Name: a micro-ct-based method for characterizing lesions and locating electrodes in small animal brains
Uploaded: 2018-11-08T14:00:00.000+00:00
Duration: 5 min 12 s
Description: Watch this Scientific Journal Video about A Micro-CT-based Method for Characterizing Lesions and Locating Electrodes in Small Animal Brains at JoVE.com

The authors thank Greg Lin and Arthur McClelland for their expertise with the micro-CT machine, David Richmond and Hunter Elliott at the Image and Data Analysis Core (IDAC) at Harvard Medical School for their image processing advice, and William Liberti at Boston University for graciously providing a zebra finch brain. This work was performed in part at the Center for Nanoscale Systems (CNS), a member of the National Nanotechnology Coordinated Infrastructure Network (NNCI), which is supported by the National Science Foundation under NSF award no. 1541959. CNS is a part of Harvard University. This work was supported by the Richard and Susan Smith Family Foundation and IARPA (contract #D16PC00002). S.B.E.W. was supported by fellowships from the Human Frontier Science Program (HFSP; LT000514/2014) and the European Molecular Biology Organization (EMBO; ALTF1561-2013). G.G. was supported by the National Science Foundation (NSF) Graduate Research Fellowship Program (GRFP).

All care and experimental manipulation of animals were reviewed and approved by the Harvard Institutional Animal Care and Use Committee. The perfusion described here is specific for rats, but the procedure is applicable to any animals with smaller or similarly sized brains.
1. Perfusion
<ol>
	<li>Prepare 1x phosphate-buffered saline (PBS). For a rat (age: 0.5&#8211;1.5 years old, weight: 250&#8211;600 g), 800&#8211;1,000 mL should be sufficient. Use 400 mL to perfuse the animal and an additional 400 mL to dilute the fixative.</li>
	<li>Prepare the fixative consisting of 2% (w/v) paraformaldehyde (PFA) and 2.5% (w/v) glutaraldehyde (GA) in 1x PBS. For a rat, 400 mL is sufficient. Save 50 mL in a 50 mL conical tube for post-fixation of the brain after perfusion.</li>
	<li>Anesthetize the rat with 4&#8211;5% isoflurane gas (at 0.8 L/min O2 at 1.0 bar at 21 &#176;C) for 15 min.</li>
	<li>Inject a lethal dose of sodium pentobarbital intraperitoneally (180 mg/kg).</li>
	<li>Test for reflex loss in the animal by conducting a toe-pinch reflex exam. Wait to begin the perfusion until the animal has lost its reflex response.</li>
	<li>Follow the previously described intracardial perfusion and brain extraction protocol14 with the following solutions: perfuse the animal with 400 mL of 1x PBS at 125 mm Hg to remove the blood. Once all blood has been removed and replaced with 1x PBS, begin perfusing with 400 mL of a solution of 2% PFA and 2.5% GA dissolved in 1x PBS at 125 mm Hg. 
	NOTE: If the procedure is being conducted in an animal that is not a rat, the only important components of the perfusion procedure are the use of 1x PBS and 2% PFA, 2.5% GA in 1x PBS. The solution volumes and perfusion pressure may be adjusted according to the species.</li>
</ol>
2. Post-fixation
<ol>
	<li>Place the extracted brain in 2% PFA, 2.5% GA in 1x PBS solution (same solution used to perfuse the animal previously). Ensure that the solution volume is at least 10x the volume of the brain. For rats, place the brain in a 50 mL conical tube with 50 mL of solution. Store the sample in post-fixation for 2&#8211;3 days, shaking lightly at 4 &#176;C. 
	NOTE: If the sample is in a 50 mL conical tube, placing it horizontally on an orbital shaker will ensure the best results.</li>
	<li>After the sample has been post-fixed for long enough, wash the sample in double-distilled water (ddH2O), de-ionized water (diH2O), or ultrapure water (see Table of Materials) four times for the following durations: 1, 1, 1, and 15 min. 
	NOTE: For this protocol, ddH2O, diH2O, or ultrapure water should be interchangeable. For simplicity, ddH2O will be used to refer to purified water henceforth.</li>
</ol>
3. Staining
CAUTION: For this step, conduct all solution preparations under a hood while using gloves.
<ol>
	<li>Prepare at least 10x the brain volume of staining solution. For rat brains, prepare 50 mL of 2% (w/v) osmium tetroxide (OsO4) in ddH2O by combining 25 mL of stock 4% OsO4 solution and 25 mL of ddH2O. 
	CAUTION: Osmium tetroxide is volatile and may cause temporary blindness and respiratory problems if not handled appropriately. Discard all materials that contact the osmium tetroxide in an appropriate chemical hazard container within a secondary container.</li>
	<li>Place the brain in a new 50 mL conical tube and add the OsO4 solution. The brain should begin to turn brown as OsO4 reacts with lipids in the tissue.</li>
