Journal of Experimental Biology,
Год журнала:
2024,
Номер
227(10)
Опубликована: Май 1, 2024
ABSTRACT
Hibernation
is
an
extreme
state
of
seasonal
energy
conservation,
reducing
metabolic
rate
to
as
little
1%
the
active
state.
During
hibernation
season,
many
species
hibernating
mammals
cycle
repeatedly
between
(aroused)
and
(torpid)
states
(T–A
cycling),
using
brown
adipose
tissue
(BAT)
drive
cyclical
rewarming.
The
regulatory
mechanisms
controlling
this
process
remain
undefined
but
are
presumed
involve
thermoregulatory
centres
in
hypothalamus.
Here,
we
used
golden
hamster
(Mesocricetus
auratus),
high-resolution
monitoring
BAT,
core
body
temperature
ventilation
rate,
sample
at
precisely
defined
phases
T–A
cycle.
Using
c-fos
a
marker
cellular
activity,
show
that
although
dorsomedial
hypothalamus
during
torpor
entry,
neither
it
nor
pre-optic
area
shows
any
significant
changes
earliest
stages
spontaneous
arousal.
Contrastingly,
three
non-neuronal
sites
previously
linked
control
physiology
over
daily
time
scales
–
choroid
plexus,
pars
tuberalis
third
ventricle
tanycytes
peak
expression
seen
arousal
initiation.
We
suggest
through
their
sensitivity
factors
blood
or
cerebrospinal
fluid,
these
may
mediate
feedback-based
initiation
process.
Frontiers in Physiology,
Год журнала:
2021,
Номер
11
Опубликована: Янв. 20, 2021
Torpor
and
hibernation
are
powerful
strategies
enabling
animals
to
survive
periods
of
low
resource
availability.
The
state
torpor
results
from
an
active
drastic
reduction
individual’s
metabolic
rate
(MR)
associated
with
a
relatively
pronounced
decrease
in
body
temperature.
To
date,
several
forms
have
been
described
all
three
mammalian
subclasses,
i.e.,
monotremes,
marsupials,
placentals,
as
well
few
avian
orders.
This
review
highlights
some
the
characteristics,
whole
organism
down
cellular
molecular
aspects,
phenotype.
first
part
this
focuses
on
specific
adaptations
torpor,
it
is
used
by
many
species
temperate
zones.
notably
includes
endocrine
changes
involved
fat-
food-storing
hibernating
species,
explaining
biomedical
implications
MR
depression.
We
further
compare
adaptive
mechanisms
occurring
opportunistic
vs.
seasonal
heterotherms,
such
tropical
sub-tropical
species.
Such
comparisons
bring
new
insights
into
origins
among
including
resistance
oxidative
stress.
second
section
emphasizes
heterotherms
protect
their
key
organs
against
potential
threats,
reactive
oxygen
torpid
state.
address
rehabilitation
protection
during
hibernation,
emphasis
brain,
central
organ
requiring
recovery.
Also,
special
focus
given
role
ubiquitous
readily-diffusing
molecule,
hydrogen
sulfide
(H
2
S),
protecting
ischemia-reperfusion
damage
various
over
torpor-arousal
cycle
conclude
that
(i)
flexibility
use
strategy
enables
different
heterothermic
substantially
suppress
energy
needs
severely
reduced
food
availability,
(ii)
phenotype
implies
marked
levels,
(iii)
highly
efficient
protective
ensuring
continuity
proper
bodily
functions.
Comparison
monotremes
marsupials
warranted
for
understanding
origin
evolution
torpor.
Annual Review of Vision Science,
Год журнала:
2023,
Номер
9(1), С. 245 - 267
Опубликована: Май 17, 2023
We
live
on
a
planet
that
is
bathed
in
daily
and
seasonal
sunlight
cycles.
In
this
context,
terrestrial
life
forms
have
evolved
mechanisms
directly
harness
light
energy
(plants)
or
decode
information
for
adaptive
advantage.
animals,
the
main
sensors
are
family
of
G
protein-coupled
receptors
called
opsins.
Opsin
function
best
described
visual
sense.
However,
most
animals
also
use
opsins
extraocular
sensing
behavior
camouflage.
While
it
has
long
been
believed
mammals
do
not
an
capacity,
recent
evidence
suggests
otherwise.
Notably,
encephalopsin
(OPN3)
neuropsin
(OPN5)
both
known
to
mediate
mice.
