We have previously demonstrated that the HMG-CoA reductase inhibitor pravastatin is efficiently taken up by the liver via the 'multispecific anion transporter' in an active manner.3 To further examine the fate of pravastatin within the liver, its biliary excretion was studied in a single-pass liver
Functional integrity of hepatocyte canalicular membrane transport of taurocholate and bilirubin diglucuronide in eisai hyperbilirubinuria rats
โ Scribed by Yukihiko Adachi; Hiroaki Kobayashi; Mika Shouji; Motokazu Kitano; Yoshifumi Okuyama; Toshio Yamamoto
- Book ID
- 118345876
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 379 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0024-3205
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๐ SIMILAR VOLUMES
We have previously demonstrated that the HMG-CoA reductase inhibitor pravastatin is efficiently taken up by the liver via the 'multispecific anion transporter' in an active manner.3 To further examine the fate of pravastatin within the liver, its biliary excretion was studied in a single-pass liver
Isolated rat hepatocyte couplets were used to study the effect of S-adenosyl-L methionine (SAMe) treatment on disruption of canalicular function caused by cyclosporin A (CyA). Canalicular function was assessed by counting the percentage of couplets that were able to accumulate the fluorescent cholep