	<li>Close the tube and seal it thoroughly with paraffin film (see Table of Materials) to ensure that it does not leak during incubation. 
	NOTE: The osmium is volatile and will react mildly with the plastic of the tube, so sealing the tube properly is very important. The tube may be wrapped with aluminum foil for added protection.</li>
	<li>Store the sealed tube at 4 &#176;C, shaking lightly on an orbital shaker at 50 rpm for 2 weeks. Place the tube horizontally to ensure the best mixing. Ensure that the sample is fully submerged in the solution while shaking. 
	NOTE: If the osmium is not allowed to circulate continuously, it may not fully penetrate the sample, so horizontal placement on the shaker is very important.</li>
</ol>
4. Embedding
<ol>
	<li>After the sample has been incubated in OsO4 for 2 weeks, wash it with ddH2O 5 times at room temperature (RT) for the following durations: 1, 1, 1, 15, and 60 min to remove all the unbound OsO4 in the sample. 
	NOTE: The multiple exchanges, including the last 60 min&#160;exchange, are necessary to allow all the osmium in the circulatory system to diffuse out.</li>
	<li>Wash the sample with ddH2O for 30 min at 4 &#176;C. 
	&#8203;NOTE: Osmium may continue to diffuse out of the sample, but its quantity should be greatly reduced from the previous step.</li>
	<li>Dehydrate the sample with ethanol to eventually infiltrate it with resin. To dehydrate, replace the ddH2O with 10&#8211;20 mL of the following ethanol dilutions (for 30 min each at 4 &#176;C): 20% (v/v) ethanol and 80% (v/v) ddH2O; 50% (v/v) ethanol and 50% (v/v) ddH2O; 70% (v/v) ethanol and 30% (v/v) ddH2O; 90% (v/v) ethanol and 10% (v/v) ddH2O; 100% ethanol.</li>
	<li>Prepare the acetone/resin dilutions as follows.
	<ol>
		<li>Prepare 100 mL of the resin for embedding (see Table of Materials) as per the manufacturer&#39;s instructions.</li>
		<li>To make the 33% (v/v) resin-67% acetone solution, pour 15 mL of resin into a 50 mL conical tube and add 30 mL of 100% glass-distilled acetone.</li>
		<li>To make the 50% (v/v) resin-50% acetone, pour 22.5 mL of resin into a 50 mL conical tube and add 22.5 mL of 100% glass-distilled acetone.</li>
		<li>To make the 67% (v/v) resin-33% acetone solution, pour 30 mL of resin into a 50 mL conical tube and add 15 mL of 100% glass-distilled acetone.</li>
		<li>Use the remaining 32.5 mL of resin as the first solution of 100% resin below.</li>
	</ol>
	</li>
	<li>Begin the resin infiltration process by moving the sample through 10-20 mL of the following acetone and acetone/resin dilutions: 100% acetone for 30 min at 4 &#176;C; 100% acetone for 30 min at 4 &#176;C; and 100% acetone for 30 min at room temperature (RT). 
	NOTE: The rest of the infiltration process will take place at RT.</li>
	<li>Immerse the sample in 33% (v/v) resin 67% acetone for 3 h at RT, then 50% (v/v) resin-50% acetone for 3 h at RT, 67% (v/v) resin 33% acetone for 3 h at RT, and 100% resin for 12 h at RT.</li>
	<li>Make a fresh 50 mL batch of resin following the instructions on the bottle. Transfer the sample to the container in which it will be cured (e.g., the disposable molds described in Table of Materials). Infuse the sample with fresh 100% resin for 4 hours at RT. 
	NOTE: If fresh resin is not used, the resin made the previous day will begin to harden prematurely, and the sample will be hard to manipulate.</li>
	<li>Degas the sample in a vacuum oven for 15 min at 45 &#176;C. 
	NOTE: This step will help remove any trapped air bubbles within the sample, but it is non-essential and will not affect quality of the data.</li>
	<li>Finally, cure the sample in an oven for 48 h at 60 &#176;C.</li>
</ol>
5. micro-CT
<ol>
	<li>Once the sample has been cured, peel off the disposable mold and scan it with the micro-CT machine. 
	NOTE: Depending on the machine used, the settings will be different. For the scanner used by the authors listed in the Table of Materials, the recommended settings are 130 kV, 135 &#181;A with a 0.1 mm copper filter and a molybdenum source, a 1-second exposure, and an average of 4 frames per projection. However, experimenters should calibrate the scanner individually, as many factors will affect optimal settings during a particular session.</li>
	<li>Once the scan is completed, reconstruct the sample with the recommended parameters for the experimenter&#39;s scanner/software combination on a computer with the scanner software.</li>
	<li>Finally, visualize and analyze the reconstructed digital volume using the experimenter&#39;s software of choice (see Table of Materials for examples).</li>
</ol>

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The authors have nothing to disclose.

The following are critical steps to the protocol: first, the use of a combination of PFA and GA to perfuse the animal and subsequently post-fix the brain was paramount to achieving consistent full osmium penetration of the tissue. Although we did not test this explicitly, a plausible explanation is that PFA fixation is reversible15, whereas GA fixation is not reversible16,17. Because a two-week incubation in osmium tetroxide is required fo...

Neuroscientists have relied on lesions for a long time in order to understand the relationship between function and location in the brain. For example, our understanding of the hippocampus as being indispensable for learning and memory and of the prefrontal cortex as being key for impulse control were both products of serendipitous lesions in humans1,2. The use of animal models, however, has allowed neuroscientists to harness the power of lesions by going beyond serendipity, and the function of countless brain areas has been elucidated through systematic studies of structure-function relationships through lesions3,4.
To correctly assign function to a structure, however, lesion studies require precise quantification procedures, which is an area that has been lacking. The current gold standard for quantifying lesions is to section, mount, and image brains with a light microscope. The imaged slices are then matched to the closest sections on an atlas, and the approximate coordinates of the lesions across subjects are indirectly reported, often through the use of camera lucida images or example histological slices3,4,5,6,7,8,9,10.
Beyond the imprecision of current lesion quantification procedures, these techniques are time-consuming and prone to failure. Small changes in brain stiffness, blade sharpness, and temperature can lead to botched, warped, or torn sections. Sections can also stain unevenly and be improperly imaged because of bubbles in the mounting medium. Importantly, upon sectioning, the three-dimensional context of the lesion&#39;s location in the brain is lost, making precise 3D reconstruction of the lesion in the brain challenging.
Another common application for lesions has been to determine the location of single and multiple electrode recordings in the brain. At the end of the final recording session, researchers induce small electrolytic lesions at the electrode tip and process the brain histologically as done in a conventional lesion experiment11. This technique suffers from the same drawbacks described above, with additional problems being that the electrolytic lesions are usually larger than the electrodes used to make them but are usually small enough that they are challenging to find histologically. When multiple electrodes are inserted, as in the case of a tetrode array, verification through electrolytic lesions is even more challenging. An alternative to electrolytic lesions is the use of a dye on the electrode to later verify histologically12, but this technique suffers from the same drawbacks that come with conventional histology.
Here, we describe in-depth a recently described method13 based on staining techniques in electron microscopy (EM) and X-ray computed tomography (micro-CT) that quantifies lesions and locates electrodes in small animal brains better than current methods. Micro-CT is an imaging technique in which X-rays are shot at a sample that is rotated 360&#176; while a scintillator collects the X-rays not deflected by the sample. The result is a high-resolution digital 3D reconstruction of the sample that can be visualized in any orientation and quantified precisely. Many academic institutions have micro-CT scanners, which are also available commercially.

<table><tbody><tr><td>Paraformaldehyde (PFA)</td><td>Electron Microscopy Sciences (EMS)</td><td>15710</td><td>2% (w/v/) in 1X PBS</td></tr><tr><td>Glutaraldehyde (GA)</td><td>EMS</td><td>16220</td><td>2.5% (w/v) GA in 1x PBS</td></tr><tr><td>OsO&lt;sub&gt;4&lt;/sub&gt;</td><td>EMS</td><td>19190</td><td>Work in fume hood</td></tr><tr><td>Ethanol</td><td>Decon Labs</td><td>Koptec</td><td>140, 190, 200 proof</td></tr><tr><td>Acetone</td><td>EMS</td><td>10015</td><td>Glass-distilled</td></tr><tr><td>Durcupan ACM resin</td><td>Sigma-Aldrich</td><td>44610</td><td>A, B, C and D components, resin for embedding</td></tr><tr><td>Disposable molds</td><td>Ted Pella</td><td>27114</td><td>Suggested</td></tr><tr><td>milliQ water (ultrapure water)</td><td>Millipore Sigma</td><td>QGARD00R1 (or related purifier)</td><td>Suggested</td></tr><tr><td>Parafilm (paraffin film)</td><td>Millipore Sigma</td><td>P7793</td><td>Suggested paraffin film</td></tr><tr><td>Micro-CT scanner</td><td>Nikon Metrology Ltd., Tring, UK</td><td>X-Tek HMS ST 225</td><td>Used by authors</td></tr><tr><td>&lt;strong&gt;Software for visualizing and analyzing micro-CT scans:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td></td><td>Volume Graphics</td><td>VG Studio Max</td><td>Used by authors</td></tr><tr><td></td><td>FEI / Thermo Scientific</td><td>Avizo</td><td>Used by authors</td></tr><tr><td></td><td>FEI / Thermo Scientific</td><td>Amira</td><td>Similar to Avizo</td></tr><tr><td></td><td>Mark Sutton &amp;amp; Russell Garwood</td><td>Spiers</td><td>Free, http://spiers-software.org/</td></tr><tr><td></td><td>Pixmeo Sarl</td><td>Osirix Lite</td><td>Free, https://www.osirix-viewer.com/</td></tr><tr><td></td><td>Open Source</td><td>FIJI</td><td>Free, https://fiji.sc/</td></tr><tr><td></td><td>Adobe</td><td>Photoshop</td><td>Good for analyzing one slice at a time</td></tr></tbody></table>

a micro-ct-based method for characterizing lesions and locating electrodes in small animal brains

Lesion and electrode location verification are traditionally done via histological examination of stained brain slices, a time-consuming procedure that requires manual estimation. Here, we describe a simple, straightforward method for quantifying lesions and locating electrodes in the brain that is less laborious and yields more detailed results. Whole brains are stained with osmium tetroxide, embedded in resin, and imaged with a micro-CT scanner. The scans result in 3D digital volumes of the brains with resolutions and virtual section thicknesses dependent on the sample size (12&#8211;15 and 5&#8211;6 &#181;m&#160;per voxel for rat and zebra finch brains, respectively). Surface and deep lesions can be characterized, and single tetrodes, tetrode arrays, electrolytic lesions, and silicon probes can also be localized. Free and proprietary software allows experimenters to examine the sample volume from any plane and segment the volume manually or automatically. Because this method generates whole brain volume, lesions and electrodes can be quantified to a much higher degree than in current methods, which will help standardize comparisons within and across studies.

