Quantitative MRI of Gd‐DOTA Accumulation in the Mouse Brain After Intraperitoneal Administration: Validation by Mass Spectrometry

Author:

Tessier Anthony12,Ruze Anthony J.1,Varlet Isabelle1ORCID,Laïb Estelle M.H.1,Royer Emilien1ORCID,Bernard Monique1ORCID,Viola Angèle1ORCID,Perles‐Barbacaru Teodora‐Adriana1ORCID

Affiliation:

1. CNRS, Center for Magnetic Resonance Imaging in Biology and Medicine (CRMBM, UMR CNRS 7339), Aix‐Marseille University Marseille France

2. Department of Medical Imaging Sainte‐Anne Military Teaching Hospital (Hôpital d'Instruction des Armées) Toulon France

Abstract

BackgroundIn 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.PurposeTo validate a quantitative time‐resolved MRI technique for mapping the CA kinetics in brain upon ip administration.Study TypeProspective, animal model.Specimen25 C57Bl/6JRj mice underwent MRI.Field Strength/Sequence7‐T, gradient echo sequence.AssessmentGd‐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 T1‐maps were acquired in 8 of 25 mice.Statistical TestsOne‐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.ResultsMRI 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 ConclusionThe 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 LevelN/ATechnical EfficacyStage 1

Publisher

Wiley

Subject

Radiology, Nuclear Medicine and imaging

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