<ol>
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S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Functional+connectivity+in+the+motor+cortex+of+resting+human+brain+using+echo-planar+MRI.">Functional connectivity in the motor cortex of resting human brain using echo-planar MRI.</a> Magn Reson Med. 34 (4), 537-541 (1995).</li><li>Sanchez-Catasus, C. A., Diercke, R. A. J. O., de Vries, E. F. J., van Waarde, A., Leenders, K. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Use+of+nuclear+medicine+molecular+neuroimaging+to+model+brain+molecular+connectivity.">Use of nuclear medicine molecular neuroimaging to model brain molecular connectivity.</a> PET and SPECT in neurology. , 181-207 (2021).</li><li>Wehrl, H. F., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Simultaneous+PET-MRI+reveals+brain+function+in+activated+and+resting+state+on+metabolic,+hemodynamic+and+multiple+temporal+scales.">Simultaneous PET-MRI reveals brain function in activated and resting state on metabolic, hemodynamic and multiple temporal scales.</a> Nat Med. 19 (9), 1184-1189 (2013).</li><li>Rosenberg, G. 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L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Optimizing+experimental+protocols+for+quantitative+behavioral+imaging+with+18F-FDG+in+rodents.">Optimizing experimental protocols for quantitative behavioral imaging with 18F-FDG in rodents.</a> J Nucl Med. 48 (2), 277-287 (2007).</li><li>Fueger, B. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Impact+of+animal+handling+on+the+results+of+18F-FDG+PET+studies+in+mice.">Impact of animal handling on the results of 18F-FDG PET studies in mice.</a> J Nucl Med. 47 (6), 999-1006 (2006).</li><li>Gold, M. E. L., Norell, M. A., Budassi, M., Vaska, P., Schulz, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Rapid+18F-FDG+uptake+in+brain+of+awake,+behaving+rat+and+anesthetized+chicken+has+implications+for+behavioral+PET+studies+in+species+with+high+metabolisms.">Rapid 18F-FDG uptake in brain of awake, behaving rat and anesthetized chicken has implications for behavioral PET studies in species with high metabolisms.</a> Front Behav Neurosci. 12, 115 (2018).</li><li>Miranda, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=PET+imaging+of+freely+moving+interacting+rats.">PET imaging of freely moving interacting rats.</a> NeuroImage. 191, 560-567 (2019).</li><li>Miranda, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Awake+18F-FDG+PET+imaging+of+memantine-induced+brain+activation+and+test-retest+in+freely+running+mice.">Awake 18F-FDG PET imaging of memantine-induced brain activation and test-retest in freely running mice.</a> J Nucl Med. 60 (6), 844-850 (2019).</li><li>Jahreis, I., Bascu&#241;ana, P., Ross, T. L., Bankstahl, J. P., Bankstahl, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Choice+of+anesthesia+and+data+analysis+method+strongly+increases+sensitivity+of+18F-FDG+PET+imaging+during+experimental+epileptogenesis.">Choice of anesthesia and data analysis method strongly increases sensitivity of 18F-FDG PET imaging during experimental epileptogenesis.</a> PLOS ONE. 16 (11), e0260482 (2021).</li><li>Pawela, C. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+protocol+for+use+of+medetomidine+anesthesia+in+rats+for+extended+studies+using+task-induced+BOLD+contrast+and+resting-state+functional+connectivity.">A protocol for use of medetomidine anesthesia in rats for extended studies using task-induced BOLD contrast and resting-state functional connectivity.</a> NeuroImage. 46 (4), 1137-1147 (2009).</li><li>Rubinov, M., Sporns, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Complex+network+measures+of+brain+connectivity:+Uses+and+interpretations.">Complex network measures of brain connectivity: Uses and interpretations.</a> NeuroImage. 52 (3), 1059-1069 (2010).</li><li>Engel, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Connectomics+and+epilepsy.">Connectomics and epilepsy.</a> Curr Opin Neurol. 26 (2), 186 (2013).</li></ol>

