Orally delivered perilla (Perilla frutescens) leaf extract effectively inhibits SARS-CoV-2 infection in a Syrian hamster model

J Food Drug Anal. 2022 Jun 15;30(2):252-270. doi: 10.38212/2224-6614.3412.

Abstract

On analyzing the results of cell-based assays, we have previously shown that perilla (Perilla frutescens) leaf extract (PLE), a food supplement and orally deliverable traditional Chinese medicine approved by the Taiwan Food and Drug Administration, effectively inhibits SARS-CoV-2 by directly targeting virions. PLE was also found to modulate virus-induced cytokine expression levels. In this study, we explored the anti-SARS-CoV-2 activity of PLE in a hamster model by examining viral loads and virus-induced immunopathology in lung tissues. Experimental animals were intranasally challenged with different SARS-CoV-2 doses. Jugular blood samples and lung tissue specimens were obtained in the acute disease stage (3-4 post-infection days). As expected, SARS-CoV-2 induced lung inflammation and hemorrhagic effusions in the alveoli and perivascular areas; additionally, it increased the expression of several immune markers of lung injury - including lung Ki67-positive cells, Iba-1-positive macrophages, and myeloperoxidase-positive neutrophils. Virus-induced lung alterations were significantly attenuated by orally administered PLE. In addition, pretreatment of hamsters with PLE significantly reduced viral loads and immune marker expression. A purified active fraction of PLE was found to confer higher antiviral protection. Notably, PLE prevented SARS-CoV-2-induced increase in serum markers of liver and kidney function as well as the decrease in serum high-density lipoprotein and total cholesterol levels in a dose-dependent fashion. Differently from lung pathology, monitoring of serum biomarkers in Syrian hamsters may allow a more humane assessment of the novel drugs with potential anti-SARS-CoV-2 activity. Our results expand prior research by confirming that PLE may exert an in vivo therapeutic activity against SARS-CoV-2 by attenuating viral loads and lung tissue inflammation, which may pave the way for future clinical applications.

Grants and funding

This research was financially supported by the Chang Gung Memorial Hospital, Taoyuan, Taiwan (grants BMRP416, CMRPD1G0301-3, CMRPD1F0581-3, and CMRPD1K0241-2), the Ministry of Science and Technology of Taiwan (grants 106-2320-B-182-004-MY3, 106-2811-B-182-011, 106-2632-B-182-001, 107-2811-B-182-512, 108- 2320-B-182-039-, and 109-2320-B-182-026-MY3), the Research Center for Epidemic Prevention Science (grants MOST 109-2327-B-182-002, 109-2327-B-182-003, and 111-2321-B-182-001 to JT Horng; grants 109-2327-B-016-002 and 110-2740-B-016-001 to JH Kau), the Research Center for Emerging Viral Infections from The Featured Areas Research Centre Program within the framework of the Higher Education Sprout Project by the Ministry of Education in Taiwan and the Ministry of Science and Technology, Taiwan (grants MOST 110-2634- F-182-001 and MOST 109-2327-B-182-002).