The arcuate nucleus mediates GLP-1 receptor agonist liraglutide-dependent weight loss.
By A. Secher, J. Jelsing, Arian F. Baquero, J. Hecksher-Sørensen, M. Cowley, L. S. Dalbøge, G. Hansen, K. Grove, C. Pyke, K. Raun and 6 more. Journal of Clinical Investigation, 2014
833 citations recorded by the source corpus.
Subfields: Endocrine and Autonomic Systems, Endocrinology, Diabetes and Metabolism, Physiology
View Paper: https://www.semanticscholar.org/paper/25a76beacceb1bbb6f6d3436151a47152c14e156
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Endocrine and Autonomic Systems
In Endocrinology, Diabetes and Metabolism
In Physiology
Citations in the corpus
- Incretin hormones: Their role in health and disease (2018, background): “The relevant GLP-1 receptors seem to be in the hypothalamus.(45) GLP-1 may enter the brain from the blood stream through circumventricular organs, which are characterized by a leaky blood–brain barrier.”
- Mechanisms of Action and Therapeutic Application of Glucagon-like Peptide-1. (2018, background): “Moreover, a fluorescent liraglutide analog was detected within the ARC, PVN, supraoptic nucleus, and supraoptic decussation in both rats and mice after peripheral administration, with brain uptake dependent on a functional GLP-1R (Secher et al., GLP-1 levels rise following Roux-en-Y gastric bypass (”
- Semaglutide lowers body weight in rodents via distributed neural pathways. (2020, background): “Furthermore, the efficacy of liraglutide is not altered by area postrema (AP) or PVH ablation or by vagal lesions (8, 20).”
- GLP-1 receptor agonists in the treatment of type 2 diabetes – state-of-the-art (2020, background): “POMC/CART neurons expressing GLP-1 receptors activate PB neurons and directly or indirectly suppress NPY/AgRP neurons [72,73], leading to disinhibition of suppressive signals to the PB (Figure 6).”
- Glucagon-like peptide 1 (GLP-1) (2019, background): “While these studies suggest that GLP-1 influx into the brain might be a GLP-1R-independent process with passive diffusion of GLP-1 through the BBB [750e752], other studies suggest that uptake of liraglutide into the brain is GLP-1R-dependent [686,753].”