Yu Teng-Fei, Wang Kun, Yin Lu, Li Wen-Zhe, Li Chuan-Ping, Zhang Wei, Tian Jie, He Wen
Department of Ultrasound, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
CAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, China.
Neural Regen Res. 2023 Jun;18(6):1321-1324. doi: 10.4103/1673-5374.357907.
In vivo imaging of cerebral ischemia/reperfusion injury remains an important challenge. We injected porous Ag/Au@SiO bimetallic hollow nanoshells carrying anti-tropomyosin 4 as a molecular probe into mice with cerebral ischemia/reperfusion injury and observed microvascular changes in the brain using photoacoustic imaging with ultrasonography. At each measured time point, the total photoacoustic signal was significantly higher on the affected side than on the healthy side. Twelve hours after reperfusion, cerebral perfusion on the affected side increased, cerebrovascular injury worsened, and anti-tropomyosin 4 expression increased. Twenty-four hours after reperfusion and later, perfusion on the affected side declined slowly and stabilized after 1 week; brain injury was also alleviated. Histopathological and immunohistochemical examinations confirmed the brain injury tissue changes. The nanoshell molecular probe carrying anti-tropomyosin 4 has potential for use in early diagnosis of cerebral ischemia/reperfusion injury and evaluating its progression.
脑缺血/再灌注损伤的体内成像仍然是一项重大挑战。我们将携带抗原肌球蛋白4作为分子探针的多孔Ag/Au@SiO双金属中空纳米壳注射到患有脑缺血/再灌注损伤的小鼠体内,并使用超声光声成像观察大脑中的微血管变化。在每个测量时间点,患侧的总光声信号明显高于健侧。再灌注12小时后,患侧脑灌注增加,脑血管损伤加重,抗原肌球蛋白4表达增加。再灌注24小时及以后,患侧灌注缓慢下降,1周后稳定;脑损伤也得到缓解。组织病理学和免疫组织化学检查证实了脑损伤组织的变化。携带抗原肌球蛋白4的纳米壳分子探针具有用于脑缺血/再灌注损伤早期诊断及其进展评估的潜力。