I11 Longitudinal MRI and MRSI characterisation of the quinolinic acid rat model for excitotoxicity: unique recovery of N-acetyl aspartate levels. (16th November 2010)

• Record Type: Journal Article
• Authors: Sadan, O; Shemesh, N; Melamed, E; Offen, D; Cohen, Y
• Is Part Of: Journal of neurology, neurosurgery and psychiatry. Volume 81(2010)Supplement 1
• Page Start: A39
• Page End: A39
• Publication Date: 2010-11-16
• Subjects: quinolinic acid -- magnetic resonance imaging -- spectroscopy -- N-acetyl aspartate -- apparent diffusion coefficients; Neurology -- Periodicals; Nervous system -- Surgery -- Periodicals; Psychiatry -- Periodicals; 616.8
• DOI: 10.1136/jnnp.2010.222679.11
• Languages: English
• ISSNs: 0022-3050

Abstract

Abstract : Introduction: Quinolinic acid (QA) induced striatal lesion is an important model for excitotoxicity that is also used for efficacy studies. To date, the morphological and spectroscopic indices of this model have not been studied longitudinally by MRI. Aims: This study aimed to monitor the lesion progression and changes in N-acetyl aspartate (NAA) as viewed by MRI and MRSI, respectively, in vivo over a period of 49 days. Results: We found that the affected areas exhibited both high and low apparent diffusion coefficients (ADC) even 49 days post QA injection in three of the six tested animals. MRI guided histological analysis correlated areas characterised by high ADCs on day 49 with cellular loss, while areas characterised by lower ADCs correlated with macrophage infiltration (CD68 positive stain). Our MRSI study revealed an initial reduction of NAA levels in the lesioned striatum, which significantly recovered with time, although not to control levels. Total striatum normalised NAA levels recovered from 0.67±0.15 (of the contralateral row) on day 1 to 0.90±0.12 on day 49. Conclusions: Our findings suggest that NAA should be considered as a marker for neuronal dysfunction, in addition to neuronal viability. Some behavioural indices could be correlated to permanent neuronal damage while others demonstrated a spontaneous recovery parallel to the NAA recovery. Our findings may have implications in efficacy oriented studies performed on the QA model.