作者
Sriram Venneti, Brian J Lopresti, Guoji Wang, Stephanie J Bissel, Chester A Mathis, Carolyn C Meltzer, Fernando Boada, Saverio Capuano, Geraldine J Kress, Denise K Davis, James Ruszkiewicz, Ian J Reynolds, Michael Murphey-Corb, Anita M Trichel, Stephen R Wisniewski, Clayton A Wiley
发表日期
2004/4/1
期刊
The Journal of clinical investigation
卷号
113
期号
7
页码范围
981-989
出版商
American Society for Clinical Investigation
简介
HIV infection in humans and simian immunodeficiency virus (SIV) infection in macaques result in encephalitis in approximately one-quarter of infected individuals and is characterized by infiltration of the brain with infected and activated macrophages. 1-(2-chlorphenyl)-N-methyl-N-(1-methylpropyl)-3-isoquinoline-carboxamide (PK11195) is a ligand specific for the peripheral benzodiazepine receptor abundant on macrophages and is expressed in low levels in the noninfected brain. We hypothesized that positron-emission tomography (PET) with the carbon-11–labeled, R-enantiomer form of PK11195 ([11C](R)-PK11195) could image brain macrophages and hence the development of encephalitis in vivo. [11C](R)-PK11195 binding was assessed in the brain using PET in 11 SIV infected macaques, six of which showed increased binding in vivo. Postmortem examination of the brain in these six macaques …
引用总数
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