Traditionally, brains are sectioned and stained in order to quantify lesions and locate electrodes, but this method is error-prone, labor-intensive, and typically requires estimation of the results. By preparing whole brains for micro-CT imaging, the probability of damaging the samples is greatly reduced, features of interest may be analyzed in the context of the entire brain, and the method lends itself to parallel processing of many samples, considerably speeding up sample preparation.<...

Watch this Scientific Journal Video about A Micro-CT-based Method for Characterizing Lesions and Locating Electrodes in Small Animal Brains at JoVE.com

A Micro-CT-based Method for Characterizing Lesions and Locating Electrodes in Small Animal Brains

This article describes a straightforward method to prepare small animal brains for micro-CT imaging, in which lesions can be quantified and electrodes located with high precision in the context of the whole brain.

Lesion and electrode location verification are traditionally done via histological examination of stained brain slices, a time-consuming procedure that ...

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Research

JoVE Journal

Neuroscience

8.4K Views.  Harvard University. This article describes a straightforward method to prepare small animal brains for micro-CT imaging, in which lesions can be quantified and electrodes located with high precision in the context of the whole brain.

Video: A Micro-CT-based Method for Characterizing Lesions and Locating Electrodes in Small Animal Brains

Simultaneous fMRI and Electrophysiology in the Rodent Brain

To examine the neural basis of the blood oxygenation level dependent (BOLD) magnetic resonance imaging (MRI) signal, we have developed a rodent model in which functional MRI data and in vivo intracortical recording can be performed simultaneously. The combination of MRI and electrical recording is technically challenging because the electrodes used for recording distort the MRI images and the MRI acquisition induces noise in the electrical recording. To minimize the mutual interference of the two modalities, glass microelectrodes were used rather than metal and a noise removal algorithm was implemented for the electrophysiology data. In our studies, two microelectrodes were separately implanted in bilateral primary somatosensory cortices (SI) of the rat and fixed in place. One coronal slice covering the electrode tips was selected for functional MRI. Electrode shafts and fixation positions were not included in the image slice to avoid imaging artifacts. The removed scalp was replaced with toothpaste to reduce susceptibility mismatch and prevent Gibbs ringing artifacts in the images. The artifact structure induced in the electrical recordings by the rapidly-switching magnetic fields during image acquisition was characterized by averaging all cycles of scans for each run. The noise structure during imaging was then subtracted from original recordings. The denoised time courses were then used for further analysis in combination with the fMRI data. As an example, the simultaneous acquisition was used to determine the relationship between spontaneous fMRI BOLD signals and band-limited intracortical electrical activity. Simultaneous fMRI and electrophysiological recording in the rodent will provide a platform for many exciting applications in neuroscience in addition to elucidating the relationship between the fMRI BOLD signal and neuronal activity.

We have developed a method for simultaneous functional magnetic resonance imaging and electrophysiological recording in the rodent brain, providing a platform for the investigation of the relationship between neural activity and the blood oxygenation level dependent (BOLD) MRI signal.

To examine the neural basis of the blood oxygenation level dependent (BOLD) magnetic resonance imaging (MRI) signal, we have developed a rodent model in ...

Targeted Labeling of Neurons in a Specific Functional Micro-domain of the Neocortex by Combining Intrinsic Signal and Two-photon Imaging

