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  • Conference proceedings
  • © 2006

N-Acetylaspartate

A Unique Neuronal Molecule in the Central Nervous System

  • Covers topics that both researchers and clinicians have interest in
  • Includes supplementary material: sn.pub/extras

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Table of contents (27 papers)

  1. Front Matter

    Pages i-xvii
  2. N-Acetylaspartate Metabolism in Neural Cells

    • Kishore K. Bhakoo, Timothy Craig, Daniel Pearce
    Pages 27-47
  3. Naa Synthesis and Functional Roles

    • Chikkathur N. Madhavarao, Aryan M. A. Namboodiri
    Pages 49-66
  4. Canavan Disease: Studies on the Knockout Mouse

    • Reuben Matalon, Kimberlee Michals-Matalon, Sankar Surendran, Stephen K. Tyring
    Pages 77-93
  5. Functions Of N-Acetylaspartate and N-Acetylaspartylglutamate in Brain

    • Morris H. Baslow, David N. Guilfoyle
    Pages 95-112
  6. Physiological Role of N-Acetylaspartate

    • Robert W. Ledeen, Jianfeng Wang, Gusheng Wu, Zi-Hua Lu, Goutam Chakraborty, Markus Meyenhofer et al.
    Pages 131-143
  7. Defective Myelin Lipid Synthesis as a Pathogenic Mechanism of Canavan Disease

    • Aryan M. A. Namboodiri, John R. Moffett, Peethambaran Arun, Raji Mathew, Sreela Namboodiri, Asha Potti et al.
    Pages 145-163
  8. Mutation Analysis of the Aspartoacylase Gene in Non-Jewish Patients with Canavan Disease

    • Bai-Jin Zeng, Gregory M. Pastores, Paola Leone, Srinivasa Raghavan, Zhao-Hui Wang, Lucilene A. Ribeiro et al.
    Pages 165-173
  9. Does ASPA Gene Mutation in Canavan Disease Alter Oligodendrocyte Development?

    • Shalini Kumar, Rasika Sowmyalakshmi, Sarah L. Daniels, Ruth Chang, Sankar Surendran, Reuben Matalon et al.
    Pages 175-182
  10. Quantitation of NAA in the Brain by Magnetic Resonance Spectroscopy

    • Peter B. Barker, David Bonekamp, Gerard Riedy, Mari Smith
    Pages 183-197
  11. N-Acetyl-L-Aspartate in Multiple Sclerosis

    • Gerson A. Criste, Bruce D. Trapp
    Pages 199-214
  12. NAA and Higher Cognitive Function in Humans

    • Ronald A. Yeo, William M. Brooks, Rex E. Jung
    Pages 215-226
  13. In Vivo NMR Measures of NAA and the Neurobiology of Schizophrenia

    • Stefano Marenco, Alessandro Bertolino, Daniel R. Weinberger
    Pages 227-240
  14. N-Acetylaspartate as a Marker of Neuronal Injury in Neurodegenerative Disease

    • Norbert Schuff, Dieter J. Meyerhoff, Susanne Mueller, Linda Chao, Diana Truran Sacrey, Kenneth Laxer et al.
    Pages 241-262
  15. Regulation of NAA-Synthesis in the Human Brain in Vivo: Canavan’s Disease, Alzheimer’s Disease and Schizophrenia

    • Kent Harris, Alexander Lin, Pratip Bhattacharya, Thao Tran, Willis Wong, Brian Ross
    Pages 263-273

About this book

N-acetylaspartate, or NAA, is the acetylated form of the amino acid aspartate, and it is present exclusively in the nervous system. Indeed, NAA is one of the most highly concentrated chemicals found in the brain of humans and animals, and yet the functions served by this brain-specific metabolite remain elusive, and controversial. Despite the uncertainties surrounding the functions of NAA in the development and operation of the nervous system, this molecule has attracted the attention of researchers and clinicians for two distinct reasons.

First, the acetyl proton on NAA gives off a very prominent signal in water-suppressed, proton magnetic resonance spectroscopy (MRS), which permits clinicians to monitor levels of NAA in the brains of patients in a non-invasive manner. Because NAA is found primarily in neurons, and because the levels in the brain have been found to change rapidly after injury, or slowly during neurodegenerative diseases, MRS has become a preferred method of analyzing nerve cell dysfunction and death without surgical intervention.

The second reason that NAA has attracted attention in recent years is that a congenital genetic disorder of NAA metabolism has been found to be the cause of the neurodegenerative disorder known as Canavan’s disease. Canavan’s disease is an inherited leukodystrophy that involves myelination pathologies of cortical white matter, leading to death within 10 years of birth. The genetic mutation results in a defective enzyme that de-acetylates NAA in the brain, resulting in a significant rise in NAA levels in the brain and urine. This enzyme, known as aspartoacylase (ASPA), appears to be involved in the process of myelination, such that a defective enzyme results in a disruption of the myelination of nerve fibers during development.

The purpose of this symposium is to bring together investigators from around the world who are interested in the study of NAA, and the roles it plays in neuronaldevelopment and functioning. It is hoped that bringing researchers and clinicians together in such a forum will facilitate rapid progress in this emerging field, and will help lead to discoveries that can alleviate the suffering caused by a deadly, inheritable infantile disease.

Editors and Affiliations

  • Uniformed Services University of the Health Sciences, Bethesda, USA

    John R. Moffett, Aryan M. A. Namboodiri

  • University of Albany, Albany, USA

    Suzannah B. Tieman

  • National Institute of Mental Health, Bethesda, USA

    Daniel R. Weinberger

  • McLean Hospital, Belmont, USA

    Joseph T. Coyle

Bibliographic Information

  • Book Title: N-Acetylaspartate

  • Book Subtitle: A Unique Neuronal Molecule in the Central Nervous System

  • Editors: John R. Moffett, Suzannah B. Tieman, Daniel R. Weinberger, Joseph T. Coyle, Aryan M. A. Namboodiri

  • DOI: https://doi.org/10.1007/0-387-30172-0

  • Publisher: Springer New York, NY

  • eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)

  • Copyright Information: The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2006

  • Hardcover ISBN: 978-0-387-30171-6Published: 28 March 2006

  • Softcover ISBN: 978-1-4899-8888-1Published: 25 November 2014

  • eBook ISBN: 978-0-387-30172-3Published: 21 October 2006

  • Edition Number: 1

  • Number of Pages: XVII, 375

  • Topics: Neurosciences

Buy it now

Buying options

eBook USD 169.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book USD 229.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book USD 219.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access