Effect of codeine on CYP450 isoform activity of rats
Context: Codeine, also known as 3-methylmorphine, is an opiate used to treat pain, as a cough medicine and for diarrhoea. No study on the effects of codeine on the metabolic capacity of CYP enzyme is reported. Objective: In order to investigate the effects of codeine on the metabolic capacity of cyt...
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doaj-cb2bdca0eb1b466c93ef9d9a1a0db7552020-11-25T03:43:20ZengTaylor & Francis GroupPharmaceutical Biology1388-02091744-51162017-01-015511223122710.1080/13880209.2017.12974661297466Effect of codeine on CYP450 isoform activity of ratsShuanghu Wang0Yanwen Dong1Ke Su2Jing Zhang3Linyi Wang4Anyue Han5Congcong Wen6Xianqin Wang7Yan He8The People's Hospital of LishuiLaboratory Animal Centre of Wenzhou Medical UniversityLaboratory Animal Centre of Wenzhou Medical UniversityLaboratory Animal Centre of Wenzhou Medical UniversityLaboratory Animal Centre of Wenzhou Medical UniversityLaboratory Animal Centre of Wenzhou Medical UniversityLaboratory Animal Centre of Wenzhou Medical UniversityAnalytical and Testing Center of Wenzhou Medical UniversityThe Institute of Molecular Medicine, School of Optometry and Ophthalmology and Eye Hospital, Wenzhou Medical UniversityContext: Codeine, also known as 3-methylmorphine, is an opiate used to treat pain, as a cough medicine and for diarrhoea. No study on the effects of codeine on the metabolic capacity of CYP enzyme is reported. Objective: In order to investigate the effects of codeine on the metabolic capacity of cytochrome P450 (CYP) enzymes, a cocktail method was employed to evaluate the activities of CYP2B1, CYP2D1, CYP1A2, CYP3A2 and CYP2C11. Materials and methods: Sprague–Dawley rats were randomly divided into codeine group (low, medium, high) and control group. The codeine group rats were given 4, 8, 16 mg/kg (low, medium, high) codeine by continuous intragastric administration for 14 days. Five probe drugs bupropion, metroprolol, phenacetin, midazolam and tolbutamide were given to rats through intragastric administration, and the plasma concentrations were determined by UPLC-MS/MS. Results and conclusion: The pharmacokinetic parameters of bupropion and metroprolol experienced obvious change with AUC(0-t), Cmax increased and CL decreased for bupropion in medium dosage group and midazolam low dosage group. This result indicates that the 14 day-intragastric administration of codeine may inhibit the metabolism of bupropion (CYP2B1) and midazolam (CYP3A2) in rat. Additional, there are no statistical differences for albumin (ALB), alkaline phosphatase (ALP), creatinine (Cr) after 14 intragastric administration of codeine, while alanine aminotransferase (ALT), aspartate aminotransferase (AST), uric acid (UA) increased compared to control group. The biomedical test results show continuous 14 day-intragastric administration of codeine would cause liver damage.http://dx.doi.org/10.1080/13880209.2017.1297466cocktailuplc-ms/msbupropionmidazolambiochemical |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shuanghu Wang Yanwen Dong Ke Su Jing Zhang Linyi Wang Anyue Han Congcong Wen Xianqin Wang Yan He |
spellingShingle |
Shuanghu Wang Yanwen Dong Ke Su Jing Zhang Linyi Wang Anyue Han Congcong Wen Xianqin Wang Yan He Effect of codeine on CYP450 isoform activity of rats Pharmaceutical Biology cocktail uplc-ms/ms bupropion midazolam biochemical |
author_facet |
Shuanghu Wang Yanwen Dong Ke Su Jing Zhang Linyi Wang Anyue Han Congcong Wen Xianqin Wang Yan He |
author_sort |
Shuanghu Wang |
title |
Effect of codeine on CYP450 isoform activity of rats |
title_short |
Effect of codeine on CYP450 isoform activity of rats |
title_full |
Effect of codeine on CYP450 isoform activity of rats |
title_fullStr |
Effect of codeine on CYP450 isoform activity of rats |
title_full_unstemmed |
Effect of codeine on CYP450 isoform activity of rats |
title_sort |
effect of codeine on cyp450 isoform activity of rats |
publisher |
Taylor & Francis Group |
series |
Pharmaceutical Biology |
issn |
1388-0209 1744-5116 |
publishDate |
2017-01-01 |
description |
Context: Codeine, also known as 3-methylmorphine, is an opiate used to treat pain, as a cough medicine and for diarrhoea. No study on the effects of codeine on the metabolic capacity of CYP enzyme is reported. Objective: In order to investigate the effects of codeine on the metabolic capacity of cytochrome P450 (CYP) enzymes, a cocktail method was employed to evaluate the activities of CYP2B1, CYP2D1, CYP1A2, CYP3A2 and CYP2C11. Materials and methods: Sprague–Dawley rats were randomly divided into codeine group (low, medium, high) and control group. The codeine group rats were given 4, 8, 16 mg/kg (low, medium, high) codeine by continuous intragastric administration for 14 days. Five probe drugs bupropion, metroprolol, phenacetin, midazolam and tolbutamide were given to rats through intragastric administration, and the plasma concentrations were determined by UPLC-MS/MS. Results and conclusion: The pharmacokinetic parameters of bupropion and metroprolol experienced obvious change with AUC(0-t), Cmax increased and CL decreased for bupropion in medium dosage group and midazolam low dosage group. This result indicates that the 14 day-intragastric administration of codeine may inhibit the metabolism of bupropion (CYP2B1) and midazolam (CYP3A2) in rat. Additional, there are no statistical differences for albumin (ALB), alkaline phosphatase (ALP), creatinine (Cr) after 14 intragastric administration of codeine, while alanine aminotransferase (ALT), aspartate aminotransferase (AST), uric acid (UA) increased compared to control group. The biomedical test results show continuous 14 day-intragastric administration of codeine would cause liver damage. |
topic |
cocktail uplc-ms/ms bupropion midazolam biochemical |
url |
http://dx.doi.org/10.1080/13880209.2017.1297466 |
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