Current Medicinal Chemistry,
Год журнала:
2021,
Номер
29(24), С. 4138 - 4151
Опубликована: Ноя. 30, 2021
Alzheimer's
disease
(AD)
is
the
most
common
form
of
dementia
worldwide,
with
approximately
6
million
cases
reported
in
America
2020.
The
clinical
signs
AD
include
cognitive
dysfunction,
apathy,
anxiety
and
neuropsychiatric
signs,
pathogenetic
mechanisms
that
involve
amyloid
peptide-β
extracellular
accumulation
tau
hyperphosphorylation.
Unfortunately,
current
drugs
to
treat
can
provide
only
symptomatic
relief
but
are
not
disease-modifying
molecules
able
revert
progression.
endogenous
modulator
adenosine,
through
A2A
receptor
activation,
plays
a
role
synaptic
loss
neuroinflammation,
which
crucial
for
impairment
memory
damage.In
this
review,
recent
advances
covering
adenosine
antagonists
will
be
extensively
reviewed,
providing
basis
rational
design
future
inhibitors.Herein,
literature
on
receptors
their
plasticity
as
well
effects
antagonism
animal
models
humans,
reviewed.
Furthermore,
chemical
structure-based
strategies
presented.Caffeine,
widely
consumed
natural
product
stimulant
an
antagonist,
improves
human
memory.
Similarly,
synthetic
antagonists,
described
may
means
fight
AD.This
review
highlights
potential
novel
approach
patients
AD.
Frontiers in Aging Neuroscience,
Год журнала:
2022,
Номер
14
Опубликована: Апрель 12, 2022
Alzheimer's
disease
(AD)
is
the
most
prevalent
form
of
age-related
dementia
in
world,
and
its
main
pathological
features
consist
amyloid-β
(Aβ)
plaque
deposits
neurofibrillary
tangles
formed
by
hyperphosphorylated
tau
protein.
So
far,
only
a
few
AD
treatments
approved
have
been
applied
clinic,
but
effects
these
drugs
are
limited
for
partial
symptomatic
relief
to
patients
with
unable
alter
progression.
Later,
all
efforts
targeting
pathogenic
factors
were
unsuccessful
over
past
decades,
which
suggested
that
pathogenesis
complex.
Recently,
disease-modifying
therapies
(DMTs)
can
change
underlying
pathophysiology
AD,
anti-Aβ
monoclonal
antibodies
(mabs)
(e.g.,
aducanumab,
bapineuzumab,
gantenerumab,
solanezumab,
lecanemab)
developed
successively
conducted
clinical
trials
based
on
theory
systemic
failure
cell-mediated
Aβ
clearance
contributes
occurrence
In
review,
we
summarized
recent
studies
therapeutic
trial
results
mabs
AD.
Specifically,
focused
discussion
impact
aducanumab
lecanemab
pathology
profiles.
The
review
provides
possible
evidence
applying
immunotherapy
analyzes
lessons
learned
from
order
further
study
adverse
Drugs in Context,
Год журнала:
2021,
Номер
10, С. 1 - 9
Опубликована: Сен. 30, 2021
Alzheimer's
disease
(AD)
is
the
most
common
cause
for
dementia
worldwide.
Until
recently,
all
approved
treatments
AD
were
symptomatic
and
not
modifying.
On
7
June
2021,
US
FDA
aducanumab,
a
human
IgG1
anti-Aβ
monoclonal
antibody
selective
Aβ
aggregates,
as
first
disease-modifying
treatment
AD.
Aducanumab
in
United
States
of
mild
cognitive
impairment
or
mild-dementia
stage
In
this
Editorial,
we
review
trial
data
aducanumab
controversies
that
its
approval
has
generated.
Antioxidants,
Год журнала:
2021,
Номер
10(9), С. 1479 - 1479
Опубликована: Сен. 16, 2021
The
pathogenesis
of
Alzheimer's
disease
involves
β
amyloid
(Aβ)
accumulation
known
to
induce
synaptic
dysfunction
and
neurodegeneration.
brain's
vulnerability
oxidative
stress
(OS)
is
considered
a
crucial
detrimental
factor
in
disease.
OS
Aβ
are
linked
each
other
because
induces
OS,
increases
the
deposition.
Thus,
answer
question
"which
comes
first:
chicken
or
egg?"
remains
extremely
difficult.
In
any
case,
evidence
for
primary
occurrence
AD
attractive.
indicates
that
long
period
gradual
damage
precedes
results
appearance
clinical
pathological
symptoms,
including
deposition,
neurofibrillary
tangle
formation,
metabolic
dysfunction,
cognitive
decline.
Moreover,
plays
role
many
risk
factors
AD.
begins
years
before
its
antioxidant
treatment
can
be
an
important
therapeutic
target
attacking
Pharmaceutics,
Год журнала:
2022,
Номер
14(6), С. 1117 - 1117
Опубликована: Май 24, 2022
Alzheimer’s
disease
(AD)
is
the
most
common
cause
of
dementia.
The
pathophysiology
this
characterized
by
accumulation
amyloid-β,
leading
to
formation
senile
plaques,
and
intracellular
presence
neurofibrillary
tangles
based
on
hyperphosphorylated
tau
protein.
