由ivermectin引起的非特异性膜双层干扰是SARS-CoV-2in vitro活动的基础
Richard T Eastman1, Radda Rusinova2, Karl F Herold3
1Division of Preclinical Innovation, National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD, USA.
bioRxiv : the preprint server for biology
|November 14, 2023
概括
在实验室研究中,甲显示出对SARS-CoV-2的抗病毒活性,但是在对细胞有毒的度. 它的机制涉及非特异性膜破坏,因此不太可能成为有效的抗病毒药物.
科学领域:
- 药理学 药理学是指药理学的学科.
- 病毒学 病毒学
- 药物重用 药物重用
背景情况:
- 作为一种抗寄生虫药物,Ivermectin被研究为SARS-CoV-2的潜在宿主导抗病毒药物.
- 临床试验没有充分证实ivermectin对抗SARS-CoV-2的有效性.
结论:
- 非特定的膜干扰是ivermectin体外抗病毒作用的可能机制.
- 由于其毒性和机制,甲不太可能是安全有效的抗病毒药物.
- 这项研究为药物重用候选人的临床前评估提供了一个模型.
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