Site and mechanism of the colokinetic action of the ghrelin receptor agonist, HM01
| Autor: | Brid Callaghan, A J Chan, Leni R. Rivera, Mitchell T Ringuet, K. Naitou, Ruslan V Pustovit, C. Pietra, John B. Furness, T P Mamerto |
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| Rok vydání: | 2015 |
| Předmět: |
Male
Agonist medicine.medical_specialty Physiology medicine.drug_class media_common.quotation_subject Stimulation Transfection Rats Sprague-Dawley Growth hormone secretagogue Internal medicine medicine Animals Humans Defecation Receptors Ghrelin Receptor media_common Endocrine and Autonomic Systems business.industry Lumbosacral Region Gastroenterology Parkinson Disease Appetite Rats Disease Models Animal HEK293 Cells Endocrinology Spinal Cord Hypothalamus Ghrelin Gastrointestinal Motility business Constipation |
| Zdroj: | Neurogastroenterology & Motility. 27:1764-1771 |
| ISSN: | 1350-1925 |
| Popis: | Background It has been recently demonstrated that the ghrelin receptor agonist, HM01, caused defecation in rats that were treated to provide a model for the constipation of Parkinson's disease. HM01 significantly increased fecal output and increased Fos activity in neurons of the hypothalamus and hindbrain, but not in the spinal defecation center. Other ghrelin agonists act on the defecation center. Methods Receptor pharmacology was examined in ghrelin receptor (GHSR1a) transfected cells. Anesthetized rats were used to investigate sites and mechanisms of action. Key Results HM01 activated rat GHSR1a at nanomolar concentrations and was antagonized by the GHSR1a antagonist, YIL781. HM01, intravenous, was potent to activate propulsive colorectal contractions. This was prevented by pelvic nerve section and by intravenous YIL781, but not by spinal cord section rostral to the defecation centers. Direct intrathecal application of HM01 to the defecation center at spinal level L6-S1 initiated propulsive contractions of the colorectum. Conclusions & Inferences HM01 stimulates GHSR1a receptors on neurons in the lumbosacral defecation centers to cause propulsive contractions and emptying of the colorectum. It has greater potency when given systemically, compared with other GHSR1a agonists. |
| Databáze: | OpenAIRE |
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