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Fat: The largest endocrine organ (Proceedings)

April 1, 2009
P. Jane Armstrong, DVM, MS, MBA, DACVIM

The past decade has seen a revolution in our understanding of adipose tissue.

Adipokines

The past decade has seen a revolution in our understanding of adipose tissue. The functions of fat have traditionally been understood as energy storage, thermal insulation, and structural support for some organs. It is now known that adipose tissue is metabolically active and constitutes the largest endocrine organ in the body with unlimited growth potential at any stage of life. Recognizing that adipose tissue is not inert has helped us understand the complex relationship between obesity and some of the diseases associated with obesity in humans (i.e., heart disease, diabetes and chronic degenerative joint disease).

The relationship of obesity to other types of diseases, such as type 2 diabetes mellitus, is not easily understood. The link is a group of proteins, collectively called adipokines, which are secreted by adipose tissue and adipose-resident macrophages and fibrocytes. Adipokines exert their effects in the central nervous system and peripherally, in tissues such as skeletal muscle and the liver. Leptin, adiponectin, resistin, visfatin, retinol-binding protein and tumor necrosis factor-alpha (TNFalpha) are some of the main adipokines of interest. Enzymes such as lipoprotein lipase are also abundantly produced and released from adipose tissue. Finally, many pro-inflammatory cytokines and acute-phase proteins originate in adipocytes.

Of the adiopkines, leptin has received the most attention. In 1995, leptin was identified as the fat cell-specific secretory factor that mediates the hormonal axis between fat and the brain. Leptin concentrations increase with increased body fat in all species studied including dogs and cats. Adequate energy stores are signaled by leptin and permit reproduction and normal immune function. Leptin also functions to reduce appetite. Despite high hopes that leptin would be the long-sought "lipostat", it is now known that leptin resistance develops with increasing obesity. The ability of low leptin levels to stimulate appetite is greater than the ability of high leptin levels to suppress appetite. Leptin, however, may provide a link between osteoarthritis and obesity. In humans, increased leptin in synovial fluid has been seen in patients with either rheumatoid arthritis or osteoarthritis.

Genomics and Obesity

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As indicated earlier, the relationship of obesity to other diseases is complicated and only recently is being recognized as a key factor affecting overall health. New research tools such as genomics have enabled scientists to shed some light on the underlying mechanisms which link obesity with other diseases. By performing microarray analysis on lean and obese adipose tissue and lymphocyte samples, scientists have begun to understand the processes behind obesity and, importantly, how obesity links to other diseases.

When comparing lean vs obese adipose tissue, the gene expression of obese adipocytes showed a down regulation of PPAR-gamma, uncoupling protein-2, carnitine O-palmitoyltransferase 1 A and acyl-CoA synthetase. When functioning properly these genes are important in the beta-oxidation of fatty acids. The down-regulation of these genes may explain why obese animals are fat storing instead of fat burning. In addition, the obese adipose tissue also had down-regulation of genes associated with glucose metabolism. Down-regulation of pyruvate dehydrogenase kinase-4 and glucose-6-phosphatase may be a potential link between diabetes and obesity.

Many of the same pathways altered in the obese adipose tissue have also found to be altered in lymphocytes from obese dogs. Microarray analysis of lymphocytes revealed that overweight dogs had decreased carbohydrate metabolism, interleukin signaling, PPAR signaling, IGF-1 signaling, insulin receptor signaling, amino acid metabolism, branch chain amino acid degradation and lipid metabolism compared to results of similar analyses in lean dogs. These observations of both adipocytes and lymphocytes may explain why obese animals become insulin resistant and have increased circulating glucose, insulin, IGF-1 and inflammation.

