R-α lipoic acid γ-cyclodextrin complex increases energy expenditure: a 4-month feeding study in mice.

Authors:
Sibylle Nikolai, Patricia Huebbe, Cornelia C Metges, Anke Schloesser, Janina Dose, Naoko Ikuta, Keiji Terao, Seiichi Matsugo, Gerald Rimbach
Year of publication:
2014
Volume:
30
Issue:
2
Issn:
0899-9007
Journal title abbreviated:
Nutrition
Journal title long:
Nutrition (Burbank, Los Angeles County, Calif.)
Abstract:
A high-fat diet (HFD) affects energy expenditure in laboratory rodents. R-α lipoic acid cyclodextrin (RALA-CD) complex is a stable form of lipoic acid (LA) and may improve energy expenditure. The aim of this study was to determine the effect of RALA-CD on energy expenditure and underlying molecular targets in female laboratory mice.Female C57BL/6J mice were fed a HFD containing 0.1% LA for about 16 wk. The effects on energy expenditure, gene and protein expression were assessed using indirect calorimetry, real-time reverse transcriptase polymerase chain reaction, and Western blot, respectively.Supplementing mice with RALA-CD resulted in a significant increase in energy expenditure. However, both RALA per se (without γ-cyclodextrin) and S-α lipoic acid cyclodextrin did not significantly alter energy expenditure. Furthermore RALA-CD changed expression of genes encoding proteins centrally involved in energy metabolism. Transcriptional key regulators sirtuin 3 and peroxisome proliferator-activated receptor-γ, coactivator 1 alpha, as well as thyroid related enzyme type 2 iodothyronine deiodinase were up-regulated in brown adipose tissue (BAT) of RALA-CD-fed mice. Importantly, mRNA and/or protein expression of downstream effectors uncoupling protein (Ucp) 1 and 3 also were elevated in BAT from RALA-CD-supplemented mice.Overall, present data suggest that RALA-CD is a regulator of energy expenditure in laboratory mice.