PubMed,
Journal Year:
2023,
Volume and Issue:
22, P. 1280 - 1310
Published: Jan. 1, 2023
It
is
now
an
accepted
principle
that
epigenetic
alterations
cause
cellular
dyshomeostasis
and
functional
changes,
both
of
which
are
essential
for
the
initiation
completion
tumor
cycle.
Oral
carcinogenesis
no
exception
in
this
regard,
as
most
tumors
different
subsites
oral
cavity
arise
from
cross-reaction
between
(epi)genetic
inheritance
huge
challenge
environmental
stressors.
Currently,
biochemical
machinery
put
at
service
program,
halting
cell
cycle,
triggering
uncontrolled
proliferation,
driving
angiogenesis
resistance
to
apoptosis,
until
archetypes
phenotype
reached.
Melatonin
has
ability
dynamically
affect
code.
become
melatonin
can
reverse
aberrations
present
other
cancers,
suggesting
possibility
enhancing
oncostatic
capacity
standard
multimodal
treatments
by
incorporating
indolamine
adjuvant.
First
steps
direction
confirm
potential
a
countermeasure
mitigate
detrimental
side
effects
conventional
first-line
radiochemotherapy.
This
single
effect
could
produce
synergies
extraordinary
clinical
importance,
allowing
doses
be
increased
not
interrupted,
ultimately
improving
patients'
quality
life
prognosis.
Motivated
urgency
medical
management
cancer,
many
authors
advocate
moving
Biological reviews/Biological reviews of the Cambridge Philosophical Society,
Journal Year:
2024,
Volume and Issue:
99(5), P. 1772 - 1790
Published: April 30, 2024
Melatonin,
a
product
of
tryptophan
metabolism
via
serotonin,
is
molecule
with
an
indole
backbone
that
widely
produced
by
bacteria,
unicellular
eukaryotic
organisms,
plants,
fungi
and
all
animal
taxa.
Aside
from
its
role
in
the
regulation
circadian
rhythms,
it
has
diverse
biological
actions
including
cytoprotective
responses
other
functions
crucial
for
survival
across
different
species.
The
latter
properties
are
also
shared
metabolites
kynuric
products
generated
reactive
oxygen
species
or
phototransfomation
induced
ultraviolet
radiation.
Vitamins
D
related
photoproducts
originate
phototransformation
∆5,7
sterols,
which
7-dehydrocholesterol
ergosterol
examples.
Their
bonds
B
ring
absorb
solar
radiation
[290-315
nm,
(UVB)
radiation]
resulting
opening
to
produce
previtamin
D,
referred
as
secosteroid.
Once
formed,
can
either
undergo
thermal-induced
isomerization
vitamin
UVB
be
transformed
into
lumisterol
tachysterol.
Vitamin
well
tachysterol,
hydroxylated
cyochrome
P450
(CYP)
enzymes
biologically
active
hydroxyderivatives.
best
known
these
1,25-dihydroxyvitamin
(1,25(OH)
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(21), P. 15963 - 15963
Published: Nov. 4, 2023
Human
skin
aging
is
associated
with
functional
deterioration
on
multiple
levels
of
physiology,
necessitating
the
development
effective
senotherapeutics.
The
well-tolerated
neurohormone
melatonin
unfolds
anti-aging
properties
in
vitro
and
vivo,
but
it
remains
unclear
whether
these
effects
translate
to
aged
human
ex
vivo.
We
tested
this
organ-cultured,
full-thickness
eyelid
(5-6
donors;
49-77
years)
by
adding
culture
medium,
followed
assessment
core
biomarkers
via
quantitative
immunohistochemistry.
Over
6
days,
200
µM
significantly
downregulated
intraepidermal
activity
aging-promoting
mTORC1
pathway
(as
visualized
reduced
S6
phosphorylation)
MMP-1
protein
expression
epidermis
compared
vehicle-treated
control
skin.
Conversely,
transmembrane
collagen
17A1,
a
key
stem
cell
niche
matrix
molecule
that
declines
aging,
mitochondrial
markers
(e.g.,
TFAM,
MTCO-1,
VDAC/porin)
were
upregulated.
Interestingly,
100
also
increased
epidermal
VEGF-A
protein,
which
required
sufficient
for
inducing
rejuvenation.