<table><tbody><tr><td>Antisedan</td><td>Orion Pharma</td><td></td><td>Atipamezole hydrochloride 5 mg/mL</td></tr><tr><td>BD Micro-Fine+ insulin syringe 1 mL</td><td>BD</td><td>324827</td><td>0.33 mm (29G) x 12.7 mm</td></tr><tr><td>BD Microlance 3 Needles 30 G x 1/2&quot;</td><td>BD</td><td>304000</td><td>30 G x 1/2&quot;; 0,3 x 13 mm</td></tr><tr><td>BD Plastipak syringe 1 mL</td><td>BD</td><td>303172</td><td>for infusion pump</td></tr><tr><td>BTPE-10 Polyethylene tubing</td><td>Instech</td><td></td><td>0.11x.024in (.28x60mm)</td></tr><tr><td>Domitor</td><td>Orion Pharma</td><td>1070499</td><td>Medetomidine hydrochloride 1 mg/mL</td></tr><tr><td>Fusion 100 infusion pump</td><td>Chemyx Inc.</td><td>07100</td><td>Newer model available: Fusion 100X</td></tr><tr><td>Isoflutek 1000 mg/g</td><td>Alivira</td><td></td><td>Isoflurane</td></tr><tr><td>MOLECUBES &amp;beta;-CUBE with CUBEFLOW software</td><td>MOLECUBES NV</td><td></td><td>Preclinical PET scanner</td></tr><tr><td>PMOD Software version 4.4&amp;nbsp;</td><td>Bruker Corporation</td><td></td><td>http://www.pmod.com; quantification of PET data</td></tr><tr><td>Saline</td><td>B. Braun</td><td>394496</td><td>NaCl 0.9%</td></tr><tr><td>Vidisic eye gel</td><td>Vidisic</td><td></td><td>Carbomerum 980 2 mg/g</td></tr></tbody></table>

studying metabolic brain connectivity using 2-deoxy-2-[18f]fluoro-d-glucose dynamic positron emission tomography at the single-subject level

単一被験者レベルでの2-デオキシ-2-[18F]フルオロ-D-グルコース動的陽電子放出断層撮影法を使用した代謝脳接続性の研究

To this day, metabolic brain connectivity is mostly studied on a group level through the acquisition of static positron emission tomography (PET) data of ...

studying-metabolic-brain-connectivity-using-2-deoxy-2-18ffluoro-d

Universidad San Sebastian

Research

JoVE Journal

Neuroscience

Studying Metabolic Brain Connectivity Using 2-Deoxy-2-[18F]Fluoro-D-Glucose Dynamic Positron Emission Tomography at the Single-subject Level

209 ビュー.  Ghent University. 動的陽電子放出断層撮影法(PET)データを取得し、時間枠に再構成することで、単一被験者レベルでの代謝脳接続性分析が可能になります。ラット脳の[18F]FDG動的PETデータを取得し、対象ボリュームの時間活動曲線を抽出して接続性マトリックスを取得する方法を説明します。

ビデオ: 単一被験者レベルでの2-デオキシ-2-[18F]フルオロ-D-グルコース動的陽電子放出断層撮影法を使用した代謝脳接続性の研究

Studying the Integration of Adult-born Neurons

Neurogenesis occurs in adult mammalian brains in the sub-ventricular zone (SVZ) of the lateral ventricle and in the sub-granular zone (SGZ) of the hippocampal dentate gyrus throughout life. Previous reports have shown that adult hippocampal neurogenesis is associated with diverse brain disorders, including epilepsy, schizophrenia, depression and anxiety (1). Deciphering the process of normal and aberrant adult-born neuron integration may shed light on the etiology of these diseases and inform the development of new therapies.
SGZ adult neurogenesis mirrors embryonic and post-natal neuronal development, including stages of fate specification, migration, synaptic integration, and maturation. However, full integration occurs over a prolonged, 6-week period. Initial synaptic input to adult-born SGZ dentate granule cells (DGCs) is GABAergic, followed by glutamatergic input at 14 days (2). The specific factors which regulate circuit formation of adult-born neurons in the dentate gyrus are currently unknown.
Our laboratory uses a replication-deficient retroviral vector based on the Moloney murine leukemia virus to deliver fluorescent proteins and hypothesized regulatory genes to these proliferating cells. This viral technique provides high specificity and resolution for analysis of cell birth date, lineage, morphology, and synaptogenesis.
A typical experiment often employs two or three viruses containing unique label, transgene, and promoter elements for single-cell analysis of a desired developmental process in vivo. The following protocol describes a method for analyzing functional newborn neuron integration using a single green (GFP) or red (dTomato) fluorescent protein retrovirus and patch-clamp electrophysiology.

