The Effect of DA-9701 in Opioid-induced Bowel Dysfunction of Guinea Pig.
- Author:
Zahid HUSSAIN
1
;
Kwang Won RHEE
;
Young Ju LEE
;
Hyojin PARK
Author Information
- Publication Type:Clinical Trial ; Original Article
- Keywords: DA-9701; Gastrointestinal transit; Ileum; Morphine; Opioid
- MeSH: Analgesics, Opioid; Animals; Baths; Charcoal; Colon; Corydalis; Gastrointestinal Transit; Guinea Pigs*; Guinea*; Ileum; Morphine; Muscle Contraction; Muscles; Semen
- From:Journal of Neurogastroenterology and Motility 2016;22(3):529-538
- CountryRepublic of Korea
- Language:English
- Abstract: 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.
