Launch week offerEnds in00h00m00s

Teodora‐Adriana Perles‐Barbacaru

Has grant

Associate Professor

Aix-Marseille University
Country flagFrance

Research Interests

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Explore related searches

Recent Grants

Grant: Close

postdoctoral research fellowship

Open Date: 2010-01-01

Close Date: 2013-01-01

Grant: Close

Pharmacological MRI of the response to cocaine in dopamine transporter knockout mice

Open Date: 2008-01-01

Close Date: 2009-12-01

Grant: Close

graduate research fellowship

Open Date: 2004-01-01

Close Date: 2007-01-01

Articles (7)

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Background In mice, intraperitoneal (ip) contrast agent (CA) administration is convenient for mapping microvascular parameters over a long‐time window. However, continuous quantitative MRI of CA accumulation in brain over hours is still missing. Purpose To validate a quantitative time‐resolved MRI technique for mapping the CA kinetics in brain upon ip administration. Study Type Prospective, animal model. Specimen 25 C57Bl/6JRj mice underwent MRI. Field Strength/Sequence 7‐T, gradient echo sequence. Assessment Gd‐DOTA concentration was monitored by MRI (25 s/repetition) over 135 minutes with (N = 15) and without (N = 10) ip mannitol challenge (5 g/kg). After the final repetition, the brains were sampled to quantify gadolinium by mass spectrometry (MS). Upon manual brain segmentation, the average gadolinium concentration was compared with the MS quantification in transcardially perfused (N = 20) and unperfused (N = 5) mice. Precontrast T 1 ‐maps were acquired in 8 of 25 mice. Statistical Tests One‐tailed Spearman and Pearson correlation between gadolinium quantification by MRI and by MS, D'Agostino‐Pearson test for normal distribution, Bland–Altman analysis to evaluate the agreement between MRI and MS. Significance was set at P ‐value <0.05. Results MRI showed that ip administered CA reached the blood compartment (>5 mM) within 10 minutes and accumulated continuously for 2 hours in cerebrospinal fluid (>1 mM) and in brain tissue. The MRI‐derived concentration maps showed interindividual differences in CA accumulation (from 0.47 to 0.81 mM at 2 hours) with a consistent distribution resembling the pathways of the glymphatic system. The average in‐vivo brain concentration 2 hours post‐CA administration correlated significantly ( r = 0.8206) with the brain gadolinium quantification by MS for N = 21 paired observations available. Data Conclusion The presented experimental and imaging protocol may be convenient for monitoring the spatiotemporal pattern of CA uptake and clearance in the mouse brain over 2 hours. The quantification of the CA from the MRI signal in brain is corroborated by MS. Evidence Level N/A Technical Efficacy Stage 1

Year:

2023

Year:

2020

Year:

2020

Collaborators (6)

Meysam Hashemi

Senior Research Fellow

INSERM

FRANCE
View details

Juan Iovanna

DRCE

INSERM

FRANCE
View details

Ling Peng

Research Director

CNRS

FRANCE
View details

Nelson Dusetti

Cancer Research Center of Marseille

INSERM Délégation régionale Provence Alpes Cote d'Azur et Corse

FRANCE
View details

Kai-Hsiang Chuang

Associate Professor

University of Queensland

AUSTRALIA
View details

Parul Verma

Assistant Professor

Indian Institute of Technology Madras

View details