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Alzheimer's beta-amyloid vasoactivity: identification of a novel beta-amyloid conformational intermediate.
[hereditary cerebral hemorrhage with amyloidosis]
The
beta
-amyloid
(
A
beta
)
peptide
has
previously
been
shown
to
enhance
phenylephrine
or
endothelin-
1
induced
constriction
of
aortic
rings
in
vitro
.
The
characteristics
of
A
beta
vasoactivity
(
dose
,
fragment
length
,
timing
)
suggest
that
the
mechanism
is
distinct
from
A
beta
cytotoxicity
.
To
identify
which
properties
of
A
beta
determine
its
biological
activity
on
vessels
,
we
investigated
a
number
of
A
beta
analogues
and
fragments
,
individually
and
in
combination
,
including
those
that
are
known
to
be
associated
with
Alzheimer
's
disease
(
A
beta
(
1
-
42
)
)
and
hereditary
cerebral
hemorrhage
with
amyloidosis
--
Dutch
type
(
A
beta
(
22
Q
)
(
1
-
40
)
)
.
The
vasoactivity
appears
to
be
related
to
the
conformation
adopted
by
the
peptide
in
solution
.
The
beta
-pleated
sheet
rich
A
beta
(
1
-
42
)
and
A
beta
(
22
Q
)
(
1
-
40
)
were
each
less
vasoactive
than
the
mainly
random
coil
wild
type
A
beta
(
1
-
40
)
.
However
,
the
most
vasoactive
A
beta
peptides
were
combinations
which
contain
mixtures
of
random
coil
and
beta
-sheet
structure
.
The
finding
that
peptides
containing
low
or
high
levels
of
beta
-pleated
conformation
are
less
vasoactive
than
those
containing
intermediate
amounts
of
this
structural
motif
allows
us
to
propose
the
existence
of
a
transitional
form
between
random
coil
and
beta
-pleated
that
is
the
vasoactive
species
of
A
beta
.
This
is
the
first
time
that
A
beta
conformational
intermediates
have
been
identified
and
a
biological
activity
associated
with
them
.
Diseases
Validation
Diseases presenting
"induced constriction of aortic rings in vitro"
symptom
hereditary cerebral hemorrhage with amyloidosis
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