In the primary visual cortex of non-rodent mammals, neurons are clustered according to their preference for stimulus features such as orientation1-4, direction5-7, ocular dominance8,9 and binocular disparity9. Orientation selectivity is the most widely studied feature and a continuous map with a quasi-periodic layout for preferred orientation is present across the entire primary visual cortex10,11. Integrating the synaptic, cellular and network contributions that lead to stimulus selective responses in these functional maps requires the hybridization of imaging techniques that span sub-micron to millimeter spatial scales. With conventional intrinsic signal optical imaging, the overall layout of functional maps across the entire surface of the visual cortex can be determined12. The development of in vivo two-photon microscopy using calcium sensitive dyes enables one to determine the synaptic input arriving at individual dendritic spines13 or record activity simultaneously from hundreds of individual neuronal cell bodies6,14. Consequently, combining intrinsic signal imaging with the sub-micron spatial resolution of two-photon microscopy offers the possibility of determining exactly which dendritic segments and cells contribute to the micro-domain of any functional map in the neocortex. Here we demonstrate a high-yield method for rapidly obtaining a cortical orientation map and targeting a specific micro-domain in this functional map for labeling neurons with fluorescent dyes in a non-rodent mammal. With the same microscope used for two-photon imaging, we first generate an orientation map using intrinsic signal optical imaging. Then we show how to target a micro-domain of interest using a micropipette loaded with dye to either label a population of neuronal cell bodies or label a single neuron such that dendrites, spines and axons are visible in vivo. Our refinements over previous methods facilitate an examination of neuronal structure-function relationships with sub-cellular resolution in the framework of neocortical functional architectures.

A method is described for labeling neurons with fluorescent dyes in predetermined functional micro-domains of the neocortex. First, intrinsic signal optical imaging is used to obtain a functional map. Then two-photon microscopy is used to label and image neurons within a micro-domain of the map.

In the primary visual cortex of non-rodent mammals, neurons are clustered according to their preference for stimulus features such as orientation1-4, ...

Intact Histological Characterization of Brain-implanted Microdevices and Surrounding Tissue

Research into the design and utilization of brain-implanted microdevices, such as microelectrode arrays, aims to produce clinically relevant devices that interface chronically with surrounding brain tissue. Tissue surrounding these implants is thought to react to the presence of the devices over time, which includes the formation of an insulating "glial scar" around the devices. However, histological analysis of these tissue changes is typically performed after explanting the device, in a process that can disrupt the morphology of the tissue of interest.
Here we demonstrate a protocol in which cortical-implanted devices are collected intact in surrounding rodent brain tissue. We describe how, once perfused with fixative, brains are removed and sliced in such a way as to avoid explanting devices. We outline fluorescent antibody labeling and optical clearing methods useful for producing an informative, yet thick tissue section. Finally, we demonstrate the mounting and imaging of these tissue sections in order to investigate the biological interface around brain-implanted devices.

Here we present a histological method for capturing, labeling, optically clearing, and imaging the intact brain tissue interface around chronically implanted microdevices in rodent brain tissue. Results from the techniques comprising this method are useful for understanding the impact of various penetrating brain-implants on their surrounding tissue.

Research  into the design and utilization of brain-implanted microdevices, such as  microelectrode arrays, aims to produce clinically relevant devices ...

A Method to Make a Craniotomy on the Ventral Skull of Neonate Rodents

The use of a craniotomy for in vivo experiments provides an opportunity to investigate the dynamics of diverse cellular processes in the mammalian brain in adulthood and during development. Although most in vivo approaches use a craniotomy to study brain regions located on the dorsal side, brainstem regions such as the pons, located on the ventral side remain relatively understudied. The main goal of this protocol is to facilitate access to ventral brainstem structures so that they can be studied in vivo using electrophysiological and imaging methods. This approach allows study of structural changes in long-range axons, patterns of electrical activity in single and ensembles of cells, and changes in blood brain barrier permeability in neonate animals. Although this protocol has been used mostly to study the auditory brainstem in neonate rats, it can easily be adapted for studies in other rodent species such as neonate mice, adult rodents and other brainstem regions.

A surgical method is described to expose the ventral skull in neonate rats. Using this approach it is possible to open a craniotomy to perform acute electrophysiology and two-photon microscopy experiments in the brainstem of anesthetized pups.

The use of a craniotomy for in vivo experiments provides an opportunity to investigate the dynamics of diverse cellular processes in the mammalian brain ...

