Abstract

Functional neuroimaging modalities vary in spatial and temporal resolution. One major limitation of most functional neuroimaging modalities is that only neural activation taking place inside the scanner can be imaged. This limitation makes functional neuroimaging in many clinical scenarios extremely difficult or impossible. The most commonly used radiopharmaceutical in Single Photon Emission Tomography (SPECT) functional brain imaging is Technetium 99 m-labeled Ethyl Cysteinate Dimer (ECD). ECD is a lipophilic compound with unique pharmacodynamics. It crosses the blood brain barrier and has high first pass extraction by the neurons proportional to regional brain perfusion at the time of injection. It reaches peak activity in the brain 1 min after injection and is then slowly cleared from the brain following a biexponential mode. This allows for a practical imaging window of 1 or 2 h after injection. In other words, it freezes a snapshot of brain perfusion at the time of injection that is kept and can be imaged later. This unique feature allows for designing functional brain imaging studies that do not require the patient to be inside the scanner at the time of brain activation. Functional brain imaging during severe burn wound care is an example that has been extensively studied using this technique. Not only does SPECT allow for imaging of brain activity under extreme pain conditions in clinical settings, but it also allows for imaging of brain activity modulation in response to analgesic maneuvers whether pharmacologic or non-traditional such as using virtual reality analgesia. Together with its utility in extreme situations, SPECTS is also helpful in investigating brain activation under typical pain conditions such as experimental controlled pain and chronic pain syndromes.

Highlights

  • Pain is one of the most challenging clinical entities in medicine

  • The majority of functional neuroimaging techniques focus on detecting changes in regional blood flow as a surrogate of neuronal activation. functional Magnetic Resonance Imaging (fMRI) measures/images changes in brain activation while the subject is inside the scanner. fMRI allows real time imaging of brain functional changes during minor or experimental pain experiences with a relatively good temporal resolution

  • Brain perfusion Single Photon Emission Computed Tomography (SPECT) using commercially available radiotracers has a unique characteristic that allows freezing an image of brain activation at the time of injection, which can be done in virtually any clinical scenario

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Summary

Utility of SPECT Functional Neuroimaging of Pain

Mohammed Bermo 1*, Mohammed Saqr 2,3, Hunter Hoffman 4, David Patterson 4, Sam Sharar 4, Satoshi Minoshima 5 and David H. One major limitation of most functional neuroimaging modalities is that only neural activation taking place inside the scanner can be imaged. ECD is a lipophilic compound with unique pharmacodynamics It crosses the blood brain barrier and has high first pass extraction by the neurons proportional to regional brain perfusion at the time of injection. It reaches peak activity in the brain 1 min after injection and is slowly cleared from the brain following a biexponential mode. It freezes a snapshot of brain perfusion at the time of injection that is kept and can be imaged later This unique feature allows for designing functional brain imaging studies that do not require the patient to be inside the scanner at the time of brain activation. Together with its utility in extreme situations, SPECTS is helpful in investigating brain activation under typical pain conditions such as experimental controlled pain and chronic pain syndromes

INTRODUCTION
Pain Imaging by SPECT
SPECT RADIOPHARMACEUTICALS
IMAGE RECONSTRUCTION
IMAGING OF PAIN
CHRONIC PAIN
Episodic Pain
Response to Therapy
Limitations
Full Text
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