β-Adrenoceptors regulate myoelectric activity in the small intestine of rats: stimulation by β2 and inhibition by β3 subtypes |
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Authors: | Mikael Thollander,T. H. SVENSSON,P. M. HELLSTR
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Affiliation: | Mikael Thollander,T. H. SVENSSON,P. M. HELLSTRÖM |
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Abstract: | Abstract Using β-adrenergic agonists and antagonists this study investigated the importance of three different adrenoceptor subtypes for the regulation of migrating myoelectric complexes (MMCs) of the upper small intestine in conscious, naive rats. After a control period of 60 min with four activity fronts, agonists were given as an intravenous infusion for another 60 min. The non-selective β-adrenoceptor agonist isoprenaline (1 μg kg?1 min?1) inhibited MMCs and induced irregular spiking during the infusion period. This effect was blocked by intravenous administration of a bolus dose of either the non-selective β-adrenoceptor antagonist propranolol (1 mg kg?1), or the β2-antagonist ICI 118 551 (1 mg kg?1), both given prior to isoprenaline. However, acebutolol (1 mg kg?1), a selective β1-antagonist, failed to antagonize the effect of isoprenaline. Furthermore, prenalterol, a selective β1-agonist (12.5–800.0 μg kg?1 min?1), had no effect on the MMC pattern, whereas the β2-selective agonist ritodrine (25–100 μg kg?1 min?1) induced a myoelectric pattern similar to one induced by isoprenaline. The partial β3-adrenoceptor agonist D7114 (50–100 μg kg?1 min?1), disrupted the MMCs and induced quiescence. Neither of the antagonists, i.e. propranolol (1 mg kg?1), acebutolol (1 mg kg?1) nor ICI 118 551 (1 mg kg?1), given alone induced changes in the MMC pattern. In conclusion, β2-adrenoceptors in particular but also β3-adrenoceptors seem to be of importance in the regulation of small intestinal motility by disrupting the regular MMC pattern in rats. |
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Keywords: | acebutol β -adrenoceptor agonists β -adrenoceptor antagonists isoprenaline migrating myoelectric complex (MMC) prenalterol ritodrine |
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