Psychopharmacology,
Journal Year:
2023,
Volume and Issue:
240(4), P. 983 - 1000
Published: March 4, 2023
Diabetes
causes
a
variety
of
molecular
changes
in
the
brain,
making
it
real
risk
factor
for
development
cognitive
dysfunction.
Complex
pathogenesis
and
clinical
heterogeneity
impairment
makes
efficacy
current
drugs
limited.
Sodium-glucose
cotransporter
2
inhibitors
(SGLT2i)
gained
our
attention
as
with
potential
beneficial
effects
on
CNS.
In
present
study,
these
ameliorated
associated
diabetes.
Moreover,
we
verified
whether
SGLT2i
can
mediate
degradation
amyloid
precursor
protein
(APP)
modulation
gene
expression
(Bdnf,
Snca,
App)
involved
control
neuronal
proliferation
memory.
The
results
research
proved
participation
multifactorial
process
neuroprotection.
attenuate
neurocognitive
through
restoration
neurotrophin
levels,
neuroinflammatory
signaling,
Bdnf,
App
brain
diabetic
mice.
targeting
above-mentioned
genes
is
currently
seen
one
most
promising
developed
therapeutic
strategies
diseases
this
work
could
form
basis
future
administration
diabetics
impairment.
Hypertension Research,
Journal Year:
2024,
Volume and Issue:
47(8), P. 2094 - 2103
Published: May 23, 2024
Abstract
The
sodium-glucose
cotransporter
2
(SGLT2)
is
a
glucose
transporter
that
located
within
the
proximal
tubule
of
kidney’s
nephrons.
While
it
typically
associated
with
kidney,
was
later
identified
in
various
areas
central
nervous
system,
including
modulating
cardiorespiratory
regulation
like
blood
pressure.
In
SGLT2
functions
by
reabsorbing
from
nephron’s
into
bloodstream.
inhibitors
are
medications
hinder
function
SGLT2,
thus
preventing
absorption
and
allowing
for
its
excretion
through
urine.
not
first-line
choice,
they
given
conjunction
other
pharmaceutical
interventions
to
manage
hyperglycemia
individuals
diabetes
mellitus.
also
have
surprising
secondary
effect
decreasing
pressure
independent
levels.
implication
lowering
presence
system
brings
question
role
brain.
Here,
we
evaluate
review
inhibitors,
their
control,
future
as
antihypertensive
agents,
possible
mechanisms
control
system.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
206, P. 107295 - 107295
Published: July 4, 2024
The
lack
of
effective
treatments
for
dementia
has
led
to
explore
the
potential
antidiabetic
agents
as
a
possible
approach.
This
cross-sectional
and
population-based
study
aimed
investigate
relationship
between
each
drug
their
defined
daily
doses
(DDDs)
use
anti-Alzheimer's
disease
(AD)
drugs
in
order
establish
new
hypotheses
about
role
AD.
For
that
purpose,
database
containing
information
on
medications
prescribed
233183
patients
aged
50
years
or
older
2018
2020
was
used.
DDDs
were
calculated
according
ATC/DDD
index
2023.
Statistical
analyses,
with
logistic
regression,
carried
out
assess
anti-AD
consumption.
A
total
91836
who
at
least
one
antihypertensive,
antidiabetic,
lipid-modifying
agent
included
study;
specifically,
29260
medication.
Among
agents,
glucagon-like
peptide-1
analogs
(GLP-1)
likely
have
positive
association
people
70
80
years.
Additionally,
sodium-glucose
cotransporter
2
inhibitors
(SGLT2i)
prone
usage
across
almost
every
age.
However,
insulin
associated
an
increased
agents.
In
conclusion,
there
is
evidence
suggesting
correlation
certain
dementia.
Specifically,
GLP-1
SGLT2i
might
be
lower
odds
usage,
while
insulins
linked
higher
using
drugs.
Translational Neurodegeneration,
Journal Year:
2024,
Volume and Issue:
13(1)
Published: Aug. 9, 2024
The
rising
prevalence
of
diabetes
mellitus
has
casted
a
spotlight
on
one
its
significant
sequelae:
cognitive
impairment.
Sodium-glucose
cotransporter-2
(SGLT2)
inhibitors,
originally
developed
for
management,
are
increasingly
studied
their
benefits.
These
benefits
may
include
reduction
oxidative
stress
and
neuroinflammation,
decrease
amyloid
burdens,
enhancement
neuronal
plasticity,
improved
cerebral
glucose
utilization.
multifaceted
effects
the
relatively
favorable
side-effect
profile
SGLT2
inhibitors
render
them
promising
therapeutic
candidate
disorders.
Nonetheless,
application
impairment
is
not
without
limitations,
necessitating
more
comprehensive
research
to
fully
determine
potential
treatment.
In
this
review,
we
discuss
role
in
neural
function,
elucidate
diabetes-cognition
nexus,
synthesize
current
knowledge
based
animal
studies
clinical
evidence.
