# Low‐Intensity Pulsed Ultrasound Alleviation of LPS‐Induced Depression‐Like Behavior via Microglial P2X4R Inhibition and BDNF/TrkB Pathway Activation

## TL;DR

Low-intensity pulsed ultrasound reduces depression-like behavior in mice by targeting microglial P2X4R and boosting BDNF/TrkB signaling.

## Contribution

This study reveals a novel mechanism by which LIPUS alleviates depression through P2X4R inhibition and BDNF/TrkB activation.

## Key findings

- LIPUS reduces LPS-induced depression-like behavior and neuroinflammation in mice.
- LIPUS suppresses microglial activation and pro-inflammatory cytokines via P2X4R downregulation.
- LIPUS activates the BDNF/TrkB pathway and reduces neuronal apoptosis in the hippocampus.

## Abstract

Low‐intensity pulsed ultrasound (LIPUS) shows promising anti‐inflammatory and neuroprotective effects for different types of neurological disorders. This study aims to investigate the therapeutic effects of LIPUS on LPS‐induced depression‐like behavior and neuroinflammation and to elucidate the underlying molecular mechanisms.

A depressive mouse model is established by intraperitoneal injection of LPS (1.0 mg/kg/day for 7 days). LIPUS is applied to the hippocampal region (30 min/day). Behavioral assessments include the open field test (OFT), forced swim test (FST), and tail suspension test (TST). Molecular analyses, including Western blotting, immunofluorescence, and qPCR, are performed to evaluate the expression of P2X4R, IBA1, inflammatory cytokines (IL‐1β, IL‐6, TNF‐α), BDNF/TrkB signaling pathway, and apoptosis‐related proteins (Bax, Bcl‐2). The involvement of P2X4R is further examined using ivermectin (IVM), a selective P2X4R agonist.

LIPUS significantly alleviates the LPS‐induced depression‐like behavior, suppresses hippocampal pro‐inflammatory cytokine expression, inhibits microglial activation, and reduces neuronal apoptosis. Mechanistically, LIPUS downregulates P2X4R and IBA1, upregulates BDNF protein levels and TrkB phosphorylation, and modulates the Bax and Bcl‐2 expression. Co‐localization studies confirm that P2X4R is predominantly expressed in microglia, and LIPUS markedly reduces the overlap. Notably, the anti‐inflammatory, neuroprotective, and antidepressant effects of LIPUS are significantly attenuated by IVM, highlighting the critical role of P2X4R suppression in mediating therapeutic effects.

LIPUS mitigates LPS‐induced neuroinflammation, neuronal apoptosis, and depression‐like behavior by targeting microglial P2X4R and activating the BDNF/TrkB pathway. The findings provide mechanistic insights and demonstrate that LIPUS is a promising non‐pharmacological intervention for depression, underscoring the translational potential of P2X4R as a therapeutic target.

LIPUS alleviates LPS‐induced depressive‐like behavior by suppressing microglial P2X4R in the hippocampus. P2X4R downregulation restores BDNF/TrkB signaling, thereby reducing microglial activation, pro‐inflammatory cytokine release, and neuronal apoptosis.