Abstract
Parkinson's disease (PD) is characterized by the decrease of dopamine (DA) production and release in the substantia nigra and striatum regions of the brain. Transcranial ultrasound has been exploited recently for neuromodulation of the brain in a number of fields. We have stimulated DA release in PC12 cells using low-intensity continuous ultrasound (0.1 W/cm2 − 0.3 W/cm2, 1 MHz), 12 h after exposure at 0.2 W/cm2, 40 s, the amount of DA content eventually increased 78.5% (p = 0.004). After 10-day ultrasonic treatment (0.3 W/cm2, 5 min/d), the DA content in the striatum of PD mice model restored to 81.07% of the control (vs 43.42% in the untreated PD mice model). In addition to this the locomotion activity was restored to the normal level after treatment. We suggest that the low intensity ultrasound-induced DA release can be attributed to a combination of neuron regeneration and improved membrane permeability produced by the mechanical force of ultrasound. Our study indicates that the application of transcranial ultrasound applied below FDA limits, could provide a candidate for relatively safe and noninvasive PD therapy through an amplification of DA levels and the stimulation of dopaminergic neuron regeneration without contrast agents.
| Original language | English |
|---|---|
| Article number | 104955 |
| Number of pages | 10 |
| Journal | Ultrasonics Sonochemistry |
| Volume | 63 |
| Early online date | 31 Dec 2019 |
| DOIs | |
| Publication status | Published - May 2020 |
Bibliographical note
Publisher Copyright:© 2020 Elsevier B.V.
Keywords
- Dopamine
- Low intensity ultrasound
- Mechanical force
- MPTP-induced mice model
- Parkinson's disease
- PC12
ASJC Scopus subject areas
- Environmental Chemistry
- Chemical Engineering (miscellaneous)
- Radiology Nuclear Medicine and imaging
- Acoustics and Ultrasonics
- Organic Chemistry
- Inorganic Chemistry
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