pubmed-article:16206186 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0011923 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0031268 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0927232 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0032743 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0050423 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0597354 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C1708632 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0539266 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C1522485 | lld:lifeskim |
pubmed-article:16206186 | lifeskim:mentions | umls-concept:C0302995 | lld:lifeskim |
pubmed-article:16206186 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:16206186 | pubmed:dateCreated | 2005-10-10 | lld:pubmed |
pubmed-article:16206186 | pubmed:abstractText | A series of brain uptake studies and PET imaging studies were conducted with the sigma(1) selective imaging agent, [(18)F]FBFPA. The results of the study indicate that this radiotracer readily crosses the blood-brain barrier and labels sigma(1) receptors in vivo. In vivo blocking studies with a sigma(1) selective ligand and a nonselective sigma(1)/sigma(2) receptor ligand indicates that [(18)F]FBFPA labels sigma(1) and not sigma(2) receptors in rodent brain. PET imaging studies demonstrated a high uptake in regions of rhesus monkey brain having a high density of sigma(1) receptors. The uptake of [(18)F]FBFPA was displaced by the sigma ligand, haloperidol (1 mg/kg, i.v.). In vivo blocking studies indicate that the progesterone blocked the brain uptake of [(18)F]FBFPA in rat brain. These data indicate that [(18)F]FBFPA is a potential radiotracer for imaging sigma(1) receptors in the CNS in vivo with PET. | lld:pubmed |
pubmed-article:16206186 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:language | eng | lld:pubmed |
pubmed-article:16206186 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16206186 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16206186 | pubmed:month | Dec | lld:pubmed |
pubmed-article:16206186 | pubmed:issn | 0887-4476 | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:DuaG LGL | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:GageH... | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:MachRobert... | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:BuchheimerNan... | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:EhrenkauferRi... | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:HuangYunsheng... | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:KuhnerRossR | lld:pubmed |
pubmed-article:16206186 | pubmed:author | pubmed-author:MortonThomas... | lld:pubmed |
pubmed-article:16206186 | pubmed:copyrightInfo | Copyright 2005 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:16206186 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16206186 | pubmed:day | 15 | lld:pubmed |
pubmed-article:16206186 | pubmed:volume | 58 | lld:pubmed |
pubmed-article:16206186 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16206186 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16206186 | pubmed:pagination | 267-74 | lld:pubmed |
pubmed-article:16206186 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:16206186 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16206186 | pubmed:articleTitle | N-[18F]4'-fluorobenzylpiperidin-4yl-(2-fluorophenyl) acetamide ([18F]FBFPA): a potential fluorine-18 labeled PET radiotracer for imaging sigma-1 receptors in the CNS. | lld:pubmed |
pubmed-article:16206186 | pubmed:affiliation | Department of Radiology-PET Center Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA. rhmach@mir.wustl.edu | lld:pubmed |
pubmed-article:16206186 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16206186 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |