THE ENHANCING MECHANISM OF CAPRIC ACID (C10) FROM A SUPPOSITORY ON RECTAL DRUG ABSORPTION THROUGH A PARACELLULAR PATHWAY

Citation
H. Takahashi et al., THE ENHANCING MECHANISM OF CAPRIC ACID (C10) FROM A SUPPOSITORY ON RECTAL DRUG ABSORPTION THROUGH A PARACELLULAR PATHWAY, Biological & pharmaceutical bulletin, 20(4), 1997, pp. 446-448
Citations number
11
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
09186158
Volume
20
Issue
4
Year of publication
1997
Pages
446 - 448
Database
ISI
SICI code
0918-6158(1997)20:4<446:TEMOCA>2.0.ZU;2-7
Abstract
Capric acid (C10) enhanced the absorption of cefoxitin sodium in a con centration-dependent manner following the rectal administration as a s uppository in rats, Tile optimal concentration of C10 was 13%. CIO adm inistered as a suppository also reduced rectal membrane resistance (R- m), showing that the above enhancing effect was induced by widening th e paracellular pathway. Both the enhancing Effect. on the absorption a nd the reducing effect on R-m were inhibited by W7, an inhibitor of my osin light chain kinase, These results supported that, as shown in the ill vitro Caco-2 cell sg stem, tile C10 effect on the paracellular pa thway is due to activating the contraction of Ca2+-calmodulin-dependen t actin filament.