Atipamezole is a promising non-discriminative inhibitor against pan-CYP450 including diclofenac 4'-hydroxylation: A comparison with ABT for drug ADME optimization and mechanism study.
Clicks: 242
ID: 58205
2019
Article Quality & Performance Metrics
Overall Quality
Improving Quality
0.0
/100
Combines engagement data with AI-assessed academic quality
Reader Engagement
Emerging Content
4.8
/100
16 views
16 readers
Trending
AI Quality Assessment
Not analyzed
Abstract
1-aminobenzotriazole (ABT) is a known P450 enzyme non-selective inactivator that serves as a tool for assessing P450-mediated metabolism. However, many findings demonstrated that ABT was ineffective with human CYP2C9. A profound pan-CYP450 inhibitor is desired avoid the risk of incomplete inhibition of P450, especially CYP2C9. Atipamezole is commonly used to recover animals from sedation-anesthesia induced by αadrenoceptor agonists. The purpose of this study is to evaluate atipamezole as a non-selective inhibitor of P450 enzymes and compare it with ABT. Inhibition toward seven major human CYP450 isoform was determined for atipamezole and ABT in human, rat, and dog liver microsomes for the direct and time-dependent inhibition potentials. IC values toward human and animal CYPs without preincubation are 0.02-7.93 μM and 20.9-1798 μM for atipamezole and ABT, respectively. The IC values of ABT after preincubation shift to 4.06-460 μM. Atipamezole has more effective inhibition to CYP2C9 mediated diclofenac hydroxylation in human and animal liver microsomes with IC values of 1.50-5.20 μM than that of ABT at 74.7-460 μM. No IC shift was observed for atipamezole to CYP isoforms. In vivo utility of atipamezole was assessed by co-dosing with diclofenac in rats. At 30 mg/kg via oral, atipamezole enhanced the AUC of diclofenac by 13.1-fold and the C by 5.6-fold. Similar enhancement also achieved for ABT (100 mg/kg) with AUC and C increased 9.5 and 4.8-fold. As a reversible pan-CYP inhibitor, atipamezole showed less species difference than ABT. It provides a better and easier to use alternative to ABT for ADME optimization and elucidating mechanistic drug metabolism or toxicity studies.
| Reference Key |
li2019atipamezoleeuropean
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Li, Zheng;Zhang, Yunxia;Gao, You;Xiang, Yanan;Zhang, Wenpeng;Lu, Chuang;Zhuang, Xiaomei; |
| Journal | European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences |
| Year | 2019 |
| DOI |
S0928-0987(19)30018-1
|
| URL | |
| Keywords |
inhibitor
p450
adme
1-aminobenzotriazole (abt) (pubchem cid:1367)
abt
amodiaquine (pubchem cid: 2165)
atipamezole
atipamezole hydrochloride (pubchem cid: 13649426)
bupropion (pubchem cid: 444)
dextromethorphan (pubchem cid: 5360696)
diclofenac (pubchem cid: 3033)
fexofenadine (pubchem cid: 3348)
mdz, midazolam (pubchem cid: 4192)
phenacetin (pubchem cid: 4754)
s-mephenytoin (pubchem cid: 107921)
|
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.