4.5 Article Proceedings Paper

Imaging microglial activation in Huntington's disease

期刊

BRAIN RESEARCH BULLETIN
卷 72, 期 2-3, 页码 148-151

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.brainresbull.2006.10.029

关键词

Huntington's disease; microglial activation; emission tomography; PK11195

资金

  1. Medical Research Council [G0300723B, MC_U120036861] Funding Source: researchfish
  2. MRC [MC_U120036861] Funding Source: UKRI
  3. Medical Research Council [MC_U120036861] Funding Source: Medline
  4. Wellcome Trust Funding Source: Medline

向作者/读者索取更多资源

Activated microglia have been proposed to play a major role in the pathogenesis of Huntington's Disease (HD). PK11195 is a ligand which binds selectively to peripheral benzodiazepine binding sites, a type of receptor selectively expressed by activated nucroglia in the central nervous system. Using C-11-(R)-PK11195 positron emission tomography (PET), we have recently shown in vivo evidence of increased microglial activation in both symptomatic and presymptomatic HD gene carriers and that the degree of microglial activation in the striatum correlates with the severity of striatal dopamine D2 receptor dysfunction measured with C-11-raclopride PET. Our findings indicate that microglial activation is an early process in the HD pathology, occurring before the onset of symptoms. The close spatial and temporal relationship between microglial activation and neuronal dysfunction lends further support to the pathogenic: link between the two processes in HD. Further longitudinal studies are needed to fully elucidate this link. (c) 2006 Elsevier Inc. All rights reserved.

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