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Antiviral Properties of R. tanguticum Nanoparticles on Herpes Simplex Virus Type I In Vitro and In Vivo
Herpes simplex virus type 1 (HSV-1), an enveloped DNA virus, plays a key role in varieties of diseases including recurrent cold sores, keratoconjunctivitis, genital herpes and encephalitis in humans. Great efforts have been made in developing more effective and less side-effects anti-herpes simplex...
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Published in: | Frontiers in pharmacology 2019-09, Vol.10, p.959-959 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Herpes simplex virus type 1 (HSV-1), an enveloped DNA virus, plays a key role in varieties of diseases including recurrent cold sores, keratoconjunctivitis, genital herpes and encephalitis in humans. Great efforts have been made in developing more effective and less side-effects anti-herpes simplex virus agents, including traditional Chinese herbal medicines. In the present study, we evaluated the antiviral efficacy of
Rheum tanguticum
nanoparticles against HSV-1
in vitro
and
in vivo
.
R. tanguticum
nanoparticles could inactivate the HSV-1 virions and block the viral attachment and entry into cells. Time-of-addition assay indicated that
R. tanguticum
nanoparticles could interfere with the entire phase of viral replication. Besides,
R. tanguticum
nanoparticles showed the ability to inhibit the mRNA expression of HSV-1 immediate early gene
ICP4
and early gene
ICP8
as well as the expression of viral protein
ICP4
and
ICP8
. Moreover,
R. tanguticum
nanoparticles have been proved to protect mice against HSV-1 induced lethality by decreasing the viral load and alleviated pathological changes in brain tissues. In conclusion, we demonstrated that
R. tanguticum
nanoparticles could inhibit HSV-1 infection through multiple mechanisms. These results suggest that
R. tanguticum
nanoparticles may have novel roles in the treatment of HSV-1 infection. |
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ISSN: | 1663-9812 1663-9812 |
DOI: | 10.3389/fphar.2019.00959 |