Searchable abstracts of presentations at key conferences in endocrinology

ea0104s3.2 | Bone Update | SFEIES24

Gut-derived peptides and bone disorders in obesity and diabetes

Irwin Nigel

Bone remodelling is regulated by many endogenous factors, with recent attention on the pivotal role of gut-derived peptide hormones in this regard. Indeed, a gut-bone axis has now been described, that is coordinated largely by the secretion and action of intestinal-derived peptide hormones. In addition to this, obesity and diabetes are highly prevalent metabolic disorders that negatively affect health, and there is now a clear link between these diseases and impaired bone heal...

ea0037oc4.1 | Diabetes | ECE2015

Novel glucagon receptor antagonist peptides improve glycaemic control and partially protect against streptozotocin induced diabetes in mice

O'Harte Finbarr , McShane Laura , Irwin Nigel

Glucagon receptor KO mice are resistant to the clinical manifestations of diabetes induced by streptozotocin (STZ) and retain normal glycaemic control and glucose tolerance. In the present study the effects of chronic (18 days) once daily i.p. administration of two different glucagon receptor antagonists (GRA); desHis1Pro4Glu9-glucagon (GRA-1) and its related acylated peptide desHis1Pro4Glu9(Lys12PAL)...

ea0104op7 | Oral Posters 2 – Diabetes/Obesity/Metabolism 1 | SFEIES24

Hybrid acylated and non-acylated GLP-1 and apelin receptor co-agonist peptides, show promising acute in vivo anti-hyperglycaemic actions in normal healthy and insulin resistant diet-induced obese mice

O'Harte Finbarr , Palmer Ethan , Craig Sarah , Irwin Nigel

Incretin mimetics, alongside associated hybrid co-agonist peptides, which activate GLP-1 and other receptors are leading the way to more effective therapeutic options for management of obesity and type 2 diabetes. The adipokine apelin, which activates the APJ receptor, has shown anti-diabetic and obesity related therapeutic utility following pre-clinical testing. The present study investigated several novel hybrid co-agonist peptides, derived from exendin-linker-apelin (ELA) a...

ea0104p99 | Diabetes & Metabolism | SFEIES24

Differential impact of GLP-1 and GLP-2 on beta-cell function, glucose metabolism, and appetite

Ali Asif , Khan Dawood , Irwin Nigel , Flatt Peter R.

Background: Glucagon-like peptide-1 (GLP-1) and glucagon-like peptide-2 (GLP-2), are key products of the L-cell proglucagon-gene with diverse effects on metabolism. Whereas GLP-1 has been extensively studied, much less attention has been devoted to GLP-2. The current study directly compares the impact of GLP-1 and GLP-2 on pancreatic beta-cell function and turnover in vitro, as well as the effects on glucose tolerance and appetite suppression in mice.<p class="abs...

ea0104p126 | Diabetes & Metabolism | SFEIES24

Novel unimolecular peptides targeting GLP-1 and APJ receptors exert potent satiety inducing effects in mice

Palmer Ethan , Craig Sarah , Irwin Nigel , O'Harte Finbarr

Incretin mimetics and associated hybrid co-agonist peptides remain a driving force in improving metabolic control and managing type 2 diabetes and obesity. Additionally, the adipokine apelin which targets the APJ receptor, has displayed positive anti-diabetic and obesity effects in pre-clinical trials. To harness these beneficial effects, two novel dual-agonist unimolecular peptides were developed based on the amino acid sequence of GLP-1 and apelin and named Exendin-Linker-Ap...

ea0104oc9 | Oral Communications | SFEIES24

Pregnancy induced pancreatic islet expansion is compromised by consumption of cafeteria diet

Dubey Vaibhav , Tanday Neil , Irwin Nigel , Draper Matthew , Tarasov Andrei I. , Flatt Peter R. , Charlotte Moffett R

Background: Pregnancy induces pancreatic islet β-cell mass expansion, but the exact mechanisms responsible remain unclear. It is nevertheless believed that disturbances in the process contribute to the development of gestational diabetes. The current study investigates the impact of pregnancy and cafeteria diet on islet morphology, cellular proliferation/apoptosis as well as endocrine cell lineage plasticity. Methods: Non-pregnant and pregnant Ins<e...