Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 11, 2025
Glucagon-like
peptide-1
(GLP-1)
receptor
is
widely
distributed
in
the
digestive
system,
cardiovascular
adipose
tissue
and
central
nervous
system.
Numerous
GLP-1
receptor-targeting
drugs
have
been
investigated
clinical
studies
for
various
indications,
including
type
2
diabetes
obesity
(accounts
70%
of
total
studies),
non-alcoholic
steatohepatitis,
Alzheimer's
disease,
Parkinson's
disease.
This
review
presented
fundamental
information
regarding
two
categories
agonists
(GLP-1RAs):
peptide-based
small
molecule
compounds,
elaborated
their
potential
neuroprotective
effects
by
inhibiting
neuroinflammation,
reducing
neuronal
apoptosis,
ultimately
improving
cognitive
function
neurodegenerative
diseases.
As
a
new
hypoglycemic
drug,
GLP-1RA
has
unique
role
concurrent
risk
stroke
T2D
patients.
Given
infiltration
peripheral
immune
cells
into
brain
tissue,
particularly
areas
surrounding
infarct
lesion,
we
further
regulatory
mechanisms.
could
not
only
facilitate
M2
polarization
microglia
through
both
direct
indirect
pathways,
but
also
modulate
quantity
T
cell
subtypes,
CD4,
CD8,
cells,
resulting
inhibition
inflammatory
responses
promotion
regeneration
interleukin-10
secretion.
Therefore,
believe
that
"Tregs-microglia-neuron/neural
precursor
cells"
axis
instrumental
mediating
suppression
neuroprotection
context
ischemic
stroke.
benefits
rapid
diffusion,
favorable
blood-brain
barrier
permeability
versatile
administration
routes,
these
compounds
will
be
one
important
candidates
GLP-1RA.
We
look
forward
to
evidence
intervention
or
complicated
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(3), P. 624 - 624
Published: March 4, 2025
Fabry
disease
(FD)
is
an
X-linked
lysosomal
storage
disorder
characterized
by
deficiency
of
α-galactosidase
A
(α-GalA),
leading
to
the
accumulation
glycosphingolipids
and
multi-organ
dysfunction,
particularly
affecting
cardiovascular
renal
systems.
Disease-modifying
treatments
such
as
enzyme
replacement
therapy
(ERT)
oral
chaperone
(OCT)
have
limited
efficacy,
in
advanced
disease,
prompting
a
need
for
innovative
therapeutic
approaches
targeting
underlying
molecular
mechanisms
beyond
glycosphingolipid
alone.
Recent
insights
into
pathophysiology
FD
highlights
chronic
inflammation
mitochondrial,
lysosomal,
endothelial
dysfunction
key
mediators
progression.
Adjunctive
therapies
sodium-glucose
cotransporter-2
(SGLT2)
inhibitors,
glucagon-like
peptide-1
(GLP-1)
agonists,
mineralocorticoid
receptor
antagonists
(MRAs)
demonstrate
significant
benefits
conditions
including
heart
failure
kidney
disease.
These
drugs
also
modulate
pathways
involved
FD,
autophagy,
oxidative
stress,
pro-inflammatory
cytokine
signaling.
While
theoretical
foundations
support
their
utility,
dedicated
trials
are
necessary
confirm
efficacy
FD-specific
population.
This
narrative
review
importance
expanding
strategies
advocating
multi-faceted
approach
involving
evidence-based
adjunctive
improve
outcomes.
Tailored
research
focusing
on
diverse
phenotypes,
females
non-classical
variants
will
be
critical
advancing
care
improving
outcomes
this
complex
disorder.
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(3), P. 184 - 184
Published: March 10, 2025
Background:
Metabolic
syndrome
is
a
complex
disorder
characterized
by
the
coexistence
of
multiple
risk
factors,
including
dysglycemia,
hypertension,
dyslipidemia,
and
visceral
obesity.
Both
metabolic
diabetes
mellitus
are
closely
associated
with
onset
microvascular
complications
such
as
retinopathy,
polyneuropathy,
nephropathy.
Methods:
This
narrative
review
analyzed
137
studies
published
up
to
2025,
retrieved
from
PubMed
Crossref
databases.
