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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,
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          氧化应激与 JNK/Mff 信号通路之间的关系以及 UTI 能
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          否通过其他信号通路来发挥心肌保护作用尚未被完全
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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 ·
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