Adipocyte Apoptosis After Burn Injury Is Associated With Altered Fat Metabolism

Burn injury often is associated with the abnormal lipid metabolism, including hyperlipidemia, desensitization to lipolytic responses to catecholamines, and reduction in the size of the white adipose tissue. Understanding the biological mechanisms for the decrease in fat mass despite desensitization to catecholamines is important both for the study of lipid metabolism and for the study of its relationship to concomitant insulin resistance. Using epididymal adipose tissue from adult male Sprague–Dawley rats after burn injury (n = 102) or sham-burn injury (n = 102), we tested the hypothesis that a whole-body burn injury causes apoptosis in that tissue. At 1, 3, and 7 days after 40% to 50% body burn injury to the rat, epidydimal adipose tissue was harvested and studied for apoptotic changes and lipolytic properties. For apoptosis, paraformaldehyde-fixed tissue sections were analyzed by in situ TdT-mediated dUTP-X nick-end labeling (TUNEL) staining, and tissue homogenates were also analyzed for DNA fragmentation by enzyme-linked immunoassay and ligation-mediated polymerase chain reaction ladder assay. Isolated adipocytes were stimulated with isoprotenerol, and glycerol production was measured as a reflector of effectiveness of lipolysis. Epididymal adipose tissue showed increased apoptosis manifested by the positive TUNEL staining and increased DNA fragmentation by enzyme-linked immunoassay at day 3 and 7 after burn injury. The DNA fragmentation was confirmed further by the ligation-mediated polymerase chain reaction ladder assay. This elevated DNA fragmentation persisted in the burned animals from day 3 until day 7 after burn injury, the end of observation period. Increase in apoptosis was correlated with decrease in DNA content and tissue weight in the epidydimis. At the functional level, a significant decrease in isoproterenol-induced lipolytic activity (glycerol production) was observed to almost 50% of control level at day 3 and 7 but was not decreased at day 1. Apoptosis of adipocytes may play a role in the altered lipid metabolism, including hyperlipidemia observed in burned subjects.

[1]  R. Panettieri,et al.  Cytokines regulate beta-2-adrenergic receptor responsiveness in airway smooth muscle via multiple PKA- and EP2 receptor-dependent mechanisms. , 2005, Biochemistry.

[2]  M. Mittlböck,et al.  Serum cholesterol and triglycerides: potential role in mortality prediction. , 2003, Burns : journal of the International Society for Burn Injuries.

[3]  E. Ulvestad,et al.  Concentrations of cytokines in plasma of patients with large burns: their relation to time after injury, burn size, inflammatory variables, infection, and outcome. , 2003, The European journal of surgery = Acta chirurgica.

[4]  A. Rosenzweig,et al.  Comparison of Comet Assay, Electron Microscopy, and Flow Cytometry for Detection of Apoptosis , 2003, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[5]  R. Hegele,et al.  The molecular basis of genetic lipodystrophies. , 2002, Clinical biochemistry.

[6]  E. Scarpini,et al.  Interleukin-1beta and interferon-gamma induce proliferation and apoptosis in cultured Schwann cells , 2002, Journal of Neuroimmunology.

[7]  S. Kumar,et al.  Resistin, central obesity, and type 2 diabetes , 2002, The Lancet.

[8]  Y. Terauchi,et al.  The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity , 2001, Nature Medicine.

[9]  S. Coppack Pro-inflammatory cytokines and adipose tissue , 2001, Proceedings of the Nutrition Society.

[10]  M. Lazar,et al.  The hormone resistin links obesity to diabetes , 2001, Nature.

[11]  J. Flier Diabetes: The missing link with obesity? , 2001, Nature.

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

[13]  J. Friedman,et al.  Obesity in the new millennium , 2000, Nature.

[14]  Joseph L. Goldstein,et al.  reply: Leptin and diabetes in lipoatrophic mice , 2000, Nature.

[15]  R. Tompkins,et al.  A unique mechanism of desensitization to lipolysis mediated by beta(3)-adrenoceptor in rats with thermal injury. , 1999, American Journal of Physiology.

[16]  R. Tompkins,et al.  A unique mechanism of desensitization to lipolysis mediated by β3-adrenoceptor in rats with thermal injury. , 1999, American journal of physiology. Endocrinology and metabolism.

