4.6 Article

Using perfusion MRI to measure the dynamic changes in neural activation associated with tonic muscular pain

期刊

PAIN
卷 148, 期 3, 页码 375-386

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/j.pain.2009.10.003

关键词

Muscle pain; Tonic pain; Hypertonic saline; Arterial spin labelling; Functional magnetic resonance imaging; Neural activation; Cerebral blood flow

资金

  1. Canadian Institutes of Health Research

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Knowledge regarding neural pain processing is primarily the result of studies involving models of brief cutaneous pain; however, clinical pain generally originates in deep tissue and is prolonged. This study measured the dynamic neural activation associated with a muscular pain model incorporating both acute and tonic states. Hypertonic saline (5% NaCl) was infused into the brachioradialis muscle of eleven healthy volunteers for 15 min after an initial bolus of 0.5 mL. Ten controls followed the same protocol with normal saline (0.9% NaCl). Magnetic resonance images of cerebral blood flow (CBF) were acquired using an arterial spin labelling method. The imaging volume extended from the thalamus to the primary somatosensory cortices, but did not include the brainstem and cerebellum. Using a numerical scale from 0 to 10, ratings of pain intensity peaked at 5.9 +/- 0.6 and remained near 5 for the remainder of the trial. Controls experienced minimal pain, reporting a peak value of 1.8 +/- 0.4. Significant CBF increases in rostral and caudal anterior insula bilaterally, anterior mid-cingulate cortex (aMCC), bilateral thalamus, and contralateral posterior insula were observed. The time courses of CBF revealed significant differences in the activation pattern during tonic pain. In particular, a more rapid return to baseline in aMCC versus insula was interpreted as a preferential decrease in the affective component of pain. This conclusion was supported by the strong correlation between pain intensity ratings and CBF in the contralateral insula (R-2 = 0.911, p < 0.01), which is a region believed to be responsible for pain intensity processing. (c) 2009 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved.

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