Journal of Infection and Chemotherapy,
Journal Year:
2023,
Volume and Issue:
29(11), P. 1054 - 1060
Published: July 26, 2023
We
previously
reported
the
finding
of
symptom
relief
in
a
randomized
controlled
trial
with
combined
use
kakkonto
and
shosaikotokakikyosekko
added
to
conventional
treatment
patients
coronavirus
disease
2019
(COVID-19).
For
further
evaluation,
we
performed
post
hoc
analysis
focused
on
disappearance
without
recurrence,
determine
clearer
effect
Kampo
medicine.
Patients
mild
moderate
COVID-19
were
randomly
allocated
control
group
receiving
symptomatic
therapy
or
(2.5
g)
three
times
daily
addition
therapy.
The
data
161
(Kampo
group,
n
=
81;
80)
analyzed
for
time
disappearance.
Kaplan-Meier
Cox
proportional
hazard
estimates
symptoms
showed
that
all
each
targeted
this
study
disappeared
faster
than
although
not
statistically
significant
(all
cases;
ratio
[HR]
3.73,
95%
confidence
interval
[CI]
0.46-29.98,
log-rank
p
0.1763).
In
supplemental
assessment
using
covariate
adjustment
competing
risk
analysis,
fever
cases,
HR
1.62,
CI
0.99-2.64,
0.0557;
unvaccinated
1.68,
1.00-2.83,
0.0498)
shortness
breath
significantly
1.92,
1.07-3.42,
0.0278;
2.15,
1.17-3.96,
0.0141).
These
results
demonstrate
advantages
acute
COVID-19.
Heliyon,
Journal Year:
2023,
Volume and Issue:
9(9), P. e19341 - e19341
Published: Aug. 20, 2023
SARS-CoV-2
is
a
novel
coronavirus
that
emerged
as
an
epidemic,
causing
respiratory
disease
with
multiple
severe
symptoms
and
deadly
consequences.
ACE-2
TMPRSS2
play
crucial
synergistic
roles
in
the
membrane
fusion
viral
entry
of
(COVID-19).
The
spike
(S)
protein
binds
to
receptor
for
entry,
while
proteolytically
cleaves
S
into
S1
S2
subunits,
promoting
fusion.
Therefore,
are
potential
drug
targets
treating
COVID-19,
their
inhibition
promising
strategy
treatment
prevention.
This
study
proposes
ginsenoside
compound
K
(G-CK),
triterpenoid
saponin
abundant
Panax
Ginseng,
dietary
medicinal
herb
highly
consumed
Korea
China,
effectively
inhibits
expression.
We
initially
conducted
in-silico
evaluation
where
G-CK
showed
high
affinity
binding
sites
two
target
proteins
SARS-CoV-2.
Additionally,
we
evaluated
stability
using
molecular
dynamics
(MD)
simulations
100
ns,
followed
by
MM-PBSA
calculations.
MD
free
energy
calculations
revealed
has
stable
favorable
energies,
leading
strong
targets.
Furthermore,
suppressed
ACE2
mRNA
expression
A549,
Caco-2,
MCF7
cells
at
concentration
12.5
μg/mL
LPS-induced
RAW
264.7
6.5
μg/mL,
without
significant
cytotoxicity.ACE2
were
significantly
lower
A549
following
treatment.
These
findings
suggest
may
evolve
therapeutic
against
COVID-19.
ACS Food Science & Technology,
Journal Year:
2023,
Volume and Issue:
3(12), P. 2108 - 2116
Published: Nov. 29, 2023
The
pathogenesis
of
coronavirus
disease
2019
(COVID-19)
is
facilitated
by
the
binding
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
spike
protein
to
angiotensin-converting
enzyme
(ACE2)
in
a
host;
hence,
interfering
with
interaction
between
SARS-CoV-2's
and
ACE2
could
possibly
reduce
risk
COVID-19.
This
study
aimed
analyze
chemical
compositions
evaluate
antiviral
free
radical
scavenging
effects
parsley
leaf
extracts.
Twenty-two
compounds
were
tentatively
identified,
octadecenamide
being
reported
for
first
time
parsley.
Parsley
extract
was
able
inhibit
SARS-CoV-2-ACE2
70%
at
concentration
3.3
mg
dry
parsley/mL
activity
86%
5.0
mg/mL.
showed
capacity
against
HO•,
DPPH•,
ABTS•+
values
184.09,
0.03,
9.58
μmol
Trolox
equivalent/gram,
respectively.
Findings
from
this
suggest
parsley's
potential
ability
mitigate
risks
symptoms
Journal of Infection and Chemotherapy,
Journal Year:
2023,
Volume and Issue:
29(11), P. 1054 - 1060
Published: July 26, 2023
We
previously
reported
the
finding
of
symptom
relief
in
a
randomized
controlled
trial
with
combined
use
kakkonto
and
shosaikotokakikyosekko
added
to
conventional
treatment
patients
coronavirus
disease
2019
(COVID-19).
For
further
evaluation,
we
performed
post
hoc
analysis
focused
on
disappearance
without
recurrence,
determine
clearer
effect
Kampo
medicine.
Patients
mild
moderate
COVID-19
were
randomly
allocated
control
group
receiving
symptomatic
therapy
or
(2.5
g)
three
times
daily
addition
therapy.
The
data
161
(Kampo
group,
n
=
81;
80)
analyzed
for
time
disappearance.
Kaplan-Meier
Cox
proportional
hazard
estimates
symptoms
showed
that
all
each
targeted
this
study
disappeared
faster
than
although
not
statistically
significant
(all
cases;
ratio
[HR]
3.73,
95%
confidence
interval
[CI]
0.46-29.98,
log-rank
p
0.1763).
In
supplemental
assessment
using
covariate
adjustment
competing
risk
analysis,
fever
cases,
HR
1.62,
CI
0.99-2.64,
0.0557;
unvaccinated
1.68,
1.00-2.83,
0.0498)
shortness
breath
significantly
1.92,
1.07-3.42,
0.0278;
2.15,
1.17-3.96,
0.0141).
These
results
demonstrate
advantages
acute
COVID-19.