In
dermis,
fibrillin-1
improved
fibrillin
structural
organization,
indicating
an
elastic
fiber
network.
contrast,
other
(SIRT-1,
lamin-B1,
p16INK4,
I)
remained
unchanged.
This
vivo
study
provides
proof
principle
indeed
exerts
long-suspected
never
conclusively
demonstrated
surprisingly
differential
dermis.
Frontiers in Physiology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 7, 2025
Access
to
electric
light
has
exposed
living
organisms
varying
intensities
of
throughout
the
24
h
day.
Dim
at
night
(DLAN)
is
an
inappropriate
signal
for
biological
clock,
which
responsible
circadian
organization
physiology.
During
gestational
period,
physiological
adaptations
occur
ensure
a
successful
pregnancy
and
optimal
fetal
development.
Environmental
maternal
conditions,
such
as
disruptions
rhythms,
could
negatively
affect
offspring
health.
We
have
previously
demonstrated
that
exposure
female
Wistar
rats
DLAN
results
in
circadian,
metabolic,
behavioral
alterations.
A
relevant
behavior
during
adolescence
social
play,
primarily
regulated
by
nucleus
accumbens
(NAc)
crucial
proper
performance
important
behaviors
adulthood.
Throughout
development,
microglia
are
remodeling
diverse
brain
regions
via
synaptic
pruning.
adolescence,
this
process
occurs
within
NAc,
where
immune-mediated
directly
impacts
play
behavior.
This
study
investigated
effects
or
light-dark
cycle
(LD)
before
(5
weeks)
period
(21-23
days)
on
metabolism
Body
mass
was
measured
every
5
days
from
postnatal
day
1
(PN1)
PN25
10
PN40
PN90;
food
consumption
monitored
weekly
PN90.
Social
evaluated
PN40.
The
quantification
morphology
NAc
were
PN30.
An
open
field
test
conducted
PN60,
anhedonia
assessed
Male
mothers
showed
increased
body
gain
PN25.
male
had
lower
consumption,
while
females
exhibited
consumption.
In
behavior,
no
differences
found
between
LD
offspring.
contrast,
significant
decrease
compared
animals,
associated
with
higher
numbers
more
ramified
morphology.
Importantly,
PN90,
presented
anxiety-like
behaviors.
These
demonstrate
induces
intergenerational
alterations
persist
until
Veterinary Sciences,
Journal Year:
2025,
Volume and Issue:
12(2), P. 87 - 87
Published: Jan. 23, 2025
Melatonin
(MLT),
produced
by
the
pineal
gland
and
other
tissues,
is
known
for
its
anti-inflammatory
effects,
particularly
in
regulating
inflammatory
markers
cytokines
intestinal
cells.
Our
study
aimed
to
investigate
how
MLT
influences
expression
of
genes
through
histone
modification
canine
ileum
epithelial
cells
(cIECs).
In
our
experiment,
cIECs
were
cultured
divided
into
a
control
group
(CON)
an
MLT-treatment
group.
did
not
significantly
affect
cell
growth
or
death
compared
CON.
However,
treatment
led
upregulation
CD40,
ZAP70,
IL7R
downregulation
LCK,
RPL37,
TNFRSF13B,
CD4,
CD40LG,
BLNK,
CIITA
at
mRNA
level.
Moreover,
altered
NF-kappa
B
signaling
pathway
upregulating
genes,
such
as
TICAM1,
VCAMI,
GADD45B,
IRAK1,
TRADD,
RELA,
RIPK1,
RELB,
downregulating
PRKCB,
LY96,
ILIB,
TNFRSF11A.
Using
ChIP-qPCR,
we
discovered
that
enhanced
acetylation
marks
H3K9ac,
H3K18ac,
H3K27ac,
methylation
H3K4me1
H3K4me3
ZAP70
CD40
gene
loci
(p
<
0.05).
Additionally,
enrichment
RNA
polymerase
II
phosphorylated
Ser5
pol-II
these
was
increased
MLT-treated
0.05),
indicating
heightened
transcriptional
activity.
conclusion,
findings
suggest
mitigates
inflammation
modulating
transcription
modifications,
offering
potential
therapeutic
insights
bowel
diseases.
GeroScience,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Abstract
Aging
is
driven
by
fundamental
mechanisms
like
oxidative
stress,
telomere
shortening
and
changes
in
DNA
methylation,
which
together
prepare
the
ground
for
age-related
diseases.
