0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      A large-scale optogenetic neurophysiology platform for improving accessibility in NHP behavioral experiments

      Preprint
      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Optogenetics has been a powerful scientific tool for two decades, yet its integration with non-human primate (NHP) electrophysiology has been limited due to several technical challenges. These include a lack of electrode arrays capable of supporting large-scale and long-term optical access, inaccessible viral vector delivery methods for transfection of large regions of cortex, a paucity of hardware designed for large-scale patterned cortical illumination, and inflexible designs for multi-modal experimentation. To address these gaps, we introduce a highly accessible platform integrating optogenetics and electrophysiology for behavioral and neural modulation with neurophysiological recording in NHPs. We employed this platform in two rhesus macaques and showcased its capability of optogenetically disrupting reaches, while simultaneously monitoring ongoing electrocorticography activity underlying the stimulation-induced behavioral changes. The platform exhibits long-term stability and functionality, thereby facilitating large-scale electrophysiology, optical imaging, and optogenetics over months, which is crucial for translationally relevant multi-modal studies of neurological and neuropsychiatric disorders.

          Graphical Abstract

          Related collections

          Most cited references69

          • Record: found
          • Abstract: not found
          • Article: not found

          The Psychophysics Toolbox

            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            The VideoToolbox software for visual psychophysics: transforming numbers into movies

              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Basomedial amygdala mediates top–down control of anxiety and fear

              Anxiety-related conditions are among the most difficult neuropsychiatric diseases to treat pharmacologically, but respond to cognitive therapies. There has therefore been interest in identifying relevant top-down pathways from cognitive control regions in medial prefrontal cortex (mPFC). Identification of such pathways could contribute to our understanding of the cognitive regulation of affect, and provide pathways for intervention. Previous studies have suggested that dorsal and ventral mPFC subregions exert opposing effects on fear, as do subregions of other structures. However, precise causal targets for top-down connections among these diverse possibilities have not been established. Here we show that the basomedial amygdala (BMA) represents the major target of ventral mPFC in amygdala in mice. Moreover, BMA neurons differentiate safe and aversive environments, and BMA activation decreases fear-related freezing and high-anxiety states. Lastly, we show that the ventral mPFC–BMA projection implements top-down control of anxiety state and learned freezing, both at baseline and in stress-induced anxiety, defining a broadly relevant new top-down behavioural regulation pathway.
                Bookmark

                Author and article information

                Journal
                bioRxiv
                BIORXIV
                bioRxiv
                Cold Spring Harbor Laboratory
                2692-8205
                29 June 2024
                : 2024.06.25.600719
                Affiliations
                [1 ]University of Washington, Seattle, Department of Electrical and Computer Engineering
                [2 ]Washington National Primate Research Center
                [3 ]University of Washington, Seattle, Department of Bioengineering
                [4 ]University of Washington, Seattle, Department of Radiology
                [5 ]Weill Neurohub
                Author notes
                [* ]Corresponding author
                Author information
                http://orcid.org/0000-0001-7059-7699
                http://orcid.org/0000-0002-2337-8976
                http://orcid.org/0009-0000-0091-1056
                http://orcid.org/0000-0001-9063-9518
                http://orcid.org/0000-0002-9293-2221
                http://orcid.org/0000-0001-5212-509X
                Article
                10.1101/2024.06.25.600719
                11230395
                38979206
                7d37bb46-d94f-452a-bc1d-5fa7436e5dd6

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.

                History
                Funding
                R01 NS119395 (DJG, JB, JZ, AY), R01 NS116464-01 (AY), University of Washington Big Data for Genomics & Neuroscience Training Grant (JB), Weill Neurohub (SF), Washington National Primate Research Center P51 OD010425 (DJG, JB, NS, JZ, SF, AY), American Heart Association (AY), 1T32 MH132518 (NS), R01 MH125429 (NS, AY), and K01 AG071798 (HJ).
                Categories
                Article

                Comments

                Comment on this article