Therapeutic targeting of obesity-induced neuroinflammation and neurodegeneration
Jialiu Zeng,
No information about this author
Lenny Yi Tong Cheong,
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Chih Hung Lo
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et al.
Frontiers in Endocrinology,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 17, 2025
Obesity
is
a
major
modifiable
risk
factor
leading
to
neuroinflammation
and
neurodegeneration.
Excessive
fat
storage
in
obesity
promotes
the
progressive
infiltration
of
immune
cells
into
adipose
tissue,
resulting
release
pro-inflammatory
factors
such
as
cytokines
adipokines.
These
inflammatory
mediators
circulate
through
bloodstream,
propagating
inflammation
both
periphery
central
nervous
system.
Gut
dysbiosis,
which
results
leaky
intestinal
barrier,
exacerbates
plays
significant
role
linking
pathogenesis
neurodegeneration
gut-brain/gut-brain-liver
axis.
Inflammatory
states
within
brain
can
lead
insulin
resistance,
mitochondrial
dysfunction,
autolysosomal
increased
oxidative
stress.
disruptions
impair
normal
neuronal
function
subsequently
cognitive
decline
motor
deficits,
similar
pathologies
observed
neurodegenerative
diseases,
including
Alzheimer's
disease,
multiple
sclerosis,
Parkinson's
disease.
Understanding
underlying
disease
mechanisms
crucial
for
developing
therapeutic
strategies
address
defects
these
metabolic
pathways.
In
this
review,
we
summarize
provide
insights
different
strategies,
methods
alter
gut
lifestyle
changes,
dietary
supplementation,
well
pharmacological
agents
derived
from
natural
sources,
that
target
obesity-induced
Language: Английский
Lysosomal acidification impairment in astrocyte-mediated neuroinflammation
Jialiu Zeng,
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Jonathan Indajang,
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David Pitt
No information about this author
et al.
Journal of Neuroinflammation,
Journal Year:
2025,
Volume and Issue:
22(1)
Published: March 10, 2025
Abstract
Astrocytes
are
a
major
cell
type
in
the
central
nervous
system
(CNS)
that
play
key
role
regulating
homeostatic
functions,
responding
to
injuries,
and
maintaining
blood-brain
barrier.
also
regulate
neuronal
functions
survival
by
modulating
myelination
degradation
of
pathological
toxic
protein
aggregates.
have
recently
been
proposed
possess
both
autophagic
activity
active
phagocytic
capability
which
largely
depend
on
sufficiently
acidified
lysosomes
for
complete
cellular
cargos.
Defective
lysosomal
acidification
astrocytes
impairs
their
resulting
accumulation
debris,
excessive
myelin
lipids,
aggregates,
ultimately
contributes
propagation
neuroinflammation
neurodegenerative
pathology.
Restoration
impaired
represent
new
neuroprotective
strategy
therapeutic
direction.
In
this
review,
we
summarize
pathogenic
factors,
including
neuroinflammatory
signaling,
metabolic
stressors,
lipid
mediated
toxicity,
contribute
impairment
associated
dysfunction
astrocytes.
We
discuss
astrocyte-mediated
primarily
context
diseases
along
with
other
brain
injuries.
then
highlight
re-acidification
as
restore
well
degradative
capacity
conclude
providing
future
perspectives
phagocytes
crosstalk
CNS
cells
impart
or
effects.
Language: Английский