Imaging opioid release after stimulants in adults with ADHD

  • Research type

    Research Study

  • Full title

    A [11C]Carfentanil PET study to investigate endogenous opioid release in adults with ADHD after one oral dose of Dexamphetamine

  • IRAS ID

    126904

  • Contact name

    Katya Rubia

  • Contact email

    katya.rubia@kcl.ac.uk

  • Duration of Study in the UK

    1 years, 5 months, 0 days

  • Research summary

    The main purpose of this study is to investigate the role of a specific brain messenger system, called “the opioid system”, in male adults with ADHD. It is possible to measure opioid receptor levels using a special chemical that has been labeled with a tiny does of radioactivity and that can be detected with a type of brain scan called Positron Emission Tomography (PET). Furthermore, if the opioid system is stimulated to release opioid molecules, such a release can be detected by a reduction in binding of the radioactive agent used to label the opioid receptors. The brain’s release of opioids can be triggered by a dose of amphetamine. Thus, two [11C]carfentanil PET scans are required to measure the aspects of the opioid system of interest in this study; one scan to measure the baseline level without any stimulation, and one scan after giving a dose of amphetamine.

    It is hypothesized that:
    1) A dose of Dexamphetamine will reduce [11C]Cartenfanil binding (i.e., increase µ-opioid release) in ADHD adults (as in controls)).
    2) The [11C]cartenfanil binding potential (i.e., amount of µ-opioid release) after one dose of Dexamphetamine in ADHD adults is lower from that in healthy adults (lower)
    3) ADHD adults will have higher [11C]carfentanil binding potential (i.e., decreased µ-opioid release) than healthy controls at baseline.

    The findings of this study have important clinical implications:
    1) Opioid release in ADHD patients after dexamphetamine could be the basis for the addictive potential of stimulants.
    2) Differential µ-opioid release after stimulant medication would suggest differences between healthy controls and ADHD patients in mechanisms of action and in the abuse potential of amphetamines.
    3) Differences in µ-opioid receptor availability at baseline in ADHD relative to controls could reflect a new underlying neurobiological mechanism for ADHD leading to new research and treatment development.

  • REC name

    London - West London & GTAC Research Ethics Committee

  • REC reference

    14/LO/1795

  • Date of REC Opinion

    1 Dec 2014

  • REC opinion

    Further Information Favourable Opinion