Low-intensity transcranial focused ultrasound suppresses pain by modulating pain-processing brain circuits

被引:4
|
作者
Kim, Min Gon [1 ]
Yu, Kai [1 ]
Yeh, Chih-Yu [1 ]
Fouda, Raghda [2 ]
Argueta, Donovan [2 ]
Kiven, Stacy [2 ]
Ni, Yunruo [1 ]
Niu, Xiaodan [1 ]
Chen, Qiyang [3 ]
Kim, Kang [3 ,4 ]
Gupta, Kalpna [2 ]
He, Bin [1 ,5 ]
机构
[1] Carnegie Mellon Univ, Dept Biomed Engn, 5000 Forbes Ave, Pittsburgh, PA 15213 USA
[2] Univ Calif Irvine, Dept Med, Irvine, CA USA
[3] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[4] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA USA
[5] Carnegie Mellon Univ, Neurosci Inst, Pittsburgh, PA USA
关键词
SICKLE HEMOGLOBIN; STIMULATION; MICE; AGE; FREQUENCY; BETA; SEX; NEUROMODULATION; SENSITIZATION; MECHANISMS;
D O I
10.1182/blood.2023023718
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is an urgent and unmet clinical need to develop nonpharmacological interventions for chronic pain management because of the critical side effects of opioids. Low-intensity transcranial focused ultrasound (tFUS) is an emerging noninvasive neuromodulation technology with high spatial specificity and deep brain penetration. Here, we developed a tightly focused 128-element ultrasound transducer to specifically target small mouse brains using dynamic focus steering. We demonstrate that tFUS stimulation at painprocessing brain circuits can significantly alter pain-associated behaviors in mouse models in vivo. Our findings indicate that a single-session focused ultrasound stimulation to the primary somatosensory cortex (S1) significantly attenuates heat pain sensitivity in wild-type mice and modulates heat and mechanical hyperalgesia in a humanized mouse model of chronic pain in sickle cell disease. Results further revealed a sustained behavioral change associated with heat hypersensitivity by targeting deeper cortical structures (eg, insula) and multisession focused ultrasound stimulation to S1 and insula. Analyses of brain electrical rhythms through electroencephalography demonstrated a significant change in noxious heat hypersensitivity-related and chronic hyperalgesia-associated neural signals after focused ultrasound treatment. Validation of efficacy was carried out through control experiments, tuning ultrasound parameters, adjusting interexperiment intervals, and investigating effects on age, sex, and genotype in a head-fixed awake model. Importantly, tFUS was found to be safe, causing no adverse effects on motor function or the brain's neuropathology. In conclusion, the validated proof-of-principle experimental evidence demonstrates the translational potential of novel focused ultrasound neuromodulation for next-generation pain treatment without adverse effects.
引用
收藏
页码:1101 / 1115
页数:15
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