It triggers a surprising metabolic mechanism: white fat cells are transformed into cells similar to brown fat ( ‘beige fat’), that protects the body against excess weight and its damaging consequences. In healthy humans, white adipose tissue constitutes ~25% of body mass. However, when in excess, white fat contributes to insulin resistance and diabetes. Conversely, brown fat improves insulin sensitivity and is reversely correlated to obesity.
In response to cold or exercise, cells similar to brown fat – the beige fat – can appear within the white fat, a phenomenon known as “browning.” Although the origin of these beige cells seems alike to that of the white fat, their function differs: the more beige fat appear within the white adipose tissue, the more calories are burned. This suggests that stimulating beige fat growth could be a way to reduce obesity and limit insulin resistance.
Today, researchers from UNIGE Faculty of Medicine demonstrate that it also has a direct impact on obesity: microbiota of obese people has a specific composition, different from the microbiota of lean people. Indeed, germ-free mice (born and kept in sterile conditions, i.e. without microbiota), which receive gut microbiota transplant from obese people, tend to develop obesity and insulin resistance. “Having observed that microbiota can affect the obesity onset, we suspected that microbiota depletion can change the insulin sensitivity by modifying the amount and balance of these various types of fat,” explains Prof Mirko Trajkovski.
METHOD/RESULTS: Researchers fed 3 groups of mice with a high-calorie diet: germ-free mice, standard mice and mice previously treated with high doses of antibiotics that have the effect of totally depleting their microbiota. While normal mice exposed to a high-calorie diet did develop obesity and insulin resistance, the 2 other groups remained lean, had an improved sensitivity to insulin and tolerated glucose better. Importantly, their amount of white fat decreased, and this was accompanied with increased levels of brown fat markers. The scientists observed that depleting microbiota – either through antibiotics or in germ-free mice – stimulated the development of functional beige fat within the white fat, in the same way as when exposed to cold or exercise.
MOA: Macrophages are an essential component of the immune system and fulfil various metabolic functions, including tissue remodelling. They express different functional programmes in response to micro-environmental signals, a process called “polarization.” Polarized macrophages can be broadly classified in two main groups: M1 and M2, the latter being able to act on the adipose and increase the production of beige fat. When the microbiota is depleted, the number of eosinophils increases in white fat, which secretes “type 2 cytokines” that act on macrophages polarization. Thanks to these proteins, M1 macrophages turn into M2 macrophages, which activate the browning of white fat and reduce obesity.
To search for effective clinical treatments of obesity, the scientists will use particular antibiotics, as well as bacterial phages, a kind of virus that kills only specific bacterial strains. The possibility of microbiota transplant from a lean to an obese person whose microbiota would have been previously depleted will also be studied. http://www.eurekalert.org/pub_releases/2015-11/udg-hdt111115.php
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