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1.
Bipolar Disord ; 2(3 Pt 2): 207-16, 2000 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-11249799

RESUMEN

OBJECTIVES: Alterations in choline and myo-inositol metabolism have been noted in bipolar disorder, and the therapeutic efficacy of lithium in mania may be related to these effects. We wished to determine the relationship between anterior cingulate cortex choline and myo-inositol levels, assessed using proton magnetic resonance spectroscopic imaging (MRSI), and mood state in subjects with bipolar disorder. METHODS: Serial assessments of anterior cingulate cortex choline and myo-inositol metabolism were performed in nine subjects with bipolar disorder, taking either lithium or valproate, and 14 controls. Each bipolar subject was examined between one and four times (3.1 +/- 1.3). On the occasion of each examination, standardized ratings of both depression and mania were recorded. RESULTS: In the left cingulate cortex, the bipolar subjects' depression ratings correlated positively with MRSI measures of Cho/Cr-PCr. In the right cingulate cortex, the Cho/Cr-PCr ratio was significantly higher in subjects with bipolar disorder compared with control subjects. In addition, bipolar subjects not taking antidepressants had a significantly higher right cingulate cortex Cho/Cr-PCr ratio compared with patients taking antidepressants or controls. No clinical or drug-related changes were observed for the Ino/Cr-PCr ratio. CONCLUSIONS: The results of this study suggest that bipolar disorder is associated with alterations in the metabolism of cytosolic, choline-containing compounds in the anterior cingulate cortex. As this resonance arises primarily from phosphocholine and glycerophosphocholine, both of which are metabolites of phosphatidylcholine, these results are consistent with impaired intraneuronal signaling mechanisms.


Asunto(s)
Afecto/fisiología , Trastorno Bipolar/fisiopatología , Colina/metabolismo , Giro del Cíngulo/fisiopatología , Inositol/metabolismo , Espectroscopía de Resonancia Magnética , Adulto , Afecto/efectos de los fármacos , Trastorno Bipolar/diagnóstico , Trastorno Bipolar/tratamiento farmacológico , Mapeo Encefálico , Dominancia Cerebral/efectos de los fármacos , Dominancia Cerebral/fisiología , Femenino , Giro del Cíngulo/efectos de los fármacos , Humanos , Carbonato de Litio/uso terapéutico , Masculino , Persona de Mediana Edad , Fosfocreatina/metabolismo , Escalas de Valoración Psiquiátrica , Ácido Valproico/uso terapéutico
2.
Biol Psychiatry ; 45(9): 1197-202, 1999 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-10331112

RESUMEN

BACKGROUND: Cerebrospinal fluid levels of myo-Inositol (m-Ino) are reported to be decreased in patients with affective disorder, and dietary supplements of m-Ino have been shown to reduce the symptoms of major depression. Myo-Inositol transport across the blood-brain barrier is mediated by a low capacity, saturable system. This study tests whether dietary m-Ino increases brain m-Ino or changes brain metabolism of m-Ino, possibly explaining the ability of this compound to alter mood. METHODS: Using proton magnetic resonance spectroscopic imaging, we measured m-Ino levels in occipital gray and parietal white matter of seventeen healthy subjects. Magnetic resonance spectroscopic imaging was performed twice at baseline as well as at day 4 and day 8 while subjects ingested 6 g of m-Ino twice a day. RESULTS: Following 4 days of m-Ino, m-Ino/Cr was 20% higher than baseline levels in occipital gray matter (p < 0.04) and 8% higher in parietal white matter (p = ns). By day 8, m-Ino/Cr ratios had returned to baseline values. CONCLUSIONS: Brain m-Ino levels initially increase during m-Ino administration and subsequently return to baseline levels. The time-limited increases observed for brain m-Ino may reflect homeostatic mechanisms, possibly associated with the role of m-Ino as a cerebral osmolyte, or with changes in brain phosphoinositide metabolism.


Asunto(s)
Encéfalo/metabolismo , Inositol/administración & dosificación , Inositol/metabolismo , Adulto , Encéfalo/efectos de los fármacos , Mapeo Encefálico , Femenino , Humanos , Espectroscopía de Resonancia Magnética , Masculino , Protones , Factores de Tiempo
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