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The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits

BACKGROUND: Cola nitida is commonly chewed in many West African cultures to ease hunger pangs and sometimes for their stimulant and euphoriant qualities. Metoclopramide is a known substrate for P-gp, SULT2A1 and CYP2D6 and studies have revealed that caffeine- a major component of Cola nitida can ind...

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Autores principales: Amadi, Cecilia Nwadiuto, Nwachukwu, Wisdom Izuchukwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945619/
https://www.ncbi.nlm.nih.gov/pubmed/31907041
http://dx.doi.org/10.1186/s40360-019-0379-6
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author Amadi, Cecilia Nwadiuto
Nwachukwu, Wisdom Izuchukwu
author_facet Amadi, Cecilia Nwadiuto
Nwachukwu, Wisdom Izuchukwu
author_sort Amadi, Cecilia Nwadiuto
collection PubMed
description BACKGROUND: Cola nitida is commonly chewed in many West African cultures to ease hunger pangs and sometimes for their stimulant and euphoriant qualities. Metoclopramide is a known substrate for P-gp, SULT2A1 and CYP2D6 and studies have revealed that caffeine- a major component of Cola nitida can induce P-glycoprotein (P-gp), SULT2A1 and SULT1A1, hence a possible drug interaction may occur on co-administration. The aim of this study was to investigate the pharmacokinetic interactions of Cola nitida and metoclopramide in rabbits. METHODS: The study was performed in two stages using five healthy male rabbits with a 1-week washout period between treatments. Stage one involved oral administration of metoclopramide (0.5 mg/kg) alone while in the second stage, metoclopramide (0.5 mg/kg) was administered concurrently with Cola nitida (0.7 mg/kg). Blood samples were collected after each stage at predetermined intervals and analyzed for plasma metoclopramide concentration using HPLC. RESULTS: Compared with control, the metoclopramide/Cola nitida co-administration produced a decrease in plasma concentration of metoclopramide at all the time intervals except at the 7th hour. The following pharmacokinetic parameters were also decreased: area under the curve (51%), peak plasma concentration (39%), half-life (51%); while an increase in elimination rate constant (113%) and clearance rate (98%) were noted indicating rapid elimination of the drug. A minimal decrease in absorption rate (10%) was also observed. CONCLUSIONS: The results of this study reveal a possible herb-drug interaction between Cola nitida and metoclopramide.
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spelling pubmed-69456192020-01-07 The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits Amadi, Cecilia Nwadiuto Nwachukwu, Wisdom Izuchukwu BMC Pharmacol Toxicol Research Article BACKGROUND: Cola nitida is commonly chewed in many West African cultures to ease hunger pangs and sometimes for their stimulant and euphoriant qualities. Metoclopramide is a known substrate for P-gp, SULT2A1 and CYP2D6 and studies have revealed that caffeine- a major component of Cola nitida can induce P-glycoprotein (P-gp), SULT2A1 and SULT1A1, hence a possible drug interaction may occur on co-administration. The aim of this study was to investigate the pharmacokinetic interactions of Cola nitida and metoclopramide in rabbits. METHODS: The study was performed in two stages using five healthy male rabbits with a 1-week washout period between treatments. Stage one involved oral administration of metoclopramide (0.5 mg/kg) alone while in the second stage, metoclopramide (0.5 mg/kg) was administered concurrently with Cola nitida (0.7 mg/kg). Blood samples were collected after each stage at predetermined intervals and analyzed for plasma metoclopramide concentration using HPLC. RESULTS: Compared with control, the metoclopramide/Cola nitida co-administration produced a decrease in plasma concentration of metoclopramide at all the time intervals except at the 7th hour. The following pharmacokinetic parameters were also decreased: area under the curve (51%), peak plasma concentration (39%), half-life (51%); while an increase in elimination rate constant (113%) and clearance rate (98%) were noted indicating rapid elimination of the drug. A minimal decrease in absorption rate (10%) was also observed. CONCLUSIONS: The results of this study reveal a possible herb-drug interaction between Cola nitida and metoclopramide. BioMed Central 2020-01-06 /pmc/articles/PMC6945619/ /pubmed/31907041 http://dx.doi.org/10.1186/s40360-019-0379-6 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Amadi, Cecilia Nwadiuto
Nwachukwu, Wisdom Izuchukwu
The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title_full The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title_fullStr The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title_full_unstemmed The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title_short The effects of oral administration of Cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
title_sort effects of oral administration of cola nitida on the pharmacokinetic profile of metoclopramide in rabbits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945619/
https://www.ncbi.nlm.nih.gov/pubmed/31907041
http://dx.doi.org/10.1186/s40360-019-0379-6
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