Journal of Herbmed Pharmacology,
Journal Year:
2024,
Volume and Issue:
14(1), P. 90 - 96
Published: Dec. 25, 2024
Introduction:
Carbon
tetrachloride
(CCl4
)
is
a
chemical
that
can
induce
injury
in
the
liver.
The
aim
was
to
evaluate
any
potential
hepatoprotective
of
seed
extract
from
Cassia
absus
against
CCl4
-induced
liver
toxicity
Wister
rats.
Methods:
To
this
end,
an
aqueous-methanolic
C.
seeds
prepared
by
maceration.
In
vitro
testing
included
phytochemical
screening
and
high-performance
liquid
chromatography
(HPLC)
analysis
phenolic
compound
constituents.
An
vivo
study
involved
single
exposure
either
alone
or
combination
with
agent,
silymarin,
administered
orally
over
28
days.
Serum
biochemical
markers
cell
were
measured
post-mortem
tissues
examined
histopathologically
using
eosin-hematoxylin
staining
microscopy.
Results:
HPLC
specifically
identified
presence
gallic
acid,
vanillic
catechin,
p-coumaric
acid.
addition,
no
changes
observed
animal
body
weights
during
treatment
protocol.
However,
both
plant
silymarin
reversed
induced
elevated
serum
concentrations
aspartate
aminotransferase
(AST),
total
bilirubin,
alkaline
phosphatase
(ALP),
alanine
transaminase
(P<0.05)
addition
histopathological
injury.
also
had
dose-related
hepatotoxic
mitigating
effect,
findings
analogous
those
standard
comparator,
silymarin.
Conclusion:
These
outcomes
substantiate
protective
effect
hepatotoxicity
model.
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(1), P. 53 - 53
Published: Jan. 15, 2025
Hepatocellular
carcinoma
(HCC)
is
a
prevalent
and
lethal
form
of
liver
cancer
with
limited
treatment
options.
Silymarin,
flavonoid
complex
derived
from
milk
thistle,
has
shown
promise
in
disease
due
to
its
antioxidant,
anti-inflammatory,
anticancer
properties.
This
study
aims
explore
the
therapeutic
potential
silymarin
HCC
through
comprehensive
silico
approach.
employed
network
pharmacology
approach
identify
key
molecular
targets
HCC.
The
Genecards
Metascape
databases
were
used
for
target
identification
functional
annotation.
Molecular
docking
analysis
was
conducted
on
primary
components
against
VEGFA
SRC
proteins,
which
are
critical
progression.
MD
simulations
followed
assess
stability
interactions
docked
complexes.
Network
identified
several
pathways
implicated
results
revealed
strong
binding
affinities
SRC,
Silybin
A
Isosilybin
B
showing
highest
affinities.
confirmed
these
interactions,
indicating
inhibitory
effects
provides
evaluation
silymarin's
findings
suggest
that
silymarin,
particularly
B,
may
effectively
offering
promising
avenue
treatment.
Further
experimental
validation
warranted
confirm
facilitate
development
silymarin-based
therapeutics
Cureus,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 17, 2024
Chronic
liver
diseases
(CLDs)
such
as
chronic
hepatitis,
cirrhosis,
and
non-alcoholic
fatty
disease
(NAFLD)
present
significant
global
health
challenges
due
to
their
high
morbidity
mortality
rates.
Silymarin,
a
flavonoid
complex
derived
from
the
seeds
of
milk
thistle
plant
(Silybum
marianum),
has
been
extensively
studied
for
its
hepatoprotective
properties.
This
review
aims
evaluate
role
silymarin
an
antioxidant
therapy
in
managing
CLDs.
We
explore
efficacy,
safety,
mechanisms
action
through
comprehensive
analysis
clinical
trials
scientific
studies.
Silymarin
offers
protective
effects
on
shows
promise
improving
function
histological
outcomes
various
conditions.
Despite
promising
results,
further
research
is
needed
fully
elucidate
optimal
dosing
regimens,
long-term
potential
drug
interactions
silymarin.
underscores
therapeutic
CLDs
provides
foundation
future
studies
aimed
at
enhancing
application.
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(1), P. 90 - 90
Published: Jan. 13, 2025
Backgroud/Objectives:
Silymarin,
an
extract
from
milk
thistle,
is
widely
recognized
for
its
therapeutic
potential
in
treating
liver
disorders.
However,
clinical
utility
limited
by
the
poor
solubility
and
low
bioavailability
of
key
active
ingredient,
Silybin.