[17]  O. Ishiko,et al.  Metabolic and Morphologic Characteristics of Adipose Tissue Associated with the Growth of Malignant Tumors , 1999, Japanese journal of cancer research : Gann.

[18]  K. Siddle,et al.  Human Preadipocytes Display a Depot-Specific Susceptibility to Apoptosis , 1998, Diabetes.

[19]  R. Hotchkiss,et al.  Apoptosis in lymphoid and parenchymal cells during sepsis: findings in normal and T- and B-cell-deficient mice. , 1997, Critical care medicine.

[20]  A. Saraste,et al.  Apoptosis in the heart. , 1997, The New England journal of medicine.

[21]  M. Grunstein,et al.  Mechanism of cytokine-induced modulation of beta-adrenoceptor responsiveness in airway smooth muscle. , 1996, The Journal of clinical investigation.

[22]  B. Spiegelman,et al.  Tumor Necrosis Factor (TNF)-α Inhibits Insulin Signaling through Stimulation of the p55 TNF Receptor and Activation of Sphingomyelinase* , 1996, The Journal of Biological Chemistry.

[23]  T. Funahashi,et al.  cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1). , 1996, Biochemical and biophysical research communications.

[24]  C. Thompson,et al.  Apoptosis in the pathogenesis and treatment of disease , 1995, Science.

[25]  H. Steller Mechanisms and genes of cellular suicide , 1995, Science.

[26]  B. Spiegelman,et al.  Tumor necrosis factor alpha inhibits signaling from the insulin receptor. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[27]  M. Soley,et al.  Epidermal growth factor modulates the lipolytic action of catecholamines in rat adipocytes. Involvement of a Gi protein. , 1993, The Journal of biological chemistry.

[28]  D. Herndon,et al.  Evidence for Kupffer cell activation by burn injury and Pseudomonas exotoxin A. , 1993, Burns : journal of the International Society for Burn Injuries.

[29]  R. Wolfe,et al.  Effect of severe burn injury on substrate cycling by glucose and fatty acids. , 1987, The New England journal of medicine.

[30]  C. Baxter,et al.  Lipid mobilization and metabolism after thermal trauma. , 1982, The Journal of trauma.

[31]  K. Hummel,et al.  The influence of genetic background on the expression of the obese (ob) gene in the mouse , 1973, Diabetologia.

[32]  J. Hirsch,et al.  Effect of early nutrition on the development of rat epididymal fat pads: cellularity and metabolism. , 1968, The Journal of clinical investigation.

[33]  M. Rodbell,et al.  Metabolism of isolated fat cells. 3. The similar inhibitory action of phospholipase C (Clostridium perfringens alpha toxin) and of insulin on lipolysis stimulated by lipolytic hormones and theophylline. , 1966, The Journal of biological chemistry.

[34]  M. Rodbell The metabolism of isolated fat cells , 1965 .

[35]  J. Friedman,et al.  Molecular mapping of obesity genes , 2004, Mammalian Genome.

[36]  R. Unger,et al.  Lipotoxic diseases. , 2002, Annual review of medicine.

[37]  C. Niesler,et al.  Tumor necrosis factor-alpha induces apoptosis of human adipose cells. , 1997, Diabetes.

[38]  A. Blaschke,et al.  Apoptotic DNA fragmentation is detected by a semi-quantitative ligation-mediated PCR of blunt DNA ends , 1997, Cell Death and Differentiation.

[39]  S. O’Rahilly,et al.  Regulation of adipose cell number in man. , 1997, Clinical science.

[40]  P. Libby,et al.  Apoptosis of vascular smooth muscle cells induced by in vitro stimulation with interferon-gamma, tumor necrosis factor-alpha, and interleukin-1 beta. , 1996, Arteriosclerosis, thrombosis, and vascular biology.

[41]  P. Libby,et al.  Apoptosis of Vascular Smooth Muscle Cells Induced by In Vitro Stimulation With Interferon-γ, Tumor Necrosis Factor–α, and Interleukin-1β , 1996 .

[42]  L. Moldawer,et al.  Identification of a novel tumor necrosis factor alpha/cachectin from the livers of burned and infected rats. , 1990, Archives of surgery.