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pubmed-article:10707113pubmed:abstractTextThe effects of multiple-dosing with dehydroepiandrosterone sulfate (DHEA-SO4) on the pharmacokinetics and pharmacodynamics of prednisolone were examined. Prednisolone (25 mg/kg i.v.) was administered to male and female Sprague-Dawley rats (250-350 g) alone and following DHEA-SO4 (4 mg/kg i.v., every 8 h for 4 days). Male control rats cleared prednisolone faster [3.68 +/- 1.30 (males) vs 1.01 +/- 0.7 l/h/kg; p < 0.05] and had larger Vss (1.38 +/- 0.459 vs 0.394 +/- 0.500 l/kg; p < 0.05) than females both due largely to lesser plasma protein binding. Prednisolone clearance and Vss were not altered by DHEA-SO4 in males or females. The net effect of prednisolone on basophils and plasma corticosterone did not differ with gender. DHEA-SO4 had no effect on plasma corticosterone and did not alter prednisolone action. DHEA-SO4 inhibited basophil trafficking in males, but to a lesser extent than prednisolone, and antagonized the effect of prednisolone on basophil trafficking in both sexes. The steroid-sparing effect observed with DHEA clinically may not be due to an alteration of corticosteroid pharmacokinetics but partly to its ability to affect immune functions.lld:pubmed
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pubmed-article:10707113pubmed:authorpubmed-author:HonY YYYlld:pubmed
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pubmed-article:10707113pubmed:authorpubmed-author:Van WartSSlld:pubmed
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pubmed-article:10707113pubmed:pagination51-70lld:pubmed
pubmed-article:10707113pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:10707113pubmed:articleTitlePharmacokinetic and pharmacodynamic interactions between dehydroepiandrosterone and prednisolone in the rat.lld:pubmed
pubmed-article:10707113pubmed:affiliationDepartment of Pharmaceutics, School of Pharmacy, State University of New York at Buffalo 14260, USA.lld:pubmed
pubmed-article:10707113pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10707113pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed