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The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig
BACKGROUND/AIMS: Opioid induced bowel dysfunction (OIBD) is associated with decreased gastrointestinal (GI) propulsive activity due to intake of opioid analgesics. DA-9701, a novel prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber has promising effects on GI motor function. Theref...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Neurogastroenterology and Motility
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930309/ https://www.ncbi.nlm.nih.gov/pubmed/26932898 http://dx.doi.org/10.5056/jnm15194 |
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author | Hussain, Zahid Rhee, Kwang Won Lee, Young Ju Park, Hyojin |
author_facet | Hussain, Zahid Rhee, Kwang Won Lee, Young Ju Park, Hyojin |
author_sort | Hussain, Zahid |
collection | PubMed |
description | BACKGROUND/AIMS: Opioid induced bowel dysfunction (OIBD) is associated with decreased gastrointestinal (GI) propulsive activity due to intake of opioid analgesics. DA-9701, a novel prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber has promising effects on GI motor function. Therefore, we aim to evaluate the prokinetic effects of DA-9701 in an OIBD model of guinea pig. METHODS: The ileal and distal colon muscle contraction in presence of different doses of DA-9701, morphine, and combination (morphine + DA-9701) was measured by tissue bath study. The prokinetic effect of DA-9701 was assessed by charcoal transit and fecal pellet output assay in an OIBD model of guinea pig. RESULTS: DA-9701 significantly increased the amplitude and area under the curve of ileal muscle contraction, while there was insignificant effect on the distal colon compared to the control. The maximal amplitude of ileal muscle contraction was acquired at a concentration of 10 μg/mL of DA-9701. In contrast, morphine significantly decreased the amplitude of ileal and distal colon muscle contraction compared to the control. Morphine delayed both upper (P < 0.01) and lower (P < 0.05) GI transit, and delayed GI transit was restored by the administration of DA-9701. Morphine induced reduction of contractility was significantly ameliorated by addition of DA-9701 in both ileal and distal colon muscles. CONCLUSIONS: DA-9701 significantly increased the amplitude of contraction of the ileal muscle, however the distal colon muscle contraction was insignificant. Additionally, it restored delayed upper and lower GI transit in an OIBD model of guinea pig, and it might prove to be a useful candidate drug in a clinical trial for OIBD. |
format | Online Article Text |
id | pubmed-4930309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society of Neurogastroenterology and Motility |
record_format | MEDLINE/PubMed |
spelling | pubmed-49303092016-07-05 The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig Hussain, Zahid Rhee, Kwang Won Lee, Young Ju Park, Hyojin J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: Opioid induced bowel dysfunction (OIBD) is associated with decreased gastrointestinal (GI) propulsive activity due to intake of opioid analgesics. DA-9701, a novel prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber has promising effects on GI motor function. Therefore, we aim to evaluate the prokinetic effects of DA-9701 in an OIBD model of guinea pig. METHODS: The ileal and distal colon muscle contraction in presence of different doses of DA-9701, morphine, and combination (morphine + DA-9701) was measured by tissue bath study. The prokinetic effect of DA-9701 was assessed by charcoal transit and fecal pellet output assay in an OIBD model of guinea pig. RESULTS: DA-9701 significantly increased the amplitude and area under the curve of ileal muscle contraction, while there was insignificant effect on the distal colon compared to the control. The maximal amplitude of ileal muscle contraction was acquired at a concentration of 10 μg/mL of DA-9701. In contrast, morphine significantly decreased the amplitude of ileal and distal colon muscle contraction compared to the control. Morphine delayed both upper (P < 0.01) and lower (P < 0.05) GI transit, and delayed GI transit was restored by the administration of DA-9701. Morphine induced reduction of contractility was significantly ameliorated by addition of DA-9701 in both ileal and distal colon muscles. CONCLUSIONS: DA-9701 significantly increased the amplitude of contraction of the ileal muscle, however the distal colon muscle contraction was insignificant. Additionally, it restored delayed upper and lower GI transit in an OIBD model of guinea pig, and it might prove to be a useful candidate drug in a clinical trial for OIBD. Korean Society of Neurogastroenterology and Motility 2016-07 2016-06-28 /pmc/articles/PMC4930309/ /pubmed/26932898 http://dx.doi.org/10.5056/jnm15194 Text en © 2016 The Korean Society of Neurogastroenterology and Motility This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hussain, Zahid Rhee, Kwang Won Lee, Young Ju Park, Hyojin The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title | The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title_full | The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title_fullStr | The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title_full_unstemmed | The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title_short | The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig |
title_sort | effect of da-9701 in opioid-induced bowel dysfunction of guinea pig |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930309/ https://www.ncbi.nlm.nih.gov/pubmed/26932898 http://dx.doi.org/10.5056/jnm15194 |
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