UDP-glucose modulates gastric function through P2Y14 receptor-dependent and -independent mechanisms
| Autor: | Lorraine Punter, Karen Townson, Alastair Morrison, Judith Latcham, Evelyn Grau, Sophie Bourdu, Alan Wheeldon, Wendy J. Winchester, Anna K. Bassil, Noureddine Zebda, Emma M. Jarvie, Angela M. Grimes, George P. Livi, Alejandro Abuin, Gary B.T. Moore, David P. Hurp, Kelly M. Downham, Gareth J. Sanger |
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| Rok vydání: | 2009 |
| Předmět: |
Uridine Diphosphate Glucose
medicine.medical_specialty P2Y receptor UDP Glucose Physiology Biology Contractility Uridine Diphosphate Galactose Mice Physiology (medical) Internal medicine medicine Animals RNA Messenger Receptor Mice Knockout Messenger RNA Hepatology Gastric emptying Dose-Response Relationship Drug Receptors Purinergic P2 Stomach Gastroenterology Muscle Smooth Rats medicine.anatomical_structure Endocrinology Gastric Emptying Gene Expression Regulation Lac Operon Receptors Purinergic P2Y Function (biology) Muscle Contraction |
| Zdroj: | American journal of physiology. Gastrointestinal and liver physiology. 296(4) |
| ISSN: | 0193-1857 |
| Popis: | P2Y receptors have been reported to modulate gastrointestinal functions. The newest family member is the nucleotide-sugar receptor P2Y14. P2ry14 mRNA was detected throughout the rat gut, with the highest level being in the forestomach. We investigated the role of the receptor in stomach motility using cognate agonists and knockout (KO) mice. In rat isolated forestomach, 100 μM UDP-glucose and 100 μM UDP-galactose both increased the baseline muscle tension (BMT) by 6.2 ± 0.6 and 1.6 ± 0.6 mN ( P < 0.05, n = 3–4), respectively, and the amplitude of contractions during electrical field stimulation (EFS) by 3.7 ± 1.7 and 4.3 ± 2.5 mN ( P < 0.05, n = 3–4), respectively. In forestomach from wild-type (WT) mice, 100 μM UDP-glucose increased the BMT by 1.0 ± 0.1 mN ( P 14 receptor associated with contractility in the rodent stomach that does not lead to altered gastric emptying after receptor deletion and an ability of UDP-glucose to delay gastric emptying without involving the P2Y14 receptor. |
| Databáze: | OpenAIRE |
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