Studies on Intestinal Absorption of Sulpiride (3): Intestinal Absorption of Sulpiride in Rats

Accession number;04A0042354
Title;Studies on Intestinal Absorption of Sulpiride (3): Intestinal Absorption of Sulpiride in Rats
Author; WATANABE K (Hokkaido Coll. Of Pharmacy, Hokkaido, Jpn) SAWANO T (Hokkaido Coll. Of Pharmacy, Hokkaido, Jpn) JINRIKI T (Hokkaido Coll. Of Pharmacy, Hokkaido, Jpn) SATO J (Hokkaido Coll. Of Pharmacy, Hokkaido, Jpn)
Journal Title;Biol Pharm Bull
Journal Code:S0989A
ISSN:0918-6158
VOL.27;NO.1;PAGE.77-81(2004)
Figure&Table&Reference;FIG.2, TBL.2, REF.20
Pub. Country;Japan
Language;English
Abstract;The aim of this study was to investigate whether the concomitant administration of the substrates or inhibitors of PEPT1, OCTN1, OCTN2, and P-glycoprotein affects the intestinal absorption of sulpiride in rats. The absorption of sulpiride from rat intestine was decreased by the substrates or inhibitors of PEPT1, OCTN1, and OCTN2. On the other hand, the absorption was increased by the substrates of P-glycoprotein. The effects of these concomitantly administered drugs on the pharmacokinetic behavior of sulpiride after oral administration in rats were investigated. Peak concentration (Cmax) and area under the plasma concentration-time curve (AUC0-8h) of sulpiride were decreased by the concomitant administration of the substrates or inhibitors of PEPT1, OCTN1, and OCTN2. However, the same parameters were significantly increased by the concomitant administration of the substrates of P-glycoprotein. The present results suggest the possibility of drug-drug interaction during the absorption process in the small intestine due to the coadministration of sulpiride and these agents. These findings provide important information for preventing adverse effects and for ensuring the effectiveness of sulpiride and concomitantly administered drugs. (author abst.)
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