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Thiorphan improves motor function after spinal cord injury by inhibiting neuronal ferroptosis in female mice.

Created on 17 Aug 2026

Authors

Yuyu Liu, Nan Xia, Huimin Qiu, Dake Wang, Jianye Li, Guoqiang Zhang, Wenxia Liu, Lailai Wei

Published in

Biochemical and biophysical research communications. Volume 833. Pages 154437. Aug 13, 2026. Epub Aug 13, 2026.

Abstract

Spinal cord injury (SCI) causes severe motor dysfunction, yet effective pharmacological treatments remain scarce, underscoring the urgent need for novel therapeutic agents. Thiorphan has shown therapeutic potential in central nervous system disorders due to its ability to modulate oxidative stress and neuroinflammation; however, its role in SCI remains largely unknown. Therefore, we selected Thiorphan and investigated whether it improves motor recovery after SCI. Our study found Thiorphan treatment significantly enhanced motor function, as evidenced by increased BMS scores (increased from 2.2 ± 0.8 to 4.9 ± 0.6), improved performance in the Oblique Board Test (improved by approximately 1.7-fold) and footprint assay, and prolonged latency of fall. Histological and biochemical analyses revealed that Thiorphan ameliorated SCI-induced pathological changes, reduced iron accumulation (about 2.8-fold), MDA and 4-HNE levels (all exceeded 2-fold), and restored GPX4 expression (improved by approximately 3.2-fold). Mechanistically, Thiorphan reversed the SCI-induced downregulation of Nrf2 in neurons. Moreover, neuron-specific Nrf2 deletion abolished the protective effects of Thiorphan, including the improvements in survival, motor function, and neuronal viability. Collectively, these results demonstrate that Thiorphan improves motor function after SCI by inhibiting neuronal ferroptosis through the reversal of Nrf2 reduction, highlighting its potential as a therapeutic agent for SCI.

PMID:
42604632
Bibliographic data and abstract were imported from PubMed on 17 Aug 2026.

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