Literature DB >> 23169269

The vesicular transport assay: validated in vitro methods to study drug-mediated inhibition of canalicular efflux transporters ABCB11/BSEP and ABCC2/MRP2.

Krisztina Herédi-Szabó1, Emese Kis, Peter Krajcsi.   

Abstract

The canalicular membrane of hepatocytes contains several transport proteins that use the energy of ATP to efflux potentially toxic molecules to the bile. Probably the two most important proteins at this location are MRP2 and BSEP, which transport phase II conjugates of xenobiotics and endobiotics and conjugated bile salts, respectively. The impaired function of either of these transporter proteins reduces the clearance of the toxic conjugates, resulting in their accumulation in the hepatocytes and eventually the plasma. Conjugated bile salts and phase II metabolites are compounds with low passive permeability; therefore, the most commonly used test system to investigate MRP2- and BSEP-mediated transport processes is the vesicular transport assay. The concentration of probe substrates and inhibitors used in the experiment is close to their free concentration in the hepatocytes, providing an advantage when calculating kinetic parameters (K(m), K(i), V(max)). The protocols aim to assist scientists to set up a transport assay for a known or potential substrate and test small molecule inhibition of the transporters.

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Year:  2012        PMID: 23169269     DOI: 10.1002/0471140856.tx2304s54

Source DB:  PubMed          Journal:  Curr Protoc Toxicol        ISSN: 1934-9254


  4 in total

1.  Major glucuronide metabolites of testosterone are primarily transported by MRP2 and MRP3 in human liver, intestine and kidney.

Authors:  Cindy Yanfei Li; Abdul Basit; Anshul Gupta; Zsuzsanna Gáborik; Emese Kis; Bhagwat Prasad
Journal:  J Steroid Biochem Mol Biol       Date:  2019-04-05       Impact factor: 4.292

2.  Assessing Transporter-Mediated Natural Product-Drug Interactions Via In vitro-In Vivo Extrapolation: Clinical Evaluation With a Probe Cocktail.

Authors:  James T Nguyen; Dan-Dan Tian; Rakshit S Tanna; Deena L Hadi; Sumit Bansal; Justina C Calamia; Christopher M Arian; Laura M Shireman; Bálint Molnár; Miklós Horváth; Joshua J Kellogg; Matthew E Layton; John R White; Nadja B Cech; Richard D Boyce; Jashvant D Unadkat; Kenneth E Thummel; Mary F Paine
Journal:  Clin Pharmacol Ther       Date:  2020-12-23       Impact factor: 6.875

3.  Partial external biliary diversion in bile salt export pump deficiency: Association between outcome and mutation.

Authors:  Philipp Ellinger; Jan Stindt; Carola Dröge; Katharina Sattler; Claudia Stross; Stefanie Kluge; Diran Herebian; Sander H J Smits; Martin Burdelski; Sebastian Schulz-Jürgensen; Antje Ballauff; Jan Schulte Am Esch; Ertan Mayatepek; Dieter Häussinger; Ralf Kubitz; Lutz Schmitt
Journal:  World J Gastroenterol       Date:  2017-08-07       Impact factor: 5.742

4.  Phase I study of PF‐04895162, a Kv7 channel opener, reveals unexpected hepatotoxicity in healthy subjects, but not rats or monkeys: clinical evidence of disrupted bile acid homeostasis.

Authors:  Michael D Aleo; Jiri Aubrecht; Paul D Bonin; Deborah A Burt; Jennifer Colangelo; Lina Luo; Shelli Schomaker; Rachel Swiss; Simon Kirby; Greg C Rigdon; Pinky Dua
Journal:  Pharmacol Res Perspect       Date:  2019-02
  4 in total

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