RESUMO
There is virtually no information on spontaneous variability of ECG body surface potential maps (BSPMs) and on dynamics of their reactive changes in healthy subjects. This study evaluated quantitatively the depolarization (QRS) and repolarization (QRST) parameters derived from the respective integral BSPMs, constructed beat-to-beat, from continual body surface ECG records in 9 healthy men resting supine, during head-up tilting and sitting. Spontaneous variability of the BSPMs parameters, both at rest and during postural reactions, was characterized by significant respiratory and low frequency oscillations, more pronounced when related to repolarization. Head-up tilting and sitting-up evoked significant decrease in the QRST-BSPM amplitudes, widening of the angle alpha and reduction of nondipolarity indexes, compared to the respective supine values. All these changes were gradual, characterized by transition phenomena and prolonged after-effects. Tilting back to horizontal restored the resting supine values. The postural effects on depolarization were individually more variable and in the average showed a minimal QRS-BSPM amplitude increase. Beat-to-beat analysis of a train of ECG BSPMs provided the first evidence of spontaneous, non-random, respiratory and low frequency oscillations of the ventricular repolarization pattern, and the first insight into the dynamics of body posture associated changes in ventricular recovery.
Assuntos
Mapeamento Potencial de Superfície Corporal , Eletrocardiografia/métodos , Frequência Cardíaca/fisiologia , Adulto , Sistema de Condução Cardíaco/fisiologia , Humanos , Masculino , Postura/fisiologiaRESUMO
The metabolism and urinary elimination of both (-)-deprenyl and (+)-deprenyl have been studied. Gas-chromatographic analysis with mass specific detection indicated that the metabolism of (-)-deprenyl results in a large excess of methamphetamine compared to amphetamine, while the metabolism of (+)-deprenyl gave nearly equal amounts of amphetamine and methamphetamine. A novel deprenyl metabolite, phenylacetone, was also identified in our studies.