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Mutations in the CCM1 (aka KRIT1), CCM2, or CCM3 (aka PDCD10) gene cause cerebral cavernous malformation (CCM) in humans. Mouse models of CCM disease have been established by tamoxifen induced deletion of Ccm genes in postnatal animals. These mouse models provide invaluable tools to investigate molecular mechanism and therapeutic approaches for CCM disease. An accurate and quantitative method to assess lesion burden and progression is essential to harness the full value of these animal models. Here, we demonstrate the induction of CCM disease in a mouse model and the use of the contrast enhanced X-ray micro computed tomography (micro-CT) method to measure CCM lesion burden in mouse brains. At postnatal day 1 (P1), we used 4-hydroxytamoxifen (4HT) to activate Cre recombinase activity from the Cdh5-CreErt2 transgene to cleave the floxed allele of Ccm2. CCM lesions in mouse brains were analyzed at P8. For micro-CT, iodine based Lugol&#39;s solution was used to enhance contrast in brain tissue. We have optimized the scan parameters and utilized a voxel dimension of 9.5 &#181;m, which lead to a minimum feature size of approximately 25 &#181;m. This resolution is sufficient to measure CCM lesion volume and number globally and accurately, and provide high-quality 3-D mapping of CCM lesions in mouse brains. This method enhances the value of the established mouse models to study the molecular basis and potential therapies for CCM and other cerebrovascular diseases.

This protocol demonstrates the induction of cerebral cavernous malformation disease in a mouse model and uses contrast enhanced micro computed tomography to measure lesion burden. This method enhances the value of established mouse models to study the molecular basis and potential therapies for cerebral cavernous malformation and other cerebrovascular diseases.

Mutations in the CCM1 (aka KRIT1), CCM2, or CCM3 (aka PDCD10) gene cause cerebral cavernous malformation (CCM) in humans. Mouse models of CCM disease have ...

Medicine

Large-scale Three-dimensional Imaging of Cellular Organization in the Mouse Neocortex

The mammalian neocortex is composed of many types of excitatory and inhibitory neurons, each with specific electrophysiological and biochemical properties, synaptic connections, and in vivo functions, but their basic functional and anatomical organization from cellular to network scale is poorly understood. Here we describe a method for the three-dimensional imaging of fluorescently-labeled neurons across large areas of the brain for the investigation of the cortical cellular organization. Specific types of neurons are labeled by the injection of fluorescent retrograde neuronal tracers or expression of fluorescent proteins in transgenic mice. Block brain samples, e.g., a hemisphere, are prepared after fixation, made transparent with tissue clearing methods, and subjected to fluorescent immunolabeling of the specific cell types. Large areas are scanned using confocal or two-photon microscopes equipped with large working distance objectives and motorized stages. This method can resolve the periodic organization of the cell type-specific microcolumn functional modules in the mouse neocortex. The procedure can be useful for the study of three-dimensional cellular architecture in the diverse brain areas and other complex tissues.

Here we describe a procedure for tissue clearing, fluorescent labeling, and large-scale imaging of mouse brain tissue which, thereby, enables visualization of the three-dimensional organization of cell types in the neocortex.

The mammalian neocortex is composed of many types of excitatory and inhibitory neurons, each with specific electrophysiological and biochemical ...

Subdural Soft Electrocorticography (ECoG) Array Implantation and Long-Term Cortical Recording in Minipigs

Neurological impairments and diseases can be diagnosed or treated using electrocorticography (ECoG) arrays. In drug-resistant epilepsy, these help delineate the epileptic region to resect. In long-term applications such as brain-computer interfaces, these epicortical electrodes are used to record the movement intention of the brain, to control the robotic limbs of paralyzed patients. However, current stiff electrode grids do not answer the need for high-resolution brain recordings and long-term biointegration. Recently, conformable electrode arrays have been proposed to achieve long-term implant stability with high performance. However, preclinical studies for these new implant technologies are needed to validate their long-term functionality and safety profile for their translation to human patients. In this context, porcine models are routinely employed in developing medical devices due to their large organ sizes and easy animal handling. However, only a few brain applications are described in the literature, mostly due to surgery limitations and integration of the implant system on a living animal.
Here, we report the method for long-term implantation (6 months) and evaluation of soft ECoG arrays in the minipig model. The study first presents the implant system, consisting of a soft microfabricated electrode array integrated with a magnetic resonance imaging (MRI)-compatible polymeric transdermal port that houses instrumentation connectors for electrophysiology recordings. Then, the study describes the surgical procedure, from subdural implantation to animal recovery. We focus on the auditory cortex as an example target area where evoked potentials are induced by acoustic stimulation. We finally describe a data acquisition sequence that includes MRI of the whole brain, implant electrochemical characterization, intraoperative and freely moving electrophysiology, and immunohistochemistry staining of the extracted brains.
This model can be used to investigate the safety and function of novel design of cortical prostheses; mandatory preclinical study to envision translation to human patients.

