Positron emission tomography imaging in multiple sclerosis-current status and future applications

被引:21
作者
Kiferle, L. [1 ,2 ,3 ]
Politis, M. [1 ,2 ]
Muraro, P. A. [1 ,2 ]
Piccini, P. [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Ctr Neurosci, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, MRC Clin Sci Ctr, Div Expt Med, London W12 0NN, England
[3] Univ Pisa, Dept Neurosci, Pisa, Italy
关键词
apoptosis; cannabinoids; gray matter; multiple sclerosis; neuroinflammation; PET; remyelination; PERIPHERAL BENZODIAZEPINE-RECEPTOR; B-CELL FOLLICLES; IN-VIVO; CANNABINOID RECEPTOR; GLUCOSE-METABOLISM; CB2; RECEPTORS; WHITE-MATTER; HUMAN BRAIN; PET; DISEASE;
D O I
10.1111/j.1468-1331.2010.03154.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Multiple Sclerosis (MS) is traditionally considered as a central nervous system (CNS) white matter inflammatory disease. However, recent studies have focused on the neurodegenerative aspects of the disease, which occur early in the pathological process, providing an opportunity for therapeutic intervention and application of neuroprotective strategies. The relationship between neural inflammation and cell death remains controversial. The recent development of new radiolabelled ligands provides positron emission tomography (PET) imaging with a role for studying early aspects of the MS pathology. Methods: We provide an overview of current PET research in MS, particularly focussing on possible applications of new radioligands for studying inflammation and neurodegenerative processes. Results: Pathological aspects of neuroinflammation, axonal degeneration and neuronal repair may be explored in vivo with selective PET tracers. Specific radioligands for the cannabinoid system may be applied in MS research to understand the role of this neurotransmitter system in the pathogenesis of the disease. Conclusions: PET imaging represents a promising tool for elucidating controversial aspects of MS pathology and for the assessment of selective and potentially neuroprotective therapies.
引用
收藏
页码:226 / 231
页数:6
相关论文
共 52 条
[1]  
Bakshi Rohit, 2005, NeuroRx, V2, P277, DOI 10.1007/BF03206672
[2]   The peripheral benzodiazepine binding site in the brain in multiple sclerosis -: Quantitative in vivo imaging of microglia as a measure of disease activity [J].
Banati, RB ;
Newcombe, J ;
Gunn, RN ;
Cagnin, A ;
Turkheimer, F ;
Heppner, F ;
Price, G ;
Wegner, F ;
Giovannoni, G ;
Miller, DH ;
Perkin, GD ;
Smith, T ;
Hewson, AK ;
Bydder, G ;
Kreutzberg, GW ;
Jones, T ;
Cuzner, ML ;
Myers, R .
BRAIN, 2000, 123 :2321-2337
[3]   Relapsing and remitting multiple sclerosis: Pathology of the newly forming lesion [J].
Barnett, MH ;
Prineas, JW .
ANNALS OF NEUROLOGY, 2004, 55 (04) :458-468
[4]   Cannabinoid CB1 and CB2 receptors and fatty acid amide hydrolase are specific markers of plaque cell subtypes in human multiple sclerosis [J].
Benito, Cristina ;
Romero, Juan Pablo ;
Tolon, Rosa Maria ;
Clemente, Diego ;
Docagne, Fabian ;
Hillard, Cecilia J. ;
Guaza, Camen ;
Romero, Julian .
JOURNAL OF NEUROSCIENCE, 2007, 27 (09) :2396-2402
[5]   A longitudinal study of cerebral glucose metabolism, MRI, and disability in patients with MS [J].
Blinkenberg, M ;
Jensen, CV ;
Holm, S ;
Paulson, OB ;
Sorensen, PS .
NEUROLOGY, 1999, 53 (01) :149-153
[6]   Microglia-mediated neurotoxicity: uncovering the molecular mechanisms [J].
Block, Michelle L. ;
Zecca, Luigi ;
Hong, Jau-Shyong .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (01) :57-69
[7]   Lack of correlation between cortical demyelination and white matter pathologic changes in multiple sclerosis [J].
Bo, Lars ;
Geurts, Jeroen J. G. ;
van der Valk, Paul ;
Polman, Chris ;
Barkhof, Frederik .
ARCHIVES OF NEUROLOGY, 2007, 64 (01) :76-80
[8]   [18F]MK-9470, a positron emission tomography (PET) tracer for in vivo human PET brain imaging of the cannabinoid-1 receptor [J].
Burns, H. Donald ;
Van Laere, Koen ;
Sanabria-Bohorquez, Sandra ;
Hamill, Terence G. ;
Bormans, Guy ;
Eng, Wai-si ;
Gibson, Ray ;
Ryan, Christine ;
Connolly, Brett ;
Patel, Shil ;
Krause, Stephen ;
Vanko, Amy ;
Van Hecken, Anne ;
Dupont, Patrick ;
De Lepeleire, Inge ;
Rothenberg, Paul ;
Stoch, S. Aubrey ;
Cote, Josee ;
Hagmann, William K. ;
Jewell, James P. ;
Lin, Linus S. ;
Liu, Ping ;
Goulet, Mark T. ;
Gottesdiener, Keith ;
Wagner, John A. ;
de Hoon, Jan ;
Mortelmans, Luc ;
Fong, Tung M. ;
Hargreaves, Richard J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (23) :9800-9805
[9]   Maturation-dependent sensitivity of oligodendrocyte lineage cells to apoptosis: implications for normal development and disease [J].
Butts, B. D. ;
Houde, C. ;
Mehmet, H. .
CELL DEATH AND DIFFERENTIATION, 2008, 15 (07) :1178-1186
[10]   Disease progression after bone marrow transplantation in a model of multiple sclerosis is associated with chronic microglial and glial progenitor response [J].
Cassiani-Ingoni, Riccardo ;
Muraro, Paolo A. ;
Magnus, Tim ;
Reichert-Scrivner, Susan ;
Schmidt, Jens ;
Huh, Jaebong ;
Quandt, Jacqueline A. ;
Bratincsak, Andras ;
Shahar, Tal ;
Eusebi, Fabrizio ;
Sherman, Larry S. ;
Mattson, Mark P. ;
Martin, Roland ;
Rao, Mahendra S. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2007, 66 (07) :637-649