Seeking the Amygdala: Novel Use of Diffusion Tensor Imaging to Delineate the Basolateral Amygdala

Author:

Obenaus Andre123ORCID,Kinney-Lang Eli12,Jullienne Amandine2ORCID,Haddad Elizabeth2ORCID,Wendel Kara M.3,Shereen A. Duke3ORCID,Solodkin Ana34,Dunn Jeffrey F.5ORCID,Baram Tallie Z.234

Affiliation:

1. Department of Pediatrics, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA

2. Department of Pediatrics, University of California, Irvine, CA 92697, USA

3. Department of Anatomy/Neurobiology, University of California, Irvine, CA 92697, USA

4. Department of Neurology, University of California, Irvine, CA 92697, USA

5. Department of Radiology, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Alberta T2N 4N1, Canada

Abstract

The amygdaloid complex, including the basolateral nucleus (BLA), contributes crucially to emotional and cognitive brain functions, and is a major target of research in both humans and rodents. However, delineating structural amygdala plasticity in both normal and disease-related contexts using neuroimaging has been hampered by the difficulty of unequivocally identifying the boundaries of the BLA. This challenge is a result of the poor contrast between BLA and the surrounding gray matter, including other amygdala nuclei. Here, we describe a novel diffusion tensor imaging (DTI) approach to enhance contrast, enabling the optimal identification of BLA in the rodent brain from magnetic resonance (MR) images. We employed this methodology together with a slice-shifting approach to accurately measure BLA volumes. We then validated the results by direct comparison to both histological and cellular-identity (parvalbumin)-based conventional techniques for defining BLA in the same brains used for MRI. We also confirmed BLA connectivity targets using DTI-based tractography. The novel approach enables the accurate and reliable delineation of BLA. Because this nucleus is involved in and changed by developmental, degenerative and adaptive processes, the instruments provided here should be highly useful to a broad range of neuroimaging studies. Finally, the principles used here are readily applicable to numerous brain regions and across species.

Funder

NIMH-supported Conte Center on Brain Programming in Adolescent Vulnerabilities, University of California Irvine, Irvine, California, United States

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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