Nanoparticle Dibenzazepine Delivery Induces Browning Of White Fat
A method to deliver a drug directly to stored white fat cells to turn them into more easily burned brown fat cells has been found by Purdue University scientists. The technique represents a potential breakthrough for the treatment of obesity and diabetes.
White adipose tissue, most associated with obesity, is a type of fat that collects in the body for long-term storage of energy. It’s possible humans evolved to store white fat to act as insulation and energy storage.
However, as we have become over-fed and less active, we have less need for the energy stored in white fat and it over accumulates, leading to metabolic diseases such as diabetes and obesity. More than one-third of Americans are obese, and nearly 10 percent have diabetes, according to the Centers for Disease Control and Prevention.
Brown fat is more readily burned by the body, dissipating energy into heat.
Notch Signaling Disruption
Assistant professor Meng Deng. Credit: Purdue Agricultural Communication photo/Tom Campbell
Scientists, including Purdue’s Meng Deng, assistant professor of agricultural and biological engineering, biomedical engineering and materials engineering, and Shihuan Kuang, professor of animal sciences, have been looking for ways to decrease white fat in favor of brown fat through a signaling pathway that is known to regulate cell differentiation and cell identity.
In Notch signaling, a cell sends a signal to a neighboring cell to control that neighbor’s gene transcription and its identity. Disrupting that signal in a progenitor cell destined to become one of the undesirable white fat cells leads to the creation of brown fat.
Deng and Kuang report that they have, for the first time, used an engineered polymeric nanoparticle for controlled delivery of a Notch-signaling inhibitor directly to white fat cells.
Controlled Dibenzazepine Delivery
In a mouse model, the nanoparticle, made of an FDA-approved polymer known as PLGA, and containing the drug Dibenzazepine, disrupted Notch signaling and led to the creation of brown fat cells.
“We can control the delivery to specific sites in the body, in this case the bad fat or white fat cells,” Deng said. “Once those engineered particles are inside the fat cells, they can slowly release the drug in the cells, potentially limiting the off-target interactions in other tissue in the body and reducing the frequency of dosing.”
Kuang said the particles, which are less than 200 nanometers in size, are readily taken up by the fat cells through a process called endocytotic trafficking and subsequently undergo a rapid endo-lysosome escape to the cytosol within the cell membrane.
“The particle was actually picked up by the cell. It’s like it’s being eaten by the cells,” Kuang said. “This limits the particle from going anywhere else.”
Since the nanoparticles containing the drug are injected into fat, Deng said it may be possible to develop therapies that target fat loss in specific parts of the body. In the mouse model, targeting a specific fat depot with weekly injections of nanoparticles is sufficient to bring about systemic improvements in glucose tolerance and insulin sensitivity.
Being overweight is also a contributing factor to developing type 2 diabetes. Removing excess fat would likely decrease the odds of developing the disease.