Wang Bo, Kovalchuk Anna, Li Dongping, Rodriguez-Juarez Rocio, Ilnytskyy Yaroslav, Kovalchuk Igor, Kovalchuk Olga
Pathway Rx Inc., Lethbridge, AB T1K 7X8, Canada.
University of Lethbridge, Lethbridge, AB T1K3M4, Canada.
Aging (Albany NY). 2020 Nov 22;12(22):22425-22444. doi: 10.18632/aging.202225.
With the current COVID-19 pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), there is an urgent need for new therapies and prevention strategies that can help curtail disease spread and reduce mortality. The inhibition of viral entry and thus spread is a plausible therapeutic avenue. SARS-CoV-2 uses receptor-mediated entry into a human host via the angiotensin-converting enzyme 2 (ACE2), which is expressed in lung tissue as well as the oral and nasal mucosa, kidney, testes and gastrointestinal tract. The modulation of ACE2 levels in these gateway tissues may be an effective strategy for decreasing disease susceptibility. , especially those high in the anti-inflammatory cannabinoid cannabidiol (CBD), has been found to alter gene expression and inflammation and harbour anti-cancer and anti-inflammatory properties. However, its effects on ACE2 expression remain unknown. Working under a Health Canada research license, we developed over 800 new cultivars and hypothesized that high-CBD extracts may be used to down-regulate ACE2 expression in target COVID-19 tissues. Using artificial 3D human models of oral, airway and intestinal tissues, we identified 13 high-CBD extracts that decrease ACE2 protein levels. Some extracts down-regulate serine protease TMPRSS2, another critical protein required for SARS-CoV-2 entry into host cells. While our most effective extracts require further large-scale validation, our study is important for future analyses of the effects of medical cannabis on COVID-19. The extracts of our most successful novel high-CBD lines, pending further investigation, may become a useful and safe addition to the prevention/treatment of COVID-19 as an adjunct therapy.
在由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引发的当前新冠疫情中,迫切需要新的治疗方法和预防策略来帮助遏制疾病传播并降低死亡率。抑制病毒进入从而阻止传播是一条可行的治疗途径。SARS-CoV-2通过血管紧张素转换酶2(ACE2)以受体介导的方式进入人类宿主,ACE2在肺组织以及口腔和鼻腔黏膜、肾脏、睾丸和胃肠道中均有表达。调节这些门户组织中ACE2的水平可能是降低疾病易感性的有效策略。大麻,尤其是那些富含抗炎大麻素大麻二酚(CBD)的大麻,已被发现可改变基因表达和炎症反应,并具有抗癌和抗炎特性。然而,其对ACE2表达的影响尚不清楚。在加拿大卫生部的研究许可下,我们培育了800多个新的大麻品种,并推测高CBD提取物可用于下调新冠病毒相关靶组织中ACE2的表达。利用口腔、气道和肠道组织的人工3D人体模型,我们鉴定出13种可降低ACE2蛋白水平的高CBD提取物。一些提取物还下调了丝氨酸蛋白酶TMPRSS2,这是SARS-CoV-2进入宿主细胞所需的另一种关键蛋白。虽然我们最有效的提取物需要进一步的大规模验证,但我们的研究对于未来分析医用大麻对新冠病毒的影响具有重要意义。我们最成功的新型高CBD品系的提取物,有待进一步研究,作为辅助疗法,可能会成为新冠病毒预防/治疗中有用且安全的补充。