OxTalks will soon move to the new Halo platform and will become 'Oxford Events.' There will be a need for an OxTalks freeze. This was previously planned for Friday 14th November – a new date will be shared as soon as it is available (full details will be available on the Staff Gateway).
In the meantime, the OxTalks site will remain active and events will continue to be published.
If staff have any questions about the Oxford Events launch, please contact halo@digital.ox.ac.uk
Seminars this term will be held remotely on Zoom. Links for joining will be sent out before each seminar. Please contact the host if you would like to set up a remote meeting with a speaker. If you have suggestions for future speakers, please contact Lauren (lauren.burgeno@dpag.ox.ac.uk), or Nima (nima.khalighinejad@psy.ox.ac.uk).
ABSTRACT:
Identification of distinct neuronal subpopulations has been essential for understanding brain function, but clinical applications struggle to access specific neurons in heterogeneously mingled populations. Recently, optogenetic protocols targeting neuronal subpopulations in the external globus pallidus (GPe) were shown to provide long-lasting therapeutic effects in dopamine depleted mice.
Here, we leverage underlying synaptic differences between Parvalbumin (PV) and Lim homeobox 6 (Lhx6) subpopulations to drive population-specific neuromodulation in the GPe, using brief bursts of electrical stimulation. We then apply these findings to strategically design a clinically appropriate deep brain stimulation (DBS) protocol, which we show induces long-lasting therapeutic effects that far exceed those of conventional DBS, extending for hours beyond stimulation. These results establish the feasibility of transforming knowledge about circuit architecture into quickly translatable therapeutic approaches.
Recent Publication related to this talk: www.science.org/doi/10.1126/science.abi7852