A way to study the integration of newborn dentate granule cells in adult animals is described. This technique uses an engineered retrovirus to label newborn neurons, followed by electrophysiological recordings to determine in vivo functional integration.

アダルト生まれのニューロンの統合を検討し

Neurogenesis occurs in adult mammalian brains in the sub-ventricular zone (SVZ) of the lateral ventricle and in the sub-granular zone (SGZ) of the ...

神経科学

Imaging Cleared Intact Biological Systems at a Cellular Level by 3DISCO

Tissue clearing and subsequent imaging of transparent organs is a powerful method to analyze fluorescently labeled cells and molecules in 3D, in intact organs. Unlike traditional histological methods, where the tissue of interest is sectioned for fluorescent imaging, 3D imaging of cleared tissue allows examination of labeled cells and molecules in the entire specimen. To this end, optically opaque tissues should be rendered transparent by matching the refractory indices throughout the tissue. Subsequently, the tissue can be imaged at once using laser-scanning microscopes to obtain a complete high-resolution 3D image of the specimen. A growing list of tissue clearing protocols including 3DISCO, CLARITY, Sca/e, ClearT2, and SeeDB provide new ways for researchers to image their tissue of interest as a whole. Among them, 3DISCO is a highly reproducible and straightforward method, which can clear different types of tissues and can be utilized with various microscopy techniques. This protocol describes this straightforward procedure and presents its various applications. It also discusses the limitations and possible difficulties and how to overcome them.

To obtain high-resolution images of fluorescently labeled cells within large tissues, ideally, the biological samples should be imaged without sectioning. 3DISCO is a straightforward tissue clearing procedure based on sequential incubation with organic solvents. Upon clearing, the organs become transparent allowing an end-to-end laser scan of the specimen.

イメージングは​​3DISCOにより、細胞レベルで無傷生物系をクリア

Tissue clearing and subsequent imaging of transparent organs is a powerful method to analyze fluorescently labeled cells and molecules in 3D, in intact ...

A Simple One-step Dissection Protocol for Whole-mount Preparation of Adult Drosophila Brains

There is an increasing interest in using Drosophila to model human brain degenerative diseases, map neuronal circuitries in adult brains, and study the molecular and cellular basis of higher brain functions. A whole-mount preparation of adult brains with well-preserved morphology is critical for such whole brain-based studies, but can be technically challenging and time-consuming. This protocol describes an easy-to-learn, one-step dissection approach of an adult fly head in less than 10 s, while keeping the intact brain attached to the rest of the body to facilitate subsequent processing steps. The procedure helps remove most of the eye and tracheal tissues normally associated with the brain that can interfere with the later imaging step, and also places less demand on the quality of the dissecting forceps. Additionally, we describe a simple method that allows convenient flipping of the mounted brain samples on a coverslip, which is important for imaging both sides of the brains with similar signal intensity and quality. As an example of the protocol, we present an analysis of dopaminergic (DA) neurons in adult brains of WT (w1118) flies. The high efficacy of the dissection method makes it particularly useful for large-scale adult brain-based studies in Drosophila.

A Simple One-step Dissection Protocol for Whole-mount Preparation of Adult Drosophila Brains

The adult Drosophila brain is a valuable system for studying neuronal circuitry, higher brain functions, and complex disorders. An efficient method to dissect whole brain tissue from the small fly head will facilitate brain-based studies. Here we describe a simple, one-step dissection protocol of adult brains with well-preserved morphology.

大人のホールマウントの準備のためのシンプルなワンステップ解剖プロトコル<em&gt;ショウジョウバエ</em&gt;ブレインズ

There is an increasing interest in using Drosophila to model human brain degenerative diseases, map neuronal circuitries in adult brains, and study the ...

In Vivo Single-Molecule Tracking at the Drosophila Presynaptic Motor Nerve Terminal

An increasing number of super-resolution microscopy techniques are helping to uncover the mechanisms that govern the nanoscale cellular world. Single-molecule imaging is gaining momentum as it provides exceptional access to the visualization of individual molecules in living cells. Here, we describe a technique that we developed to perform single-particle tracking photo-activated localization microscopy (sptPALM) in Drosophila larvae. Synaptic communication relies on key presynaptic proteins that act by docking, priming, and promoting the fusion of neurotransmitter-containing vesicles with the plasma membrane. A range of protein-protein and protein-lipid interactions tightly regulates these processes and the presynaptic proteins therefore exhibit changes in mobility associated with each of these key events. Investigating how mobility of these proteins correlates with their physiological function in an intact live animal is essential to understanding their precise mechanism of action. Extracting protein mobility with high resolution in vivo requires overcoming limitations such as optical transparency, accessibility, and penetration depth. We describe how photoconvertible fluorescent proteins tagged to the presynaptic protein Syntaxin-1A can be visualized via slight oblique illumination and tracked at the motor nerve terminal or along the motor neuron axon of the third instar Drosophila larva.