In
therapeutic
approach
AD,
we
can
identify
three
important
fronts:
approved
drugs
currently
available
for
treatment
disease,
which
include
aducanumab,
donepezil,
galantamine,
rivastigmine,
memantine,
a
combination
memantine
donepezil;
therapies
under
investigation
that
work
mainly
Aβ
pathology
pathology,
γ-secretase
inhibitors,
β-secretase
α-secretase
modulators,
aggregation
metal
interfering
drugs,
enhance
clearance,
inhibitors
protein
hyperphosphorylation,
promote
clearance
tau,
finally,
other
alternative
designed
improve
lifestyle,
thus
contributing
prevention
disease.
Therefore,
aim
review
was
analyze
describe
current
treatments
possible
future
alternatives
in
AD.
Frontiers in Neurology,
Год журнала:
2022,
Номер
13
Опубликована: Март 23, 2022
Second-generation
anti-amyloid
monoclonal
antibodies
are
emerging
as
a
viable
therapeutic
option
for
individuals
with
prodromal
and
mild
dementia
due
to
Alzheimer's
disease
(AD).
Passive
immunotherapy
aducanumab
(Aduhelm),
lecanemab,
donanemab,
gantenerumab
all
lower
CNS
amyloid
(Aβ)
burden
but
come
significant
risk
of
amyloid-related
imaging
abnormality
(ARIA)—the
most
common
side
effect
this
class
drugs.
While
usually
asymptomatic
detected
only
on
brain
MRI,
ARIA
may
lead
new
signs
symptoms
including
headache,
worsening
confusion,
dizziness,
visual
disturbances,
nausea,
seizures.
In
addition,
one
fatality
related
ARIA-E
(edema)
ARIA-H
(hemorrhage)
donanemab
reported
date.
be
associated
excessive
neuroinflammation
saturation
perivascular
clearance
pathways,
while
vascular
weakening
rupture
small
blood
vessels.
The
is
higher
at
treatment
initiation,
in
ApoE4
carriers,
dosage,
>4
microhemorrhages
baseline
MRI.
increases
age
cerebrovascular
disease.
Dose
titration
mitigates
the
ARIA,
contraindications
include
those
prescribed
anti-platelet
or
anti-coagulant
A
MRI
required
before
initiated,
each
scheduled
dose
escalation,
any
neurologic
sign
symptom.
Management
ranges
from
continued
antibody
monthly
monitoring
temporary
permanent
suspension
symptomatic
moderate
severe
Controlled
studies
regarding
prevention
lacking,
anecdotal
evidence
suggests
that
pulse
intravenous
corticosteroids
benefit,
well
course
anticonvulsant
JAMA Neurology,
Год журнала:
2022,
Номер
79(5), С. 478 - 478
Опубликована: Март 28, 2022
Several
anti-amyloid
monoclonal
antibodies
have
been
developed
for
slowing
the
progression
of
Alzheimer
disease
(AD).
Among
furthest
are
aducanumab,
which
received
accelerated
approval
from
US
Food
and
Drug
Administration
in
2021,
donanemab,
is
currently
undergoing
phase
3
trials.
The
cost-effectiveness
these
treatments
has
not
established.
Biomedicine & Pharmacotherapy,
Год журнала:
2023,
Номер
162, С. 114581 - 114581
Опубликована: Март 24, 2023
Puerarin
is
an
isoflavone
compound
derived
from
Pueraria
lobata
in
traditional
Chinese
medicine.
Accumulating
evidence
has
indicated
that
puerarin
demonstrates
multiple
pharmacological
effects
and
exhibits
treatment
potential
for
various
neurological
disorders.
Based
on
the
latest
research
progress
as
a
neuroprotective
agent,
its
activity,
molecular
mechanism,
therapeutic
application
were
systematically
reviewed
with
emphasis
pre-clinical
studies.
The
related
information
was
extracted
compiled
major
scientific
databases,
including
PubMed,
ScienceDirect,
SpringerLink,
National
Knowledge
Infrastructure,
using
'Puerarin',
'Neuroprotection',
'Apoptosis',
'Autophagy',
'Antioxidant',
'Mitochondria',
'Anti-inflammation'
keywords.
This
review
complied
Preferred
Reporting
Items
Systematic
Reviews
criteria.
Forty-three
articles
met
established
inclusion
exclusion
shown
against
variety
of
disorders,
ischemic
cerebrovascular
disease,
subarachnoid
hemorrhage,
epilepsy,
cognitive
traumatic
brain
injury,
Parkinson's
Alzheimer's
anxiety,
depression,
diabetic
neuropathy,
neuroblastoma/glioblastoma.
anti-apoptosis,
proinflammatory
mediator
inhibitory,
autophagy
regulatory,
anti-oxidative
stress,
mitochondria
protection,
Ca2+
influx
anti-neurodegenerative
activities.
exerts
noticeable
models
disorders
vivo
(animal).
will
contribute
to
development
novel
clinical
drug
candidate
However,
well-designed,
high-quality,
large-scale,
multicenter
randomized
studies
are
needed
determine
safety
utility
patients
Frontiers in Cellular Neuroscience,
Год журнала:
2023,
Номер
17
Опубликована: Март 6, 2023
Neuronal
loss
is
one
of
the
striking
causes
various
central
nervous
system
(CNS)
disorders,
including
major
neurodegenerative
diseases,
such
as
Alzheimer’s
disease
(AD),
Parkinson’s
(PD),
Huntington’s
(HD),
and
Amyotrophic
lateral
sclerosis
(ALS).
