Mechanisms of ketamine action on lipid metabolism in rats

Summary Background and objective: This study was conducted to determine the effect of ketamine on metabolic homoeostasis and particularly in lipoprotein lipase (LPL) activity in adipose tissue. Methods: Sixty male Wistar rats were divided into six groups of 10 each. Group A served as controls, while...

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Veröffentlicht in:European journal of anaesthesiology 2005-03, Vol.22 (3), p.222-226
Hauptverfasser: Saranteas, T., Zotos, N., Lolis, E., Stranomiti, J., Mourouzis, C., Chantzi, C., Tesseromatis, C.
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Sprache:eng
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Zusammenfassung:Summary Background and objective: This study was conducted to determine the effect of ketamine on metabolic homoeostasis and particularly in lipoprotein lipase (LPL) activity in adipose tissue. Methods: Sixty male Wistar rats were divided into six groups of 10 each. Group A served as controls, while Groups B–F received, respectively, ketamine 60, 80, 100, 120 and 140 mg kg−1 intraperitoneally. The animals were sacrificed 20 min after the administration of ketamine. Insulin concentrations in plasma and total cholesterol, triglyceride, high-density lipoprotein (HDL) and free fatty acid (FFA) concentrations in serum were measured. LPL activity in adipose tissue and medium-chain acyl-CoA dehydrogenase (MCAD) content in muscle were determined. Results: FFA concentrations in serum significantly increased from the second lowest dose of ketamine. Insulin concentrations in plasma did not exhibit any significant difference between groups. MCAD levels were 0.5-fold more in Group F than in Group A, while there were no significant differences between control group and Groups B–E. Furthermore, high concentrations (120 and 140 mg kg−1) of ketamine interfered with in metabolic homoeostasis by significantly reducing LPL activity, thus elevating triglyceride concentrations in serum without affecting cholesterol and HDL metabolism. Conclusions: Ketamine induces various metabolic effects due to changes in adipose LPL activity and MCAD levels in muscles. These findings seem to be significant only at high doses.
ISSN:0265-0215
1365-2346
DOI:10.1017/S0265021505000384