In Vivo Single-Molecule Tracking at the Drosophila Presynaptic Motor Nerve Terminal

Here we illustrate how single molecule photo-activated localization microscopy can be carried out on the motor nerve terminal of a live Drosophila melanogaster third instar larva.

生体内で1 分子追跡ショウジョウバエ運動神経がシナプス前ターミナルで

An increasing number of super-resolution microscopy techniques are helping to uncover the mechanisms that govern the nanoscale cellular world. ...

Analyzing Neural Activity and Connectivity Using Intracranial EEG Data with SPM Software

Measuring neural activity and connectivity associated with cognitive functions at high spatial and temporal resolutions is an important goal in cognitive neuroscience. Intracranial electroencephalography (EEG) can directly record electrical neural activity and has the unique potential to accomplish this goal. Traditionally, averaging analysis has been applied to analyze intracranial EEG data; however, several new techniques are available for depicting neural activity and intra- and inter-regional connectivity. Here, we introduce two analytical protocols we recently applied to analyze intracranial EEG data using the Statistical Parametric Mapping (SPM) software: time-frequency SPM analysis for neural activity and dynamic causal modeling of induced responses for intra- and inter-regional connectivity. We report our analysis of intracranial EEG data during the observation of faces as representative results. The results revealed that the inferior occipital gyrus (IOG) showed gamma-band activity at very early stages (110 ms) in response to faces, and both the IOG and amygdala showed rapid intra- and inter-regional connectivity using various types of oscillations. These analytical protocols have the potential to identify the neural mechanisms underlying cognitive functions with high spatial and temporal profiles.

We present two analytical protocols that can be used to analyze intracranial electroencephalography data using the Statistical Parametric Mapping (SPM) software: time-frequency statistical parametric mapping analysis for neural activity, and dynamic causal modeling of induced responses for intra- and inter-regional connectivity.

神経活動と Spm と頭蓋内脳波データを使用した接続の分析

Measuring neural activity and connectivity associated with cognitive functions at high spatial and temporal resolutions is an important goal in cognitive ...

Studying Brain Function in Children Using Magnetoencephalography

Magnetoencephalography (MEG) is a non-invasive neuroimaging technique which directly measures magnetic fields produced by the electrical activity of the human brain. MEG is quiet and less likely to induce claustrophobia compared with magnetic resonance imaging (MRI). It is therefore a promising tool for investigating brain function in young children. However, analysis of MEG data from pediatric populations is often complicated by head movement artefacts which arise as a consequence of the requirement for a spatially-fixed sensor array that is not affixed to the child's head. Minimizing head movements during MEG sessions can be particularly challenging as young children are often unable to remain still during experimental tasks. The protocol presented here aims to reduce head movement artefacts during pediatric MEG scanning. Prior to visiting the MEG laboratory, families are provided with resources that explain the MEG system and the experimental procedures in simple, accessible language. An MEG familiarization session is conducted during which children are acquainted with both the researchers and the MEG procedures. They are then trained to keep their head still whilst lying inside an MEG simulator. To help children feel at ease in the novel MEG environment, all of the procedures are explained through the narrative of a space mission. To minimize head movement due to restlessness, children are trained and assessed using fun and engaging experimental paradigms. In addition, children's residual head movement artefacts are compensated for during the data acquisition session using a real-time head movement tracking system. Implementing these child-friendly procedures is important for improving data quality, minimizing participant attrition rates in longitudinal studies, and ensuring that families have a positive research experience.

This article introduces a child-friendly research protocol designed to improve data quality by reducing head movement during pediatric magnetoencephalography (MEG). We familiarize families with the MEG environment, train children to remain still using an MEG simulator, and correct for residual head movement artefacts using a real-time head movement detection system.

子供の脳磁図を用いた脳機能の研究

Magnetoencephalography (MEG) is a non-invasive neuroimaging technique which directly measures magnetic fields produced by the electrical activity of the ...

