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Effects of acidosis on leptin secretion from 3T3-L1 adipocytes and on serum leptin in the uraemic rat
- Source :
- Clinical Science. 97:363-368
- Publication Year :
- 1999
- Publisher :
- Portland Press Ltd., 1999.
-
Abstract
- 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.
- Subjects :
- Leptin
medicine.medical_specialty
Biology
Mice
chemistry.chemical_compound
Internal medicine
Adipocyte
Gene expression
Blood plasma
Adipocytes
medicine
Animals
Secretion
Rats, Wistar
Uremia
Acidosis
business.industry
digestive, oral, and skin physiology
Metabolic disorder
Glucose transporter
Skeletal muscle
Metabolic acidosis
3T3-L1
3T3 Cells
General Medicine
Hydrogen-Ion Concentration
medicine.disease
Rats
medicine.anatomical_structure
Endocrinology
chemistry
Female
medicine.symptom
business
Subjects
Details
- ISSN :
- 14708736 and 01435221
- Volume :
- 97
- Database :
- OpenAIRE
- Journal :
- Clinical Science
- Accession number :
- edsair.doi.dedup.....a9ee3085818d7a3ab994ceb6a7febd32
- Full Text :
- https://doi.org/10.1042/cs0970363