidence supporting a role for N-acetyl-L-aspartate as a molecular water pump in myelinated neurons in the central nervous system -: An analytical review [J].
Baslow, MH .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (04) :295-300