导航抗生素安全的景观:传统的方法和新兴的策略,以克服宿主核糖核酸 (RNA) 的目标外毒性
Tanya Jamal1,2, Rinni Singh1, Mukul Bajpai1
1Computational Toxicology Group, Regulatory, GLP Compliant Studies, and Computational Toxicology (REACT), CSIR-Indian Institute of Toxicology Research, Vishvigyan Bhavan, 31, Mahatma Gandhi Marg, Lucknow 226001 Uttar Pradesh, India.
ACS pharmacology & translational science
|February 19, 2026
概括
本综述探讨了抗生素如何通过与RNA相互作用来伤害宿主细胞. 它建议使用天然化合物和计算工具来开发更安全的抗生素,减少非目标效应.
科学领域:
- 药理学 药理学是指药理学的学科.
- 微生物学 微生物学
- 药物开发 药物开发
背景情况:
- 抗生素向细菌的过程,如细胞壁和蛋白质合成.
- 关于抗生素的非向毒性,特别是与宿主核酸机制的相互作用,存在着关键的知识差距.
- 了解这些意外相互作用对于有效的抗生素治疗至关重要.
研究的目的:
- 审查抗生素对宿主RNA表现出非目标效应的证据.
- 探索传统抗生素设计关于3Rs原则 (替代,减少,改进) 的局限性.
- 建议利用自然化合物和计算方法来开发更安全的抗生素.
主要方法:
- 文献综述重点关注影响宿主RNA的抗生素.
- 对传统药物设计局限性的分析.
- 探索天然化合物和用于抗生素发现的计算方法.
主要成果:
- 有证据表明,某些抗生素可以与宿主RNA相互作用,这是一个重要的但未被充分研究的领域.
- 与合成抗生素相比,天然化合物具有较低的目标外毒性.
- 计算工具可以加快自然类型的识别,并减轻药物诱导的毒性.
结论:
- 开发具有降低目标外毒性的抗生素对于患者安全至关重要.
- 自然化合物为制造更安全的抗生素提供了一个有希望的途径.
- 跨学科的计算方法和高通量查是确定有效和安全的抗生素类型的关键.
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