Single Hind Limb Burn Injury to Mice Alters Nuclear Factor-&kgr;B Expression and [18F] 2-Fluoro-2-Deoxy-D-Glucose Uptake

Burn trauma to the extremities can produce marked systemic effects in mice. Burn injury to the dorsal surface of mice is also associated with changes in glucose metabolism ([18F] 2-fluoro-2-deoxy-D-glucose [18FDG] uptake) by brown adipose tissue (BAT) and nuclear factor (NF)-&kgr;B activity in several tissues including skeletal muscle. This study examined the effect of a single hind limb burn in mice on 18FDG uptake by NF-&kgr;B activity in vivo, and blood flow was determined by laser Doppler techniques. Male NF-&kgr;B luciferase reporter mice (28–30 g) were anesthetized, both legs were shaven, and the right leg was subjected to scald injury by immersion in 90°C water for 5 seconds. Sham-treated animals were used as controls. Each burned and sham mouse was resuscitated with saline (2 mL, i.p.). The individual animals were placed in wire bottom cages with no food and free access to water. After 24 hours, the animals were imaged with laser Doppler for measuring blood flow in the hind limb. The animals were then unanesthetized with 50 &mgr;Ci of FDG or luciferin (1.0 mg, i.v.) via tail vein. Five minutes after luciferin injection, NF-&kgr;B mice were studied by bioluminescence imaging with a charge-coupled device camera. One hour after 18FDG injection, the animals were killed with carbon dioxide overdose, and 18FDG biodistribution was measured. Tissues were also analyzed for NF-&kgr;B luciferase activity. The scalding procedure used here produced a full-thickness burn injury to the leg with sharp margins. 18FDG uptake by the burned leg was lower than that in the contralateral limb. Similarly, luciferase activity and blood flow in the burned leg were lower than those in the contralateral leg. 18FDG uptake by BAT and heart increased, whereas that by brain decreased. In conclusion, the present study suggests that burn injury to a single leg decreased 18FDG uptake by skeletal muscle but increased 18FDG uptake by BAT. The injury to the leg reduced NF-&kgr;B expression compared with the contralateral leg and the uninjured skeletal muscle of the sham but activated NF-&kgr;B expression in a number of other organs. These findings are consistent with the hypothesis that burn trauma to the extremities can produce marked systemic effects, including activation of NF-&kgr;B expression and activation of 18FDG uptake by BAT.

[1]  R. Tompkins,et al.  Effects of burn injury, cold stress and cutaneous wound injury on the morphology and energy metabolism of murine brown adipose tissue (BAT) in vivo. , 2011, Life sciences.

[2]  C. K. Song,et al.  Sympathetic and sensory innervation of brown adipose tissue , 2010, International Journal of Obesity.

[3]  Michael E. Phelps,et al.  Quantification of Cerebral Glucose Metabolic Rate in Mice Using 18F-FDG and Small-Animal PET , 2009, Journal of Nuclear Medicine.

[4]  Touqir Zahra,et al.  Targeted photodynamic therapy of established soft-tissue infections in mice , 2004, SPIE BiOS.

[5]  W. Chapman,et al.  Systemic nf-?B activation in a transgenic mouse model of acute pancreatitis 1 1 Supported by a VA/HB , 2003 .

[6]  S. Kandarian,et al.  Activation of an alternative NF‐ΚB pathway in skeletal muscle during disuse atrophy , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  D. Maass,et al.  The Time Course of Cardiac NF-&kgr;B Activation and TNF-&agr; Secretion by Cardiac Myocytes After Burn Injury: Contribution to Burn-Related Cardiac Contractile Dysfunction , 2002, Shock.

[8]  J. Fischer,et al.  The transcription factors NF-kappab and AP-1 are differentially regulated in skeletal muscle during sepsis. , 2001, Biochemical and biophysical research communications.

[9]  M. Kaneki,et al.  Skeletal muscle apoptosis after burns is associated with activation of proapoptotic signals. , 2000, American journal of physiology. Endocrinology and metabolism.

[10]  D. Brenner,et al.  Gene expression and cytokine and enzyme activation in the liver after a burn injury. , 2000, The Journal of burn care & rehabilitation.

[11]  R. Tompkins,et al.  Decreased cerebral glucose utilization in rats during the ebb phase of thermal injury. , 1996, The Journal of trauma.

[12]  S. Shackford,et al.  The neurohumoral response to burn injury in patients resuscitated with hypertonic saline. , 1988, The Journal of trauma.

[13]  J. Turinsky Hepatic and skeletal muscle phospholipid metabolism in recovering burned rats. , 1986, Experimental and molecular pathology.

[14]  J. Turinsky,et al.  Prostaglandin E2 and muscle proteolysis: effect of burn injury and cycloheximide. , 1986, The American journal of physiology.

[15]  J. Turinsky,et al.  Altered protein kinetics in vivo after single-limb burn injury. , 1984, The Biochemical journal.

[16]  H. Jacobson,et al.  Effect of thermal injury on glucocorticoid and androgen binding in skeletal muscles with different fiber populations. , 1982, Journal of Trauma.

[17]  K. M. Nelson,et al.  Analysis of postburn insulin unresponsiveness in skeletal muscle. , 1981, The Journal of surgical research.

[18]  J. Turinsky,et al.  Proximity to a burn wound as a new factor in considerations of postburn insulin resistance. , 1979, The Journal of surgical research.

[19]  J. Turinsky,et al.  Dynamics of insulin secretion and resistance after burns. , 1977, The Journal of trauma.

[20]  Michael Karin,et al.  NF-kappaB: linking inflammation and immunity to cancer development and progression. , 2005, Nature reviews. Immunology.

[21]  W. Chapman,et al.  Systemic nf-kappaB activation in a transgenic mouse model of acute pancreatitis. , 2003, The Journal of surgical research.

[22]  S. Kandarian,et al.  Activation of an alternative NF-kappaB pathway in skeletal muscle during disuse atrophy. , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.