| Literature DB >> 32890967 |
Andresa Aparecida Berretta1, Marcelo Augusto Duarte Silveira2, José Manuel Cóndor Capcha3, David De Jong4.
Abstract
Propolis, a resinous material produced by honey bees from plant exudates, has long been used in traditional herbal medicine and is widely consumed as a health aid and immune system booster. The COVID-19 pandemic has renewed interest in propolis products worldwide; fortunately, various aspects of the SARS-CoV-2 infection mechanism are potential targets for propolis compounds. SARS-CoV-2 entry into host cells is characterized by viral spike protein interaction with cellular angiotensin-converting enzyme 2 (ACE2) and serine protease TMPRSS2. This mechanism involves PAK1 overexpression, which is a kinase that mediates coronavirus-induced lung inflammation, fibrosis, and immune system suppression. Propolis components have inhibitory effects on the ACE2, TMPRSS2 and PAK1 signaling pathways; in addition, antiviral activity has been proven in vitro and in vivo. In pre-clinical studies, propolis promoted immunoregulation of pro-inflammatory cytokines, including reduction in IL-6, IL-1 beta and TNF-α. This immunoregulation involves monocytes and macrophages, as well as Jak2/STAT3, NF-kB, and inflammasome pathways, reducing the risk of cytokine storm syndrome, a major mortality factor in advanced COVID-19 disease. Propolis has also shown promise as an aid in the treatment of various of the comorbidities that are particularly dangerous in COVID-19 patients, including respiratory diseases, hypertension, diabetes, and cancer. Standardized propolis products with consistent bioactive properties are now available. Given the current emergency caused by the COVID-19 pandemic and limited therapeutic options, propolis is presented as a promising and relevant therapeutic option that is safe, easy to administrate orally and is readily available as a natural supplement and functional food.Entities:
Keywords: Anti-inflammatory; Antiviral; COVID-19; PAK1 blocker; Propolis; SARS-CoV-2
Mesh:
Substances:
Year: 2020 PMID: 32890967 PMCID: PMC7430291 DOI: 10.1016/j.biopha.2020.110622
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529
Potential pathways through which propolis and its components could attenuate SARS-CoV-2 infection and its consequences.
| N | Targets | Aspect of SARS-CoV-2 infection | Propolis Components | Effect of the components and type of evidence |
|---|---|---|---|---|
| Viral component that attaches to host cell | Limonin, Quercetin and Kaempferol | Inhibitory potential with high binding energy to viral components from -9 to -7.1 kcal/mol ( | ||
| Viral component that attaches to host cell | Kaempferol | Blocks the 3a channel that is encoded by ORF 3a of SARS-CoV ( | ||
| Main receptor for viral entry | Myricetin, Caffeic Acid Phenethyl Ester, Hesperetin and Pinocembrin | Inhibitory potential with high binding energy to ACE2 (-8.97 kcal/mol) ( | ||
| Kaempferol | Inhibitory potential with high binding energy to ACE2 (-7.5 kcal/mol) ( | |||
| Quercetin | Inhibitory potential with high binding energy to ACE2 (-10.4 kcal/mol) ( | |||
| Serine protease that mediates spike protein priming for viral entry | Kaempferol | Downregulates androgen receptors such as PSA and TMPRSS2 in a prostate cancer model ( | ||
| PAK-1 (RAC/CDC42-activated kinases) - Responsible for suppression of immune system in hosts | Caffeic Acid and Caffeic Acid Phenethyl Ester | Downregulates PAK-1 associated with Rac1 activation ( | ||
| Inhibits PAK-1 directly or up-stream, blocking coronaviral infection (Review) [ | ||||
| Mediates the proteolytic processing of replicase polypeptides 1a and 1ab into functional proteins in SARS-CoV-2 infection | Hesperetin | Inhibits cleavage activity of 3CLpro ( | ||
| Response to viral infection that leads to organ injury | Propolis Extract | Inhibits NF-kB activation ( | ||
| Induces Ca2+ signaling in dendritic cells in Peyer’s patches, improving the immune response ( | ||||
| Attenuates the inflammatory response through intracellular ROS and NO levels with downregulation of IL‐1β and IL‐6 expression ( | ||||
| Regulates IFN-γ, IL-6, and IL-10 cytokines in an experimental asthma model ( | ||||
| Increases TGF-β and IL-10 levels, which contribute to the regulation of the inflammatory process in Acute Pulmonary Inflammation ( | ||||
| Inhibits the production of ROS, RNS, NO, cytokines IL-1α, IL-1β, IL-4, IL-6, IL-12p40, IL-13, TNF-α, G-CSF, GM-CSF, MCP-1, MIP-1α, MIP-1β, and RANTES in stimulated J774A.1 macrophages ( | ||||
| Kaempferol | Reduces TNF-α, IL-6, VEGF via the ERK-NFkB-cMyc-p21 pathway ( | |||
| Caffeic Acid Phenethyl Ester | Inhibits NF-kB activation in HTLV-1 infection ( | |||
| Modulates JAK/STAT signaling and attenuates oxidative stress and inflammation [ | ||||
| Adaptive immune response against viral infection | Propolis Extract | Increases humoral and cellular response in mice immunized with Suid herpesvirus type 1[ | ||
| Suppresses the differentiation of Th17 cells by inhibition of IL-6-induced phosphorylation of signal transducer and activator of transcription 3 (STAT3) ( | ||||
| Blood clotting dysregulation caused by viral infection | Quercetin | Inhibits thrombin in thrombotic manifestations ( | ||
| 8 | Viral translation | Kaempferol and Hesperetin | Inhibits internal ribosomal entry site (IRES) activity required for viral protein translation ( | |
| Transcription | Kaempferol | Inhibits human immunodeficiency virus reverse transcriptase-associated DNA polymerase as well as RNAase H and RNase H activities ( | ||
| Presents potent anti-HIV-1 reverse transcriptase activity ( | ||||
| Endocytosis | Quercetin | Decreases Akt phosphorylation and viral endocytosis of Rhinovirus ( | ||
| Replication and virion integrity | Prevents up-regulation of diacylglycerol acyltransferase (DGAT) required for hepatitis C virus replication ( | |||
| Replication | Decreases heat shock proteins and Hepatitis B virus transcription levels ( | |||
| Endocytosis | Caffeic Acid | Inhibits Hepatitis B virus-DNA replication ( | ||
| Endocytosis | Inhibits influenza A virus (IAV) replication ( | |||
| Endocytosis | Inhibits influenza A virus (IAV) activity through neuraminidases ( | |||
| Transcription | Caffeic Acid Phenethyl Ester | Inhibits HIV-1 integrase (Review) [ |
Fig. 1Major pathways through which propolis can interfere with SARS-CoV-2 attachment to the host cell, viral replication, and pathophysiological consequences. SARS-CoV-2 entry into target cells requires spike protein binding to ACE2 and activation by TMPRSS2. After binding, several signals are triggered, allowing viral endocytosis and PAK1 activation, which reduces the adaptive immune response and antibody production against the virus. PAK1 also stimulates CCL2 production, which generates a fibrotic response. Viral infection induces nuclear transition factor NF-KB activation, generating local pro-inflammatory cytokine production. Propolis-derived compounds downregulate the expression of TMPRSS2 and the anchoring ACE2, which limits entry of the virus. Furthermore, they promote NF-KB and monocyte/macrophage immunomodulation, reducing pro-inflammatory cytokine overproduction, and they reduce PAK1 activation, increasing the production of antibodies against SARS-CoV-2.