Diabetes Obesity and Metabolism,
Год журнала:
2024,
Номер
unknown
Опубликована: Сен. 23, 2024
We
evaluated
the
efficacy
and
safety
of
cofrogliptin,
a
novel
dipeptidyl
peptidase-4
inhibitor
taken
once
every
2
weeks
(Q2W),
compared
with
linagliptin
(taken
daily)
in
patients
type
diabetes
inadequately
controlled
on
metformin
China.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(17), С. 13381 - 13381
Опубликована: Авг. 29, 2023
Diabetes
mellitus
is
a
chronic
multifaceted
disease
with
multiple
potential
complications,
the
treatment
of
which
can
only
delay
and
prolong
terminal
stage
disease,
i.e.,
type
2
diabetes
(T2DM).
The
World
Health
Organization
predicts
that
will
be
seventh
leading
cause
death
by
2030.
Although
many
antidiabetic
medicines
have
been
successfully
developed
in
recent
years,
such
as
GLP-1
receptor
agonists
SGLT-2
inhibitors,
single-target
drugs
are
gradually
failing
to
meet
therapeutic
requirements
owing
individual
variability,
diversity
pathogenesis,
organismal
resistance.
Therefore,
there
remains
need
investigate
pathogenesis
T2DM
more
depth,
identify
targets,
provide
improved
glycemic
control
solutions.
This
review
presents
an
overview
mechanisms
action
development
latest
agents
targeting
years.
It
also
discusses
emerging
target-based
therapies
new
targets
emerged
within
last
three
aim
our
theoretical
basis
for
further
advancement
targeted
T2DM.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(2), С. 1646 - 1646
Опубликована: Янв. 13, 2023
Diabetes
Mellitus
is
a
multifactorial
disease
with
critical
impact
worldwide.
During
prediabetes,
the
presence
of
various
inflammatory
cytokines
and
oxidative
stress
will
lead
to
pathogenesis
type
2
diabetes.
Furthermore,
insulin
resistance
chronic
hyperglycemia
micro-
macrovascular
complications
(cardiovascular
disease,
heart
failure,
hypertension,
kidney
atherosclerosis).
The
development
through
years
pharmacological
options
allowed
us
reduce
persistence
diabetic
complications.
This
review
aims
highlight
specific
mechanisms
which
new
treatments
for
diabetes
improve
cardiovascular
outcomes.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Фев. 6, 2024
The
global
prevalence
of
diabetes
mellitus
(DM)
has
led
to
widespread
multi-system
damage,
especially
in
cardiovascular
and
renal
functions,
heightening
morbidity
mortality.
Emerging
antidiabetic
drugs
sodium-glucose
cotransporter
2
inhibitors
(SGLT2i),
glucagon-like
peptide-1
receptor
agonists
(GLP-1RAs),
dipeptidyl
peptidase-4
(DPP-4i)
have
demonstrated
efficacy
preserving
cardiac
function,
both
type
diabetic
non-diabetic
individuals.
To
understand
the
exact
impact
these
on
cardiorenal
protection
underlying
mechanisms,
we
conducted
a
comprehensive
review
recent
large-scale
clinical
trials
basic
research
focusing
SGLT2i,
GLP-1RAs,
DPP-4i.
Accumulating
evidence
highlights
diverse
mechanisms
including
glucose-dependent
independent
pathways,
revealing
their
potential
disease.
This
provides
critical
insights
into
protective
effects
DPP-4i
underscores
importance
medications
mitigating
progression
complications,
broader
implications
beyond
glycemic
management.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Фев. 9, 2024
Insulin
resistance
in
brain
and
amyloidogenesis
are
principal
pathological
features
of
diabetes-related
cognitive
decline
development
Alzheimer’s
disease
(AD).
A
growing
body
evidence
suggests
that
maintaining
glucose
under
control
diabetic
patients
is
beneficial
for
preventing
AD
development.
Dipeptidyl
peptidase
4
inhibitors
(DDP4is)
a
class
novel
glucose-lowering
medications
through
increasing
insulin
excretion
decreasing
glucagon
levels
have
shown
neuroprotective
potential
recent
studies.
This
review
consolidates
extant
from
earlier
new
studies
investigating
the
association
between
DPP4i
use,
AD,
other
outcomes.
Beyond
DPP4i’s
benefits
alleviating
glucose-lowering,
underlying
mechanisms
neuroprotection
with
were
categorized
into
following
sections:
(Ferrari
et
al.,
Physiol
Rev,
2021,
101,
1,047–1,081):
DPP4is
on
directly
ameliorating
burden
β-amyloid
plaques
reducing
formation
neurofibrillary
tangles;
bioactivity
DPP4
substrates
including
glucagon-like
peptide-1
(GLP-1),
glucose-dependent
insulinotropic
peptide
(GIP),
stromal-derived
factor-1α
(SDF-1α)
etc.;
pleiotropic
effects
neuronal
cells
intracerebral
structure
anti-inflammation,
anti-oxidation,
anti-apoptosis.
We
further
revisited
recently
published
epidemiological
provided
supportive
data
to
compliment
preclinical
evidence.
Given
there
remains
lack
completed
randomized
trials
aim
at
assessing
effect
progression,
this
expected
provide
useful
insight
inhibition
as
therapeutic
target
prevention
treatment.
The
helpful
informing
rationales
future
clinical
research
guiding
evidence-based
practice.
