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Chimeric Mice with Hepatocyte-humanized Liver as an Appropriate Model to Study Human Peroxisome Proliferator-activated Receptor-α
[severe combined immunodeficiency]
Peroxisome
proliferator
(
PP
)
-
activated
receptor-α
(
PPAR
α
)
agonists
exhibit
species-
specific
effects
on
livers
of
the
rodent
and
human
(
h
)
,
which
has
been
considered
to
reside
in
the
difference
of
PPARα
gene
structures
.
However
,
the
contribution
of
h-hepatocytes
(
heps
)
to
the
species-specificity
remains
to
be
clarified
.
In
this
study
,
the
effects
of
fenofibrate
were
investigated
using
a
hepatocyte-humanized
chimeric
mouse
(
m
)
model
whose
livers
were
replaced
with
h-heps
at
>
70
%
.
Fenofibrate
induced
hepatocellular
hypertrophy
,
cell
proliferation
,
and
peroxisome
proliferation
in
livers
of
severe
combined
immunodeficiency
(
SCID
)
mice
,
but
not
in
the
h-hep
of
chimeric
mouse
livers
.
Fenofibrate
increased
the
expression
of
the
enzymes
of
β-
and
ω-hydroxylation
and
deoxygenation
of
lipids
at
both
gene
and
protein
levels
in
SCID
mouse
livers
,
but
not
in
the
h-heps
of
chimeric
mouse
livers
,
supporting
the
studies
with
h-
PPAR
α-transgenic
mice
,
a
hitherto
reliable
model
for
studying
the
regulation
of
h-
PPARα
in
the
h-
liver
in
most
respects
,
except
the
induction
of
the
peroxisome
proliferation
.
This
study
indicates
the
importance
of
not
only
h-
PPARα
gene
but
also
h-heps
themselves
to
correctly
predict
effects
of
fibrates
on
h-livers
,
and
,
therefore
,
suggests
that
the
chimeric
mouse
is
a
currently
available
,
consistent
,
and
reliable
model
to
obtain
pharmaceutical
data
concerning
the
effects
of
fibrates
on
h-livers
.
Diseases
Validation
Diseases presenting
"human"
symptom
severe combined immunodeficiency
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