Zusammenfassung
Die pharmakokinetischen Einflußgrößen der Neuroleptikawirkung sind in Abb. 2.1.1 dargestellt. Während stark polare oder hydrophile Substanzen einem Ein-Kompartment-Modell folgen, sind zur Beschreibung der pharmakokinetischen Verhältnisse lipophiler Substanzen wie der Neuroleptika Multi-Kompartment-Modelle notwendig. Nach Resorption eines oral gegebenen Neuroleptikums kommt es zu einer teilweisen präsystemischen Verstoffwechselung, die bei parenteraler Gabe z. B. eines Depotneuroleptikums umgangen werden kann. Aus dem Plasma wird das Pharmakon in die verschiedenen Kompartimente verteilt und dort gebunden, in der Leber metabolisiert und renal sowie biliär ausgeschieden. Nur der Anteil des Neuroleptikums, der nicht an Plasmaproteine gebunden ist, also in freier Form vorliegt, kann mit dem Hirngewebe und dem Liquorraum im Gleichgewicht stehen. An einem idealisierten Plasmaspiegel-Kurvenverlauf (Abb. 2.1.2) lassen sich eine initiale Absorptionsphase, die Verteilung und Äquilibrierung mit den einzelnen Körperkompartimenten, die Elimination sowie das Zurückfluten aus den äquilibrierenden Kompartimenten unterscheiden.
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Heininger, K., Sieberns, S., Gaebel, W. (1992). Pharmakologie. In: Riederer, P., Laux, G., Pöldinger, W. (eds) Neuro-Psychopharmaka Ein Therapie-Handbuch. Springer, Vienna. https://doi.org/10.1007/978-3-7091-3282-1_2
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