(588.10) The Effect of Lipolysis Inhibitor Acipimox on Brown Adipose Tissue Bioenergetics and Uncoupling Protein Abundance in Severely Burned Rats

Poster Board Number: E360

Victoria Rontoyanni (University of Texas Medical Branch), Amina El Ayadi (University of Texas Medical Branch), Anesh Prasai (University of Texas Medical Branch), Ye Wang (University of Texas Medical Branch), Nisha Bhattarai (University of Texas Medical Branch), Emre Vardarli (University of Texas Medical Branch), Craig Porter (University of Arkansas for Medical Sciences, University of Arkansas for Medical Sciences), Andrew Murton (University of Texas Medical Branch)

Introduction: Uncoupling protein 1 (UCP1) activation in brown adipose tissue (BAT) contributes to the hypermetabolic stress response to burn trauma. Strategies that target BAT UCP1 could be beneficial in controlling burn-induced hypermetabolism. Acipimox, an inhibitor of adipose tissue lipolysis, has been shown to be effective at blunting burn-induced lipolysis and expression of UCP1 protein in rodent white adipose tissue. The impact of acipimox on BAT bioenergetics and uncoupling protein abundance is currently unknown. We hypothesized that acipimox would blunt burn-induced UCP-1 dependent respiration and UCP-1 protein levels in BAT.

Methods: Sixty-four male Sprague-Dawley rats received a 60% TBSA scald burn (n=32) or sham procedure (n=32) and were subsequently randomized to receive either acipimox (n=16/group; 50 mg/kg/day i.p.) or vehicle (n=16/group) daily for 7d. BAT was harvested from the interscapular fat pad on day 7 after burn and mitochondrial respiratory function assessed by high-resolution respirometry. GDP-sensitive respiration was assayed as a direct measure of UCP1 function. UCP1 and adenine nucleotide translocator (ANT2) protein levels were determined by western blot.

Results: UCP1-dependent and UCP1-independent uncoupled respiration in BAT was reduced at 7d after severe burn, independent of treatment (injury effect, Plt;0.01). Post-burn, UCP1-dependent respiration accounted for 65% of total uncoupled respiration compared to 59% in sham rats (injury effect, Plt;0.05), independent of treatment. Acipimox appeared to exert a lowering effect on UCP1-dependent respiration (treatment effect, P=0.07) but not on UCP1-independent respiration. Neither burn nor treatment with acipimox had a significant effect on UCP1 protein levels. Protein levels of ANT2, a carrier protein involved in fatty acid-induced uncoupling, were greater in response to acipimox (treatment effect, Plt;0.05).

Conclusion: BAT UCP1 function than UCP1 protein content is greater in severely burned rats. Acipimox appears to reduce UCP1-dependent respiration, independent of UCP1 protein levels. The effect of acipimox on BAT ANT2 protein content may partly explain the absence of an effect on UCP1-independent respiration, but this warrants further investigation.

The protocol was approved by the University of Texas Medical Branch IACUC.

University of Texas Medical Branch Institutional funds