期刊
NUCLEAR MEDICINE AND BIOLOGY
卷 40, 期 7, 页码 906-911出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2013.06.008
关键词
[C-11]PBR28; TSPO; Systemic adjuvant arthritis; Carrageenan-induced inflammation macrophages, RAW 264.7 cells
资金
- National Institutes of Health (NIH) [R01 AR060350, R01 AR055179]
Introduction: [C-11] PBR28 binding to translocator protein (TSPO) was evaluated for imaging of acute and chronic inflammation using two established rat models. Methods: Acute inflammation was induced by local carrageenan injection into the paw of Fisher 344 rats (model A). T-cell mediated adjuvant arthritis was induced by heat-inactivated Mycobacterium butyricum injection in Lewis rats (model B). Micro-PET scan was performed after injection of approximately 35 MBq [C-11]PBR28. In model A. volumes of interest (VOls) were defined in the paw of Fisher 344 rats (n=6) with contralateral sham treatment as control. For model B, VOls were defined in the tail, sacroiliac joints, hips, knees and thigh muscles of M. butyricum treated animals (n=8) and compared with sham-treated controls (n=4). The peak C-11-PBR28 SUV (SUVpeak) under area under the curve (AUC(SUV)) peak, of 60-minute time-activity data were calculated. Immunohistochemistry for CD68, a macrophage stain, was performed from paw tissues. In addition, the [C-11]PBR28 cell uptake was measured in lipopolysaccharide (LPS)-stimulated and non-stimulated macrophage cultures. Results: LPS-stimulated macrophages displayed dose-dependent increased [C-11]PBR28 uptake, which was blocked by non-labeled PBR28. In both models, radiotracer uptake of treated lesions increased rapidly within minutes and displayed overall accumulative kinetics. The SW peak and AUC(SUV) of carrageenan-treated paws was significantly increased compared to controls. Also, the [C-11]PBR28 uptake ratio of carrageenan-treated vs. sham-treated paw correlated significantly with CD68 staining ratios of the same animals. In adjuvant arthritis, significantly increased [C-11]PBR28 SW peak and AUC(SUV) values were identified at the tail, knees, and sacroiliac joints, while no significant differences were identified in the lumbar spine and hips. Conclusions: Based on our initial data, [C-11]PBR28 PET appears to have potential for imaging of various inflammatory processes involving macrophage activation. (C) 2013 Elsevier Inc. All rights reserved.
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