Linus Pauling Institute, Department of Pharmaceutical Sciences, College of Pharmacy, Oregon State University, 2900 SW Campus Way, Corvallis, Oregon 97331, United States.
Molecular Microbiology & Immunology, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, United States.
J Nat Prod. 2022 Jan 28;85(1):176-184. doi: 10.1021/acs.jnatprod.1c00946. Epub 2022 Jan 10.
As a complement to vaccines, small-molecule therapeutic agents are needed to treat or prevent infections by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and its variants, which cause COVID-19. Affinity selection-mass spectrometry was used for the discovery of botanical ligands to the SARS-CoV-2 spike protein. Cannabinoid acids from hemp () were found to be allosteric as well as orthosteric ligands with micromolar affinity for the spike protein. In follow-up virus neutralization assays, cannabigerolic acid and cannabidiolic acid prevented infection of human epithelial cells by a pseudovirus expressing the SARS-CoV-2 spike protein and prevented entry of live SARS-CoV-2 into cells. Importantly, cannabigerolic acid and cannabidiolic acid were equally effective against the SARS-CoV-2 alpha variant B.1.1.7 and the beta variant B.1.351. Orally bioavailable and with a long history of safe human use, these cannabinoids, isolated or in hemp extracts, have the potential to prevent as well as treat infection by SARS-CoV-2.
作为疫苗的补充,需要小分子治疗药物来治疗或预防由严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)及其变体引起的 COVID-19 感染,这些变体导致 COVID-19。亲和筛选-质谱法用于发现针对 SARS-CoV-2 刺突蛋白的植物配体。从大麻中发现的大麻素酸是变构和正位配体,对刺突蛋白具有微摩尔亲和力。在后续的病毒中和测定中,大麻萜酚酸和大麻二酚酸可防止表达 SARS-CoV-2 刺突蛋白的假病毒感染人上皮细胞,并防止活 SARS-CoV-2 进入细胞。重要的是,大麻萜酚酸和大麻二酚酸对 SARS-CoV-2 的 alpha 变体 B.1.1.7 和 beta 变体 B.1.351 同样有效。这些大麻素具有口服生物利用度和长期安全的人类使用历史,无论是单独使用还是从大麻提取物中分离出来,都有可能预防和治疗 SARS-CoV-2 感染。