The
objective
was
identify
evaluate
potential
biomarkers
that
could
facilitate
early
detection
in
patients
syndrome.
Results:
Several
demonstrated
strong
correlation
individuals
These
findings
suggest
their
role
diagnosis
assessment.
Conclusions:
identification
reliable
may
enhance
targeted
interventions
for
Further
research
essential
validate
these
markers
establish
clinical
applicability
routine
medical
practice.
Peptides,
Journal Year:
2025,
Volume and Issue:
187, P. 171380 - 171380
Published: March 11, 2025
Recent
studies
with
peptide-based
incretin
herapies
have
focussed
mainly
on
the
glucagon-like
peptide-1
(GLP-1)
receptor
agonist
semaglutide
and
dual
tirzepatide
that
engages
receptors
for
GLP-1
glucose-dependent
insulinotropic
polypeptide
(GIP).
Randomised
clinical
trials
'real-world'
confirmed
marked
glucose-lowering
weight-lowering
efficacy
of
these
agents
across
diverse
populations.
These
include
different
ethnic
groups,
young
elderly
individuals
without
diabetes
and/or
overweight
or
obesity.
also
protections
against
development
progression
cardiovascular
renal
diseases
are
additive
to
benefits
conferred
by
improved
control
blood
glucose
body
weight.
Emerging
evidence
suggests
therapies
could
additionally
ameliorate
fatty
liver
disease,
chronic
inflammation,
sleep
apnea
possibly
degenerative
bone
disorders
cognitive
decline.
New
incretin-based
peptide
in
a
long-acting
glucagon
(LY3324954),
GLP-1/glucagon
agonists
(survodutide,
pemvidutide,
mazdutide,
G49),
triple
GLP-1/GIP/glucagon
(retatrutide,
efocipegtrutide),
combination
amylin
analogue
cagrilintide
(CagriSema),
unimolecular
GLP-1/amylin
(amycretin),
GIP
antibody
agonism
(MariTide).
The
creation
multi-targeting
synthetic
peptides
provides
opportunities
management
type
2
obesity
as
well
new
therapeutic
approaches
an
expanding
list
associated
co-morbidities.
aim
review
is
acquaint
reader
developments
field
from
2023
present
(February
2025).
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 11, 2025
Glucagon-like
peptide-1
(GLP-1)
receptor
is
widely
distributed
in
the
digestive
system,
cardiovascular
adipose
tissue
and
central
nervous
system.
Numerous
GLP-1
receptor-targeting
drugs
have
been
investigated
clinical
studies
for
various
indications,
including
type
2
diabetes
obesity
(accounts
70%
of
total
studies),
non-alcoholic
steatohepatitis,
Alzheimer's
disease,
Parkinson's
disease.
This
review
presented
fundamental
information
regarding
two
categories
agonists
(GLP-1RAs):
peptide-based
small
molecule
compounds,
elaborated
their
potential
neuroprotective
effects
by
inhibiting
neuroinflammation,
reducing
neuronal
apoptosis,
ultimately
improving
cognitive
function
neurodegenerative
diseases.
As
a
new
hypoglycemic
drug,
GLP-1RA
has
unique
role
concurrent
risk
stroke
T2D
patients.
Given
infiltration
peripheral
immune
cells
into
brain
tissue,
particularly
areas
surrounding
infarct
lesion,
we
further
regulatory
mechanisms.
could
not
only
facilitate
M2
polarization
microglia
through
both
direct
indirect
pathways,
but
also
modulate
quantity
T
cell
subtypes,
CD4,
CD8,
cells,
resulting
inhibition
inflammatory
responses
promotion
regeneration
interleukin-10
secretion.
Therefore,
believe
that
"Tregs-microglia-neuron/neural
precursor
cells"
axis
instrumental
mediating
suppression
neuroprotection
context
ischemic
stroke.
benefits
rapid
diffusion,
favorable
blood-brain
barrier
permeability
versatile
administration
routes,
these
compounds
will
be
one
important
candidates
GLP-1RA.
We
look
forward
to
evidence
intervention
or
complicated