Neuroscience & Biobehavioral Reviews,
Год журнала:
2014,
Номер
47, С. 122 - 153
Опубликована: Авг. 10, 2014
The
energy
allocation
(EA)
model
defines
behavioral
strategies
that
optimize
the
temporal
utilization
of
to
maximize
reproductive
success.
This
proposes
all
species
animal
kingdom
share
a
universal
sleep
function
shunts
waking
toward
sleep-dependent
biological
investment.
For
endotherms,
REM
evolved
enhance
appropriation
for
somatic
and
CNS-related
processes
by
eliminating
thermoregulatory
defenses
skeletal
muscle
tone.
Alternating
with
NREM
conserves
decreasing
need
core
body
temperature
defense.
Three
EA
phenotypes
are
proposed:
sleep-wake
cycling,
torpor,
continuous
(or
predominant)
wakefulness.
Each
phenotype
carries
inherent
costs
benefits.
Sleep-wake
cycling
downregulates
specific
in
upregulates
them
sleep,
thereby
demands
imposed
wakefulness,
reducing
cellular
infrastructure
requirements,
resulting
overall
conservation.
Torpor
achieves
greatest
savings,
but
critical
operations
compromised.
Continuous
wakefulness
maximizes
niche
exploitation,
endures
demands.
advances
new
construct
understanding
organization
ontogenetic
phylogenetic
domains.
Biology of Reproduction,
Год журнала:
2001,
Номер
65(5), С. 1311 - 1323
Опубликована: Ноя. 1, 2001
All
mammalian
uteri
contain
endometrial
glands
that
synthesize
or
transport
and
secrete
substances
essential
for
survival
development
of
the
conceptus
(embryo/fetus
associated
extraembryonic
membranes).
In
rodents,
uterine
secretory
products
are
unequivocally
required
establishment
receptivity
implantation.
Analyses
ovine
gland
knockout
model
support
a
primary
role
and,
by
default,
their
secretions
in
peri-implantation
development.
Uterine
adenogenesis
is
process
whereby
develop.
humans,
this
begins
fetus,
continues
postnatally,
completed
during
puberty.
contrast,
primarily
postnatal
event
sheep,
pigs,
rodents.
Typically,
involves
differentiation
budding
glandular
epithelium
from
luminal
epithelium,
followed
invagination
extensive
tubular
coiling
branching
morphogenesis
throughout
stroma
to
myometrium.
This
requires
site-specific
alterations
cell
proliferation
extracellular
matrix
(ECM)
remodeling
as
well
paracrine
cell-cell
cell-ECM
interactions
actions
specific
hormones
growth
factors.
Studies
neonatal
ungulates
implicate
prolactin,
estradiol-17β,
receptors
mechanisms
regulating
adenogenesis.
These
same
appear
regulate
menstruating
primates
humans
reconstruction
functionalis
basalis
endometrium
after
menses.
sheep
hyperplasia
hypertrophy
occur
gestation,
presumably
provide
increasing
histotrophic
rabbit,
pig,
servomechanism
proposed
differentiated
function
pregnancy
sequential
ovarian
steroid
hormones,
recognition
signals,
lactogenic
pituitary
placenta.
That
disruption
critical
organizational
periods
can
alter
functional
capacity
embryotrophic
potential
adult
uterus
reinforces
importance
understanding
developmental
biology
glands.
Unexplained
high
rates
embryonic
loss
livestock
may
reflect
defects
due
genetic
errors,
epigenetic
influences
endocrine
disruptors,
pathological
lesions.
Annual Review of Physiology,
Год журнала:
2002,
Номер
64(1), С. 47 - 67
Опубликована: Март 1, 2002
▪
Abstract
Prolactin
(PRL)
is
a
paradoxical
hormone.
Historically
known
as
the
pituitary
hormone
of
lactation,
it
has
had
attributed
to
more
than
300
separate
actions,
which
can
be
correlated
quasi-ubiquitous
distribution
its
receptor.
Meanwhile,
PRL-related
knockout
models
have
mainly
highlighted
irreplaceable
role
in
functions
lactation
and
reproduction,
suggests
that
most
other
reported
target
tissues
are
presumably
modulated
by,
rather
strictly
dependent
on,
PRL.
The
multiplicity
PRL
actions
animals
direct
opposition
paucity
arguments
suggest
involvement
human
pathophysiology
effects
on
reproduction.
Although
many
experimental
data
argue
for
progression
some
tumors,
such
breast
prostate
cancers,
drugs
lowering
circulating
levels
ineffective.
This
observation
opens
new
avenues
research
into
understanding
whether
local
production
involved
tumor
growth
and,
if
so,
how
extrapituitary
synthesis
regulated.
