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Herling, Andreas W.; Schwab, Dietmar; Burger, Hans-Joerg; Maas, Jochen; Hammerl, Roland; Schmidt, Dietmar; Strohschein, Sabine; Hemmerle, Horst; Schubert, Gerrit; Petry, Stefan; Kramer, Werner
Biochimica et biophysica acta, 01/2002, Letnik: 1569, Številka: 1Journal Article
Chlorogenic acid derivatives are potent inhibitors of hepatic glucose production by inhibition of the glucose-6-phosphate translocase component of the hepatic glucose-6-phosphatase system. The pharmacological proof of concept was clearly demonstrated during i.v. infusion of potent derivatives (S 4048, S 3483) in rats. However, the blood glucose lowering effect of S 4048 after bolus i.v. injection lasted only 60–90 min. Plasma clearance of S 4048 was very high, and the parent compound was rapidly and efficiently excreted into the bile of Wistar and GY/TR − rats, indicating that mrp-2 was not involved in this hepatobiliary elimination process. About 72% of the total administered radioactivity appeared in the bile within 20 min after i.v. bolus injection of the radiolabeled analogue 3HS 1743 in a Wistar rat. However, in GY/TR − rats the dicarboxylic analogue of S 4048, S 3025, was cleared from the plasma less rapidly than its parent compound and its biliary elimination was comparatively low. In contrast, S 3025 exhibited comparable pharmacokinetics and biliary elimination profile as S 4048 in Wistar rats, suggesting that biliary elimination of S 3025 is facilitated by mrp-2, functionally absent in GY/TR − rats. Targeting to mrp-2 resulted in a significantly prolonged reduction of blood glucose levels in GY/TR − rats after i.v. bolus administration of S 3025.
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