Dynamic Inter-subject Functional Connectivity Reveals Moment-to-Moment Brain Network Configurations Driven by Continuous or Communication Paradigms

Task-based functional magnetic resonance imaging bears great potential to understand how our brain reacts to various types of stimulation; however, this is often achieved without considering the dynamic facet of functional processing, and analytical outputs typically account for merged influences of task-driven effects and underlying spontaneous fluctuations of brain activity. Here, we introduce a novel methodological pipeline that can go beyond these limitations: the use of a sliding-window analytical scheme permits tracking of functional changes over time, and through cross-subject correlational measurements, the approach can isolate purely stimulus-related effects. Thanks to a rigorous thresholding process, significant changes in inter-subject functional correlation can be extracted and analyzed.
On a set of healthy subjects who underwent naturalistic audio-visual stimulation, we demonstrate the usefulness of the approach by tying the unraveled functional reconfigurations to particular cues of the movie. We show how, through our method, one can capture either a temporal profile of brain activity (the evolution of a given connection), or focus on a spatial snapshot at a key time point. We provide a publicly available version of the whole pipeline, and describe its use and the influence of its key parameters step by step.

The goal of the described approach is to determine at what moments of the paradigm (temporal perspective), and between which regions (spatial perspective), significant reconfigurations in functional connectivity occur on functional magnetic resonance imaging recordings during which a time-locked stimulus is played.

動的な被験者間の機能的結合連続によって駆動される瞬間に脳ネットワーク構成を明らかにするまたは通信パラダイム

Task-based functional magnetic resonance imaging bears great potential to understand how our brain reacts to various types of stimulation; however, this ...

A Benchtop Approach to the Location Specific Blood Brain Barrier Opening using Focused Ultrasound in a Rat Model

Stereotaxic surgery is the gold standard for localized drug and gene delivery to the rodent brain. This technique has many advantages over systemic delivery including precise localization to a target brain region and reduction of off target side effects. However, stereotaxic surgery is highly invasive which limits its translational efficacy, requires long recovery times, and provides challenges when targeting multiple brain regions. Focused ultrasound (FUS) can be used in combination with circulating microbubbles to transiently open the blood brain barrier (BBB) in millimeter sized regions. This allows intracranial localization of systemically delivered agents that cannot normally cross the BBB. This technique provides a noninvasive alternative to stereotaxic surgery. However, to date this technique has yet to be widely adopted in neuroscience laboratories due to the limited access to equipment and standardized methods. The overall goal of this protocol is to provide a benchtop approach to FUS BBB opening (BBBO) that is affordable and reproducible and can therefore be easily adopted by any laboratory.

Focused ultrasound with microbubble agents can open the blood brain barrier focally and transiently. This technique has been used to deliver a wide range of agents across the blood brain barrier. This article provides a detailed protocol for the localized delivery to the rodent brain with or without MRI guidance.

ラットモデルにおける集中超音波を用いた位置特異的血液脳関門開口へのベンチトップアプローチ

Stereotaxic surgery is the gold standard for localized drug and gene delivery to the rodent brain. This technique has many advantages over systemic ...

Extraction and Dissection of the Domesticated Pig Brain

Use of the pig as a preclinical and translatable animal model has been well-documented and accepted by research fields investigating cardiovascular systems, gastrointestinal systems, and nutrition, and the pig is increasingly being used as a large animal model in neuroscience. Furthermore, the pig is an accepted model to study neurodevelopment as it displays brain growth and development patterns similar to what occurs in humans. As a less common animal model in neuroscience, surgical and dissection procedures on pigs may not be as familiar or well-practiced among researchers. Therefore, a standardized visual protocol detailing consistent extraction and dissection methods may prove valuable for researchers working with the pig. The following video showcases a technique to remove the pig brain while keeping the cortex and brainstem intact and reviews methods to dissect several commonly investigated brain regions including the brainstem, cerebellum, midbrain, hippocampus, striatum, thalamus, and medial prefrontal cortex. The purpose of this video is to provide researchers with the tools and knowledge necessary to consistently perform a brain extraction and dissection on the four-week-old pig.

This protocol details the technique for removal of the pig brain in its entirety and dissection of several brain regions commonly studied in neuroscience.

家畜豚脳の抽出と解剖

Use of the pig as a preclinical and translatable animal model has been well-documented and accepted by research fields investigating cardiovascular ...

