A Metabolic Intravascular Platform to Study FDG Uptake in Vascular Injury.
A Metabolic Intravascular Platform to Study FDG Uptake in Vascular Injury.
复制标题
用于研究血管损伤中 FDG 摄取的代谢血管内平台。
DOI:
10.1007/s13239-020-00457-z
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发表时间:
2020
影响因子:
1.8
通讯作者:
Rodriguez-Porcel,M
中科院分区:
文献类型:
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作者:
Franchi,F;Olthoff,M;Krier,J;Noble,C;Al-Hijji,M;Ramaswamy,V;Witt,T;Burke,M;Benscoter,M;Lerman,A;Sandhu,GS;Rodriguez-Porcel,M
PurposeMetabolic alterations underlie many pathophysiological conditions, and their understanding is critical for the development of novel therapies. Although the assessment of metabolic changesin vivohas been historically challenging, recent developments in molecular imaging have allowed us to study novel metabolic research concepts directly in the living subject, bringing us closer to patients. However, in many instances, there is need for sensors that are in close proximity to the organ under investigation, for example to study vascular metabolism.MethodsIn this study, we developed and validated a metabolic detection platform directly in the living subject under an inflammatory condition. The signal collected by a scintillating fiber is amplified using a photomultiplier tube and decodified by an in-house tunable analysis platform. Forin vivotesting, we based our experiments on the metabolic characteristics of macrophages, cells closely linked to inflammation and avid for glucose and its analog18F-fluorodeoxyglucose (18F-FDG). The sensor was validated in New Zealand rabbits, in which inflammation was induced by either a) high cholesterol (HC) diet for 16 weeks or b) vascular balloon endothelial denudation followed by HC diet.ResultsThere was no difference in weight, hemodynamics, blood pressure, or heart rate between the groups. Vascular inflammation was detected by the metabolic sensor (Inflammation: 0.60 ± 0.03 AU vs. control: 0.48 ± 0.03 AU,p= 0.01), even though no significant inflammation/atherosclerosis was detected by intravascular ultrasound, underscoring the high sensitivity of the system. These findings were confirmed by the presence of macrophages on ex vivo aortic tissue staining.ConclusionIn this study, we validated a tunable very sensitive metabolic sensor platform that can be used for the detection of vascular metabolism, such as inflammation. This sensor can be used not only for the detection of macrophage activity but, with alternative probes, it could allow the detection of other pathophysiological processes.