Implications of amylin receptor agonism: integrated neurohormonal mechanisms and therapeutic applications.

Article Details

Citation

Roth JD, Maier H, Chen S, Roland BL

Implications of amylin receptor agonism: integrated neurohormonal mechanisms and therapeutic applications.

Arch Neurol. 2009 Mar;66(3):306-10. doi: 10.1001/archneurol.2008.581.

PubMed ID
19273748 [ View in PubMed
]
Abstract

Amylin receptor agonism is emerging as part of an integrated neurohormonal therapeutic approach for managing diabetes mellitus (DM) and body weight. Pramlintide acetate, an analogue of the pancreatic hormone amylin, has been studied in the United States as an antihyperglycemic agent in patients with type 1 or type 2 DM treated with mealtime insulin(1). Further clinical testing of pramlintide in subjects with obesity demonstrated that pramlintide monotherapy induced significant, sustained, and dose-dependent weight loss(2). Recent clinical observations point to its compatibility as a combination therapy with the hormone leptin, eliciting double-digit weight loss in patients with overweight and obesity(3). Herein, we link amylin activation of central neural circuits to these therapeutic effects, and we speculate on other potential therapeutic applications of amylin receptor agonism.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
PramlintideCalcitonin receptorProteinHumans
Yes
Agonist
Details
PramlintideReceptor activity-modifying protein 1ProteinHumans
Yes
Agonist
Details
PramlintideReceptor activity-modifying protein 2ProteinHumans
Yes
Agonist
Details
PramlintideReceptor activity-modifying protein 3ProteinHumans
Yes
Agonist
Details