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Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats

The potential pharmacokinetic (PK) interaction of conventional western drug, baclofen, and oriental medications Oyaksungisan (OY) and Achyranthes bidentata radix (AB) extract for the treatment of spasticity has been evaluated. Rats were pretreated with distilled water (DW), OY, or AB extract by oral...

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Autores principales: Kim, Tae Hwan, Park, Gi-Young, Shin, Soyoung, Kwon, Dong Rak, Seo, Won Sik, Shin, Jeong Cheol, Choi, Jin Ho, Joo, Sang Hoon, Weon, Kwon-Yeon, Min, Byung Sun, Baek, Kyung Min, Upadhyay, Mahesh, Zhao, Bing Tian, Woo, Mi Hee, Kwon, So Hee, Shin, Beom Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229966/
https://www.ncbi.nlm.nih.gov/pubmed/25530781
http://dx.doi.org/10.1155/2014/402126
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author Kim, Tae Hwan
Park, Gi-Young
Shin, Soyoung
Kwon, Dong Rak
Seo, Won Sik
Shin, Jeong Cheol
Choi, Jin Ho
Joo, Sang Hoon
Weon, Kwon-Yeon
Min, Byung Sun
Baek, Kyung Min
Upadhyay, Mahesh
Zhao, Bing Tian
Woo, Mi Hee
Kwon, So Hee
Shin, Beom Soo
author_facet Kim, Tae Hwan
Park, Gi-Young
Shin, Soyoung
Kwon, Dong Rak
Seo, Won Sik
Shin, Jeong Cheol
Choi, Jin Ho
Joo, Sang Hoon
Weon, Kwon-Yeon
Min, Byung Sun
Baek, Kyung Min
Upadhyay, Mahesh
Zhao, Bing Tian
Woo, Mi Hee
Kwon, So Hee
Shin, Beom Soo
author_sort Kim, Tae Hwan
collection PubMed
description The potential pharmacokinetic (PK) interaction of conventional western drug, baclofen, and oriental medications Oyaksungisan (OY) and Achyranthes bidentata radix (AB) extract for the treatment of spasticity has been evaluated. Rats were pretreated with distilled water (DW), OY, or AB extract by oral administration every day for 7 days. After 10 min of the final dose of DW or each herbal medication, baclofen (1 mg/kg) was given by oral administration and plasma concentrations of baclofen were determined by LC/MS/MS. The plasma baclofen concentration-time profiles were then analyzed by noncompartmental analysis and a population PK model was developed. Baclofen was rapidly absorbed, showed biexponential decline with elimination half-life of 3.42–4.10 hr, and mostly excreted into urine. The PK of baclofen was not affected by AB extract pretreatment. However, significantly lower maximum plasma concentration (C (max)) and longer time to reach C (max) (T (max)) were observed in OY pretreated rats without changes in the area under the curve (AUC) and the fraction excreted into urine (F (urine)). The absorption rate (K (a)) of baclofen was significantly decreased in OY pretreated rats. These data suggested that repeated doses of OY might delay the absorption of baclofen without changes in extent of absorption, which needs further evaluation for clinical significance.
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spelling pubmed-42299662014-12-21 Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats Kim, Tae Hwan Park, Gi-Young Shin, Soyoung Kwon, Dong Rak Seo, Won Sik Shin, Jeong Cheol Choi, Jin Ho Joo, Sang Hoon Weon, Kwon-Yeon Min, Byung Sun Baek, Kyung Min Upadhyay, Mahesh Zhao, Bing Tian Woo, Mi Hee Kwon, So Hee Shin, Beom Soo Evid Based Complement Alternat Med Research Article The potential pharmacokinetic (PK) interaction of conventional western drug, baclofen, and oriental medications Oyaksungisan (OY) and Achyranthes bidentata radix (AB) extract for the treatment of spasticity has been evaluated. Rats were pretreated with distilled water (DW), OY, or AB extract by oral administration every day for 7 days. After 10 min of the final dose of DW or each herbal medication, baclofen (1 mg/kg) was given by oral administration and plasma concentrations of baclofen were determined by LC/MS/MS. The plasma baclofen concentration-time profiles were then analyzed by noncompartmental analysis and a population PK model was developed. Baclofen was rapidly absorbed, showed biexponential decline with elimination half-life of 3.42–4.10 hr, and mostly excreted into urine. The PK of baclofen was not affected by AB extract pretreatment. However, significantly lower maximum plasma concentration (C (max)) and longer time to reach C (max) (T (max)) were observed in OY pretreated rats without changes in the area under the curve (AUC) and the fraction excreted into urine (F (urine)). The absorption rate (K (a)) of baclofen was significantly decreased in OY pretreated rats. These data suggested that repeated doses of OY might delay the absorption of baclofen without changes in extent of absorption, which needs further evaluation for clinical significance. Hindawi Publishing Corporation 2014 2014-10-29 /pmc/articles/PMC4229966/ /pubmed/25530781 http://dx.doi.org/10.1155/2014/402126 Text en Copyright © 2014 Tae Hwan Kim et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kim, Tae Hwan
Park, Gi-Young
Shin, Soyoung
Kwon, Dong Rak
Seo, Won Sik
Shin, Jeong Cheol
Choi, Jin Ho
Joo, Sang Hoon
Weon, Kwon-Yeon
Min, Byung Sun
Baek, Kyung Min
Upadhyay, Mahesh
Zhao, Bing Tian
Woo, Mi Hee
Kwon, So Hee
Shin, Beom Soo
Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title_full Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title_fullStr Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title_full_unstemmed Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title_short Pharmacokinetic Alteration of Baclofen by Multiple Oral Administration of Herbal Medicines in Rats
title_sort pharmacokinetic alteration of baclofen by multiple oral administration of herbal medicines in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4229966/
https://www.ncbi.nlm.nih.gov/pubmed/25530781
http://dx.doi.org/10.1155/2014/402126
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