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Received for publication October 31, 2006.
Revised April 26, 2007.
Accepted for publication April 26, 2007.
S-8921 is a novel inhibitor of the ileal apical sodium-dependent bile acid transporter (ASBT/SLC10A2) developed for the treatment of hypercholesterolemia. The present study investigated the hypocholesterolemic action of S-8921 glucuronide (S-8921G) in rats. The plasma concentration of S-8921G was higher than that of S-8921 after single oral administration of S-8921 in normal rats, and S-8921G was excreted into the bile (13% of dose). Oral administration of either S-8921 or S-8921G reduced the serum total cholesterol, particularly non-high density lipoprotein cholesterol, in hypercholesterolemic normal rats. In Gunn rats devoid of UGT1A activity, S-8921G was undetectable both in the plasma and bile specimens, and only S-8921G administration significantly reduced the serum non-high density lipoprotein cholesterol. An in vitro inhibition study showed that glucuronidation converts S-8921 to a 6,000-fold more potent inhibitor of hASBT (Ki 18 nM versus 109 µM). S-8921G was detected both in the portal plasma and loop when S-8921 was administered into the loop of the rat jejunum although the cumulative amount of S-8921G recovered in the bile was 5-fold greater than that in the loop. The uptake of S-8921G by freshly prepared rat hepatocytes was saturable, and sodium-dependent and -independent systems were involved. Organic anions, such as bromosulfophthalein, estrone 3-sulfate and taurocholic acid, inhibited the uptake. These results suggest that UDP-glucuronosyltransferase-1 isoforms play a critical role in the hypocholesterolemic action of S-8921 by converting S-8921 to a more potent ASBT inhibitor, and organic anion transporter(s) are also involved in its pharmacological action through the biliary excretion of S-8921G.
Key words:
ASBT, Gunn rats, UGT1, glucuronidation, hypocholesterolemic action, transport