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  4. Cerium Oxide Nanoparticles Alleviate Neuropathic Pain by Modulating Macrophage Polarization in a Rat SCI Model

Cerium Oxide Nanoparticles Alleviate Neuropathic Pain by Modulating Macrophage Polarization in a Rat SCI Model

Journal of Pain Research, 2022 · DOI: https://doi.org/10.2147/JPR.S371789 · Published: October 25, 2022

Spinal Cord InjuryPain ManagementGenetics

Simple Explanation

Chronic neuropathic pain (NP) frequently occurs after spinal cord injury (SCI) but lacks effective therapeutic options in the clinic. Numerous evidence indicates the involvement of macrophages activation in the NP, and the modulation of macrophages is promising for NP treatment. Macrophages are the main immune cells and have a significant function in mediating neuroinflammation. They are highly plastic and can polarize into the classical phenotype (M1) and the alternative phenotype (M2). Cerium oxide nanoparticles (CONPs) are redox-active rare earth nanomaterials. It has shown many fascinating biological properties such as anti-inflammation, anti-oxidation, anti-tumor, as well as free radical scavenging, and attracts increased interest for therapeutic application.

Study Duration
4 Weeks
Participants
Adult female Wistar rats (180–250 g)
Evidence Level
Not specified

Key Findings

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    The synthesized CONPs were 6.8 ± 0.5 nm in size, presenting a cubic morphology.
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    Intrathecal injection of CONPs could significantly increase the mechanical PWT and thermal PWL of SCI rats.
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    Molecular experiments results showed the expression of M2 macrophage-related markers (CD206, Arg-1, IL-10) were significantly increased, while that of M1 macrophage-related markers (CD86, TNF-α, iNOS) were downregulated after CONPs treatment.

Research Summary

Our study suggests that CONPs can relive the NP following SCI by promoting M2 macrophages polarization, which provides a novel insight for the treatment of SCI induced NP. Many researchers in the SCI region mainly focused on neuron regeneration and motor function recovery while ignoring the assessment of NP. However, NP is frequently complicated with SCI and usually causes depression, and sleep disturbance and seriously compromises patients’ life quality. Overall, the present study demonstrated that CONPs could alleviate neuropathic pain after rats’ SCI by promoting macrophage polarization towards M2 phenotypes.

Practical Implications

Therapeutic Potential

CONPs hold promise as a novel therapeutic agent for alleviating neuropathic pain associated with spinal cord injury.

Macrophage Modulation

The study highlights the importance of modulating macrophage polarization as a strategy for treating SCI-induced NP.

Motor Function Improvement

CONPs treatment also led to improved motor function recovery in the SCI rat model, suggesting broader benefits.

Study Limitations

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