Journal of Molecular Endocrinology,
Год журнала:
2014,
Номер
52(3), С. R199 - R222
Опубликована: Фев. 27, 2014
Lipolysis
is
the
process
by
which
triglycerides
(TGs)
are
hydrolyzed
to
free
fatty
acids
(FFAs)
and
glycerol.
In
adipocytes,
this
achieved
sequential
action
of
adipose
TG
lipase
(ATGL),
hormone-sensitive
(HSL),
monoglyceride
lipase.
The
activity
in
lipolytic
pathway
tightly
regulated
hormonal
nutritional
factors.
Under
conditions
negative
energy
balance
such
as
fasting
exercise,
stimulation
lipolysis
results
a
profound
increase
FFA
release
from
tissue
(AT).
This
response
crucial
order
provide
organism
with
sufficient
supply
substrate
for
oxidative
metabolism.
However,
failure
efficiently
suppress
when
demands
low
can
have
serious
metabolic
consequences
believed
be
key
mechanism
development
type
2
diabetes
obesity.
As
discovery
ATGL
2004,
substantial
progress
has
been
made
delineation
remarkable
complexity
regulatory
network
controlling
adipocyte
lipolysis.
Notably,
mechanisms
identified
on
multiple
levels
pathway,
including
gene
transcription
translation,
post-translational
modifications,
intracellular
localization,
protein–protein
interactions,
protein
stability/degradation.
Here,
we
an
overview
recent
advances
field
AT
particular
focus
molecular
regulation
two
main
lipases,
HSL,
extracellular
signals
affecting
their
activity.
Physiological Reviews,
Год журнала:
2018,
Номер
98(4), С. 2133 - 2223
Опубликована: Авг. 1, 2018
The
1921
discovery
of
insulin
was
a
Big
Bang
from
which
vast
and
expanding
universe
research
into
action
resistance
has
issued.
In
the
intervening
century,
some
discoveries
have
matured,
coalescing
solid
fertile
ground
for
clinical
application;
others
remain
incompletely
investigated
scientifically
controversial.
Here,
we
attempt
to
synthesize
this
work
guide
further
mechanistic
investigation
inform
development
novel
therapies
type
2
diabetes
(T2D).
rational
such
necessitates
detailed
knowledge
one
key
pathophysiological
processes
involved
in
T2D:
resistance.
Understanding
resistance,
turn,
requires
normal
action.
review,
both
physiology
pathophysiology
are
described,
focusing
on
three
target
tissues:
skeletal
muscle,
liver,
white
adipose
tissue.
We
aim
develop
an
integrated
physiological
perspective,
placing
intricate
signaling
effectors
that
carry
out
cell-autonomous
response
context
tissue-specific
functions
generate
coordinated
organismal
response.
First,
section
II,
effects
direct,
tissue
reviewed,
beginning
at
receptor
working
downstream.
Section
III
considers
critical
underappreciated
role
crosstalk
whole
body
action,
especially
essential
interaction
between
lipolysis
hepatic
gluconeogenesis.
is
then
described
IV.
Special
attention
given
pathways
become
resistant
setting
chronic
overnutrition,
alternative
explanation
phenomenon
‟selective
resistanceˮ
presented.
Sections
V,
VI,
VII
critically
examine
evidence
against
several
putative
mediators
V
reviews
linking
bioactive
lipids
diacylglycerol,
ceramide,
acylcarnitine
resistance;
VI
impact
nutrient
stresses
endoplasmic
reticulum
mitochondria
discusses
non-cell
autonomous
factors
proposed
induce
including
inflammatory
mediators,
branched-chain
amino
acids,
adipokines,
hepatokines.
Finally,
VIII,
propose
model
links
these
final
common
metabolite-driven
gluconeogenesis
ectopic
lipid
accumulation.
World Journal of Diabetes,
Год журнала:
2015,
Номер
6(6), С. 850 - 850
Опубликована: Янв. 1, 2015
The
epidemic
nature
of
diabetes
mellitus
in
different
regions
is
reviewed.The
Middle
East
and
North
Africa
region
has
the
highest
prevalence
adults
(10.9%)
whereas,
Western
Pacific
number
diagnosed
with
countries
(37.5%).Different
classes
mellitus,
type
1,
2,
gestational
other
types
are
compared
terms
diagnostic
criteria,
etiology
genetics.The
molecular
genetics
received
extensive
attention
recent
years
by
many
prominent
investigators
research
groups
biomedical
field.A
large
array
mutations
single
nucleotide
polymorphisms
genes
that
play
a
role
various
steps
pathways
involved
glucose
metabolism
development,
control
function
pancreatic
cells
at
levels
major
advances
understanding
relation
to
comparison
previous
this
field
briefly
reviewed
here.Despite
accumulation
data
cellular
levels,
mechanism
development
complications
still
not
fully
understood.Definitely,
more
needed
will
eventually
reflect
on
ultimate
objective
improve
diagnoses,
therapy
minimize
chance
chronic
development.
