Effects of acidosis on leptin secretion from 3T3-L1 adipocytes and on serum leptin in the uraemic rat.
Détails
ID Serval
serval:BIB_E78C74DF76C2
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Effects of acidosis on leptin secretion from 3T3-L1 adipocytes and on serum leptin in the uraemic rat.
Périodique
Clinical Science
ISSN
0143-5221
Statut éditorial
Publié
Date de publication
09/1999
Peer-reviewed
Oui
Volume
97
Numéro
3
Pages
363-368
Langue
anglais
Résumé
Marked hyperleptinaemia and metabolic acidosis are common findings in patients with chronic renal failure. In animal models, both leptin administration and acidosis reduce food intake. However, leptin causes loss of body fat, while acidosis induces muscle wasting. Whether a low pH and leptin production are related has not been studied. Leptin secretion was measured in cultured 3T3-L1 adipocytes exposed to acid or control pH for up to 96 h. In addition, serum leptin was compared between acidotic and bicarbonate-treated uraemic Wistar rats using the remnant model. Leptin levels in the culture medium were decreased at an acid pH of 7.1 compared with a control pH of 7.5 at 96 h (562+/-78 and 831+/-103 pg.48 h(-1). well(-1) respectively; mean+/-S.E.M.; P=0.037). Similarly, serum leptin in uraemic rats was found to be lower in the acidotic group than in the bicarbonate-treated group, although this observation fell just short of statistical significance (1273+/-171 compared with 2059+/-376 pg/ml; P=0.07). In conclusion, acidosis decreases leptin secretion from cultured adipocytes. Accordingly, acidotic uraemic rats seem to exhibit lower serum leptin levels than their bicarbonate-supplemented counterparts. This study is the first report providing a link between acidosis and leptin levels.
Mots-clé
3T3 Cells, Acidosis/metabolism, Adipocytes/metabolism, Animals, Female, Hydrogen-Ion Concentration, Leptin/blood, Leptin/metabolism, Mice, Rats, Rats, Wistar, Uremia/blood
Pubmed
Web of science
Création de la notice
25/01/2008 13:01
Dernière modification de la notice
20/08/2019 16:10