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Effect of vitamin D3 intake on the onset of disease in a murine model of human Krabbe disease.
[krabbe disease]
Low
vitamin
D
level
is
a
risk
factor
for
various
late-onset
CNS
demyelinating
disorders
.
We
investigated
whether
vitamin
D
deficiency
influences
disease
in
twitcher
mice
(
GALC
(
twi
/
twi
)
;
twi
)
,
a
murine
model
of
Krabbe
disease
(
KD
)
,
an
inherited
disorder
caused
by
galactocerebrosidase
(
GALC
)
deficiency
that
leads
to
psychosine
accumulation
,
oligodendrocyte
(
OL
)
loss
,
and
CNS
demyelination
.
We
found
that
the
in
situ
1
,
25
-
dihydroxyvitamin
D
3
level
was
reduced
,
with
a
parallel
increase
in
the
expression
of
inflammatory
cytokines
and
vitamin
D-
catabolizing
enzymes
in
the
brains
of
KD
and
twi
mice
compared
with
age-matched
controls
.
Pups
maintained
on
milk
from
lactating
heterozygous
(
GALC
(
twi
/
+
)
)
mothers
that
were
fed
a
vitamin
D
3
-
supplemented
diet
until
weaning
and
then
fed
a
vitamin
D
3
-
supplemented
diet
demonstrated
delayed
body
weight
loss
and
development
of
disease
in
twi
mice
.
This
delayed
the
onset
of
tremors
and
locomotor
disabilities
that
eventually
impacted
the
life
span
of
twi
mice
(
50
 
±
 
2
days
)
.
Accordingly
,
the
expression
of
antioxidant
enzymes
was
increased
with
delayed
psychosine
accumulation
,
lipid
peroxidation
,
and
inflammatory
response
that
eventually
protected
CNS
myelin
and
axonal
integrity
in
twi
mice
.
In
vitro
studies
revealed
that
1
,
25
-
dihydroxyvitamin
D
3
enhances
antioxidant
defenses
in
OLs
deficient
for
GALC
or
incubated
with
psychosine
.
Together
these
data
provide
the
first
evidence
that
vitamin
D
deficiency
affects
disease
development
in
twi
mice
and
that
vitamin
D
3
supplementation
has
the
potential
to
improve
the
efficacy
of
KD
therapeutics
.
©
2014
Wiley
Periodicals
,
Inc
.
Diseases
Validation
Diseases presenting
"inflammatory cytokines"
symptom
alpha-thalassemia
congenital toxoplasmosis
cystinuria
esophageal adenocarcinoma
hydrocephalus with stenosis of the aqueduct of sylvius
inclusion body myositis
krabbe disease
oculocutaneous albinism
omenn syndrome
primary effusion lymphoma
severe combined immunodeficiency
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