Finally,
physiological
relevance
variants,
antiangiogenic
16K-like
fragments,
needs
elucidated.
review
aimed
at
critically
discussing
these
recent
findings
renewed
manner
should
considered
multifunctional
Journal of Endocrinology,
Год журнала:
2005,
Номер
186(3), С. 411 - 427
Опубликована: Авг. 31, 2005
The
relevance
of
testosterone,
oestradiol
and
certain
peptides
(oxytocin
(OT),
beta-endorphin
prolactin
(PRL))
to
sexual
arousal
in
humans
is
reviewed.
In
addition
behavioural
studies,
evidence
distribution
gonadal
steroid
receptors
the
brain
limited
from
imaging
are
also
considered.
Testosterone
plays
a
key
role
adult
male,
with
clear,
consistent
studies
hypogonadal
eugonadal
men.
roles
testosterone
development
arousability,
aging
less
clear.
aromatization
non-sexual
effects
which
might
indirectly
influence
not
well
understood.
female
presents
more
complex,
picture.
One
possible
explanation
much
greater
variability
across
women
responsiveness
testosterone.
A
'desensitization
hypothesis'
account
for
striking
gender
differences
offered.
There
direct
effect
on
arousability
women.
extent
acts
by
conversion
or
increase
free
yet
remains
uncertain,
partly
because
multiple
sites
action
most
peptides.
OT
appear
have
both
excitatory
inhibitory
effects.
PRL
has
been
proposed
as
an
factor
via
inhibition
dopaminergic
activity,
but
this
inconclusive.
Whereas
traditional
concept
'hormone'
continues
apply
arousal,
present
complex
role.
Journal of Psychopharmacology,
Год журнала:
2008,
Номер
22(2_suppl), С. 12 - 19
Опубликована: Март 1, 2008
Dopamine
(DA)
holds
a
predominant
role
in
the
regulation
of
prolactin
(PRL)
secretion.
Through
direct
effect
on
anterior
pituitary
lactotrophs,
DA
inhibits
basally
high-secretory
tone
cell.
It
accomplishes
this
by
binding
to
D2
receptors
expressed
cell
membrane
lactotroph,
activation
which
results
reduction
PRL
exocytosis
and
gene
expression
variety
intracellular
signalling
mechanisms.
The
hypothalamic
dopaminergic
neurons,
provide
gland,
are
themselves
regulated
feedback
from
through
short-loop
mechanism
.
A
other
modulators
secretion
act
at
level
either
disinhibition
(e.g.
serotonin,
GABA,
oestrogens
opioids)
or
reinforcing
it
substance
P).
All
typical
antipsychotic
medications
associated
with
sustained
hyperprolactinaemia
due
their
high
affinity
for
receptor
slow
dissociation
once
bound,
but
atypicals
differ
quite
dramatically
propensity
cause
prolonged
levels.
Of
those
that
elevation,
main
causative
factor
appears
be
higher
peripheral-to-central
dopamine
potency
parent
drug
its
active
metabolite
risperidone,
9-hydroxy-risperidone
amisulpride).
Antipsychotics
easily
cross
blood—brain
barrier
exhibit
fast
bound
do
not
result
hyperprolactinaemia.
Environmental Health Perspectives,
Год журнала:
2005,
Номер
113(4), С. 431 - 439
Опубликована: Янв. 14, 2005
Xenoestrogens
(XEs)
are
widespread
in
our
environment
and
known
to
have
deleterious
effects
animal
(and
perhaps
human)
populations.
Acting
as
inappropriate
estrogens,
XEs
thought
interfere
with
endogenous
estrogens
such
estradiol
(E2)
disrupt
normal
estrogenic
signaling.
We
investigated
the
of
E2
versus
several
representing
organochlorine
pesticides
(dieldrin,
endosulfan,
o',p'-dichlorodiphenylethylene),
plastics
manufacturing
by-products/detergents
(nonylphenol,
bisphenol
A),
a
phytoestrogen
(coumestrol),
synthetic
estrogen
(diethylstilbestrol)
on
pituitary
tumor
cell
subline
GH3/B6/F10,
previously
selected
for
expression
high
levels
membrane
receptor-alpha.
Picomolar
nanomolar
concentrations
both
caused
intracellular
Ca2+
changes
within
30
sec
administration.
Each
XE
produced
unique
temporal
pattern
elevation.
Removing
from
extracellular
solution
abolished
spontaneous
XE-induced
changes,
did
10
microM
nifedipine.
This
suggests
that
mediate
their
actions
via
voltage-dependent
L-type
channels
plasma
membrane.
None
fluxes
came
stores.
each
also
time-
concentration-dependent
patterns
prolactin
(PRL)
secretion
were
largely
complete
3
min
PRL
was
blocked
by
nifedipine,
demonstrating
correlation
between
influx
secretion.
These
data
indicate
at
very
low
concentrations,
membrane-initiated
CCa2+
increases
resulting
mechanism
similar
E2,
but
distinct
potencies
could
explain
abilities
endocrine
functions.