Can slowing down ‘fat burning’ genes reduce obesity?October 4th, 2008 - 3:26 pm ICT by IANS
Washington, Oct 4 (IANS) Inactivating a pair of key genes involved in ‘fat burning’ actually increases energy expenditure and helps lower obesity, according to a new study. Humans and other warm-blooded animals need to continually “burn fat” in order to maintain body temperature, and it’s currently believed that an individual’s fat-burning capacity, or thermogenic potential, is connected with obesity risk. In fact, bodybuilders and dieters looking to burn fat commonly use thermogenic supplements like ephedra.
In theory, lowering thermogenesis should increase the chances of obesity, but Leslie Kozak and colleagues at Pennington Biomedical Research Centre found that this may not be the case, according to a release of the centre.
They knocked-out two thermogenic genes in mice, Ucp1 (mitochondrial uncoupling protein) and Gdm (glycerol 3-phosphate dehydrogenase) and then fed the mice a high-fat diet while rearing them at a cool 20 degrees Celsius.
Surprisingly, these mice were actually quite resistant to obesity, which resulted from the mice turning on backup heat generators, so to speak. Lacking Ucp1 and Gdm, genes that have been designed for the efficient production of heat, their white fat cells activated alternate, and more inefficient, fat burning pathways.
In this case the inefficiency was beneficial, as the mice had to burn more fat than normal to stay warm (by analogy you burn more wood by warming your house with an open fire then with a well designed wood stove).
Importantly, after spending 10 weeks at 20 degrees Celsius the mice retained these alternate pathways even after transferring to 28 degrees, suggesting their bodies had adapted to the change.
Thus, Kozak and colleagues noted, fat burning does not necessarily require making thermogenesis easier; by making it harder and forcing the body to use inefficient methods to stay warm, the same goals can be reached.
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Tags: biomedical research centre, energy expenditure, fat cells, kozak, pennington biomedical research, phosphate dehydrogenase, study humans, thermogenic supplements, uncoupling protein, warm blooded animals