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PET imaging of [11C]MPC-6827, a microtubule-based radiotracer in non-human primate brains

  • Naresh Damuka
  • , Paul W. Czoty
  • , Ashley T. Davis
  • , Michael A. Nader
  • , Susan H. Nader
  • , Suzanne Craft
  • , Shannon L. Macauley
  • , Lindsey K. Galbo
  • , Phillip M. Epperly
  • , Christopher T. Whitlow
  • , April T. Davenport
  • , Thomas J. Martin
  • , James B. Daunais
  • , Akiva Mintz
  • , Kiran Kumar Solingapuram Sai

Producción científica: Article › revisión exhaustiva

15 Citas (Scopus)

Resumen

Dysregulation of microtubules is commonly associated with several psychiatric and neurological disorders, including addiction and Alzheimer’s disease. Imaging of microtubules in vivo using positron emission tomography (PET) could provide valuable information on their role in the development of disease pathogenesis and aid in improving therapeutic regimens. We developed [11C]MPC-6827, the first brain-penetrating PET radiotracer to image microtubules in vivo in the mouse brain. The aim of the present study was to assess the reproducibility of [11C]MPC-6827 PET imaging in non-human primate brains. Two dynamic 0–120 min PET/CT imaging scans were performed in each of four healthy male cynomolgus monkeys approximately one week apart. Time activity curves (TACs) and standard uptake values (SUVs) were determined for whole brains and specific regions of the brains and compared between the “test” and “retest” data. [11C]MPC-6827 showed excellent brain uptake with good pharmacokinetics in non-human primate brains, with significant correlation between the test and retest scan data (r = 0.77, p = 0.023). These initial evaluations demonstrate the high translational potential of [11C]MPC-6827 to image microtubules in the brain in vivo in monkey models of neurological and psychiatric diseases.

Idioma originalEnglish
Número de artículo2289
PublicaciónMolecules
Volumen25
N.º10
DOI
EstadoPublished - may 2020

Nota bibliográfica

Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Financiación

Funding: The authors acknowledge financial support for these studies provided by NIH-NIA: R01AG065839-01 (KKSS), Wake Forest Center for Research on Substance Use and Addiction (CRSUA) pilot grant (KKSS), Wake Forest Translational Alcohol Research Center P50AA026117 (Czoty), Wake Forest Center for Neurobiology of Addiction Treatment, P50DA006634-27 (Nader), NIH-NIDA: R01 DA017763 (Nader), and TIP-CTSA ULTR001420 (McClain).

FinanciadoresNúmero del financiador
KKSS
NIA/NIHR01AG065839-01
NIH/NIDAR01 DA017763, TIP-CTSA ULTR001420
Wake Forest Center for Neurobiology of Addiction TreatmentP50DA006634-27
Wake Forest Translational Alcohol Research CenterP50AA026117
National Center for Advancing Translational Sciences (NCATS)UL1TR001420

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Analytical Chemistry
    • Chemistry (miscellaneous)
    • Molecular Medicine
    • Pharmaceutical Science
    • Drug Discovery
    • Physical and Theoretical Chemistry
    • Organic Chemistry

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