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肠道微生物群在多克索鲁比诱导心脏毒性的作用:从致病源到相关干预措施
Chao Huang1, Xiaoxia Li2, Hanqing Li3
1Department of Cardiology, The Affiliated Hospital of Qingdao University, No. 59 Haier Road, Qingdao, Shandong, 266100, China.
Journal of translational medicine
|May 9, 2024
概括
多克索鲁比 (DOX) 化疗会导致心脏损伤 (心脏毒性),与肠道细菌的变化有关. 本综述探讨了肠道微生物群失生症如何影响DOX诱导的心脏毒性 (DIC),并讨论了微生物向疗法.
科学领域:
- 心脏病学 心脏病学
- 微生物学 微生物学
- 药理学 药理学是指药理学的学科.
背景情况:
- doxorubicin (DOX) 是一种有效的抗癌药物,但由于严重的心脏毒性,其使用受到限制.
- 新出现的证据将肠道微生物失调与DOX诱导心脏毒性 (DIC) 的进展联系起来.
- 肠道-微生物群-心脏 (GMH) 轴与DIC有关,但机制尚不清楚.
研究的目的:
- 阐明连接肠道微生物群失调和DIC的机制.
- 为DIC的病理生理学提供新的见解.
- 总结DIC的微生物向治疗干预措施.
主要方法:
- 对肠道微生物群,DOX和心脏毒性现有文献的综述.
- 在DIC.中分析肠道-微生物群-心脏 (GMH) 轴.
- 综合了各种微生物向干预措施的数据.
主要成果:
- 肠道微生物群失生症在DIC的发展和进展中起着重要作用.
- 特定的微生物代谢物和改变的肠道功能有助于心脏毒性.
- 针对肠道微生物群的各种干预措施显示出缓解DIC的潜力.
结论:
- 肠道微生物群失调是DOX诱导心脏毒性的关键因素.
- 针对微生物的治疗方法为预防和治疗DIC提供了有希望的途径.
- 对GMH轴的进一步研究对于DIC患者的临床应用至关重要.
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