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UTI 后,JNK、Drp1 蛋白的表达被抑制得更明显,心肌促 p38-MAPK,and JAK1/STAT3/NF-κB signals[J]. Naunyn
凋亡蛋白和细胞凋亡指数的下降也更显著,但UTI的效 Schmiedebergs Arch Pharmacol,2024,397(8):5649-
应强度是否与剂量存在潜在关联尚需通过多剂量实验 5662.
予以验证。 [10] SAMAVATI I,RANJBAR A,HADDADI R. Cardioprotec‐
综上所述,UTI 可改善 CP 诱导的心肌损伤,其潜在 tive effect of vitamin D3 on cisplatin-induced cardiotoxi-
city in male mice:role of oxidative stress[J]. Naunyn
机制可能与拮抗氧化应激和抑制 JNK/Mff 信号通路有
Schmiedebergs Arch Pharmacol,2024,397(7):4761-
关。这为UTI的临床应用提供了基础实验数据。但是,
4769.
氧化应激与 JNK/Mff 信号通路之间的关系以及 UTI 能
[11] KARASAWA T,STEYGER P S. An integrated view of
否通过其他信号通路来发挥心肌保护作用尚未被完全
cisplatin-induced nephrotoxicity and ototoxicity[J]. Toxi‐
阐明,有待后续研究进一步完善。
col Lett,2015,237(3):219-227.
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cisplatin-induced heart toxicity by suppressing oxidative (收稿日期:2024-10-15 修回日期:2025-03-06)
stress and inflammation and modulating Nrf2,TLR4/ (编辑:张元媛)
中国药房 2025年第36卷第8期 China Pharmacy 2025 Vol. 36 No. 8 · 925 ·