Botanical
extracts,
rich
bioactive
phytoconstituents,
represent
a
promising
resource
developing
therapies
that
target
these
to
promote
healthy
aging.
This
study
explores
geroprotective
potential
of
Monarda
didyma
L.
extract.
In
vitro
analyses
revealed
extract’s
strong
antioxidant
activity,
ability
reduce
shortening,
capacity
protect
against
damage,
thereby
decreasing
cellular
senescence
improving
endothelial
function.
The
randomized,
double-blind
clinical
trial
demonstrated
daily
oral
supplementation
with
extract
significantly
improved
leukocyte
length
(LTL)
stabilized
methylation
age
(DNAmAge)
intervention
group,
while
placebo
group
experienced
accelerated
epigenetic
aging
hypermethylation
critical
genes
(ELOVL2
FHL2).
also
reported
enhanced
quality
life,
particularly
physical
domain,
along
movement
sleep
indices
detected
questionnaire
wearable
sensors.
These
compelling
findings
position
as
powerful
candidate
future
therapies,
impact
Behavioral and Brain Functions,
Journal Year:
2025,
Volume and Issue:
21(1)
Published: March 18, 2025
Alzheimer's
disease
(AD)
is
characterized
by
progressive
cognitive
decline
and
synaptic
dysfunction,
largely
driven
amyloid
plaques
neurofibrillary
tangles
(NFTs)
composed
of
hyperphosphorylated
tau.
These
pathological
hallmarks
disrupt
glutamate
signaling,
which
essential
for
plasticity
memory
consolidation.
This
study
investigates
the
therapeutic
potential
melatonin
on
in
an
AD-like
mouse
model,
with
a
focus
its
regulatory
effects
homeostasis
metabotropic
receptors
(mGluRs).
The
began
in-silico
bioinformatics
analysis
RNA-seq
datasets
from
hippocampal
tissues
AD
patients
to
identify
differentially
expressed
genes
(DEGs)
related
signaling
tau
pathology.
An
model
was
induced
via
intra-hippocampal
injection
cis-phospho
C57BL/6
mice.
Memory
function
assessed
using
behavioral
tests.
Synaptic
evaluated
vitro
field
recording
slices.
Histological
analyses
included
Nissl
staining
neuronal
density,
Luxol
Fast
Blue
myelin
integrity,
immunofluorescence
hyperphosphorylation.
Molecular
studies
employed
qPCR
Western
blot
assess
glutamate-related
markers
phosphorylation.
Melatonin
(10
mg/kg)
administered
intraperitoneally,
starting
either
two
weeks
(early
intervention)
or
four
(late
post-induction.
Key
molecular
targets
pathways
were
identified
bioinformatics.
mice
displayed
deficits
dysfunction.
improved
function,
especially
early
intervention,
as
confirmed
revealed
reduced
loss,
decreased
findings
showed
restored
mGluR
expression
GSK3
activity.
Early
intervention
yielded
superior
outcomes,
partial
restoration
observed
LTP
recordings.
underscore
neuroprotective
properties
melatonin,
mediated
ability
modulate
activity,
offering
new
insights
into
agent
AD.
Additionally,
results
suggest
that
earlier
administration
may
significantly
enhance
efficacy,
highlighting
importance
timely
neurodegenerative
diseases.
Antioxidants,
Journal Year:
2025,
Volume and Issue:
14(4), P. 387 - 387
Published: March 26, 2025
Kidney
disease
and
hypertension
are
interconnected,
prevalent
conditions
that
affect
both
pregnant
women
children.
Oxidative
stress
occurs
when
reactive
oxygen
species
or
nitrogen
exceed
the
capacity
of
antioxidant
systems.
It
plays
a
critical
role
in
kidney
development,
resulting
programming
increased
risks
for
across
life
course.
Animal
models
have
significantly
advanced
our
understanding
oxidative
stress-related
programming,
molecular
mechanisms
involved,
early-life
interventions
to
prevent
disease.
This
review
critically
examines
influence
perinatal
on
highlighting
its
long-term
effects
outcomes
susceptibility
hypertension.
also
explores
potential
antioxidant-based
preventing
Furthermore,
addresses
existing
gap
between
insights
gained
from
animal
their
translation
into
clinical
practices,
emphasizing
challenges
opportunities
future
research
this
area.