Recent studies researched the effects of weight loss on the gene expression profiles of obese dogs and cats. (Data thanks to Ryan M. Yamka, PhD, MS, MBA, Hill's Pet Nutrition, Inc., Topeka, KS). These dogs (> 35% % body fat by DEXA) were fed a dry low-fat, fiber-enhanced therapeutic food (33.2% crude protein, 8.7% crude fat and 26.7% total dietary fiber on dry matter basis) for a period of 4 months. On average, dogs lost 2.8 ± 0.8 kg body fat (41.2% of initial fat mass) in 4 months. The nutrigenomic effect of the food can be seen in the shift from an obese to a lean gene expression profile. Of the genes identified, there was a down regulation of genes associated with fat accumulation (i.e., leptin and IGF-1) once the dogs lost weight. These data suggest that obese dogs fed the weight loss food had a shift in metabolism to a lean genomic profile. However, weight loss alone does not alter gene expression. Changes in gene expression occur as a result of foods with specific nutrient profiles and weight loss working together.

The effect of weight loss on the gene expression profiles of obese cats has also been examined. In one study, obese cats (> 30% body fat by DEXA) were fed Hill's Prescription Diet® feline r/d® dry for a period of 4 months. On average, cats lost 0.61 ± 0.13 kg body fat (30.7% of initial fat mass) in 4 months. The nutrigenomic effect of the food was associated with the down regulation of genes associated with inflammation, obesity and T2DM. These data suggest that weight loss can correct the systemic effects of obesity.

In summary, obesity is not just a weight issue. The biochemical changes occurring with obesity result in an increased susceptibility to other diseases. Genomics may provide valuable insights into the underlying mechanisms which link obesity with other diseases. The biochemical changes which occur in the adipocyte influence the adipokines released which ultimately will affect the body systemically. These changes can be quantitated by studying the genomics of lymphocytes and adipose tissue, and by measuring circulating adipokines. Weight loss appears to reverse many of the changes that occur with obesity.

Selected Readings

Scherer PE. Adipose tissue: from lipid storage compartment to endocrine organ. Diabetes 2006; 55, 1537.

Henson MS and O'Brien TD. Feline models of type 2 diabetes mellitus. ILAR Journal 2006; 47: 234.

Hoenig M. The cat as a model for human nutrition and disease. Curr Opin Clin Nutr Metab Care 2006; 9:584.

Lund EM, Armstrong PJ, et al. Prevalence and risk factors for obesity in adult cats from United States private veterinary practices. Intern J Appl Vet Res 2005; (3): 2.

Laflamme DP. Understanding and managing obesity in dogs and cats. Vet Clin Small An Pract 2006; 36; 1283-95, vii.

Center SA, Harte J, Watrous D et al. The clinical and metabolic effects of rapid weight loss in obese pet cats and the influence of supplemental oral L-carnitine. J Vet Intern Med. 2000 Nov-Dec;14:598.

Rand JS, Marshall RD. Diabetes mellitus in cats. Vet Clin Small Anim Prac 2005;35:211-224.

Yamka RM, Friesen KG and Frantz NZ. Identification of canine markers related to obesity and the effects of weight loss on the markers of interest. Intern J Appl Res Vet Med. 2006; 4:282-292.

Yamka RM, Frantz NZ and Friesen KG. Effects of three canine weight loss foods on body composition and obesity markers. Intern J Appl Res Vet Med. 2007; 5:125-132.

Diez M, Michaux C, Jeusette I, et al. Evolution of blood parameters during weight loss in experimental obese beagle dogs. J Anim Physiol Anim Nutr 2004;88:166-171.

Blanchard G, Nguyen P, Gayet C, et al. Rapid weight loss and a high-protein low-energy diet allows the recovery of ideal body composition and insulin sensitivity in obese dogs. J Nutr 2004;134:2148S-2150S.

Yamka, R.M. and K.G. Friesen. 2006. Identification of markers related to feline obesity. J. Anim. Sci. 84 (Suppl. 1): 171-172 (T31).

Yamka, R.M., K.G. Friesen, X. Gao, S. Malladi, S. Al-Murrani and L Bernal. The effects of weight loss on gene expression in dogs. 2008 ACVIM Meeting, San Antonio.

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