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Yang, Han, Ye, Fei, Chen, Liuxu, Yang, Linyu, Kang, Jianping. (1404). EGCG attenuated spinal cord injury by inhibiting ferroptosis via activation of HMOX1 expression and suppression of HIF-1 signaling pathway. , 28(6), 799-807. doi: 10.22038/ijbms.2025.82651.17864
Han Yang; Fei Ye; Liuxu Chen; Linyu Yang; Jianping Kang. "EGCG attenuated spinal cord injury by inhibiting ferroptosis via activation of HMOX1 expression and suppression of HIF-1 signaling pathway". , 28, 6, 1404, 799-807. doi: 10.22038/ijbms.2025.82651.17864
Yang, Han, Ye, Fei, Chen, Liuxu, Yang, Linyu, Kang, Jianping. (1404). 'EGCG attenuated spinal cord injury by inhibiting ferroptosis via activation of HMOX1 expression and suppression of HIF-1 signaling pathway', , 28(6), pp. 799-807. doi: 10.22038/ijbms.2025.82651.17864
Yang, Han, Ye, Fei, Chen, Liuxu, Yang, Linyu, Kang, Jianping. EGCG attenuated spinal cord injury by inhibiting ferroptosis via activation of HMOX1 expression and suppression of HIF-1 signaling pathway. , 1404; 28(6): 799-807. doi: 10.22038/ijbms.2025.82651.17864

EGCG attenuated spinal cord injury by inhibiting ferroptosis via activation of HMOX1 expression and suppression of HIF-1 signaling pathway

Iranian Journal of Basic Medical Sciences
مقاله 13، دوره 28، شماره 6، شهریور 2025، صفحه 799-807    اصل مقاله (758.26 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2025.82651.17864
نویسندگان
Han Yang؛ Fei Ye؛ Liuxu Chen؛ Linyu Yang؛ Jianping Kang*
Department of Orthopaedics, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, P.R. China
چکیده
Objective(s): Epigallocatechin gallate (EGCG) exhibits various biological effects, including antiviral, anti-inflammatory, cardioprotective, and lipid-regulating properties. This study aims to investigate the therapeutic effects and mechanisms of EGCG in spinal cord injury (SCI).
Materials and Methods: TThe bioinformatic databases were used to screen therapeutic target genes for drugs against SCI. Component-Target-Disease networks were constructed with Cytoscape software, and inter-target interactions were analyzed using the String database. Additionally, KEGG pathway enrichment analyses were conducted on the identified target genes. SCI was evaluated by detecting inflammation-related factors, H&E staining, and immunohistochemistry. Furthermore, ROS and JC1 staining were performed on HT22 cells subjected to various treatments. Molecular mechanisms were investigated using western blot and qRT-PCR analyses. 
Results: Forty-four overlapping genes were identified as potential targets, with HMOX1, GPX-4, and HIF-1A emerging as central hub genes. Key pathways associated with these targets included Ferroptosis and HIF-1 signaling. In vivo studies demonstrated that EGCG effectively promotes motor function recovery and reduces the expression of proteins and genes such as IL-1β, IL-6, HIF-1α, and 4HNE. In vitro experiments showed that EGCG decreases ROS and intracellular lipid ROS levels in HT22 cells while increasing GPX-4 and HMOX1 expression to inhibit ferroptosis and HIF-1 signaling pathways. 
Conclusion: Our findings reveal a significant new mechanism by which EGCG can reduce SCI through the inhibition of ferroptosis, facilitated by the activation of HMOX1 expression and the down-regulation of the HIF-1 signaling pathway. This suggests its potential as a therapeutic option for this condition.
کلیدواژه‌ها
Epigallocatechin gallate؛ Ferroptosis؛ HIF-1؛ HMOX1؛ Spinal cord injury
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