In
this
study,
we
sought
to
address
issue
through
development
a
novel
cocrystal
Silyin.
Methods:
Silybin-L-proline
was
synthesized
physicochemical
properties
were
characterized
PXRD,
TGA,
DSC,
FTIR.
Dissolution
tests
conducted
various
pH
solutions,
impact
precipitation
inhibitors
evaluated.
Furthermore,
pharmacokinetic
study
rats
performed
assess
bioavailability.
Results:
The
dissolution
studies
demonstrated
that
has
significant
improvement
performance,
particularly
acidic
environments.
use
inhibitors,
such
as
PVP,
prolonged
supersaturation
period
adequate
absorption.
Pharmacokinetic
revealed
exhibited
16-fold
increase
compared
raw
Silybin
extract,
outperforming
commercial
Silybin–phosphatidylcholine
complex.
Conclusions:
Silybin–L-proline
significantly
enhances
bioavailability,
indicating
improve
efficacy
applications.
Panorama actual del medicamento,
Journal Year:
2025,
Volume and Issue:
unknown, P. 139 - 145
Published: Feb. 25, 2025
Silybum
marianum,
perteneciente
a
la
familia
Asteraceae
y
comúnmente
conocido
como
“cardo
mariano”,
es
una
especie
vegetal
utilizada
por
sus
propiedades
terapéuticas
desde
hace
más
de
2000
años
cuyos
frutos
contienen
mezcla
flavonolignanos
conocidos
colectivamente
silimarina,
siendo
silibina
(también
llamada
silibinina)
el
componente
principal.
Este
artículo
revisión
se
centra
en
química
planta
destaca
potencial
farmacológico
marianum.
Tanto
extracto
estandarizado
silimarina
han
mostrado
antiinflamatorias,
antioxidantes
proapoptóticas,
que
afectan
varias
vías
mecanismos
celulares.
Estas
acciones
respaldan
beneficios
demostrados
principalmente
protector
hepático,
además
neuroprotección,
cardioprotección
alteraciones
metabólicas
su
agente
anticancerígeno
antidiabético,
respaldado
estudios
extensos
datos
experimentales.
Ha
demostrado
ser
particularmente
eficaz
para
proteger
función
hepática,
reducir
mortalidad
debido
enfermedad
hepática
preservar
salud
del
hígado
al
mitigar
estrés
oxidativo
citotoxicidad.
Todo
ello,
junto
con
prácticamente
nula
toxicidad,
suponga
opción
terapéutica
frente
afecciones
hepáticas,
incluida
cirrosis
daño
hepático
inducido
alcohol,
drogas
graso.
BMC Complementary Medicine and Therapies,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 12, 2025
It
is
widely
believed
that
Silybum
marianum
(Silymarin)
alleviates
liver
injury
arising
from
various
etiologies
with
different
degrees
of
damage
through
its
anti-inflammatory
and
antioxidant
activities.
This
meta-analysis
investigated
the
effects
silymarin
administration
on
serum
levels
enzymes
including
AST,
ALT
ALP.
From
inception
to
November,
2023,
a
comprehensive
literature
search
was
conducted.
Inclusion
criteria
for
this
study
were
randomized
trials
provided
sufficient
data
each
group
at
beginning
end
follow-up
period.
Ultimately,
55
studies
total
3545
patients
included.
Comprehensive
Meta-Analysis
(CMA)
V4
software
used
meta-analysis.
Begg's
funnel
plot
symmetry
status,
rank
correlation,
Egger's
weighted
regression
tests
examine
potential
publication
bias.
According
findings
showed
significant
reduction
in
AST
(SMD
[95%
CI]:
-
0.670
[-
0.931,
0.408],
p-value
=
0.000),
0.912
1.177,
0.646],
0.000)
levels.
While
it
had
no
statistically
effect
ALP
level
0.236
1.929,
1.458],
0.159).
Meta-regression
analysis
there
association
between
dose,
age,
BMI,
treatment
duration
hepatoprotective
silymarin.
In
subgroup
analysis,
greater
observed
under
50
years
old.
The
also
decrease
BMI
less
than
30,
while
≥
30.
Silymarin
dose
400
mg
≤
2
months
decreasing
compared
high
doses
longer
duration.
significantly
decreased
NAFLD
viral
hepatitis,
drugs
induced
alcohol-related
disease.
Modifying
recommended
causes
damage.