Humans have two types of fat. White adipose tissue (WAT)
stores excess energy in large droplets of triglycerides, typically referred to
as unhealthy or "bad" fat. Brown adipose tissue (BAT) contains
smaller droplets and a high number of mitochondria that burn fat to produce
heat. When exposed to cold temperatures or when stimulated by exercise, the
body can convert adult WAT into BAT in a process known as browning. This
process can be employed to combat diabetes and obesity (Cavalera, Axling,
Berger, & Holm, 2016; Khidr, Ali, Elshafey, & Fawzy, 2017; Wankhade,
Shen, Yadav, & Thakali, 2016). However, current treatment options are
limited to pills and injections, which are do not produce strong or localized
results.
A research team at the Columbia University
Medical Center (CUMC) and the University of North Carolina (UNC) wanted to
investigate localized browning while increasing overall metabolism. They
created a microneedle skin patch that has nanoparticles containing either
rosiglitazone (Avandia), an oral diabetes medication, or CL316243, a beta
adrenergic agonist (a class of medication that relaxes muscles in the airway)
that has been shown to stimulate browning in mice (Zhang et al., 2017). The
mice two patches which were placed on either side of the lower abdomen. The
patches were replaced every three days over the course of four weeks.
Experimental mice received one patch with drug-containing nanoparticles and one
patch with empty nanoparticles, while control mice received two patches with
empty nanoparticles.
The experiment demonstrated an additional 20%
overall fat reduction on the side receiving a drug when compared to the side
receiving no drugs. Treated mice exhibited lower fasting blood glucose levels
than control mice. Genetic analyses also indicated an increase in
BAT-associated genes when exposed to the drug, and the increase was observed
locally. Applying the patch to lean mice led to an increase in oxygen
consumption, indicating a metabolic increase.
However, this technology cannot quite yet be
applied to humans. Humans lack beta3 andrenergic receptors in adipose tissues,
meaning CL316243 may not be a viable treatment option. Furthermore, this patch
only locally treats the symptoms of obesity and diabetes. For most, proper
nutrition, exercise, and sleep are key to resolving obesity and managing
diabetes.
References
Cavalera, M., Axling, U., Berger, K., &
Holm, C. (2016). Rose hip supplementation increases
energy expenditure and induces browning of white adipose tissue. Nutrition
&
Metabolism, 13, 1-9.
doi:10.1186/s12986-016-0151-5
Khidr, E. G., Ali, S. S., Elshafey, M. M., &
Fawzy, O. A. (2017). Association of irisin and
FNDC5 rs16835198 G > T gene polymorphism with type 2
diabetes mellitus and diabetic
nephropathy. An Egyptian pilot
study. Gene, 626, 26-31. doi:10.1016/j.gene.2017.05.010
Wankhade, U. D., Shen, M., Yadav, H., &
Thakali, K. M. (2016). Novel browning agents,
mechanisms, and therapeutic potentials of brown adipose tissue. Biomed
Research
International, 20,
161-15. doi:10.1155/2016/2365609
I think it's interesting how the treatment is effective, but since humans lack the correct receptors, it is not a viable option for us. I was also curious as to why the patch only treats symptoms of diabetes and obesity. Shouldn't the patch effect any source of white adipose tissue? Do you know what's the reason for that?
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