Skip to main content

In Vivo Measurement of Hepatic Drug Transporter Inhibition with Radiolabeled Bile Acids

  • Protocol
  • First Online:
Experimental Cholestasis Research

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1981))

Abstract

Drug-induced liver injury, and more specifically drug-induced cholestasis, is responsible for a large amount of hospitalizations and attrition of new drug candidates in preclinical drug development. Drug-induced cholestasis can be triggered by drugs that are inhibitors of the hepatic bile acid transporters. Therefore, it is of considerable interest in preclinical drug development to detect whether new candidate drugs can cause interference with the hepatic bile acid transporters. Although several cost-effective and fast in vitro assays are available to that end, these do not mimic the in vivo situation completely. In vivo research to monitor a new candidate drug’s cholestatic potential is still relevant, yet is time-consuming and requires invasive sampling of a lot of laboratory animals. In this chapter, a protocol is provided to determine in vivo inhibition of the hepatic bile acid transporters in mice, using the nuclear imaging techniques positron emission tomography and single photon emission computed tomography. The protocol includes detailed information on preparation of the animal, scan acquisition, processing, and (statistical) analysis.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 119.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Bleibel W, Kim S, D’Silva K et al (2007) Drug-induced liver injury: review article. Dig Dis Sci 52:2463–2471

    Article  Google Scholar 

  2. Regev A (2014) Drug-induced liver injury and drug development: industry perspective. Semin Liver Dis 34:227–239

    Article  CAS  Google Scholar 

  3. Yang K, Ock KK, Sedykh A et al (2013) An updated review on drug-induced cholestasis: mechanisms and investigation of physicochemical properties and pharmacokinetic parameters. J Pharm Sci 102:3037–3057

    Article  CAS  Google Scholar 

  4. Klaassen CD, Aleksunes LM (2014) Xenobiotic, bile acid, and cholesterol transporters: function and regulation. Pharmacol Rev 62:1–96

    Article  Google Scholar 

  5. Alrefai W, Gill RK (2007) Bile acid transporters: structure, function, regulation and pathophysiological implications. Pharm Res 24:1803–1823

    Article  CAS  Google Scholar 

  6. Bohan A, Boyer JL (2002) Mechanisms of hepatic transport of drugs: Implications for cholestatic drug reactions. Semin Liver Dis 22:123–136

    Article  CAS  Google Scholar 

  7. de Lima Toccafondo Vieira M, Tagliati CA (2014) Hepatobiliary transporters in drug-induced cholestasis: a perspective on the current identifying tools. Expert Opin Drug Metab Toxicol 10:581–597

    Article  Google Scholar 

  8. Bergman E, Hedeman M, Bondesson U et al (2010) The effect of acute administration of rifampicin and imatinib on the enterohepatic transport of rosuvastatin in vivo. Xenobiotica 40:558–568

    Article  CAS  Google Scholar 

  9. Sjögren E, Hedeland M, Bondesson U et al (2014) Effects of verapamil on the pharmacokinetics and hepatobiliary disposition of fexofenadine in pigs. Eur J Pharm Sci 57:214–223

    Article  Google Scholar 

  10. Shin DH, Park SH, Jeong SW et al (2014) Hepatic uptake of epirubicin by isolated rat hepatocytes and its biliary excretion after intravenous infusion in rats. Arch Pharm Res 37:1599–1606

    Article  CAS  Google Scholar 

  11. Cunha L, Horvath I, Ferreira S et al (2014) Preclinical imaging: an essential ally in modern biosciences. Mol Diagnosis Ther 18:153–173

    Article  Google Scholar 

  12. Neyt S, Huisman MT, Vanhove C et al (2013) In vivo visualization and quantification of (disturbed) Oatp-mediated hepatic uptake and Mrp2-mediated biliary excretion of 99mTc-mebrofenin in mice. J Nucl Med 54:624–630

    Article  CAS  Google Scholar 

  13. Neyt S, Vliegen M, Verreet B et al (2016) Synthesis, in vitro and in vivo small-animal SPECT evaluation of novel technetium labeled bile acid analogues to study (altered) hepatic transporter function. Nucl Med Biol 43:642–649

    Article  CAS  Google Scholar 

  14. Shingaki T, Takashima T, Ijuin R et al (2013) Evaluation of Oatp and Mrp2 activities in hepatobiliary excretion using newly developed positron emission tomography tracer [11C]dehydropravastatin in rats. J Pharmacol Exp Ther 347:193–202

    Article  CAS  Google Scholar 

  15. Chen X, Zhang C, Wang H et al (2009) Altered integrity and decreased expression of hepatocyte tight junctions in rifampicin-induced cholestasis in mice. Toxicol Appl Pharmacol 240:26–36

    Article  CAS  Google Scholar 

  16. Vavricka SR, Van Montfoort J, Ha HR et al (2002) Interactions of rifamycin SV and rifampicin with organic anion uptake systems of human liver. Hepatology 36:164–172

    Article  CAS  Google Scholar 

  17. De Lombaerde S, Neyt S, Kersemans K et al (2017) Synthesis, in vitro and in vivo evaluation of 3β-[18F]fluorocholic acid for the detection of drug-induced cholestasis in mice. PLoS One 12(3):e0173529

    Article  Google Scholar 

  18. Hartman JC, Brouwer K, Mandagere A et al (2010) Evaluation of the endothelin receptor antagonists ambrisentan, darusentan, bosentan, and sitaxsentan as substrates and inhibitors of hepatobiliary transporters in sandwich-cultured human hepatocytes. Can J Physiol Pharmacol 88:682–691

    Article  CAS  Google Scholar 

  19. Fattinger K, Funk C, Pantze M et al (2001) The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: a potential mechanism for hepatic adverse reactions. Clin Pharmacol Ther 69:223–231

    Article  CAS  Google Scholar 

  20. Leslie EM, Watkins PB, Kim RB et al (2007) Differential inhibition of rat and human Na+-dependent taurocholate cotransporting polypeptide (NTCP/SLC10A1) by bosentan: a mechanism for species differences in hepatotoxicity. J Pharmacol Exp Ther 321:1170–1178

    Article  CAS  Google Scholar 

  21. Ghibellini G, Johnson BM, Kowalsky RJ et al (2004) A novel method for the determination of biliary clearance in humans. AAPS J 6:45–56

    Article  Google Scholar 

  22. Ghibellini G, Leslie EM, Pollack GM et al (2008) Use of tc-99m mebrofenin as a clinical probe to assess altered hepatobiliary transport: integration of in vitro, pharmacokinetic modeling, and simulation studies. Pharm Res 25:1851–1860

    Article  CAS  Google Scholar 

  23. Diehl KH, Hull R, Morton D et al (2001) A good practice guide to the administration of substances and removal of blood, including routes and volumes. J Appl Toxicol 21:15–23

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Stef De Lombaerde .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2019 Springer Science+Business Media, LLC, part of Springer Nature

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

De Lombaerde, S., Neyt, S., Vanhove, C., De Vos, F. (2019). In Vivo Measurement of Hepatic Drug Transporter Inhibition with Radiolabeled Bile Acids. In: Vinken, M. (eds) Experimental Cholestasis Research. Methods in Molecular Biology, vol 1981. Humana, New York, NY. https://doi.org/10.1007/978-1-4939-9420-5_6

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-9420-5_6

  • Published:

  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-4939-9419-9

  • Online ISBN: 978-1-4939-9420-5

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics