Effects of lithium and amphetamine on inositol metabolism in the human brain as measured by 1H and 31P MRS

被引:25
作者
Silverstone, PH
Rotzinger, S
Pukhovsky, A
Hanstock, CC
机构
[1] Univ Alberta, Dept Psychiat, Edmonton, AB, Canada
[2] Univ Alberta, Dept Biomed Engn, Edmonton, AB, Canada
关键词
lithium; inositol; bipolar disorder; amphetamine; magnetic resonance spectroscopy;
D O I
10.1016/S0006-3223(99)00076-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The clinical effectiveness of lithium may be due to its decreasing the intracellular concentration of myo-inositol and increasing that of its inositol monophosphate precursors, which is known as the inositol depletion hypothesis. Methods: Magnetic resonance spectroscopy (MRS) was used to measure the concentration of both myo-inositol (H-1 MRS) and phosphomonoesters (PME) [P-31 MRS], in healthy volunteers in a double-blind placebo-controlled study. MRS measurements were made at baseline, again on the 7th day of lithium (1200 mg, n = 10) or placebo (n = 6) administration, and again on day 8, 2 hours following oral administration of 20 mg dextroamphetamine to stimulate the phosphoinositol (PI) cycle. Results: Subjects who received lithium showed a greater increase in PME ratios in response to amphetamine administration than did placebo-treated subjects. Conclusions: The present results support the hypothesis that lithium administration blocks the conversion of inositol monophosphates to myo-inositol, and that this effect is especially apparent following PT cycle stimulation. The effects of lithium treatment on myo-inositol in healthy volunteers in vivo are uncertain, and may have to await improvements in the ability to measure myo-inositol in the brain. Biol Psychiatry 1999;46:1634-1641 (C) 1999 Society of Biological Psychiatry.
引用
收藏
页码:1634 / 1641
页数:8
相关论文
共 54 条
  • [11] DECREASED TEMPORAL-LOBE PHOSPHOMONOESTERS IN BIPOLAR DISORDER
    DEICKEN, RF
    WEINER, MW
    FEIN, G
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 1995, 33 (03) : 195 - 199
  • [12] DEICKEN RF, 1995, AM J PSYCHIAT, V152, P915
  • [13] THE EFFECT OF LITHIUM ON RAT-BRAIN AND ERYTHROCYTE GLYCINE LEVELS
    DEUTSCH, SI
    STANLEY, M
    BANAYSCHWARTZ, M
    PESELOW, ED
    VIRGILIO, J
    GEISLER, S
    MOHS, RC
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1981, 75 (01) : 75 - 76
  • [14] MULTIPLE COMPARISONS AMONG MEANS
    DUNN, OJ
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1961, 56 (293) : 52 - &
  • [15] ALTERATION OF INOSITOL PHOSPHOLIPID-METABOLISM IN RAT CORTEX BY LITHIUM BUT NOT CARBAMAZEPINE
    ELPHICK, M
    TAGHAVI, Z
    POWELL, T
    GODFREY, PP
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 156 (03) : 411 - 414
  • [16] SUBACUTE AND CHRONIC INVIVO LITHIUM TREATMENT INHIBITS AGONIST-STIMULATED AND SODIUM FLUORIDE-STIMULATED INOSITOL PHOSPHATE PRODUCTION IN RAT CORTEX
    GODFREY, PP
    MCCLUE, SJ
    WHITE, AM
    WOOD, AJ
    GRAHAMESMITH, DG
    [J]. JOURNAL OF NEUROCHEMISTRY, 1989, 52 (02) : 498 - 506
  • [17] GORDON RE, 1984, P SOC MAGN RES MED
  • [18] PHOSPHORYLETHANOLAMINE - THE MAJOR CONSTITUENT OF THE PHOSPHOMONOESTER PEAK OBSERVED BY P-31-NMR ON DEVELOPING DOG BRAIN
    GYULAI, L
    BOLINGER, L
    LEIGH, JS
    BARLOW, C
    CHANCE, B
    [J]. FEBS LETTERS, 1984, 178 (01) : 137 - 142
  • [19] HALLCHER LM, 1980, J BIOL CHEM, V255, P896
  • [20] CEREBRAL LITHIUM, INOSITOL AND INOSITOL MONOPHOSPHATES
    HIRVONEN, MR
    [J]. PHARMACOLOGY & TOXICOLOGY, 1991, 69 (01): : 22 - 27