|
English
|
正體中文
|
简体中文
|
Items with full text/Total items : 12145/12927 (94%)
Visitors : 848421
Online Users : 1040
|
|
|
Loading...
|
Please use this identifier to cite or link to this item:
http://ir.nhri.org.tw/handle/3990099045/16245
|
Title: | Very low-intensity ultrasound facilitates glymphatic influx and clearance via modulation of the TRPV4-AQP4 pathway |
Authors: | Wu, CH;Liao, WH;Chu, YC;Hsiao, MY;Kung, Y;Wang, JL;Chen, WS |
Contributors: | Institute of Biomedical Engineering and Nanomedicine |
Abstract: | Recently, the glymphatic system has been proposed as a mechanism for waste clearance from the brain parenchyma. Glymphatic dysfunction has previously been shown to be associated with several neurological diseases, including Alzheimer's disease, traumatic brain injury, and stroke. As such, it may serve as an important target for therapeutic interventions. In the present study, very low-intensity ultrasound (VLIUS) (center frequency, 1 MHz; pulse repetition frequency, 1 kHz; duty factor, 1%; spatial peak temporal average intensity [I(spta)] = 3.68 mW cm(2); and duration, 5 min) is found to significantly enhance the influx of cerebrospinal fluid tracers into the paravascular spaces of the brain, and further facilitate interstitial substance clearance from the brain parenchyma, including exogenous β-amyloid. Notably, no evidence of brain damage is observed following VLIUS stimulation. VLIUS may enhance glymphatic influx via the transient receptor potential vanilloid-4-aquaporin-4 pathway in astrocytes. This mechanism may provide insights into VLIUS-regulated glymphatic function that modifies the natural course of central nervous system disorders related to waste clearance dysfunction. |
Date: | 2024-11-04 |
Relation: | Advanced Science. 2024 Nov 04;Article in Press. |
Link to: | http://dx.doi.org/10.1002/advs.202401039 |
Appears in Collections: | [其他] 期刊論文
|
Files in This Item:
File |
Description |
Size | Format | |
PUB39494466.pdf | | 15105Kb | Adobe PDF | 18 | View/Open |
|
All items in NHRI are protected by copyright, with all rights reserved.
|