PMID- 11787766 OWN - NLM STAT- MEDLINE DCOM- 20020924 LR - 20131121 IS - 0867-5910 (Print) IS - 0867-5910 (Linking) VI - 52 IP - 4 Pt 1 DP - 2001 Dec TI - Central nervous stimuli increase duodenal bicarbonate secretion by release of mucosal melatonin. PG - 671-8 AB - A number of common diseases in humans, including gastroduodenal ulcer and irritable bowel syndrome, show circadian rhythms in pain and discomfort. The neurohormone melatonin is released from enterochromaffin cells in the intestinal mucosa and from the pineal gland but its role in gastrointestinal function is largely unknown. We have studied the involvement of melatonin in stimulation of the mucosa-protective alkaline secretion by the duodenal mucosa. A 12-mm segment of proximal duodenum with an intact blood supply was cannulated in situ in anesthetized rats and duodenal HCO3- secretion titrated by pH-stat. Duodenal close intra-arterial infusion of melatonin or the full agonist 2-iodo-N-butanoyl- 5-methoxytryptamine significantly increased the secretion and pretreatment with the melatonin (predominantly MT2-receptor specific) antagonist luzindole almost abolished the response. Intracerebroventricular (i.c.v.) infusion of the alpha1-adrenoceptor agonist phenylephrine (12.2 micromol kg(-1) x h(-1)) caused an up to fivefold increased in the alkaline secretion and the melatonin antagonist luzindole or cutting all peri-carotid nerves abolished the duodenal secretory response to i.c.v. phenylephrine. Peripheral melatonin thus stimulates duodenal mucosal HCO3- secretion and endogenous melatonin, very likely released from mucosal enterochromaffin cells, is involved in mediating neural stimulation of the secretion. FAU - Sjoblom, M AU - Sjoblom M AD - Department of Physiology, Uppsala University, Sweden. FAU - Flemstrom, G AU - Flemstrom G LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Poland TA - J Physiol Pharmacol JT - Journal of physiology and pharmacology : an official journal of the Polish Physiological Society JID - 9114501 RN - 0 (Bicarbonates) RN - 0 (Receptors, Cell Surface) RN - 0 (Receptors, Cytoplasmic and Nuclear) RN - 0 (Receptors, Melatonin) RN - JL5DK93RCL (Melatonin) SB - IM MH - Animals MH - Bicarbonates/*metabolism MH - Brain/drug effects/*physiology MH - Duodenum/*drug effects/metabolism MH - Injections, Intraventricular MH - Male MH - Melatonin/*pharmacology MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Cell Surface/physiology MH - Receptors, Cytoplasmic and Nuclear/physiology MH - Receptors, Melatonin EDAT- 2002/01/15 10:00 MHDA- 2002/09/25 06:00 CRDT- 2002/01/15 10:00 PHST- 2002/01/15 10:00 [pubmed] PHST- 2002/09/25 06:00 [medline] PHST- 2002/01/15 10:00 [entrez] PST - ppublish SO - J Physiol Pharmacol. 2001 Dec;52(4 Pt 1):671-8.