4.6 Article

Focused ultrasound neuromodulation of the spleen activates an anti-inflammatory response in humans

Journal

BRAIN STIMULATION
Volume 16, Issue 3, Pages 703-711

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.brs.2023.04.003

Keywords

Inflammation; Cytokines; Ultrasound; Spleen; Cholinergic anti-inflammatory pathway; Bioelectronic medicine

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Focused ultrasound stimulation (FUS) has been found to be effective in noninvasive modulation of inflammatory response in humans. The study demonstrates that both continuously swept and focused pulsed ultrasound can suppress inflammation without adverse effects, regardless of the ultrasound energy level and target site, providing potential implications for noninvasive treatment of inflammatory disorders.
Focused ultrasound stimulation (FUS) activates mechanosensitive ion channels and is emerging as a method of noninvasive neuromodulation. In preclinical studies, FUS of the spleen (sFUS) activates an anti-inflammatory neural pathway which suppresses acute and chronic inflammation. However, the relevance of sFUS for regu-lating inflammatory responses in humans is unknown. Here, we used a modified diagnostic ultrasound imaging system to target the spleen of healthy human subjects with 3 min of continuously swept or stationary focused pulsed ultrasound, delivered at three different energy levels within allowable safety exposure limits. Potential anti-inflammatory effects of sFUS were assessed by measuring sFUS-elicited changes in endotoxin-induced tumor necrosis factor (TNF) production in whole blood samples from insonified subjects. We found that stimulation with either continuously swept or focused pulsed ultrasound has an anti-inflammatory effect: sFUS lowers TNF production for >2 h, with TNF returning to baseline by 24 h following sFUS. This response is independent of anatomical target (i.e., spleen hilum or parenchyma) or ultrasound energy level. No clinical, biochemical, or hematological parameters are adversely impacted. This is the first demonstration that sFUS suppresses the normal inflammatory response in humans, with potential implications for noninvasive bioelectronic therapy of inflammatory disorders.

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