Although
these
diseases
have
different
features
clinical
manifestations,
they
share
some
common
mechanisms
pathology.
Progressive
regional
neurons
in
patients
responsible
for
motor,
memory,
cognitive
dysfunctions,
leading
to
disabilities
death.
cell
death
linked
pathways
conditions.
Protein
misfolding
aggregation,
mitochondrial
dysfunction,
generation
reactive
oxygen
species
(ROS),
activation
innate
immune
response
are
most
critical
hallmarks
diseases.
Thus,
endoplasmic
reticulum
(ER)
stress,
oxidative
neuroinflammation
pathological
factors
neuronal
Even
though
exact
not
fully
discovered,
notable
role
mentioned
well
known.
On
this
basis,
researchers
been
prompted
investigate
neuroprotective
effects
targeting
underlying
determine
a
promising
therapeutic
approach
treatment.
This
review
provides
an
overview
ER
death,
mainly
discussing
or
molecules
involved
factors.
Frontiers in Pharmacology,
Год журнала:
2024,
Номер
15
Опубликована: Май 24, 2024
Alois
Alzheimer
described
the
first
patient
with
Alzheimer’s
disease
(AD)
in
1907
and
today
AD
is
most
frequently
diagnosed
of
dementias.
a
multi-factorial
neurodegenerative
disorder
familial,
life
style
comorbidity
influences
impacting
global
population
more
than
47
million
projected
escalation
by
2050
to
exceed
130
million.
In
USA
demographic
encompasses
approximately
six
individuals,
expected
increase
surpass
13
2050,
antecedent
phase
AD,
recognized
as
mild
cognitive
impairment
(MCI),
involves
nearly
12
individuals.
The
economic
outlay
for
management
AD-related
decline
estimated
at
355
billion
USD.
addition,
intensifying
prevalence
cases
countries
modest
intermediate
income
further
enhances
urgency
therapeutically
cost-effective
treatments
improving
quality
patients
their
families.
This
narrative
review
evaluates
pathophysiological
basis
an
initial
focus
on
therapeutic
efficacy
limitations
existing
drugs
that
provide
symptomatic
relief:
acetylcholinesterase
inhibitors
(AChEI)
donepezil,
galantamine,
rivastigmine,
N-methyl-D-aspartate
receptor
(NMDA)
allosteric
modulator,
memantine.
hypothesis
amyloid-β
(Aβ)
tau
are
appropriate
targets
have
potential
halt
progress
critically
analyzed
particular
clinical
trial
data
anti-Aβ
monoclonal
antibodies
(MABs),
namely,
aducanumab,
lecanemab
donanemab.
challenges
dogma
targeting
Aβ
will
benefit
majority
subjects
MABs
unlikely
be
“magic
bullet”.
A
comparison
benefits
disadvantages
different
classes
forms
determining
new
directions
research
alternative
drug
undergoing
pre-clinical
assessments.
we
discuss
stress
importance
treatment
co-morbidities,
including
hypertension,
diabetes,
obesity
depression
known
risk
developing
AD.
Health psychology research,
Год журнала:
2022,
Номер
10(1)
Опубликована: Янв. 30, 2022
Alzheimer’s
disease
(AD)
is
the
most
common
form
of
dementia
affecting
millions
individuals,
including
family
members
who
often
take
on
role
as
caregiver.
This
debilitating
reportedly
consumes
8%
total
United
States
healthcare
expenditure,
with
medical
and
nursing
outlays
accounting
for
an
estimated
$290
billion.
Cholinesterase
inhibitors
N-methyl-D-aspartate
receptor
antagonists
have
historically
been
widely
used
pharmacologic
therapies
patients
AD,
however,
these
drugs
are
not
curative.
review
discusses
epidemiology,
pathophysiology,
risk
factors,
presentation,
current
treatment
AD
followed
by
novel
monoclonal
antibody,
aducanumab,
in
AD.
Currently
aducanumab
only
Food
Drug
Administration
(FDA)
approved
drug
that
acts
to
slow
progression
this
disease.
Aducanumab
anti-amyloid
which
functions
selectively
binding
amyloid
aggregates
both
oligomeric
fibrillar
states.
Studies
show
may
help
restore
neurological
function
reducing
beta-amyloid
plaques
reestablishing
neuronal
calcium
permeability.
However,
there
concern
magnitude
drug’s
benefit
be
statistically
significant
clinically
significant.
Despite
skepticism,
has
proven
significantly
decrease
all
cortical
brain
regions
examined.
In
summary,
provided
hope
those
working
toward
goal
providing
a
safe
viable
option
management