Obesity in
humans is a contributing factor to many other health concerns, such as
arthritis and cardiovascular problems. Recently, researchers at Purdue
University utilized PLGA from PolySciTech (www.polyscitech.com) (PolyVivo AP101) to develop
nanoparticles which deliver dibenzazepine to reduce the overgrowth of
adipocytes (fat-cells). This research holds promise to provide for improved
treatments of obesity. Read more: Jiang, Chunhui, Mario Alberto Cano-Vega, Feng
Yue, Liangju Kuang, Naagarajan Narayanan, Gozde Uzunalli, Madeline P. Merkel,
Shihuan Kuang, and Meng Deng. "Dibenzazepine-loaded nanoparticles induce
local browning of white adipose tissue to counteract obesity." Molecular
Therapy (2017). http://www.cell.com/molecular-therapy-family/molecular-therapy/abstract/S1525-0016(17)30256-3
“Inhibition
of Notch signaling via systemic drug administration triggers conversion of
white adipocytes into beige adipocytes (browning) and reduces adiposity.
However, translation of this discovery into clinical practice is challenged by
potential off-target side effects and lack of control over the location and
temporal extent of beige adipocyte biogenesis. Here, we demonstrate an
alternative approach to stimulate browning using nanoparticles (NPs) composed
of FDA-approved poly(lactide-co-glycolide) that enable sustained local release
of a Notch inhibitor (dibenzazepine, DBZ). These DBZ-loaded NPs support rapid
cellular internalization and inhibit Notch signaling in adipocytes.
Importantly, focal injection of these NPs into the inguinal white adipose
tissue depots of diet-induced obese mice results in localized NP retention and
browning of adipocytes, consequently improving the glucose homeostasis and
attenuating body-weight gain of the treated mice. These findings offer new
avenues to develop a potential therapeutic strategy for clinical treatment of
obesity and its associated metabolic syndrome. Keywords: drug delivery;
nanoparticle; browning; adipocyte; Notch signaling; obesity; PLGA;
dibenzazepine; adipose tissue; Notch inhibitor”
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