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Related Experiment Video

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Bidirectional Electrical and Optoelectronic Interfaces in Healthy and Ischemic Ex Vivo Rat Hearts
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A Device for Long-Term Perfusion, Imaging, and Electrical Interfacing of Brain Tissue In vitro.

Nathaniel J Killian1, Varadraj N Vernekar2, Steve M Potter1

  • 1Laboratory for NeuroEngineering, Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University, Georgia Institute of Technology Atlanta, GA, USA.

Frontiers in Neuroscience
|April 12, 2016
PubMed
Summary

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From animal testing to <i>in vitro</i> systems: advancing standardization in microphysiological systems.

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This study introduces a new device for long-term culturing of thick brain tissue slices, improving nutrient delivery and waste removal. This innovation supports healthier, more active tissue models for neurobiology research.

Area of Science:

  • Neurobiology
  • Tissue Engineering
  • Electrophysiology

Background:

  • Thick brain tissue preparations are crucial for in vivo-like studies but suffer from necrosis due to poor nutrient and waste exchange.
  • Existing electrophysiological tools are inadequate for long-term maintenance of these thick tissue models.

Purpose of the Study:

  • To develop an integrated device for long-term maintenance and electrophysiological recording of thick, functionally active brain tissue models.
  • To overcome limitations of current methods hindering days-long experiments with tissue cultures.

Main Methods:

  • Developed an integrated device featuring interstitial perfusion for nutrient/waste exchange in thick tissue slices.
  • Utilized perforated multi-electrode arrays for distributed recordings from explanted tissue.
Keywords:
MEAbrain sliceneuronsperforated microelectrode arraythree-dimensional culture

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  • Incorporated automated culturing and in situ imaging capabilities.
  • Main Results:

    • The device enables long-term maintenance of thick, viable, and functionally active brain tissue models.
    • Convective perfusion significantly improved tissue viability, evidenced by higher firing rates in perfused vs. unperfused cultures.
    • The system is economical, easy to assemble, and integrates with standard electrophysiology equipment.

    Conclusions:

    • The novel device facilitates healthier, thicker, and more active tissue cultures for extended experimental periods.
    • This advancement supports research into normal brain function, neurological disorders, and drug screening, overcoming limitations of acute slice preparations.