Research
gaps
proposed
spur
further
investigation.
Diabetes/Metabolism Research and Reviews,
Journal Year:
2024,
Volume and Issue:
40(2)
Published: Feb. 1, 2024
Abstract
Aims
The
effectiveness
of
sodium‐glucose
co‐transporter‐2
inhibitors
(SGLT2i)
on
incident
dementia
in
patients
with
diabetes
and
atrial
fibrillation
(AF)
remains
unknown.
This
study
aimed
to
investigate
the
association
between
SGLT2i
risk
diabetic
AF,
explore
interactions
oral
anticoagulants
or
dipeptidyl
peptidase‐4
(DPP4i).
Materials
Methods
We
conducted
a
cohort
using
Taiwan's
National
Health
Insurance
Research
Database.
Patients
AFwithout
prior
history
established
cardiovascular
diseases,
were
identified.
Using
propensity
score
matching,
810
receiving
matched
1620
not
SGLT2i.
primary
outcome
was
dementia,
secondary
outcomes
included
composite
events
mortality.
Results
After
up
5
years
follow‐up,
use
associated
significantly
lower
(hazard:
0.71,
95%
confidence
interval:
0.51–0.98),
particularly
vascular
(HR:
0.44,
CI:
0.24–0.82).
related
reduced
risks
AF‐related
hospitalisation
0.72,
0.56–0.93),
stroke
0.75,
0.60–0.94),
all‐cause
death
0.33,
0.24–0.44).
protective
effects
consistent
irrespective
concurrent
non‐vitamin
K
antagonist
(NOACs)
DPP4i.
Conclusions
In
hospitalisation,
stroke,
death.
independent
either
NOACs
IBRO Neuroscience Reports,
Journal Year:
2025,
Volume and Issue:
18, P. 163 - 170
Published: Jan. 10, 2025
Alzheimer's
disease
(AD)
is
one
of
the
most
common
age-related
neurodegenerative
disorders.
The
main
medicinal
theory
for
management
AD
belongs
to
acetyl-cholinesterase-inhibition
pathway
and
NMDA
antagonism.
Recent
investigation
proposed
memory
improvement
by
sodium-glucose
co-transporter
2
(SGLT2)
inhibitors
which
indicated
improve
glycemic
control
in
adults
with
type
diabetes
mellitus.
According
lack
sufficient
evidence
about
efficacy
empagliflozin
(EMPA)
improvement,
comparison
donepezil
(DON),
present
research
was
carried
out
order
investigate
this
hypothesis
towards
scopolamine-induced
neurotoxicity
on
experimental
male
Wistar
rats.
animals
divided
into
two
sets,
each
included
4
groups:
first
set
Healthy
[Control,
EMPA
(4
or
10mg/kg),
DON
(1mg/kg)].
second
rat
Alzheimer
model,
received
2mg/kg
Scopolamine
intraperitoneal
route
10
days
followed
other
treatments
[AD,
AD+
10mg/kg)
AD+DON].
Normal
rats
rats,
group
receiving
different
substances
8
consecutive
24hours
after
accomplishment
drug
administrations,
functions
assessed
through
Morris
water
maze
(MWM)
paradigm.
This
task
decapitation
evaluate
biochemical
oxidative
stress
parameters
brain
tissue.
Our
data
that
significantly
improved
animals'
performance
behavioral
test
a
significant
decrease
antioxidant
imbalance.
In
addition,
(4mg/kg)
reduced
both
cellular
malondialdehyde
protein
carbonyl
content
while
conversely
increased
total
glutathione
content.
Besides,
levels
as
well
endogenous
antioxidants
ferric
reducing
power
assay
reported
be
augmented.
It
seems
aspects
animal
models
accordance
histopathological
assessments.
Conclusively,
4mg/kg
demonstrated
better
results
all
were
evaluated
during
research.
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
Frontiers in Endocrinology,
Journal Year:
2023,
Volume and Issue:
14
Published: Sept. 21, 2023
Type
II
diabetes
mellitus
(T2DM)
is
a
chronic
metabolic
disease
characterized
by
prolonged
hyperglycemia
and
insulin
resistance
(IR).
Its
incidence
increasing
annually,
posing
significant
threat
to
human
life
health.
Consequently,
there
an
urgent
requirement
discover
effective
drugs
investigate
the
pathogenesis
of
T2DM.
Autophagy
plays
crucial
role
in
maintaining
normal
islet
structure.
However,
state
high
glucose,
autophagy
inhibited,
resulting
impaired
function,
resistance,
complications.
Studies
have
shown
that
modulating
through
activation
or
inhibition
can
positive
impact
on
treatment
T2DM
its
it
important
note
specific
regulatory
mechanisms
vary
depending
target
organ.
This
review
explores
T2DM,
taking
into
account
both
genetic
external
factors.
It
also
provides
summary
reported
chemical
traditional
Chinese
medicine
autophagic
pathway
for