Metadata

Dataset ID: 12
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Study Design
Study Design Background To visualize LPS-induced neuroinflammation using paramagnetic micelles decorated with a peptide targeting the inflammation marker VCAM-1
Study Description VCAM-1 paramagnetic micelles to detect neuroinflammation by MRI
Study Type preclinical
Study Subtype in vivo/ex vivo
Publication
Paper Linked yes
Paper Title MRI visualization of neuroinflammation using VCAM-1 targeted paramagnetic micelles.
Paper Authors Garello Francesca, Pagoto Amerigo, Arena Francesca, Buffo Annalisa, Blasi Francesco, Alberti Diego, Terreno Enzo.
Affiliation Molecular & Preclinical Imaging Centers, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy; Department of Neuroscience Rita Levi-Montalcini, University of Torino, Torino, Italy; Neuroscience Institute Cavalieri Ottolenghi, Torino, Italy; Molecular & Preclinical Imaging Centers, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
Paper Journal Nanomedicine: Nanotechnology, Biology and Medicine
Paper Year 2018
Paper Doi https://doi.org/10.1016/j.nano.2017.10.002.
Open Access no
Updated Year 2023
Study Component
Multi Modality Images no
Imaging Modality MRI
Imaging Sub Modality T1w CE, T2w
Radiation no
Imaging Coverage brain
Imaging Target VCAM-1
Dataset Information
Institution UniTO
Pi Enzo Terreno
Country Of Institution Italy
Imaging Facility Laboratory of molecular imaging for small animal
Euro Bio Imaging Node MMMI
Country Of Imaging Facility Italy
Contact Person francesca.garello@unito.it
In Vivo Experimental Parameters
Number Of Groups 3
Types Of Groups blood half-life determination, VCAM-1 micelles, scrambled micelles, Multihance
Overall Sample Size 19
Disease Model neuroinflammation
Organ Or Tissue brain
Sample Size For Each Group 3 for half-life time, 8 for VCAM-1 micelles, 4 for scrambled micelles, 4 for Multihance
Power Calculation none
Inclusion Criteria none
Exclusion Criteria none
Randomization mice were randomly divided into treted and control group
Blinding no
Outcome Measures MRI T1 contrast
Statistical Methods t-test
Species Mice
Strain C57/BL6
Immune Status Immunocompetent
Sex female
Age older than 8 weeks
Age At Start Experiment 8 weeks
Age At Scanning Experiment S 8 weeks
Weight About 18-20 g
Weight At Start Experiment About 18-20 g
Weight At End Experiment About 18-20 g
Source Of Animals University of Torino, Italy
Experimental Procedures
Pharmacological Procedures Intervention And Control no
Blood Sampling yes
Blood Sampling Method from the tail vein
Blood Sample Volume 20-50 ul
Blood Timing 5, 15, 30 min, 1, 2, 4 and 24 h
Surgical Procedures Including Sham Surgery yes
Description Of The Surgical Procedure Acute neuroinflammatory response was induced in the right striatum. To obtain the model, mice were anesthetized, positioned in a stereotaxic apparatus (Stoelting) and the skull was exposed. The brain of the animal was then exposed via a hole, which was drilled through the skull. A glass capillary was inserted into the right striatum using the following stereotaxic coordinates from bregma: + 0.1 mm antero-posterior, ? 2.1 mm mediolateral, ? 2.6 mm dorsoventral. 1 ?L of lipopolysaccharide (LPS) (E. coli 026:B6, Sigma?Aldrich) in sterile phosphate buffered saline PBS at a concentration of 5 ?g/?l was then infused with a pneumatic pressure injection apparatus (Picospritzer II, General Valve Corporation) over 5 min followed by a 2 minutes rest period to allow the solution to diffuse into the brain prior to the removal of the capillary. For the saline control mouse, the same surgery described above was performed, but the vehicle only (1 ?L of PBS) was injected intra-striatally.
Target Organ Tissue brain
Analgesic Plan To Relieve Pain Suffering And Distress no
Anesthesia Type gas
Duration ~30 minutes
Anesthesia Drugs Isoflurane
Anesthesia Dose 1-2% isoflurane
Monitoring Regime respiratoy rate
Euthanasia yes
Method cervival dislocation
Histology yes
Tissues Collected Post Euthanasia brain
Timing Of Collection 24 h post VCAM-1 or scarmbled micelles injection
Histological Procedure frozen
Name Of Reagent S VCAM-1, F4/80, CD31
Catalogue Number rat anti-mouse CD31, Clone MEC 13:3, BD Pharmingen. Rat anti mouse F4/80 antibody, clone Cl:A3-1, Serotec.
Length Of Fixation 5 min, absolute ethanol
Frequency Of Imaging Pre, 20 min, 4 h, 24 h and 48 h post injection of micelles.
Timing Of Imaging 24h post LPS administration.
Overall Scan Length 20 min
Contrast Agent Or Radio Isotope Or Challenge With Gas Molecule contrast agent
Contrast Agent Commercial Drug Multihance / paramagnetic micelles
Contrast Agent Chemical Drug gadobenate dimeglumine
Contrast Agent Dose VCAM-1 targeted or scrambled micelles (0.05 mmolGd/kg); MultiHance (0.2 mmolGd/Kg)
Injection Volume 0,2
Injection Time 10 seconds
Vehicle saline
Route Of Administration intravenous
Housing Room not SPF
Dietary Intervention no
Respiration Rate only during scanning
Body Tempurature Etc only during scanning
Food Intake Measured no
Image Acquisition
Instrument Vendor Bruker
Instrument Type Icon, equipped with a mouse brain volume coil
Instrument Specifics 1T
Image Acquisition Parameters T2-weighted MRI images were obtained using a RARE sequence protocol (TR/TE/NAV = 2500/26.7/12). T1-weighted MRI images were acquired using a FLASH sequence (TR/TE/NAV = 75/5.8/18, field of view (FOV) = 1.2 cm)
Raw Data yes
Image Correlation
Image Type Primary image
Dimensions 2D
Field Of View 1,2 cm x 1,2 cm
Dimension Extents 128x128
Image Processing Methods default
Quality Control no
Image Smoothing Or Filtering Algorithm no
Image Registration Algorithm no
Analyzed Data
Analysis Result Type numerical
Data Used For Analysis ROI
Analysis Method And Details manual
Status complete
Ontology Terms
Ncit Imaging NCIT:C16809
Ncit Imaging Submodality NCIT:C180729,NCIT:C180727,NCIT:C46087
Ncit Anatomy NCIT:C12439
Ncit Species NCIT:C14238
Ncit Strain NCIT:C14424
Chebi Anesthesia CHEBI:6015
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