JINA de Rancho Jerez

HD-A, AA-0/0, eyes-free

(Ch.Pl. N.Cl.W.N.'03 J.W.of Pl..O'EMIR de la Douce Plaine X Ch.Pl. J.Ch.of H. BIJOU Ambassadeur des Belges)

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Monitoring parameters for metoclopramide and the effect of dosing regimen are shown in Supplementary Table 5. DISCUSSION The main feature of our study was the identification of novel pharmacodynamic effects in the context of pharmacokinetics metoclopramide. Furthermore, the finding of no difference between the different groups regarding plasma exposure of metoclopramide to brain was particularly interesting because the drug was administered subcutaneously and thus directly to the brain. observation of a decrease in peak plasma concentration with time points between 40 and 240 min also supports the hypothesis that observed pharmacogenic effects of metoclopramide may be related to the rate-limiting step, i.e. at blood and/or the brain interface, before metoclopramide is distributed across the extracellular milieu to reach brain tissues. The results of our study thus suggest that the decrease in plasma exposure with time may be the cause of observed pharmacokinetic profile metoclopramide that is of potential clinical utility. On the other hand, it is possible, that the increase of peak concentration metoclopramide between 40 and 240 min may be the reason for decreased brain exposure. Furthermore, while the observed effect is at first sight surprising because it was not observed in a clinical situation, since it would lead to a change in the dose or mode of administration, it is worth noting that the data indicate this phenomenon may be responsible for the decrease in exposure of metoclopramide