Modulation of HMGB1-mediated neuroinflammation and synaptic plasticity by ethyl pyruvate reduces methamphetamine reward and motivation in male rats

The HMGB1 inhibitor EP attenuated METH reinforcement and motivation by targeting the IL to disrupt a neuroinflammatory cascade, prevent apoptosis and pyroptosis, and restore synaptic homeostasis. These findings identify HMGB1 inhibitors as a novel therapeutic target for mitigating the neuropathology and motivational drive underlying METH addiction.

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Publication Details

Journal
Brain Behavior and Immunity
Published
2026-02-10
DOI
https://doi.org/10.1016/j.bbi.2026.106481
Primary Topic
Advanced Glycation End Products research
Type
article
Field-Weighted Citation Impact
0.00
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article

Modulation of HMGB1-mediated neuroinflammation and synaptic plasticity by ethyl pyruvate reduces methamphetamine reward and motivation in male rats

Xuyan Huang, Huifen Liu, Wenhua Zhou, Yiying Zhou et al.
Brain Behavior and Immunity
Advanced Glycation End Products research
article

Modulation of HMGB1-mediated neuroinflammation and synaptic plasticity by ethyl pyruvate reduces methamphetamine reward and motivation in male rats

Xuyan Huang, Huifen Liu, Wenhua Zhou, Yiying Zhou, Manqing Wu, Huizhen Liu, Tingting Wu, Baobao Shi, Shanshan Chen, Yuting Wang, Fangmin Wang, Miaojun Lai, Zhongyu Zhang
article en

Abstract

The HMGB1 inhibitor EP attenuated METH reinforcement and motivation by targeting the IL to disrupt a neuroinflammatory cascade, prevent apoptosis and pyroptosis, and restore synaptic homeostasis. These findings identify HMGB1 inhibitors as a novel therapeutic target for mitigating the neuropathology and motivational drive underlying METH addiction.

Brain Behavior and ImmunityVol. 134
North China University of Science and Technology (CN), Shanghai Jiao Tong University (CN), Shanghai Mental Health Center (CN), Ningbo Medical Center Lihuili Hospital (CN), Ningbo Kangning Hospital (CN)
Good health and well-being
Openalex Percentile: Top 59%
Advanced Glycation End Products research
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