Biomedicines,
Год журнала:
2022,
Номер
10(9), С. 2306 - 2306
Опубликована: Сен. 16, 2022
Dipeptidyl
peptidase
4
(DPP4)
is
a
molecule
implicated
in
the
regulation
of
metabolic
homeostasis
and
inflammatory
processes,
it
exerts
its
main
action
through
enzymatic
activity.
DPP4
represents
enzyme
most
involved
catabolism
incretin
hormones;
thus,
activity
impacts
appetite,
energy
balance,
fine
glucose
homeostasis.
Indeed,
inhibitors
represent
class
antidiabetic
agents
widely
used
for
treatment
Type
2
diabetes
mellitus
(T2DM).
also
acts
as
an
adipokine
mainly
secreted
by
adipose
tissue,
mostly
from
mature
adipocytes
visceral
compartment,
where
autocrine
paracrine
activities.
can
disrupt
insulin
signaling
within
adipocyte
other
target
cells
tissues,
favors
development
proinflammatory
environment.
This
likely
at
basis
presence
elevated
circulating
levels
several
diseases.
In
this
review,
we
summarize
recent
evidence
role
adipokine-regulating
glucose/insulin
metabolism
fat
homeostasis,
with
particular
focus
on
clinical
outcomes
associated
increased
secretion
tissue
accumulation
dysfunction.
Annals of Medicine and Surgery,
Год журнала:
2025,
Номер
87(4), С. 2133 - 2148
Опубликована: Март 7, 2025
Background:
Dipeptidyl
peptidase-4
(DPP-4)
inhibitors
are
oral
antihyperglycemic
agents
commonly
prescribed
for
type
2
diabetes
(T2DM).
Due
to
the
intricate
relationship
between
glucose
regulation
and
cardiovascular
diseases
(CVDs),
DPP-4
have
attracted
attention
their
safety
efficacy.
This
bibliometric
analysis
aims
provide
insights
into
global
research
landscape
on
outcomes
(CVOs).
Methods:
A
was
performed,
using
Web
of
Science
Core
Collection.
Data
were
analyzed
VOSviewer,
CiteSpace,
Biblioshiny.
Results:
The
United
States
led
in
publication
output,
followed
by
Japan
China.
Harvard
University
Toronto
leading
institutions.
most
influential
journals
Cardiovascular
Diabetology
Diabetes
Obesity
&
Metabolism.
Darren
K.
McGuire
prolific
author
Rury
R.
Holman.
occurring
keyword
heart
failure.
Cluster
revealed
key
thematic
areas
field,
including
“incretin-based
therapy,”
“dipeptidyl
inhibition,”
“cardiovascular
safety.”
Emerging
clusters,
such
as
“atrial
fibrillation,”
gained
recent
years,
highlighting
evolving
investigation.
Conclusion:
study
underscores
importance
CVOs
inhibitors.
high
frequency
keywords
“heart
failure,”
along
with
terms
like
“mortality”
“risk,”
highlights
a
strong
focus
complications
literature.
Our
reflected
that
studies
address
these
critical
aspects
health,
discussing
potential
role
mitigating
adverse
outcomes,
particularly
patients
T2DM.
PLoS ONE,
Год журнала:
2025,
Номер
20(3), С. e0312600 - e0312600
Опубликована: Март 10, 2025
Exploring
the
possibility
of
familiar
dietary
sources
as
additional
diabetes
treatments
is
crucial,
especially
considering
financial
difficulties
related
to
mellitus.
Using
both
in
vitro
and
silico
techniques,
this
work
aims
assess
antidiabetic
benefits
extract
from
Solanum
lasiocarpum
Dunal
.
The
evaluations
encompass
ability
scavenge
DPPH
radicals,
inhibition
α-amylase,
α-glucosidase,
DPP-4,
cytotoxicity,
glucose
absorption
kinetics.
With
an
IC50
value
0.69
±
0.14
mg/ml,
S.
showed
encouraging
inhibition.
values
2.123
mg/ml
inhibited
enzymes
DPP-4.
Furthermore,
a
notable
increase
(P
<
0.05)
uptake
by
L6
myoblasts
was
observed
with
administration
various
combinations.
In
analysis,
including
XP
docking
MM-GBSA,
revealed
that
10
21
compounds
within
combination
exhibited
substantial
interactions
stable
binding
capabilities
α-amylase
DPP-4
proteins,
indicating
their
potential
enzyme
inhibitors.
Therefore,
it
can
be
inferred
represents
promising
therapeutic
approach
for
management.
Molecules,
Год журнала:
2022,
Номер
27(14), С. 4498 - 4498
Опубликована: Июль 14, 2022
The
enzymatic
activity
of
CD26/DPP4
(dipeptidyl
peptidase
4/DPP4)
is
highlighted
in
multiple
studies
to
play
a
vital
role
glucose
metabolism
by
cleaving
and
inactivating
the
incretins
glucagon-like
peptide-1
(GLP)
gastric
inhibitory
protein
(GIP).
A
large
number
demonstrate
that
CD26
also
plays
an
integral
immune
system,
particularly
T
cell
activation.
extensively
expressed
cells,
such
as
B
NK
dendritic
macrophages.
cleaves
regulates
numerous
chomokines
cytokines.
inhibitors
have
been
widely
used
for
treatment
diabetes
mellitus,
while
it
still
under
investigation
therapy
immune-mediated
diseases.
In
addition,
CD26’s
involvement
cancer
immunology
was
described.
review
aims
summarize
therapeutic
effects
on
diseases,
well
mechanisms
underpin
them.