RESUMEN
Ataxia severity, cerebellar hemispheric blood flow (CHBF), ascorbate free radical (AFR), superoxide dismutase protein, superoxide scavenging activity, and 8-hydroxy-2'-deoxyguanosine (8-OHdG) in cerebrospinal fluid (CSF) were compared before and after an 8-week course of repetitive transcranial magnetic stimulation (rTMS) in 20 patients with spinocerebellar degenerations (SCD). SCD patients showed higher AFR, 8-OHdG, and superoxide scavenging activity than 19 controls. In SCD patients, AFR and ataxia severity declined, and CHBF increased after rTMS. As the SCD patients showed negative correlations between ataxia severity and CHBF or superoxide scavenging activity, the therapeutic mechanism of rTMS may involve decreased oxidative stress and increased CHBF.
Asunto(s)
Terapia por Estimulación Eléctrica , Depuradores de Radicales Libres/líquido cefalorraquídeo , Estrés Oxidativo , Degeneraciones Espinocerebelosas , Estimulación Magnética Transcraneal , Adulto , Ácido Ascórbico/líquido cefalorraquídeo , Circulación Cerebrovascular/fisiología , Desoxiadenosinas/líquido cefalorraquídeo , Terapia por Estimulación Eléctrica/métodos , Ensayo de Inmunoadsorción Enzimática/métodos , Humanos , Persona de Mediana Edad , Flujo Sanguíneo Regional/fisiología , Índice de Severidad de la Enfermedad , Degeneraciones Espinocerebelosas/líquido cefalorraquídeo , Degeneraciones Espinocerebelosas/clasificación , Degeneraciones Espinocerebelosas/fisiopatología , Degeneraciones Espinocerebelosas/cirugía , Superóxido Dismutasa/líquido cefalorraquídeo , Factores de TiempoRESUMEN
INTRODUCTION: Normal brain development and function depend on the active transport of folates across the blood-brain barrier. The folate receptor-1 (FR 1) protein is localized at the basolateral surface of the choroid plexus, which is characterized by a high binding affinity for circulating 5-methyltetrahydrofolate (5-MTHF). PATIENTS AND METHODS: We report on the clinical and metabolic findings among five children with normal neurodevelopmental progress during the first four to six months followed by the acquisition of a neurological condition which includes marked irritability, decelerating head growth, psychomotor retardation, cerebellar ataxia, dyskinesias (choreoathetosis, ballism), pyramidal signs in the lower limbs and occasional seizures. After the age of six years the two oldest patients also manifested a central visual disorder. Known disorders have been ruled out by extensive investigations. Cerebrospinal fluid (CSF) analysis included determination of biogenic monoamines, pterins and 5-MTHF. RESULTS: Despite normal folate levels in serum and red blood cells with normal homocysteine, analysis of CSF revealed a decline towards very low values for 5-methyltetrahydrofolate (5-MTHF), which suggested disturbed transport of folates across the blood-brain barrier. Genetic analysis of the FR 1 gene revealed normal coding sequences. Oral treatment with doses of the stable compound folinic acid (0.5-1 mg/kg/day Leucovorin(R)) resulted in clinical amelioration and normalization of 5-MTHF values in CSF. CONCLUSION: Our findings identified a new condition manifesting after the age of 6 months which was accompanied by low 5-MTHF in cerebrospinal fluid and responded to oral supplements with folinic acid. However, the cause of disturbed folate transfer across the blood-brain barrier remains unknown.