Literature DB >> 28070880

On the Molecular Basis Underlying the Metabolism of Tapentadol Through Sulfation.

Ahsan F Bairam1, Mohammed I Rasool1, Katsuhisa Kurogi1,2, Ming-Cheh Liu3.   

Abstract

BACKGROUND AND OBJECTIVES: Previous studies reported that tapentadol-sulfate represented one of the major metabolites of tapentadol excreted in urine. The current study aimed to identify the human cytosolic sulfotransferases (SULTs) that is(are) capable of sulfating tapentadol and to examine whether human cells and human organ specimens are capable of sulfating tapentadol.
METHODS: Thirteen human SULTs, previously expressed and purified, as well as human organ cytosols, were analyzed for tapentadol-sulfating activity using an established sulfotransferase assay. Cultured HepG2 human hepatoma cells and Caco-2 human colon carcinoma cells were labeled with [35S]sulfate in the presence of different concentrations of tapentadol.
RESULTS: Three of the thirteen human SULTs, SULT1A1, SULT1A3, and SULT1C4, were found to display sulfating activity toward tapentadol. Kinetic analysis revealed that SULT1A3 displayed the highest catalytic efficiency in mediating the sulfation of tapentadol, followed by SULT1A1 and SULT1C4. Using cultured HepG2 and Caco-2 cells, the generation and release of sulfated tapentadol under metabolic conditions was demonstrated. Moreover, of the four human organ specimens (kidney, liver, lung, and small intestine) tested, the cytosols prepared from small intestine and liver showed significant tapentadol-sulfating capacity (at 0.0203 and 0.0054 nmol/min/mg, respectively).
CONCLUSION: Taken together, the results derived from the current study provided a molecular basis underlying the sulfation of tapentadol in humans.

Entities:  

Keywords:  HepG2 Cell; Human Organ; Sulfating Activity; Sulfation; Tapentadol

Mesh:

Substances:

Year:  2017        PMID: 28070880     DOI: 10.1007/s13318-016-0392-8

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  48 in total

1.  Tapentadol and its two mechanisms of action: is there a new pharmacological class of centrally-acting analgesics on the horizon?

Authors:  Hans G Kress
Journal:  Eur J Pain       Date:  2010-07-24       Impact factor: 3.931

Review 2.  Structure, function and polymorphism of human cytosolic sulfotransferases.

Authors:  Julian Lindsay; Lin-Lin Wang; Yong Li; Shu-Feng Zhou
Journal:  Curr Drug Metab       Date:  2008-02       Impact factor: 3.731

3.  cDNA cloning, expression, and characterization of the human bifunctional ATP sulfurylase/adenosine 5'-phosphosulfate kinase enzyme.

Authors:  K Yanagisawa; Y Sakakibara; M Suiko; Y Takami; T Nakayama; H Nakajima; K Takayanagi; Y Natori; M C Liu
Journal:  Biosci Biotechnol Biochem       Date:  1998-05       Impact factor: 2.043

4.  Cholesterol and hydroxycholesterol sulfotransferases: identification, distinction from dehydroepiandrosterone sulfotransferase, and differential tissue expression.

Authors:  N B Javitt; Y C Lee; C Shimizu; H Fuda; C A Strott
Journal:  Endocrinology       Date:  2001-07       Impact factor: 4.736

5.  Human adult and foetal liver sulphotransferases: inhibition by mefenamic acid and salicylic acid.

Authors:  M Vietri; A Pietrabissa; F Mosca; A Rane; G M Pacific
Journal:  Xenobiotica       Date:  2001-03       Impact factor: 1.908

Review 6.  Tapentadol hydrochloride: a centrally acting oral analgesic.

Authors:  William E Wade; William J Spruill
Journal:  Clin Ther       Date:  2009-12       Impact factor: 3.393

7.  Pharmacological characterization of morphine-6-sulfate and codeine-6-sulfate.

Authors:  A Zuckerman; E Bolan; T de Paulis; D Schmidt; S Spector; G W Pasternak
Journal:  Brain Res       Date:  1999-09-18       Impact factor: 3.252

8.  Molecular cloning, expression, and characterization of novel human SULT1C sulfotransferases that catalyze the sulfonation of N-hydroxy-2-acetylaminofluorene.

Authors:  Y Sakakibara; K Yanagisawa; J Katafuchi; D P Ringer; Y Takami; T Nakayama; M Suiko; M C Liu
Journal:  J Biol Chem       Date:  1998-12-18       Impact factor: 5.157

9.  The inadequacy of perinatal glucuronidation: immunoblot analysis of the developmental expression of individual UDP-glucuronosyltransferase isoenzymes in rat and human liver microsomes.

Authors:  M W Coughtrie; B Burchell; J E Leakey; R Hume
Journal:  Mol Pharmacol       Date:  1988-12       Impact factor: 4.436

10.  Sulfation of opioid drugs by human cytosolic sulfotransferases: metabolic labeling study and enzymatic analysis.

Authors:  Katsuhisa Kurogi; Andriy Chepak; Michael T Hanrahan; Ming-Yih Liu; Yoichi Sakakibara; Masahito Suiko; Ming-Cheh Liu
Journal:  Eur J Pharm Sci       Date:  2014-05-14       Impact factor: 4.384

View more
  3 in total

1.  Effects of human SULT1A3/SULT1A4 genetic polymorphisms on the sulfation of acetaminophen and opioid drugs by the cytosolic sulfotransferase SULT1A3.

Authors:  Ahsan F Bairam; Mohammed I Rasool; Fatemah A Alherz; Maryam S Abunnaja; Amal A El Daibani; Katsuhisa Kurogi; Ming-Cheh Liu
Journal:  Arch Biochem Biophys       Date:  2018-04-26       Impact factor: 4.013

2.  Effects of the human SULT1A1 polymorphisms on the sulfation of acetaminophen,O-desmethylnaproxen, and tapentadol.

Authors:  Mohammed I Rasool; Ahsan F Bairam; Saud A Gohal; Amal A El Daibani; Fatemah A Alherz; Maryam S Abunnaja; Eid S Alatwi; Katsuhisa Kurogi; Ming-Cheh Liu
Journal:  Pharmacol Rep       Date:  2018-12-10       Impact factor: 3.024

Review 3.  Pharmacological rationale for tapentadol therapy: a review of new evidence.

Authors:  Patrizia Romualdi; Mariagrazia Grilli; Pier Luigi Canonico; Massimo Collino; Anthony H Dickenson
Journal:  J Pain Res       Date:  2019-05-16       Impact factor: 3.133

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.