Dataset ID: 12

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Dataset Details

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
Open Access
No
Study Component
Multi Modality Images
No
Imaging Modality
Imaging Sub Modality
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
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
Randomization
Mice were randomly divided into treted and control group
Blinding
No
Outcome Measures
MRI T1 contrast
Statistical Methods
T-test
Species
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 mmol Gd kg); Multi Hance (0.2 mmol Gd 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 Data
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
Updated Year
2023