Basic Research
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2003; 9(4): 779-783
Published online Apr 15, 2003. doi: 10.3748/wjg.v9.i4.779
Relative efficacy of some prokinetic drugs in morphine-induced gastrointestinal transit delay in mice
AD Suchitra, SA Dkhar, DG Shewade, CH Shashindran
AD Suchitra, SA Dkhar, DG Shewade, CH Shashindran, Department of Pharmacology, JIPMER, Pondicherry 605006, INDIA
Author contributions: All authors contributed equally to the work.
Correspondence to: DG Shewade, Department of Pharmacology, JIPMER, Pondicherry 605006, INDIA. shewade@eth.net
Telephone: +91-413-2278693 Fax: +91-413-2272067
Received: October 5, 2002
Revised: October 27, 2002
Accepted: November 4, 2002
Published online: April 15, 2003
Abstract

AIM: To study the relative efficacy of cisapride, metoclopramide, domperidone, erythromycin and mosapride on gastric emptying (GE) and small intestinal transit (SIT) in morphine treated mice.

METHODS: Phenol red marker meal was employed to estimate GE and SIT in Swiss albino mice of either sex. The groups included were control, morphine 1 mg/kg (s.c. 15 min before test meal) alone or with (45 min before test meal p.o.) cisapride 10 mg/kg, metoclopramide 20 mg/kg, domperidone 20 mg/kg, erythromycin 6 mg/kg and mosapride 20 mg/kg.

RESULTS: Cisapride, metoclopramide and mosapride were effective in enhancing gastric emptying significantly (P < 0.001) whereas other prokinetic agents failed to do so in normal mice. Metoclopramide completely reversed morphine induced delay in gastric emptying followed by mosapride. Metoclopramide alone was effective when given to normal mice in increasing the SIT. Cisapride, though it did not show any significant effect on SIT in normal mice, was able to reverse morphine induced delay in SIT significantly (P < 0.001) followed by metoclopramide and mosapride.

CONCLUSION: Metoclopramide and cisapride are most effective in reversing morphine-induced delay in gastric emptying and small intestinal transit in mice respectively.

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