Korean Chestnut Honey Suppresses HSV-1 Infection by Regulating the ROS-NLRP3 Inflammasome Pathway.
Eun-Bin KwonYoung Soo KimBuyun KimSe-Gun KimSung-Joon NaYoung-Hoon GoHong Min ChoiHye Jin LeeSang Mi HanJang-Gi ChoiPublished in: Antioxidants (Basel, Switzerland) (2023)
Herpes simplex virus 1 (HSV-1) is double-stranded DNA virus that belongs to the Orthoherpesviridae family. It causes serious neurological diseases of the central nervous system, such as encephalitis. The current U.S. Food and Drug Administration (FDA)-approved drugs for preventing HSV-1 infection include acyclovir (ACV) and valacyclovir; however, their long-term use causes severe side effects and often results in the emergence of drug-resistant strains. Therefore, it is important to discover new antiviral agents that are safe and effective against HSV-1 infection. Korean chestnut honey (KCH) has various pharmacological activities, such as antioxidant, antibacterial, and anti-inflammation effects; however, antiviral effects against HSV-1 have not yet been reported. Therefore, we determined the antiviral activity and mechanism of action of KCH after HSV-1 infection on the cellular level. KCH inhibited the HSV-1 infection of host cells through binding and virucidal steps. KCH decreased the production of reactive oxygen species (ROS) and calcium (Ca 2+ ) following HSV-1 infection and suppressed the production of inflammatory cytokines by inhibiting nuclear factor kappa-light-chain-enhancer of activated B cells (NF-кB) activity. Furthermore, we found that KCH inhibited the expression of the nod-like receptor protein 3 (NLRP3) inflammasome during HSV-1 infection. Taken together, the antiviral effects of KCH occur through multiple targets, including the inhibition of viral replication and the ROS-mediated NLRP3 inflammasome pathway. Our findings suggest that KCH has potential for the treatment of HSV-1 infection and related diseases.
Keyphrases
- herpes simplex virus
- nlrp inflammasome
- drug resistant
- nuclear factor
- oxidative stress
- signaling pathway
- dna damage
- sars cov
- multidrug resistant
- toll like receptor
- induced apoptosis
- pseudomonas aeruginosa
- cell proliferation
- cell cycle arrest
- inflammatory response
- transcription factor
- endoplasmic reticulum stress
- risk assessment
- brain injury
- single molecule
- anti inflammatory
- silver nanoparticles
- replacement therapy
- smoking cessation
- amino acid
- cell free