Department of Ultrasound, The Second Medical Center, Chinese People's Liberation Army (PLA) General Hospital, Beijing, China (mainland).
Med Sci Monit. 2020 Jun 30;26:e924832. doi: 10.12659/MSM.924832.
BACKGROUND The aim of this study was to explore the effect and duration of 2-dimensional shear wave elastography (2D-SWE) irradiation on the expression of brain-derived neurotrophic factor (BDNF) in the brains of neonatal mice and to preliminarily investigate whether its mechanism is neuronal apoptosis. MATERIAL AND METHODS Neonatal mice (within 48 hours of birth) were subjected to 2D-SWE irradiation of the brain for 10 minutes (group S1), 20 minutes (group S2), and 30 minutes (group S3). The mice were sacrificed immediately after irradiation or 24 hours after irradiation. Brains were collected for real-time polymerase chain reaction (RT-PCR) and western blot experiments to determine the expression of BDNF in each group. TdT-mediated dUTP nick-end labeling (TUNEL) was performed to observe neuronal apoptosis in the brain. RESULTS The results of PCR and western blots from the brains of neonatal mice that were sacrificed immediately after irradiation show that S1, S2, and S3 were significantly different from those in the control group. The PCR and western blot results of brain tissues from neonatal mice sacrificed at 24 hours after irradiation showed that there was no significant difference between the S1, S2, S3, and control groups. The results of TUNEL experiments showed that there was no statistically significant difference in the number of apoptotic neurons between the S1, S2, S3, and control groups. CONCLUSIONS 2D-SWE irradiation of neonatal mice for more than 10 minutes downregulated the expression of BDNF. This effect disappeared within 24 hours after the irradiation, and the 2D-SWE scan seemed not to induce neuronal apoptosis.
本研究旨在探讨二维剪切波弹性成像(2D-SWE)照射对新生小鼠大脑中脑源性神经营养因子(BDNF)表达的影响,并初步探讨其机制是否为神经元凋亡。
新生小鼠(出生后 48 小时内)接受大脑 2D-SWE 照射 10 分钟(S1 组)、20 分钟(S2 组)和 30 分钟(S3 组)。照射后立即或照射后 24 小时处死小鼠,取脑进行实时聚合酶链反应(RT-PCR)和 Western blot 实验,以确定各组 BDNF 的表达。末端转移酶介导的 dUTP 缺口末端标记(TUNEL)法观察脑内神经元凋亡。
立即处死照射后新生小鼠脑内 PCR 和 Western blot 结果显示,S1、S2 和 S3 与对照组相比差异有统计学意义。照射后 24 小时处死新生小鼠脑组织的 PCR 和 Western blot 结果显示,S1、S2、S3 与对照组之间无显著差异。TUNEL 实验结果显示,S1、S2、S3 与对照组之间凋亡神经元数量无统计学差异。
2D-SWE 照射新生小鼠超过 10 分钟会下调 BDNF 的表达。这种作用在照射后 24 小时内消失,2D-SWE 扫描似乎不会诱导神经元凋亡。