Positron Emission Tomography Imaging for In Vivo Measuring of Myelin Content in the Lysolecithin Rat Model of Multiple Sclerosis

Multiple sclerosis (MS) is a neuroinflammatory disease with expanding axonal and neuronal degeneration and demyelination in the central nervous system, leading to motor dysfunctions, psychical disability, and cognitive impairment during MS progression. Positron emission tomography (PET) is an imaging technique able to quantify in vivo cellular and molecular alterations.
Radiotracers with affinity to intact myelin can be used for in vivo imaging of myelin content changes over time. It is possible to detect either an increase or decrease in myelin content, what means this imaging technique can detect demyelination and remyelination processes of the central nervous system. In this protocol we demonstrate how to use PET imaging to detect myelin changes in the lysolecithin rat model, which is a model of focal demyelination lesion (induced by stereotactic injection) (i.e., a model of multiple sclerosis disease). 11C-PIB PET imaging was performed at baseline, and 1 week and 4 weeks after stereotaxic injection of lysolecithin 1% in the right striatum (4 &#181;L) and corpus callosum (3 &#181;L) of the rat brain, allowing quantification of focal demyelination (injection site after 1 week) and the remyelination process (injection site at 4 weeks).
Myelin PET imaging is an interesting tool for monitoring in vivo changes in myelin content which could be useful for monitoring demyelinating disease progression and therapeutic response.

Positron Emission Tomography Imaging for In Vivo Measuring of Myelin Content in the Lysolecithin Rat Model of Multiple Sclerosis

This protocol has the aim of monitoring in vivo myelin changes (demyelination and remyelination) by positron emission tomography (PET) imaging in an animal model of multiple sclerosis.

多発性硬化症のリゾレシチンラットモデルにおけるイン ビボ 含有量の測定のための陽電子放出断層撮影

Multiple sclerosis (MS) is a neuroinflammatory disease with expanding axonal and neuronal degeneration and demyelination in the central nervous system, ...

単一被験者レベルでの2-デオキシ-2-[¹⁸F]フルオロ-D-グルコース動的陽電子放出断層撮影法を使用した代謝脳接続性の研究

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この動画の章

アダルト生まれのニューロンの統合を検討し

イメージングは3DISCOにより、細胞レベルで無傷生物系をクリア

大人のホールマウントの準備のためのシンプルなワンステップ解剖プロトコル

生体内で1 分子追跡ショウジョウバエ運動神経がシナプス前ターミナルで

神経活動と Spm と頭蓋内脳波データを使用した接続の分析

子供の脳磁図を用いた脳機能の研究

動的な被験者間の機能的結合連続によって駆動される瞬間に脳ネットワーク構成を明らかにするまたは通信パラダイム

ラットモデルにおける集中超音波を用いた位置特異的血液脳関門開口へのベンチトップアプローチ

家畜豚脳の抽出と解剖

多発性硬化症のリゾレシチンラットモデルにおけるインビボ含有量の測定のための陽電子放出断層撮影

単一被験者レベルでの2-デオキシ-2-[18F]フルオロ-D-グルコース動的陽電子放出断層撮影法を使用した代謝脳接続性の研究

要約

さらに動画を探す

この動画の章

アダルト生まれのニューロンの統合を検討し

イメージングは​​3DISCOにより、細胞レベルで無傷生物系をクリア

大人のホールマウントの準備のためのシンプルなワンステップ解剖プロトコル

生体内で1 分子追跡ショウジョウバエ運動神経がシナプス前ターミナルで

神経活動と Spm と頭蓋内脳波データを使用した接続の分析

子供の脳磁図を用いた脳機能の研究

動的な被験者間の機能的結合連続によって駆動される瞬間に脳ネットワーク構成を明らかにするまたは通信パラダイム

ラットモデルにおける集中超音波を用いた位置特異的血液脳関門開口へのベンチトップアプローチ

家畜豚脳の抽出と解剖

多発性硬化症のリゾレシチンラットモデルにおけるイン ビボ 含有量の測定のための陽電子放出断層撮影

単一被験者レベルでの2-デオキシ-2-[¹⁸F]フルオロ-D-グルコース動的陽電子放出断層撮影法を使用した代謝脳接続性の研究

イメージングは3DISCOにより、細胞レベルで無傷生物系をクリア

多発性硬化症のリゾレシチンラットモデルにおけるインビボ含有量の測定のための陽電子放出断層撮影