Research Society and Development,
Journal Year:
2022,
Volume and Issue:
11(9), P. e45711932115 - e45711932115
Published: July 15, 2022
Nanoemulsões
de
cinamaldeído
(NNC)
assistidas
por
ultrassom,
surgem
como
uma
alternativa
energeticamente
viável
e
potencialmente
promissora
para
a
entrega
controlada
desse
composto
orgânico
bioativo.
Nesse
contexto,
o
objetivo
central
do
estudo
consistiu
na
otimização
das
variáveis
operacionais
processo
produção
assistida
ultrassom
NNC,
fim
avaliar
efeito
dos
elementos
estabilidade
cinética,
composição
bioativa
atividade
antibacteriana
NNC
obtidas.
A
metodologia
superfície
resposta
(MSR),
via
delineamento
rotacional
foi
utilizada
ajuste,
quando
possível,
modelos
polinomiais
segunda
ordem.
O
tempo
sonicação
(TS)
amplitude
da
potência
(AP)
ultrassônica
foram
os
fatores
estudados,
enquanto
as
respostas
corresponderam,
respectivamente
ao
diâmetro
hidrodinâmico
(DH),
índice
polidispersidade
(PDI),
potencial
zeta
(PZ),
turbidez
(T)
fenólica
total
(CFT).
in-vitro
sistemas
obtidos
realizada
meio
analítica
difusão
em
ágar-poço.
Os
resultados
mostraram
que
independentemente
TS
utilizado
no
processo,
menores
valores
DH
T
nanoemulsões
condições
otimizadas
com
baixa
ultrassônica.
PDI
revelaram
eram
monodispersas,
teores
CFT
preservados
durante
obtenção
considerável
antibacteriana.
Logo,
MSR
propor
ideais
preparo
assim
obter
características
físico-químicas
reforçam
sua
elevada
cinética
manutenção
antimicrobiana
processamento.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
165, P. 114867 - 114867
Published: June 28, 2023
With
the
growing
shortage
of
organs,
improvements
in
donor
organ
protection
are
needed
to
meet
increasing
demands
for
transplantation.
Here,
aim
was
investigate
protective
effect
cinnamaldehyde
against
ischemia-reperfusion
injury
(IRI)
hearts
exposed
prolonged
cold
ischemia.
Donor
were
harvested
from
rats
pretreated
with
or
without
cinnamaldehyde,
then
subjected
24
h
preservation
and
1
ex
vivo
perfusion.
Hemodynamic
changes,
myocardial
inflammation,
oxidative
stress,
apoptosis
evaluated.
The
PI3K/AKT/mTOR
pathway
involved
cardioprotective
effects
explored
through
RNA
sequencing
western
blot
analysis.
Intriguingly,
pretreatment
remarkably
improved
cardiac
function
coronary
flow,
left
ventricular
systolic
pressure,
+dp/dtmax,
-dp/dtmax,
decreasing
vascular
resistance
end-diastolic
pressure.
Moreover,
our
findings
indicated
that
protected
heart
IRI
by
alleviating
attenuating
reducing
apoptosis.
Further
studies
showed
activated
after
treatment
during
IRI.
abolished
LY294002.
In
conclusion,
alleviated
suffering
Cinnamaldehyde
exerted
activation
pathway.
Journal of Food and Drug Analysis,
Journal Year:
2024,
Volume and Issue:
32(2), P. 146 - 160
Published: June 10, 2024
As
cancer
continues
to
rise
globally,
there
is
growing
interest
in
discovering
novel
methods
for
prevention
and
treatment.
Due
the
limitations
of
traditional
therapies,
has
been
a
emphasis
on
investigating
herbal
remedies
exploring
their
potential
synergistic
effects
when
combined
with
chemotherapy
drugs.
Cinnamaldehyde,
derived
from
cinnamon,
gained
significant
attention
its
role
Extensive
research
demonstrated
that
cinnamaldehyde
exhibits
promising
anticancer
properties
by
modulating
various
cellular
processes
involved
tumor
growth
progression.
However,
challenges
unanswered
questions
remain
regarding
precise
mechanisms
effective
use
as
an
agent.
This
article
aims
explore
multifaceted
cells
shed
light
these
existing
issues.
Cinnamaldehyde
diverse
anti-cancer
mechanisms,
including
inducing
apoptosis
activating
caspases
damaging
mitochondrial
function,
inhibiting
angiogenesis,
anti-proliferation,
anti-inflammatory
antioxidant.
In
addition,
also
acts
reactive
oxygen
species
scavenger,
reducing
oxidative
stress
preventing
DNA
damage
genomic
instability.
emphasizes
therapeutic
treatment
underscores
need
future
unlock
strategies
combating
cancer.
By
providing
valuable
insights
into
mechanism
cancer,
this
comprehensive
understanding
paves
way
Overall,
holds
great
promise
agent,
exploration
highlights
addition
options.
