Abstract
The pancreatic hormone amylin (AMY) and the AMY-receptor-agonist salmon-calcitonin (sCT) reduce short-term food-intake after binding to the area postrema (AP), a circumventricular organ (CVO) lacking blood-brain-barrier characteristics. AMY has also been proposed to induce drinking via another CVO, the subfornical organ (SFO). In cellular systems, AMY-binding is generated by interaction of calcitonin-receptor a/b (CT((a))/CT((b))) with receptor-activity modifying proteins (RAMPs). By using in situ hybridization, the codistribution of CT((a))/CT((b)) with RAMP1-3 and c-fos was mapped in CVOs of rats. AMY and sCT induced c-fos within the SFO which contained CT((a)) and/or CT((b)) and RAMP1/2 mRNA. AMY and sCT also activated AP neurons, which express the CT((a)), but not the CT((b)), receptor and RAMP2/3 mRNA. These data emphasize the important role of these structures as primary targets for circulating AMY.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amyloid / metabolism*
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Animals
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Anti-Asthmatic Agents / pharmacology
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Behavior, Animal
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Calcitonin / pharmacology
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Eating / drug effects
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Gene Expression / drug effects
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In Situ Hybridization / methods
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Intracellular Signaling Peptides and Proteins
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Islet Amyloid Polypeptide
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Male
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Membrane Proteins / genetics
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Membrane Proteins / metabolism*
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Proto-Oncogene Proteins c-fos / genetics
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Proto-Oncogene Proteins c-fos / metabolism
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Rats
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Rats, Wistar
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Receptor Activity-Modifying Protein 1
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Receptor Activity-Modifying Protein 2
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Receptor Activity-Modifying Proteins
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Receptors, Calcitonin / genetics
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Receptors, Calcitonin / metabolism*
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Subfornical Organ / metabolism*
Substances
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Amyloid
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Anti-Asthmatic Agents
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Intracellular Signaling Peptides and Proteins
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Islet Amyloid Polypeptide
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Membrane Proteins
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Proto-Oncogene Proteins c-fos
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Ramp1 protein, rat
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Ramp2 protein, rat
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Receptor Activity-Modifying Protein 1
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Receptor Activity-Modifying Protein 2
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Receptor Activity-Modifying Proteins
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Receptors, Calcitonin
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salmon calcitonin
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Calcitonin