Subdural Soft Electrocorticography ECoG Array Implantation and Long-Term Cortical Recording in Minipigs

Here, we present a method for the long-term performance and safety assessment of soft subdural electrode arrays in a minipig model, describing surgical method and tools, postoperative magnetic resonance imaging, electrophysiology of the auditory cortex, electrochemical properties of the implant, and postmortem immunochemistry.

Neurological impairments and diseases can be diagnosed or treated using electrocorticography (ECoG) arrays. In drug-resistant epilepsy, these help ...

Bioengineering

Mouse Neonatal Brain Micro-CT Scanning and Image Processing

Micro-CT Imaging and Morphometric Analysis of Mouse Neonatal Brains

Neuroimages are a valuable tool for studying brain morphology in experiments using animal models. Magnetic resonance imaging (MRI) has become the standard method for soft tissues, although its low spatial resolution poses some limits for small animals. Here, we describe a protocol for obtaining high-resolution three-dimensional (3D) information on mouse neonate brains and skulls using micro-computed tomography (micro-CT). The protocol includes those steps needed to dissect the samples, stain and scan the brain, and obtain morphometric measurements of the whole organ and regions of interest (ROIs). Image analysis includes the segmentation of structures and the digitization of point coordinates. In sum, this work shows that the combination of micro-CT and Lugol's solution as a contrast agent is a suitable alternative for imaging the perinatal brains of small animals. This imaging workflow has applications in developmental biology, biomedicine, and other sciences interested in assessing the effect of diverse genetic and environmental factors on brain development.

Author Spotlight: High-Resolution Imaging of Mouse Neonate Brains &#8211; A Micro-CT Protocol with Lugol&#39;s Solution Contrast Agent

This study describes the steps for obtaining high-resolution images of neonatal mouse brains by combining micro-computed tomography (micro-CT) and a contrast agent in ex vivo samples. We describe basic morphometric analyses to quantify brain size and shape in these images.

Neuroimages are a valuable tool for studying brain morphology in experiments using animal models. Magnetic resonance imaging (MRI) has become the standard ...

Implanting a Wireless Bidirectional Microelectrode System in a Rat Brain

Source: Melo-Thomas, L., et al., <a href="https://app.jove.com/v/56299">A Wireless, Bidirectional Interface for In Vivo Recording and Stimulation of Neural Activity in Freely Behaving Rats.</a> J. Vis. Exp. (2017)
The video demonstrates a procedure for implanting a wireless bidirectional multichannel electrode unit into a rat brain to record and stimulate multichannel neural networks.

All procedures involving animal models have been reviewed by the local institutional animal care committee and the JoVE veterinary review board.
1. ...

JoVE Encyclopedia of Experiments

Neurophysiology

Electrophysiology Techniques

Concurrent Electroencephalographic and Local Field Potential Recordings in an Anesthetized Rat

Source: Kang, S., et al. <a href="https://app.jove.com/v/56447">Concurrent Recording of Co-localized Electroencephalography and Local Field Potential in Rodent.</a> J. Vis. Exp. (2017).
This video demonstrates the procedure for concurrent recordings of co-localized electroencephalography (EEG) and local field potentials (LFPs) in an anesthetized rat. The process involves preparing the rat and attaching stimulating electrodes to its whisker pads. An EEG spider electrode is placed on the rat&#39;s skull for surface EEG measurements. At the same time, a multi-channel microelectrode is inserted into a specific brain region through a burr hole in the skull to record neural activity from a localized brain area.