1. Fat Gain Signals Inflammatory Response
2. Fat Cells Release Inflammatory Factors
Tumor Necrosis Factor α (TNF-α) is an inflammatory molecule released from adipose tissue. Overweight and obese individuals secrete TNF-α in greater amounts, contributing to insulin resistance.3 TNF- α down regulates GLUT-4, which is responsible for transporting glucose into skeletal muscle, resulting in reduced insulin function. TNF- α also reduces the activity of the insulin receptor, diminishing insulin’s metabolic effects and potentially leading to muscle insulin resistance.5
Interleukin-6 is another molecule released in greater amounts from excessive adipose tissue. Like TNF-α, IL-6 also down regulates GLUT-4, further reducing insulin function and contributing to insulin resistance. Increased IL-6 concentrations also induce the liver to release excess amounts of C-reactive protein (CRP) and fibrinogen in the blood, which are two of the major risk factors for cardiovascular disease and type 2 diabetes.6 IL-6 also increases the concentration and activity of blood platelets, which increases the risk for blood clots.2 The activity of cells that line the blood vessels, such as endothelial cells and smooth muscle cells, is also affected by high IL-6 levels, contributing to vascular wall inflammation and damage.4
3. Fat Cells Cause Plaque Formation
Fat stores also affect your health by reducing the fat cell’s secretion of the anti-atherogenic, anti-inflammatory protein,
4. Fat Cells Can Become "Sick"
To further illustrate the dangers of accumulating excessive fat stores, a study by Bodenet al. (2008) in the Diabetes journal suggests fat cells from obese individuals are “sick,” due to significantly higher levels of stress to the cell. The authors explain that a constant influx of excess calories into fat cells can induce stress to the endoplasmic reticulum (ER), which is responsible for synthesizing lipids for storage. This stress triggers ER stress sensors, which activate various pathways in the body to alleviate stress. Researchers believe that this ER stress may be a contributor to the inflammation and insulin resistance associated with diabetes.
In conclusion, adipose tissue does much more than only serve as an energy source. Fat cells are very active, able to communicate with immune cells and initiate an inflammatory response with excess calorie storage. Both fat and immune cells secrete various inflammatory factors that negatively influence normal and healthy functions of the body. As these responses become chronic with significant fat gain, you are at greater risk for chronic inflammation, cardiovascular disease, insulin resistance, and diabetes. Therefore, no matter how active you are, it is important to keep your body fat percentage at a reasonable level in order to maintain long-term health.
References:
1. Boden, G. et al., Increase in Endoplasmic Reticulum Stress-Related Proteins and Genes in Adipose Tissue of Obese, Insulin-Resistant Individuals. Diabetes, 2008. 57: p. 2438-2444.
2. Burstein, S.A. et al., Cytokine-induced alteration of platelet and hemostatic function. Stem Cells, 1996. 14: p. 154-162.
3. Diamond, A.S. et al,The Endocrine Function of Adipose Tissue. GGH, 2002. 18(2): p. 17-23.
4. Wassmann, S. et al., Interleukin-6 induces oxidative stress and endothelial dysfunction by overexpression of the angiotensin II type 1 receptor.Circ Res, 2004. 94: p. 534-541.
5. Weisberg S.P. et al., Obesity is associated with macrophage accumulation in adipose tissue. J Clin Invest, 2003. 112: p. 1796-1808.
6. Wisse, B.E., The Inflammatory Syndrome: The Role of Adipose Tissue Cytokines in Metabolic Disorders Linked to Obesity.J Am Soc Nephrol, 2004. 15: p. 2792-2800.
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