| 總結: | <b>Background/Objectives:</b> Fibroblast activation protein (FAP) has gained tremendous traction as a target for tumor imaging and cancer treatment, while also playing a key role in fibrosis. Our study aimed to evaluate [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>.SA.FAPi for PET imaging of replacement fibrosis following myocardial infarction (MI) or interstitial fibrosis associated with hypertrophy. <b>Methods</b>: MI or transverse aortic constriction (TAC)-induced hypertrophy was induced in C57BL/6 mice, with sham-operated animals serving as controls. At multiple time points during disease progression (1, 2, and 6 weeks post-surgery), [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>.SA.FAPi PET/CT scans were performed, followed by ex vivo investigations. Additionally, in vitro cell uptake experiments simulating hypertrophy were conducted. <b>Results</b>: Cardiac uptake of [<sup>68</sup>Ga]Ga-DATA5m.SA.FAPi significantly increased two weeks after MI induction (MI: 2.1 ± 0.2%ID/g, <i>n</i> = 7 vs. SHAM: 1.1 ± 0.2%ID/g, <i>n</i> = 5; <i>p</i> = 0.002), confirmed by ex vivo autoradiography. No significant difference was observed at six weeks post-MI (MI: 1.1 ± 0.1%ID/g, <i>n</i> = 4 vs. SHAM: 0.8 ± 0.0%ID/g, <i>n</i> = 3), indicating infarct healing completion. In contrast, TAC mice showed increased uptake after six weeks (TAC: 1.8 ± 0.2%ID/g, <i>n</i> = 6; <i>p</i> = 0.007), related to interstitial fibrosis progression. Consistently, high-stretched cardiac fibroblasts demonstrated a higher uptake compared to low-stretched conditioned ones, suggesting the stretch mediates regulation of FAP. <b>Conclusions</b>: This study demonstrated the efficacy of [<sup>68</sup>Ga]Ga-DATA<sup>5m</sup>.SA.FAPi for longitudinal imaging of cardiac fibrosis in response to different cardiac injuries. In vivo FAP imaging during cardiac remodeling may serve as a valuable tool for diagnosing and predicting disease progression, ultimately aiding in the clinical management of patients.
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