Examples
mediation
include
photoentrainment
circadian
clocks
skin
(by
OPN5)
acute
light-dependent
regulation
metabolic
pathways
OPN3
OPN5).
This
review
summarizes
current
findings
expanding
field
photoreception
their
relevance
human
physiology.
Nature Communications,
Год журнала:
2020,
Номер
11(1)
Опубликована: Авг. 27, 2020
The
annual
photoperiod
cycle
provides
the
critical
environmental
cue
synchronizing
rhythms
of
life
in
seasonal
habitats.
In
1936,
Bünning
proposed
a
circadian-based
coincidence
timer
for
photoperiodic
synchronization
plants.
Formal
studies
support
universality
this
so-called
timer,
but
we
lack
understanding
mechanisms
involved.
Here
show
mammals
that
long
photoperiods
induce
circadian
transcription
factor
BMAL2,
pars
tuberalis
pituitary,
and
triggers
summer
biology
through
eyes
absent/thyrotrophin
(EYA3/TSH)
pathway.
Conversely,
long-duration
melatonin
signals
on
short
repressors
including
DEC1,
suppressing
BMAL2
EYA3/TSH
pathway,
triggering
winter
biology.
These
actions
are
associated
with
progressive
genome-wide
changes
chromatin
state,
elaborating
effect
timer.
Hence,
clock-pituitary
epigenetic
pathway
interactions
form
basis
mammalian
mechanism.
Our
results
constitute
blueprint
timekeeping
vertebrates.
Journal of Neuroendocrinology,
Год журнала:
2022,
Номер
34(5)
Опубликована: Март 15, 2022
Abstract
Synchronization
of
mammalian
breeding
activity
to
the
annual
change
photoperiod
and
environmental
conditions
is
utmost
importance
for
individual
survival
species
perpetuation.
Subsequent
early
1960s,
when
central
role
melatonin
in
this
adaptive
process
was
demonstrated,
our
comprehension
mechanisms
through
which
light
regulates
gonadal
has
increased
considerably.
The
current
model
photoperiodic
neuroendocrine
system
points
pivotal
roles
melatonin‐sensitive
pars
tuberalis
(PT)
its
seasonally‐regulated
production
thyroid‐stimulating
hormone
(TSH),
as
well
TSH‐sensitive
hypothalamic
tanycytes,
radial
glia‐like
cells
located
basal
part
third
ventricle.
Tanycytes
respond
TSH
expression
thyroid
(TH)
deiodinase
2
(
Dio2
),
leads
heightened
intrahypothalamic
triiodothyronine
(T3)
during
longer
days
spring
summer.
There
strong
evidence
that
local,
long‐day
driven,
increase
T3
links
input
at
PT
gonadotropin‐releasing
(GnRH)
output,
align
with
seasons.
mechanism(s)
impinges
upon
GnRH
remain(s)
unclear.
However,
two
distinct
neuronal
populations
medio‐basal
hypothalamus,
express
(Arg)(Phe)‐amide
peptides
kisspeptin
RFamide‐related
peptide‐3,
appear
be
well‐positioned
relay
seasonal
message
towards
neurons.
Here,
we
summarize
understanding
cellular,
molecular
players,
keep
track
ultimately
govern
output
breeding.
Biological reviews/Biological reviews of the Cambridge Philosophical Society,
Год журнала:
2023,
Номер
98(4), С. 1424 - 1458
Опубликована: Апрель 17, 2023
ABSTRACT
The
characteristic
maximum
lifespan
varies
enormously
across
animal
species
from
a
few
hours
to
hundreds
of
years.
This
argues
that
lifespan,
and
the
ageing
process
itself
dictates
are
large
extent
genetically
determined.
Although
controversial,
this
is
supported
by
firm
evidence
semelparous
display
evolutionarily
programmed
in
response
reproductive
environmental
cues.
Parabiosis
experiments
reveal
orchestrated
systemically
through
circulation,
accompanied
changes
hormone
levels
lifetime.
implies
that,
like
circadian
circannual
clocks,
there
master
‘clock
age’
(circavital
clock)
located
limbic
brain
mammals
modulates
systemic
growth
factor
secretion
over
as
well
alterations
gene
expression
revealed
genomic
methylation
analysis.
Studies
on
accelerated
mice,
human
longevity
genes,
converge
conserved
fibroblast
factors
(FGFs)
their
receptors,
including
KLOTHO,
insulin‐like
(IGFs)
steroid
hormones,
key
players
mediating
effects
ageing.
