Interactions in tissue distribution between methylphenidate and pemoline. II. Effects of methylphenidate or its metabolite on plasma and tissue concentrations of pemoline in the rat.

pemoline in rats were investigated.At 20min after intravenous administration of 3 mg/kg dose of pemoline as a loading dose,constant infusion at a rate of 139ƒÊg/h of the drug was carried out to give steady-state plasma level.In intravenous administration of 1mg/kg dose of RA during the constant infusion of pemoline,the plasma concentration of pemoline before and after the administration of RA did not change.Steady-state pemoline also did not affect the pharmacokinetics of RA.Onthe other hand,in intravenous administration of 1 mg/kg dose of MPD during the constant infusion of pemoline,the plasma concentration of pemoline slightly increased within 15min after the administration of MPD.Thereafter the concentration of pemoline returned to the level before the superimposition of MPD within 60min.The liver-,kidney-,lung-,muscleand blood cell-to-plasma concentration ratios of pemoline at5min after the administration of MPD became smaller compared with those of pemoline in the absence of MPD,and those of pemoline at 60min after the administration were approximately the same as those of pemoline in the absence of MPD.Steady-state pemoline did not affect the pharmacokinetics and tissue distribution of MPD. The increase of plasma concentration of pemoline caused by the superimposition of MPD may result in the displacement of pemoline from tissues and blood cell and/or MPD may inhibit the metabolism of pemoline.