The inhibitory effect of gadoxetate disodium on hepatic transporters: a study using indocyanine green View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-10

AUTHORS

Hiroyuki Akai, Koichiro Yasaka, Akira Kunimatsu, Masanori Nojima, Yusuke Inoue, Osamu Abe, Kuni Ohtomo, Shigeru Kiryu

ABSTRACT

OBJECTIVES: To assess the inhibitory effect of gadoxetate disodium on the transporter system using indocyanine green (ICG). MATERIALS AND METHODS: Groups of six female B6 Albino mice were injected with the test agent (0.62 mmol/kg gadoxetate disodium) or phosphate-buffered saline (control) 10 min before injection of ICG. Identical fluorescence images were subsequently obtained to create time-efficiency curves of liver parenchymal uptake. The study was performed on hypothermic and normothermic mice. The logarithms of the absorption rate constants (logKa values) and of the elimination rate constants (logKe values) were calculated for each experimental condition, and between-group differences were compared using Student's t-test. RESULTS: The logKe values of the test group were lower than those of the control group at both temperatures (-6.52 vs. -5.87 under hypothermic conditions and -4.54 vs. -4.14 under normothermic conditions), and both differences were statistically significant (p = 0.037, 0.015 respectively). In terms of the logKa values, although the difference did not reach statistical significance (p = 0.052), the test group had lower values than the control group under hypothermic conditions (-0.771 vs. -0.376). In normothermic mice, the logKa values for the test and control groups were 0.037 and 0.277 respectively, thus not significantly different (p = 0.404). CONCLUSIONS: Gadoxetate disodium inhibited ICG excretion. Thus, gadoxetate disodium inhibited the ATP-binding cassette sub-family C member 2 transporter. KEY POINTS: • Gadoxetate disodium inhibited ICG excretion. • Gadoxetate disodium tended to inhibit hepatic ICG uptake. • Drug-drug interactions of gadoxetate disodium need further investigation. More... »

PAGES

4128-4133

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00330-018-5403-5

DOI

http://dx.doi.org/10.1007/s00330-018-5403-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1103234261

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29651770


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