Journal of Cellular Physiology,
Год журнала:
2018,
Номер
234(6), С. 8152 - 8161
Опубликована: Окт. 14, 2018
Abstract
Most
human
cells
utilize
glucose
as
the
primary
substrate,
cellular
uptake
requiring
insulin.
Insulin
signaling
is
therefore
critical
for
these
tissues.
However,
decrease
in
insulin
sensitivity
due
to
disruption
of
various
molecular
pathways
causes
resistance
(IR).
IR
underpins
many
metabolic
disorders
such
type
2
diabetes
and
syndrome,
impairments
disrupting
entry
into
adipocytes,
skeletal
muscle
cells.
Although
exact
underlying
cause
has
not
been
fully
elucidated,
a
number
major
mechanisms,
including
oxidative
stress,
inflammation,
receptor
mutations,
endoplasmic
reticulum
mitochondrial
dysfunction
have
suggested.
In
this
review,
we
consider
role
mechanisms
play
development
IR.
Journal of Endocrinology,
Год журнала:
2013,
Номер
220(2), С. T1 - T23
Опубликована: Ноя. 26, 2013
Insulin
resistance
is
a
major
underlying
mechanism
responsible
for
the
‘metabolic
syndrome’,
which
also
known
as
insulin
syndrome.
The
incidence
of
metabolic
syndrome
increasing
at
an
alarming
rate,
becoming
public
and
clinical
problem
worldwide.
Metabolic
represented
by
group
interrelated
disorders,
including
obesity,
hyperglycemia,
hyperlipidemia,
hypertension.
It
significant
risk
factor
cardiovascular
disease
increased
morbidity
mortality.
Animal
studies
have
demonstrated
that
its
signaling
cascade
normally
control
cell
growth,
metabolism,
survival
through
activation
MAPKs
phosphatidylinositide-3-kinase
(PI3K),
in
PI3K
associated
with
receptor
substrate
1
(IRS1)
IRS2
subsequent
Akt→Foxo1
phosphorylation
has
central
role
nutrient
homeostasis
organ
survival.
inactivation
Akt
Foxo1,
suppression
IRS1
different
organs
following
hyperinsulinemia,
inflammation,
overnutrition,
may
act
mechanisms
humans.
Targeting
IRS→Akt→Foxo1
will
probably
provide
strategy
therapeutic
intervention
treatment
type
2
diabetes
complications.
This
review
discusses
basis
signaling,
mouse
models,
how
deficiency
components
contributes
to
features
Emphasis
placed
on
IRS1,
IRS2,
pathways
are
coupled
forkhead/winged
helix
transcription
Foxo1.
Oxidative Medicine and Cellular Longevity,
Год журнала:
2020,
Номер
2020, С. 1 - 13
Опубликована: Март 9, 2020
Type
2
diabetes
mellitus
(T2DM)
is
the
most
prevalent
metabolic
disorder
characterized
by
chronic
hyperglycemia
and
an
inadequate
response
to
circulatory
insulin
peripheral
tissues
resulting
in
resistance.
Insulin
resistance
has
a
complex
pathophysiology,
it
contributed
multiple
factors
including
oxidative
stress.
Oxidative
stress
refers
imbalance
between
free
radical
production
antioxidant
system
leading
reduction
of
sensitivity
contributing
development
T2DM
via
several
molecular
mechanisms.
In
this
review,
we
present
mechanisms
which
milieu
contributes
pathophysiology
mellitus.
Journal of Neuroinflammation,
Год журнала:
2018,
Номер
15(1)
Опубликована: Сен. 24, 2018
Alzheimer’s
disease
(AD)
is
a
neurodegenerative
disorder,
most
cases
of
which
lack
clear
causative
event.
This
has
made
the
difficult
to
characterize
and,
thus,
diagnose.
Although
some
are
genetically
linked,
there
many
diseases
and
lifestyle
factors
that
can
lead
an
increased
risk
developing
AD,
including
traumatic
brain
injury,
diabetes,
hypertension,
obesity,
other
metabolic
syndromes,
in
addition
aging.
Identifying
common
trends
between
these
conditions
could
enhance
our
understanding
AD
development
more
effective
treatments.
immune
system
one
body’s
key
defense
mechanisms,
chronic
inflammation
been
increasingly
linked
with
several
age-related
diseases.
Moreover,
it
now
well
accepted
important
role
onset
progression
AD.
In
this
review,
different
inflammatory
signals
associated
its
will
be
outlined
demonstrate
how
may
influencing
individual
susceptibility
Our
goal
bring
attention
potential
shared
presented
by
during
successful