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德克索鲁比诱导的心脏毒性:探讨分子病原和基于植物化合物的治疗策略
Harshal D Pawar1, Sanskruti Dusane1, Tanisha Sharma1
1Department of Pharmacology, Shri Vile Parle Kelavani Mandal's Institute of Pharmacy, Dhule 424001, Maharashtra, India.
Current pharmaceutical design
|November 4, 2025
概括
植物化合物可以通过向多个分子通路来防止多克索鲁比诱导的心脏毒性 (DIC). 需要进一步的研究和临床试验来确认它们的有效性,并优化它们在癌症治疗中的使用.
科学领域:
- 心脏病学 心脏病学
- 药理学 药理学是指药理学的学科.
- 在瘤学瘤学.
背景情况:
- 多克索鲁比 (DOX) 是一种重要的化疗药物,但其使用受到剂量依赖性心脏毒性的限制.
- 了解DOX诱导心脏毒性 (DIC) 的分子机制对于开发保护策略至关重要.
研究的目的:
- 系统地审查DIC背后的分子机制.
- 评估植物衍生生物活性化合物对DIC的心脏保护潜力.
主要方法:
- 在PubMed,Scopus和Web of Science (过去二十年) 的综合文献搜索.
- 专注于实验和临床前研究,研究DIC分子通路和植物化学干预.
主要成果:
- DIC涉及氧化应激,线粒体损伤,亡,自性损伤和改变的信号通路 (例如AMPK,Nrf2).
- 植物化学物质 (黄类,多类,类) 通过调节氧化还原平衡,线粒体功能和亡,显示出显著的心脏保护作用.
- 这些化合物向多种病理机制,在临床前模型中显示出前景.
结论:
- 植物衍生化合物显示了缓解DIC的潜力,并得到了临床前数据的支持.
- 挑战包括生物可用性差,缺乏标准化剂量和有限的临床数据.
- 进一步的翻译研究,新型的输送系统和临床试验对于临床应用至关重要.
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