Journal
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 88, Pages -Publisher
JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/50682
Keywords
Medicine; Issue 88; mu-opioid; opiate; migraine; headache; pain; Positron Emission Tomography; molecular neuroimaging; 3D; neuronavigation
Categories
Funding
- National Institute of Health - National Institute of Neurological Disorders and Stroke [K23 NS062946]
- Dana Foundation's Brain and Immuno-Imaging Award
- Migraine Research Foundation Research Grant Award
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A growing body of research, generated primarily from MRI-based studies, shows that migraine appears to occur, and possibly endure, due to the alteration of specific neural processes in the central nervous system. However, information is lacking on the molecular impact of these changes, especially on the endogenous opioid system during migraine headaches, and neuronavigation through these changes has never been done. This study aimed to investigate, using a novel 3D immersive and interactive neuronavigation (3D-IIN) approach, the endogenous mu-opioid transmission in the brain during a migraine headache attack in vivo. This is arguably one of the most central neuromechanisms associated with pain regulation, affecting multiple elements of the pain experience and analgesia. A 36 year-old female, who has been suffering with migraine for 10 years, was scanned in the typical headache (ictal) and nonheadache (interictal) migraine phases using Positron Emission Tomography (PET) with the selective radiotracer [C-11] carfentanil, which allowed us to measure mu-opioid receptor availability in the brain (non-displaceable binding potential mu - OR BPND). The short-life radiotracer was produced by a cyclotron and chemical synthesis apparatus on campus located in close proximity to the imaging facility. Both PET scans, interictal and ictal, were scheduled during separate mid-late follicular phases of the patient's menstrual cycle. During the ictal PET session her spontaneous headache attack reached severe intensity levels; progressing to nausea and vomiting at the end of the scan session. There were reductions in mu OR BPND in the pain-modulatory regions of the endogenous mu-opioid system during the ictal phase, including the cingulate cortex, nucleus accumbens (NAcc), thalamus (Thal), and periaqueductal gray matter (PAG); indicating that mu ORs were already occupied by endogenous opioids released in response to the ongoing pain. To our knowledge, this is the first time that changes in mu OR BPND during a migraine headache attack have been neuronavigated using a novel 3D approach. This method allows for interactive research and educational exploration of a migraine attack in an actual patient's neuroimaging dataset.
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