Age‐related
these
multiple
other
inferred
cause
progressive
decline
tissue
maintenance
failure
stem
cell
replenishment.
most
severely
affects
immune
system,
which
requires
constant
renewal
bone
marrow
cells.
increases
risk
infection
whereas
can
be
extended
germfree
animals.
suggests
major
death
higher
organisms.
Immune
also
associated
with
age‐related
diseases.
Taking
example
Alzheimer's
disease
(AD),
we
assess
AD
caused
immunosenescence
infection.
signature
protein
brain,
Aβ,
now
known
an
antimicrobial
peptide,
Aβ
deposits
may
rather
than
disease.
Because
some
cognitively
normal
elderly
individuals
show
extensive
neuropathology,
argue
location
pathology
crucial
–
specifically,
lesions
likely
accentuate
immunosenescence,
could
thus
underlie
vicious
cycle
microbial
proliferation
culminates
AD.
general
model
extend
diseases,
propose
paradigm
organismal
senescence
declining
leads
mortality.
Frontiers in Endocrinology,
Год журнала:
2019,
Номер
10
Опубликована: Июнь 25, 2019
Central
and
peripheral
mechanisms
that
modulate
energy
intake,
partition
expenditure
determine
homeostasis.
Thyroid
hormones
(TH)
regulate
through
the
control
of
basal
metabolic
rate
thermogenesis;
they
also
food
intake.
TH
concentrations
are
regulated
by
hypothalamus-pituitary-thyroid
(HPT)
axis,
transport
metabolism
in
blood
target
tissues.
In
mammals,
hypophysiotropic
thyrotropin-releasing
hormone
(TRH)
neurons
paraventricular
nucleus
hypothalamus
integrate
energy-related
information.
They
project
to
external
zone
median
eminence
(ME),
a
brain
circumventricular
organ
rich
neuron
terminal
varicosities
buttons,
tanycytes,
other
glial
cells
capillaries.
These
capillary
vessels
form
portal
system
links
base
with
anterior
pituitary.
Tanycytes
medio-basal
express
repertoire
proteins
involved
transport,
sensing,
TH;
among
them
is
type
2
deiodinase,
source
3,3',5-triiodo-L-thyronine
necessary
for
negative
feedback
on
TRH
neurons.
subtypes
distinguished
position
phenotype.
The
end-feet
β2-tanycytes
intermingle
terminals
layer
ME
terminate
close
Besides
TRH-degrading
ectoenzyme
(TRH-DE);
this
enzyme
likely
controls
amount
entering
vessels.
TRH-DE
rapidly
upregulated
TH,
contributing
HPT
axis.
Alterations
balance
expression
activity
ME,
making
hub
regulation
axis
activity.
TRH-R1,
which
mediates
positive
effects
size
β2-tanycyte
contacts
lamina
adjacent
associations
capillaries,
activity,
appear
coordinately
Thus,
down-stream
neuronal
release
action
potentials
arrival
eminence,
imbricated
intercellular
processes
may
coordinate
flux
into
conclusion,
as
critical
cellular
element
somatic
post-secretory
vessels,
mammals.
Experimental Dermatology,
Год журнала:
2020,
Номер
29(9), С. 814 - 827
Опубликована: Июнь 17, 2020
Abstract
Male‐pattern
hair
loss,
also
termed
androgenetic
alopecia
(AGA),
is
a
highly
prevalent
age‐related
condition
that
characterized
by
distinct
pattern
of
loss
from
the
frontotemporal
and
vertex
regions
scalp.
The
phenotype
heritable
hormone
dependent,
with
androgens
being
recognized
critical
hormonal
factor.
Numerous
molecular
genetic
studies
have
focused
on
variation
in
around
gene
encodes
androgen
receptor.
More
recently,
however,
availability
high‐throughput
methods,
novel
methods
data
analysis
sufficiently
large
sample
sizes
rendered
possible
systematic
investigation
contribution
other
components
receptor
pathway
or
pathways
beyond
signalling
pathways.
Over
past
decade,
genome‐wide
association
increasingly
cohorts
enabled
identification
risk
factors
for
AGA,
yielded
unprecedented
insights
into
underlying
pathobiology.
present
review
discusses
some
most
intriguing
findings
relevance
(sex)hormonal
AGA.