In vivo and in vitro characterization of GL0034, a novel long‐acting glucagon‐like peptide‐1 receptor agonist

• Published in: Diabetes, obesity & metabolism obesity & metabolism, 2022-11, Vol.24 (11), p.2090-2101
• Main Authors: Jones, Ben, Burade, Vinod, Akalestou, Elina, Manchanda, Yusman, Ramchunder, Zenouska, Carrat, Gaëlle, Nguyen‐Tu, Marie‐Sophie, Marchetti, Piero, Piemonti, Lorenzo, Leclerc, Isabelle, Thennati, Rajamannar, Vilsboll, Tina, Thorens, Bernard, Tomas, Alejandra, Rutter, Guy A.
• Format: Article
• Language: English
• Subjects: Adenosine Monophosphate; Agonists; Animals; antidiabetic drug; Antidiabetics; antiobesity drug; Arrestin; beta-Arrestins - metabolism; beta‐cell function; Blood Glucose; Body weight loss; Cyclic AMP; Cyclic AMP - metabolism; Diabetes mellitus (non-insulin dependent); Diabetes Mellitus, Type 2 - drug therapy; drug development; Endocytosis; GLP-1 receptor agonists; GLP‐1 analogue; Glucagon; Glucagon-Like Peptide-1 Receptor - agonists; HEK293 Cells; Humans; Hypoglycemic Agents - pharmacology; Hypoglycemic Agents - therapeutic use; incretin therapy; Insulin; Insulin secretion; Insulins; Ligands; Mice; Original; Peptides; Protein turnover; Weight Loss
• ISSN: 1462-8902; 1463-1326
• DOI: 10.1111/dom.14794

Aims To describe the in vitro characteristics and antidiabetic in vivo efficacy of the novel glucagon‐like peptide‐1 receptor agonist (GLP‐1RA) GL0034. Materials and Methods Glucagon‐like peptide‐1 receptor (GLP‐1R) kinetic binding parameters, cyclic adenosine monophosphate (cAMP) signalling, endocytosis and recycling were measured using HEK293 and INS‐1832/3 cells expressing human GLP‐1R. Insulin secretion was measured in vitro using INS‐1832/3 cells, mouse islets and human islets. Chronic administration studies to evaluate weight loss and glycaemic effects were performed in db/db and diet‐induced obese mice. Results Compared to the leading GLP‐1RA semaglutide, GL0034 showed increased binding affinity and potency‐driven bias in favour of cAMP over GLP‐1R endocytosis and β‐arrestin‐2 recruitment. Insulin secretory responses were similar for both ligands. GL0034 (6 nmol/kg) led to at least as much weight loss and lowering of blood glucose as did semaglutide at a higher dose (14 nmol/kg). Conclusions GL0034 is a G protein‐biased agonist that shows powerful antidiabetic effects in mice, and may serve as a promising new GLP‐1RA for obese patients with type 2 diabetes.