image: Top: near-infrared (NIR) light can pass through brain tissue and activate neurons via nanoparticles. Bottom: non-invasive activation of neurons in the reward center of the mouse brain. view more
Credit: Dr. Shuo Chen and Dr. Thomas J. McHugh
A Non-Invasive Way to Manipulate Neural Activity With Optogenetics: A new optogenetic technique allows for deep brain neural stimulation or inhibition by applying light externally to the skull, rather than via invasive optical fibers. The technique, which was tested in mice, may one day complement or extend current approaches to deep brain stimulation and therapies for neurological disorders in humans. Over recent years, scientists have benefited greatly by studying neurons engineered to be activated or inhibited in response to light, a field called optogenetics that yields valuable insights into underlying mechanisms of brain function and disease. However, the blue-green wavelengths of light that are used to activate or inhibit neurons are prone to scattering when applied within the brain, meaning that these light waves must be delivered using invasive probes that extend very close to the area that needs to be manipulated. Here, Shuo Chen and colleagues developed a non-invasive technique where special nanoparticles, in this case lanthanide-doped up conversion nanoparticles (UCNPs), are delivered to the desired brain region. Then, near-infrared light, which passes more easily through the brain, is applied externally to the skull. The nanoparticles interact with the infrared light, altering it to the blue-green wavelengths required for neural stimulation. When the researchers injected UCNPs into mouse brains, electron microscopy showed that the particles remain localized in the injection area. In mice conditioned to freeze under certain scenarios, applying the new optogenetic technique was sufficient to stop the mice's freezing behavior, the authors report. Neus Feliu et al. highlight this advance in a related Perspective.
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Journal
Science