Histological studies of the effects of chronic implantation of ceramic-based microelectrode arrays and microdialysis probes in rat prefrontal cortex

Erin R. Hascup, Sara af Bjerkén, Kevin N. Hascup, Francois Pomerleau, Peter Huettl, Ingrid Strömberg, Greg A. Gerhardt

Research output: Contribution to journalArticlepeer-review

82 Scopus citations

Abstract

Chronic implantation of neurotransmitter measuring devices is essential for awake, behavioral studies occurring over multiple days. Little is known regarding the effects of long term implantation on surrounding brain parenchyma and the resulting alterations in the functional properties of this tissue. We examined the extent of tissue damage produced by chronic implantation of either ceramic microelectrode arrays (MEAs) or microdialysis probes. Histological studies were carried out on fixed tissues using stains for neurons (cresyl violet), astrocytes (GFAP), microglia (Iba1), glutamatergic nerve fibers (VGLUT1), and the blood-brain barrier (SMI-71). Nissl staining showed pronounced tissue body loss with microdialysis implants compared to MEAs. The MEAs produced mild gliosis extending 50-100 μm from the tracks, with a significant change in the affected areas starting at 3 days. By contrast, the microdialysis probes produced gliosis extending 200-300 μm from the track, which was significant at 3 and 7 days. Markers for microglia and glutamatergic fibers supported that the MEAs produce minimal damage with significant changes occurring only at 3 and 7 days that return to control levels by 1 month. SMI-71 staining supported the integrity of the blood-brain barrier out to 1 week for both the microdialysis probes and the MEAs. This data support that the ceramic MEA's small size and biocompatibility are necessary to accurately measure neurotransmitter levels in the intact brain. The minimal invasiveness of the MEAs reduce tissue loss, allowing for long term (> 6 month) electrochemical and electrophysiological monitoring of brain activity.

Original languageEnglish
Pages (from-to)12-20
Number of pages9
JournalBrain Research
Volume1291
DOIs
StatePublished - Sep 21 2009

Funding

FundersFunder number
National Institute on Drug AbuseR01DA017186

    Keywords

    • Amperometry
    • Biosensor
    • Immunohistochemistry
    • Microelectrode
    • Microglia
    • Neurotransmitter

    ASJC Scopus subject areas

    • General Neuroscience
    • Molecular Biology
    • Clinical Neurology
    • Developmental Biology

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