| Literature DB >> 9350983 |
A P Goldstone1, J G Mercer, I Gunn, K M Moar, C M Edwards, M Rossi, J K Howard, S Rasheed, M D Turton, C Small, M M Heath, D O'Shea, J Steere, K Meeran, M A Ghatei, N Hoggard, S R Bloom.
Abstract
The adipose tissue hormone, leptin, and the neuropeptide glucagon-like peptide-1 (7-36) amide (GLP-1) both reduce food intake and body weight in rodents. Using dual in situ hybridization, long isoform leptin receptor (OB-Rb) was localized to GLP-1 neurons originating in the nucleus of the solitary tract. ICV injection of the specific GLP-1 receptor antagonist, exendin(9-39), at the onset of dark phase, did not affect feeding in saline pre-treated controls, but blocked the reduction in food intake and body weight of leptin pre-treated rats. These findings suggest that GLP-1 neurons are a potential target for leptin in its control of feeding.Entities:
Mesh:
Substances:
Year: 1997 PMID: 9350983 DOI: 10.1016/s0014-5793(97)01103-4
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124