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Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity
The present study was undertaken to investigate the food–drug interaction of carbamazepine (CBZ). Common fruit juices [grapefruit juice (GFJ), lime juice (LJ)], known to inhibit the enzyme cytochrome P450 3A4 (CYP3A4), and some widely consumed beverages [milk (M), black tea (BT)] were involved in th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taiwan Food and Drug Administration
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351769/ https://www.ncbi.nlm.nih.gov/pubmed/28911389 http://dx.doi.org/10.1016/j.jfda.2014.07.012 |
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author | Karmakar, Sanmoy Biswas, Sreerupa Bera, Rammohan Mondal, Samiran Kundu, Amit Ali, Md Asif Sen, Tuhinadri |
author_facet | Karmakar, Sanmoy Biswas, Sreerupa Bera, Rammohan Mondal, Samiran Kundu, Amit Ali, Md Asif Sen, Tuhinadri |
author_sort | Karmakar, Sanmoy |
collection | PubMed |
description | The present study was undertaken to investigate the food–drug interaction of carbamazepine (CBZ). Common fruit juices [grapefruit juice (GFJ), lime juice (LJ)], known to inhibit the enzyme cytochrome P450 3A4 (CYP3A4), and some widely consumed beverages [milk (M), black tea (BT)] were involved in this study in the presence of CBZ, as might happen during clinical therapy. The effects of the beverages on the pharmacokinetics and drug-induced toxicity of CBZ was observed after concomitant administration for a period of 28 days. Accordingly, the influence of altered bioavailability of CBZ on its antiepileptic activity was investigated. A significant shift in the C(max) as well as T(max) of CBZ was observed in the presence of LJ and GFJ. This increase in bioavailability significantly enhanced hepatotoxicity and delayed the onset of tremor and piloerection against pentylene tetrazole (PTZ)-induced seizure in experimental animals. However, increased toxicity of CBZ was found to be absent with BT. Thus, from our observation, LJ or GFJ in the presence of CBZ significantly increased the bioavailability of CBZ, which might lead to increased toxicity and antiepileptic activity of the drug. |
format | Online Article Text |
id | pubmed-9351769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Taiwan Food and Drug Administration |
record_format | MEDLINE/PubMed |
spelling | pubmed-93517692022-08-09 Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity Karmakar, Sanmoy Biswas, Sreerupa Bera, Rammohan Mondal, Samiran Kundu, Amit Ali, Md Asif Sen, Tuhinadri J Food Drug Anal Original Article The present study was undertaken to investigate the food–drug interaction of carbamazepine (CBZ). Common fruit juices [grapefruit juice (GFJ), lime juice (LJ)], known to inhibit the enzyme cytochrome P450 3A4 (CYP3A4), and some widely consumed beverages [milk (M), black tea (BT)] were involved in this study in the presence of CBZ, as might happen during clinical therapy. The effects of the beverages on the pharmacokinetics and drug-induced toxicity of CBZ was observed after concomitant administration for a period of 28 days. Accordingly, the influence of altered bioavailability of CBZ on its antiepileptic activity was investigated. A significant shift in the C(max) as well as T(max) of CBZ was observed in the presence of LJ and GFJ. This increase in bioavailability significantly enhanced hepatotoxicity and delayed the onset of tremor and piloerection against pentylene tetrazole (PTZ)-induced seizure in experimental animals. However, increased toxicity of CBZ was found to be absent with BT. Thus, from our observation, LJ or GFJ in the presence of CBZ significantly increased the bioavailability of CBZ, which might lead to increased toxicity and antiepileptic activity of the drug. Taiwan Food and Drug Administration 2014-12-03 /pmc/articles/PMC9351769/ /pubmed/28911389 http://dx.doi.org/10.1016/j.jfda.2014.07.012 Text en © 2015 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article Karmakar, Sanmoy Biswas, Sreerupa Bera, Rammohan Mondal, Samiran Kundu, Amit Ali, Md Asif Sen, Tuhinadri Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title | Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title_full | Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title_fullStr | Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title_full_unstemmed | Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title_short | Beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
title_sort | beverage-induced enhanced bioavailability of carbamazepine and its consequent effect on antiepileptic activity and toxicity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9351769/ https://www.ncbi.nlm.nih.gov/pubmed/28911389 http://dx.doi.org/10.1016/j.jfda.2014.07.012 |
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