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Inhibition of regorafenib against UDP-glucuronosyltransferases
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Xiao-ya SUN1, Guang-bo GE2, Hui TANG1, *, Ya-qiao WANG1, Xin-cheng YAO1, Le LI1
Acta Pharmaceutica Sinica | 2017, 52(11) : 1705 - 1714
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Acta Pharmaceutica Sinica | 2017, 52(11): 1705-1714
ORIGINAL ARTICLES
Inhibition of regorafenib against UDP-glucuronosyltransferases
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Xiao-ya SUN1, Guang-bo GE2, Hui TANG1, *, Ya-qiao WANG1, Xin-cheng YAO1, Le LI1
Affiliations
  • 1. Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, Pharmacy School of Shihezi University, Shihezi 832002, China
  • 2. Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China
Published: 2017-11-12 doi: 10.16438/j.0513-4870.2017-0424
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This study was designed to investigate the inhibitory effects of regorafenib (REG) on the catalytic activities of 12 kinds of human UGT isoforms and human liver microsomes (HLM) in vitro. The broader potential of REG to perpetrate drug-drug interactions (DDI) arising from UGT enzyme inhibition is predicted by in vitro-vivo extrapolation (IV-IVE). Fifty mixed HLM and 12 kinds of recombinant UGTs were utilized as enzyme sources to evaluation the inhibitory effects of REG against UGTs. 4-Methylumbelliferone (4-MU) as a nonselective substrate of UGTs except for UGT1A4, N-(3-carboxypropyl)-4-hydroxy-1, 8-napht-halimide (NCHN) and N-butyl-4-(4-hydroxyphenyl)-1, 8-naphthalimide (NPHN) as the specific fluorescent substrate of UGT1A1, and trifluoperazine (TFP) as the specific substrate of UGT1A4. The half maximal inhibitory concentration (IC50) was calculated via the nonlinear regression analysis using Graphpad Prism 6.0, the inhibition kinetic types were selected and evaluated based on the intersection location of Lineweaver-Burk plot and Dixon plot, and Ki values were determined by the second plot of slopes. The potential DDI risk based on UGT1A1 inhibition was also evaluated through the in vitro parameters. The results demonstrated that REG displayed strong inhibitory effects against UGT1A1, 1A7, 1A9, and 2B7. The IC50 values were from 0.15 to 6.6 μmol·L-1 and Ki values from 0.027 to 14 μmol·L-1. The REG exerted competitive inhibition against UGT1A1-mediated 4-MU-O-glucuronidation and UGT1A1-mediated NPHN-O-glucuronidation, while the inhibition of NCHN-4-O-glucuronide by REG was suited to noncompetitive inhibition in both HLM and recombinant UGT1A1. Likewise, REG exhibited a mixed efficacy in inhibition of UGT1A7-, UGT1A9-, and UGT2B7-catalyzed 4-MU-O-glucuronidation. The AUC ratio of UGT1A1 specific substrates NPHN and NCHN can be increased by 101% to 302% and 13% to 109%, respectively. These results suggest that much caution should be exercised when REG is co-administered with UGT1A1 substrates.

regorafenib  /  UDP-glucuronosyltransferases  /  enzyme inhibition  /  drug-drug interaction
Xiao-ya SUN, Guang-bo GE, Hui TANG, Ya-qiao WANG, Xin-cheng YAO, Le LI. Inhibition of regorafenib against UDP-glucuronosyltransferases[J]. Acta Pharmaceutica Sinica, 2017 , 52 (11) : 1705 -1714 . DOI: 10.16438/j.0513-4870.2017-0424
Year 2017 volume 52 Issue 11
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Article Info
doi: 10.16438/j.0513-4870.2017-0424
  • Receive Date:2017-05-15
  • Online Date:2026-01-14
  • Published:2017-11-12
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History
  • Received:2017-05-15
  • Revised:2017-07-22
Funding
Affiliations
    1. Key Laboratory of Xinjiang Phytomedicine Resource and Utilization, Ministry of Education, Pharmacy School of Shihezi University, Shihezi 832002, China
    2. Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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