Journal of physiological investigation.,
Journal Year:
2024,
Volume and Issue:
67(3), P. 129 - 138
Published: May 1, 2024
Ischemia-reperfusion
(IR)
injury
remains
a
pivotal
contributor
to
myocardial
damage
following
acute
coronary
events
and
revascularization
procedures.
Phosphoinositide
3-kinase
(PI3K),
key
mediator
of
cell
survival
signaling,
plays
central
role
in
regulating
inflammatory
responses
death
mechanisms.
Trans-chalcone
(Tch),
natural
compound
known
for
its
anti-inflammatory
activities,
has
shown
promise
various
disease
models.
The
aim
the
current
study
was
investigate
potential
protective
effects
Tch
against
induced
by
ischemia
reperfusion
challenges
targeting
PI3K-inflammasome
interaction.
Experimental
models
utilizing
male
rats
subjected
an
vivo
model
IR
infarction
were
employed.
Administration
(100
μg/kg,
intraperitoneally)
significantly
reduced
injury,
as
indicated
limited
infarct
size
decreased
levels
enzyme
troponin.
Mechanistically,
upregulated
PI3K
expression,
thereby
inhibiting
activity
NOD-like
receptor
protein
3
inflammasome
followed
activation
pro-inflammatory
cytokines
interleukin-1β
(IL-1β)
IL-18.
Moreover,
it
mitigated
oxidative
stress
suppressed
vascular-intercellular
adhesion
molecules,
contributing
cardioprotective
effects.
PI3K/Akt
pathway
inhibitor
LY294002
considerably
attenuated
beneficial
Tch.
These
findings
highlight
therapeutic
ameliorating
associated
with
insults
through
modulation
PI3K/Akt-inflammasome
axis.
multifaceted
mechanisms
underlying
signify
promising
candidate
further
exploration
developing
targeted
therapies
aimed
at
mitigating
ischemic
heart
improving
clinical
outcomes
cardiovascular
diseases
characterized
injury.
Oxidative Medicine and Cellular Longevity,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 23
Published: Oct. 8, 2022
Evidence
from
epidemiological
studies
has
demonstrated
that
the
incidence
and
mortality
of
cardiovascular
diseases
(CVDs)
increase
year
by
year,
which
pose
a
great
threat
on
social
economy
human
health
worldwide.
Due
to
limited
therapeutic
benefits
associated
adverse
effects
current
medications,
there
is
an
urgent
need
uncover
novel
agents
with
favorable
safety
efficacy.
Cinnamaldehyde
(CA)
bioactive
phytochemical
isolated
stem
bark
Chinese
herbal
medicine
Cinnamon
been
suggested
possess
curative
roles
against
development
CVDs.
This
integrated
review
intends
summarize
physicochemical
pharmacokinetic
features
CA
discuss
recent
advances
in
underlying
mechanisms
potential
targets
responsible
for
anti-CVD
properties
CA.
The
CA-related
protective
could
be
attributed
inhibition
inflammation
oxidative
stress,
improvement
lipid
glucose
metabolism,
regulation
cell
proliferation
apoptosis,
suppression
cardiac
fibrosis,
platelet
aggregation
promotion
vasodilation
angiogenesis.
Furthermore,
likely
inhibit
CVD
progression
via
affecting
other
possible
processes
including
autophagy
ER
stress
regulation,
gut
microbiota
immune
homeostasis,
ion
ncRNA
expression,
TRPA1
activation.
Collectively,
experiments
reported
previously
highlight
clinical
trials
are
advocated
offer
scientific
basis
compound
future
applied
practice
prophylaxis
treatment.
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 3315 - 3332
Published: April 1, 2024
Background:
Acute
myocardial
infarction
(AMI)
is
a
common
cardiovascular
disease
in
clinic.Currently,
there
no
specific
treatment
for
AMI.Carbon
dots
(CDs)
have
been
reported
to
show
excellent
biological
activities,
which
hold
promise
the
development
of
novel
nanomedicines
diseases.Methods:
In
this
study,
we
firstly
prepared
CDs
from
natural
herb
Curcumae
Radix
Carbonisata
(CRC-CDs)
by
green,
simple
calcination
method.The
aim
study
investigate
cardioprotective
effect
and
mechanism
CRC-CDs
on
isoproterenol
(ISO)
-induced
(MI)
rats.
