Radish Extract Stimulates Motility of the Intestine via the Muscarinic Receptors

Author:

Jung Kyu Yong1,Choo Young Kug12,Kim Hyung Min13,Choi Bong Kyu4

Affiliation:

1. Center of Oriental Medicinal Science, College of Natural Science, Iksan, Chonbuk 570–749, Korea

2. Division of Biological Science, College of Natural Science, Iksan, Chonbuk 570–749, Korea

3. Department of Oriental Pharmacy, College of Pharmacy, Wonkwang University, Iksan, Chonbuk 570–749, Korea

4. Department of Pharmacology, School of Medicine, Iksan, Chonbuk 570–749, Korea

Abstract

Abstract The effects of radish (Brassica oleraceae, Cruciferae) on gastrointestinal motility were examined using rat intestinal segments with myenteric plexus in-vitro and measuring the intestinal transit of charcoal in-vivo. Radish extract (10 μg mL−1 to 2 mg mL−1) caused a dose-dependent increase in contractions of the duodenum, jejunum and ileum, and 1 mg mL−1 was the maximum effective dose. The largest contraction by the extract was found in ileal segments. The extract-induced (0.5 mg ML−1) ileal contraction was remarkably inhibited by pretreatment of segments with atropine (10−7 M) for 10 min, but not by hexamethonium (0.5 mM). Moreover, antagonists of the muscarinic receptor reduced the radish-induced ileal contraction by a different ratio. The rank order of inhibitory effects was 4-diphenylacetoxy-N-methyl-(2-chloroethyl)-piperidine methiodide (90.5% of control) > tropicamide (67.4%) > pirenzepine (42.8%) > methoctramine (16.7%). Oral administration of radish extract (300–500 mg kg−1 body weight) to mice remarkably improved the intestinal transit of charcoal, and this was significantly attenuated by co-administration of atropine (50 mg kg−1). Taken together, these results suggest that radish extract stimulates gastrointestinal motility through activation of muscarinic pathways.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference20 articles.

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3. Autoradiographic localization of peripheral M1 muscarinic receptors using [3H]pir-enzepine;Buckley;Brain Res.,1986

4. International union of pharmacology. XVII. Classification of muscarinic acetylcholine receptor;Caulfield;Pharmacol. Rev.,1998

5. Effect of ganglionic blocking compounds on in-vivo fluid secretion in the rat small intestine;Delbro;J. Pharm. Pharmacol.,1997

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