Author: Xiaowei Huang, Lili Niu, Long Meng, Zhengrong Lin, Wei Zhou, Xiufang Liu, Jiqing Huang, Derek Abbott, Hairong Zheng
Conference/Journal: IEEE Trans Ultrason Ferroelectr Freq Control
Date published: 2020 Oct 5
Other: Volume ID: PP , Special Notes: doi: 10.1109/TUFFC.2020.3028619. , Word Count: 244
Autophagy, or cellular self-digestion, is an essential process for eliminating abnormal protein in mammalian cells. Accumulating evidence indicates that increased neuronal autophagy has a protective effect on neurodegenerative disorders. It has been reported that low-intensity pulsed ultrasound (LIPUS) can non-invasively modulate neural activity in the brain. Yet, the effect of LIPUS on neuronal autophagy is still unclear. The objective of this study was to examine whether LIPUS stimulation could induce neuronal autophagy. Primary neurons were treated by LIPUS with frequency of 0.68 MHz, pulse repetition frequency (PRF) of 500 Hz, spatial peak temporal-average intensities (ISPTA) of 70 and 165 mW/cm2. Then immunofluorescent analysis of LC3B was carried out for evaluating neuronal autophagy. Further, 0.5 MHz LIPUS was non-invasively delivered to the cortex and hippocampus of adult mice (n = 16) with PRF of 500 Hz and ISPTA of 235 mW/cm2. The LC3BII/LC3BI ratio and p62 (autophagic markers) were measured by western blot analysis. In in vitro study, the expression of LC3B in primary neurons was statistically improved after LIPUS stimulation was implemented for 4 hours (p < 0.01). With the increase of irradiation duration or acoustic intensity of LIPUS stimulation, the expression of LC3B in primary neurons was increased. Furthermore, transcranial LIPUS stimulation increased the LC3BII/LC3BI ratio (p < 0.05), and decreased the expression of p62 (p < 0.05) in the cortex and hippocampus. We concluded that LIPUS provides a safe and capable tool for activating neuronal autophagy in vitro and in vivo.
PMID: 33017285 DOI: 10.1109/TUFFC.2020.3028619