Results:The
results
showed
that
pretreatment
with
significantly
reduced
serum
levels
cardiac
enzymes
(CK-MB,
LDH,
AST)
lipids
(TC,
TG,
LDL)
st-segment
elevation
infarct
size
ECG
AMI
rats.Importantly,
ejection
fraction
(EF)
shortening
(FS)
were
markedly
elevated,
as
was
ATPase
activity.In
addition,
could
increase
superoxide
dismutase
(SOD),
glutathione
(GSH),
catalase
(CAT),
reduce
malondialdehyde
(MDA)
reactive
oxygen
species
(ROS)
tissue,
thereby
exerting
enhancing
antioxidant
capacity
tissue.Moreover,
TUNEL
staining
image
positive
apoptotic
cells
declined
after
treatment,
indicate
inhibit
cardiomyocyte
apoptosis.Importantly,
The
protective
H
2
O
-pretreated
H9c2
also
verified
vitro.Conclusion:
Taken
together,
has
potential
clinical
application
an
anti-myocardial
ischemia
drug
candidate,
not
only
provides
evidence
further
broadening
diseases,
but
offers
hope
nanomedicine
treat
intractable
diseases.
Journal of Agricultural and Food Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 28, 2025
Natural
spices
have
gained
much
attention
for
their
aromatic
and
pungent
flavors
as
well
multiple
beneficial
health
effects.
As
complex
organelles
that
play
a
central
role
in
energy
production,
stress
response
control,
cell
signal
transduction,
metabolism
regulation,
mitochondria
could
be
regulated
by
many
bioactive
components
spices.
In
this
review,
the
of
maintaining
cellular
homeostasis
is
summarized.
The
regulatory
effects
mitochondrial
function
major
compounds
from
natural
are
evaluated,
including
capsaicin,
6-gingerol,
6-shogaol,
allicin,
quercetin,
curcumin,
tetrahydrocurcumin,
cinnamaldehyde.
underlying
molecular
mechanisms
also
discussed.
This
work
enhance
our
understanding
toward
health-promoting
properties
spice
provide
new
insights
into
prevention
treatment
disorders
associated
with
dysfunctions
those
nutraceuticals.
Journal for Research in Applied Sciences and Biotechnology,
Journal Year:
2025,
Volume and Issue:
4(1), P. 132 - 141
Published: Feb. 28, 2025
Chronic
renal
disease
is
defined
as
the
presence
of
kidney
damage
or
impaired
function
over
a
period
at
least
three
months,
regardless
origin
condition.
Numerous
factors,
including
oxidative
stress,
inflammation,
and
cell
death,
are
frequently
responsible
for
acute
chronic
injury,
which
significant
issue
in
field
global
health.
Because
crucial
functions
that
they
play,
NF-κB
PI3K/Akt
signaling
pathways
potential
therapeutic
targets.
These
pathogenic
processes
mediated
by
these
pathways.
cinnamonaldehyde,
naturally
occurring
bioactive
component,
has
demonstrated
encouraging
nephroprotective
properties.
properties
attributed
to
fact
it
contains
anti-inflammatory,
antioxidant,
anti-apoptotic
The
purpose
this
review
investigate
molecular
role
cinnamaldehyde
preventing
modulating
Within
article,
we
examine
involved
highlight
treatment
disease.
Although
preclinical
studies
have
protective
effects,
additional
research,
clinical
trials,
required
validate
its
safety,
effectiveness,
uses
management
illness
people.
Food & Function,
Journal Year:
2024,
Volume and Issue:
15(12), P. 6217 - 6231
Published: Jan. 1, 2024
Cinnamaldehyde
(CA)
is
the
main
bioactive
component
extracted
from
internal
bark
of
cinnamon
trees
with
many
health
benefits.
In
this
paper,
bioavailability
and
biological
activities
cinnamaldehyde,
underlying
molecular
mechanism
are
reviewed
discussed,
including
antioxidant,
cardioprotective,
anti-inflammatory,
anti-obesity,
anticancer,
antibacterial
properties.
Common
delivery
systems
that
could
improve
stability
CA
also
summarized
evaluated,
such
as
micelles,
microcapsules,
liposomes,
nanoparticles,
nanoemulsions.
This
work
provides
a
comprehensive
understanding
beneficial
functions
strategies
CA,
which
useful
for
future
application
in
functional
food
industry.
Molecules,
Journal Year:
2022,
Volume and Issue:
27(19), P. 6709 - 6709
Published: Oct. 9, 2022
In
this
study,
a
series
of
coumarin
derivatives,
either
alone
or
as
hybrids
with
cinnamic
acid,
were
synthesized
and
evaluated
for
their
cytotoxicity
against
panel
cancer
cells
using
the
MTT
assay.
Then,
most
active
compounds
inspected
mechanism
by
cell-cycle
analysis,
RT-PCR,
DNA
fragmentation,
Western
blotting
techniques.
Cytotoxic
results
showed
that
compound
(4)
had
significant
cytotoxic
effect
HL60
(IC50
=
8.09
µM),
while
(8b)
noticeable
activity
HepG2
13.14
µM).
Compounds
mediated
via
PI3K/AKT
pathway
inhibition.
These
assured
molecular
docking
studies.
support
further
exploratory
research
focusing
on
therapeutic
derivatives
agents.