Evaluation of In Vitro and In Vivo Antiviral Activities of Vitamin D for SARS-CoV-2 and Variants.
Chee-Keng MokYan Ling NgBintou Ahmadou AhidjoZhen Qin AwHuixin ChenYi Hao WongRegina Ching Hua LeeMarcus Wing Choy LoeJing LiuKai Sen TanParveen KaurDe Yun WangErwei HaoXiaotao HouYong Wah TanJiagang DengJustin Jang Hann ChuPublished in: Pharmaceutics (2023)
The COVID-19 pandemic has brought about unprecedented medical and healthcare challenges worldwide. With the continual emergence and spread of new COVID-19 variants, four drug compound libraries were interrogated for their antiviral activities against SARS-CoV-2. Here, we show that the drug screen has resulted in 121 promising anti-SARS-CoV-2 compounds, of which seven were further shortlisted for hit validation: citicoline, pravastatin sodium, tenofovir alafenamide, imatinib mesylate, calcitriol, dexlansoprazole, and prochlorperazine dimaleate. In particular, the active form of vitamin D, calcitriol, exhibits strong potency against SARS-CoV-2 on cell-based assays and is shown to work by modulating the vitamin D receptor pathway to increase antimicrobial peptide cathelicidin expression. However, the weight, survival rate, physiological conditions, histological scoring, and virus titre between SARS-CoV-2 infected K18-hACE2 mice pre-treated or post-treated with calcitriol were negligible, indicating that the differential effects of calcitriol may be due to differences in vitamin D metabolism in mice and warrants future investigation using other animal models.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- healthcare
- poor prognosis
- high throughput
- weight loss
- type diabetes
- mesenchymal stem cells
- single cell
- copy number
- body mass index
- insulin resistance
- signaling pathway
- gene expression
- bone marrow
- dna methylation
- emergency department
- genome wide
- metabolic syndrome
- weight gain
- chronic myeloid leukemia
- wild type