Titre du document / Document title
Peripheral and hypothalamic leptin resistance with age-related obesity
Auteur(s) / Author(s)
SCARPACE Philip J. ;
TÜMER Nihal ;
Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)
Geriatric Research, Education and Clinical Center (182), Department of Veterans Affairs Medical Center, Gainesville, FL 32608-1197, ETATS-UNIS
Department of Pharmacology and Therapeutics, University of Florida College of Medicine, Gainesville, FL 32610, ETATS-UNIS
Résumé / Abstract
Leptin contributes to the regulation of both food intake and energy expenditure. Serum leptin is elevated in most obese humans, and that obesity persists in spite of the elevated leptin, suggesting leptin resistance. The F-344 x BN rat strain, similar to humans, demonstrates a steady increase in body fat and serum leptin into early senescence. Thus, these aged rats become obese in spite of the elevated leptin, suggesting the relationship between leptin, adiposity, and food intake is altered with age. Following both peripheral and central leptin administration, the decrease in food intake and the increase in energy expenditure are blunted in the older obese rats, The extent of the blunting is greater following peripheral leptin, suggesting both peripheral and hypothalamic components to the leptin resistance. Moreover, leptin decreased neuropeptide Y (NPY) mRNA in young but not senescent rats, suggesting that leptin signal transduction may be impaired. Leptin receptor signal transduction involves phosphorylation of cytosolic signal transducer and activator of transcription (STAT) proteins, specifically phosphorylation of STAT3 (P-STAT3). Leptin-induced P-STAT3 levels and P-STAT3 transcription factor binding were diminished with age. In summary, aged rats demonstrate a reduced responsiveness to peripheral and central leptin, and the mechanism may involve impaired suppression of hypothalamic NPY mRNA that may be a consequence of impaired leptin signal transduction. This leptin resistance may have both a peripheral and central component and may be due to either the elevated obesity and serum leptin with age or due to age itself or both.
Revue / Journal Title
Physiology & behavior
ISSN 0031-9384
Source / Source
Congrès
Society for the Study of Ingestive Behavior (SSIB) meeting, Dublin
, IRLANDE
(25/07/2000)
2001, vol. 74, n
o4-5, pp. 721-727 (37 ref.)
Langue / Language
Anglais
Editeur / Publisher
Elsevier, New York, NY, ETATS-UNIS
(1966)
(Revue)
Localisation / Location
INIST-CNRS, Cote INIST : 12876, 35400009475493.0370
Nº notice refdoc (ud4) : 13418296