4.7 Article

Imaging signal transduction via arachidonic acid in the human brain during visual stimulation, by means of positron emission tomography

期刊

NEUROIMAGE
卷 34, 期 4, 页码 1342-1351

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2006.11.018

关键词

positron emission tomography; brain; human; arachidonic acid; stimulation; phospholipase A(2); signal; transduction; blood flow; visual; flash; sensory

资金

  1. Intramural NIH HHS [Z99 NS999999] Funding Source: Medline

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Background. Arachidonic acid (AA, 20:4n-6), an important second messenger, is released from membrane phospholipid following receptor mediated activation of phospholipase A(2) (PLAD(2)). This signaling process can be imaged in brain as a regional brain AA incorporation coefficient K*. Hypothesis: K* will be increased in brain visual areas of subjects submitted to visual stimulation. Subjects and methods: Regional values of K* were measured with positron emission tomography (PET), following the intravenous injection of [1-C-11]AA, in 16 healthy volunteers subjected to visual stimulation at flash frequencies 2.9 Hz (8 subjects) or 7.8 Hz (8 subjects), compared with the dark (0 Hz) condition. Regional cerebral blood flow (rCBF) was measured with intravenous [O-15]water under comparable conditions. Results: During flash stimulation at 2.9 Hz or 7.8 Hz vs. 0 Hz, K* was increased significantly by 2.3-8.9% in Brodmann areas 17, 18 and 19, and in additional frontal, parietal and temporal cortical regions. rCBF was increased significantly by 3.1-22%, often in comparable regions. Increments at 7.8 Hz often exceeded those at 2.9 Hz for both K* and rCBF. Decrements in both parameters also were produced, particularly in frontal brain regions. Conclusions: AA plays a role in signaling processes provoked by visual stimulation, since visual stimulation at flash frequencies of 2.9 and 7.8 Hz compared to 0 Hz modifies both K* for AA and rCBF in visual and related areas of the human brain. The two-stimulus condition paradigm of this study might be used with PET to image effects of other functional activations and of drugs on brain signaling via AA. Published by Elsevier Inc.

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