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The present protocol describes a simple procedure to acquire and analyze the topography of epicranial visual evoked potentials with 32-multichannel thin-film electrodes in the mouse.
Visual evoked potentials (VEP) allow the characterization of visual function in preclinical mouse models. Various methods exist to measure VEPs in mice, from non-invasive EEG, subcutaneous single-electrodes, and ECoG to fully invasive intracortical multichannel visual cortex recordings. It can be useful to acquire a global, topographical EEG-level characterization of visual responses previous to local intracortical microelectrode measurements in acute experimental settings. For example, one use case is to assess global cross-modal changes in VEP topography in deafness models before studying its effects on a local intracortical level. Multichannel epicranial EEG is a robust method to acquire such an overview measure of cortical visual activity. Multichannel epicranial EEG provides comparable results through a standardized, consistent approach to, for example, identify cross-modal, pathological, or age-related changes in cortical visual function. The current study presents a method to obtain the topographical distribution of flash-evoked VEPs with a 32-channel thin-film EEG electrode array in anesthetized mice. Combined with analysis in the time and frequency domain, this approach allows fast characterization and screening of the topography and basic visual properties of mouse cortical visual function, which can be combined with various acute experimental settings.
Mice are a preclinical model of degenerative processes of vision and ophthalmological diseases1,2,3,4. Visual evoked potentials (VEPs) are commonly used to measure cortical visual function and, for example, to assess visual degeneration in pathological models5,6. The VEP latency, conduction time, amplitude, multifocal characteristics, or spatial acuity of cortical visual evoked potentials provide diagnostic information on the functional integrity of the visual s....
All animals were handled and housed according to German (TierSchG, BGBl. I S. 1206, 1313) and European Union (ETS 123; Directive 2010/63/EU) guidelines for animal research. The animal experiments were approved by German state authorities (Lower Saxony State Office for Consumer Protection and Food Safety, LAVES) and were monitored by the university animal welfare officer. A 3-month-old male C57BL/6J mouse was used for the present study.
1. Animal details
Recording visual evoked potentials with multichannel EEG allows the assessment of the topography of VEP amplitudes, latencies, or frequency components in mice. Figure 2A shows an example of a flash evoked VEP topography recorded with an epicranial 32-channel EEG from a 3-month-old male C57BL/6J mouse. The strongest visual evoked activity occurs in the occipital region above the visual cortex.
Figure 2B shows the voltage distribution o.......
This article describes a method for recording epi-cranial multichannel EEG with thin-film electrodes and how to acquire a consistent topographical representation of visual evoked potentials in the mouse. Here, we exemplarily showed binocular flash stimulation, but this approach can also be applied with other types of visual stimuli (i.e., monocular, spatial gratings, focal visual field) using, for example, a larger display.
A critical step in the protocol is the positioning of the electro.......
This work was supported by the German Research Foundation (Deutsche Forschungsgemeinschaft, Cluster of Excellence 2177 "Hearing4all", Project number 390895286).
....Name | Company | Catalog Number | Comments |
Bepanthen 5% Dexpantheol | Bayer | Ophtamic gel | |
Cheetah software 5.11 | Neuralnyx | Version 5.11 | Recording software for neurophysiologcal signals |
Digital Lynx SX | Neuralynx | Digital Lynx 16SX | Recording system |
ECG differential amplifier | Otoconsult | WDA2 V1.0 | |
Electric shaver | Aesculap | GT420 | |
Electrode Holder | TSE Systems | 430005-HE | |
Examination light | Heine | HL 5000 | Cold light source lamp |
Heating Pad + Temperature Control system | CWE | TC-1000 Mouse | |
Histoacryl 0.5 mL | B.Braun | Tissue adhesive | |
Infrared heat lamp | Sanitas | SIL 06 | |
Ketamine 10% | WDT | Ketaminhydrochlorid | |
LED stroboscope | Monarch | Nova Strobe PBL | Visual stimulation |
Matlab 2021a | The Mathworks | 2021a | Stimulus control and analysis |
Moria Vessel Clamp | Fine Science Tools | 18320-11 | |
Mouse EEG electrode | NeuroNexus | H32 (Reticular) | 32-channel EEG electrode. Thickness: 20 μm; length: 8.6 mm; width 6.8 mm. Platinum sites: 500 μm diameter |
Mouse Frame | custom made | Information available on request | |
Multifunction I/O device | National Instruments | PCIe-6353 with BNC 2090A | Analog stimulus generation, output, and trigger |
NaCl 0.9% | B.Braun | Isotonic, sterile, nonpyrogenic | |
Neuralynx HS36 | Neuralynx | HS-36 | Headstage |
Neuronexus probe connector | Neuralynx | ADPT-HS36-N2T-32A | Electrode connector |
Oscilloscope | Tektronix | TDS 2014B | |
Progent Intensive Cleaner | Menicon | Protein remover and disinfecting solution for rigid gas permeable lenses | |
Recording PC | HP | HP Z800 | Recording PC |
Rimadyl (Carprofen) | Zoetis | Carprofen | |
Silicon Oil M 1000 | Carl Roth | 4045.1 | |
Silver wire | Science Products | AG-8W | Diameter 203 µm; ECG and reference electrode |
Sound proof chamber | IAC acoustics | ||
Stereotactic Micromanipulator | TSE Systems | 430005-M/P | For EEG electrode placement |
Stimulation PC | Dell | Dell Precision T5810 | Stimulation PC |
Surgical microscope | Zeiss | Op-Mi Focus | |
Surgical tape | 3M | 1527-0 | 1.25 cm x 9.1 m |
Thilo-Tears 3 mg/g | Alcon Pharma GmbH | Ophtamic gel | |
Vaselin Lichtenstein | Winthrop | White vaselin ointment | |
Xylazin 2% | Bernburg | Xylazinehydrochlorid | |
Xylocaine Spray (10 mg/puff) | Aspen | Lidocaine |
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