Circadian and Photoperiodic Effects of Brief Light Pulses in Male Djungarian Hamsters
OF
BIOLOGY
35, 327-3
REPRODUCTION
Circadian
35 (1986)
and Photoperiodic
Effects of Brief
in Male Djungarian
Hamsters’
JILL
J. MILETTE2
Department
and
of Neuro
Northwestern
FRED
Illinois
Pulses
W. TUREK
biology
and
University
Evanston,
Light
Physiology
60201
The
the
effects
of brief
light
pulses
neuroendocrine-gonadal
running
in constant
locomotor
night,
darkness
activity.
animals;
phase-delays
and
Animals
exposed
in increased
levels
of light
(but
two
of
phase-advances
1 -mm
the
during
pulses)
for
testicular
weight
gains
and serum
FSH
apart,
some
animals
showed
a short-day
10
the
circadian
Djungarian
induced
induced
by
of light
testicular
days
light
subjective
rhythm
of locomotor
hamsters.
day
curve”
was
pulses
delivered
induced
phase
similar
little
resulted
in stable
entrainment
two
10-mm
pattern
(i.e.,
did-
not
in which
result
trainment
increase
productive
the
activity
in testicular
rhythm
growth
showed
in any
of
a long-day
the
animals
The
annual
variation
or photoperiod,
avian
and
to bong
days
several
(e.g.,
has
the
amount
species
sparrows,
of
light
per
activity
manipulation
that
of
breed
voles,
mice
during
and
only
hamsters)
Accepted
January
27, 1986.
Received
November
25, 1985.
‘Preliminary
reports
of this work
were
presented
at the 17th
and
18th
Annual
Meetings
of the
Society
for the Study
of Reproduction
in Laramie,
Wyoming,
July
1984,
and Montreal,
Quebec,
July
1985.
This
work
was supported
by a National
Science
Foundation
Fellowship
to J.J.M.,
the
Whitehall
Foundation
and
NIH
Research
Grant
HD-09885.
2Reprint
requests.
subjective
rhythm
presented
confined
exposure
rhythm
activity
as well
8 and
to the
activity
that
to the
confined
rhythm
of
in all the
same
showed
light
measuring
but
instead
between
clock
been
carried
(Gaston
Stetson
Zucker,
and
Menaker,
et al., 1975;
1978;
Matt
variety
of
collegues
coincident
absolute
is dependent
bight
and
(Menaker
out
and
using
length
of the
upon
the
the
animal’s
Eskin,
1967;
Clarke,
1980;
et
al.,
1974;
Darrow
1985).
of a circadian
clock
in
in mammals
have
the
golden
1967;
Elliott
et
Elliott,
1976,
1981;
and
Stetson,
1980).
experimental
have
with
measurement
the
Grocock
and
and
Zucker,
Underwood
ena rapid
on re-
time
studies
on the robe
time
measurement
cycle
a short-day
photoperiodic
circadian
as
16 h
long
neuroendocrine-gonadal
and the circadian
testicular
growth
activity
of
other
exposed
to 6L:18D
or two 10-mm
pulses
locomotor
pattern,
revealed
Detailed
photoperiodic
exposure
late
in the
of the activity
Follett
et a!.,
1974;
Elliott,
1976;
Johnston
and
Goldman,
1985;
short
days
the photo-
and
in
that
short
pulses
of light
can induce
hamster
and that
the effects
of light
the light and the circadian
system.
internal
appropriate
time
1979).
In many
days
stimulate
while
the
does not involve
day
(or night),
phase-relationship
as the primary
signal
for
species
to synchronize
activities
to the
and Campbell,
species,
long
neuroendocrine-gonadal
inhibit
it. Experimental
of
in
serves
mammalian
their
reproductive
of the year
(Turek
seasonally
breeding
period
entrainment
in which
pattern.
Taken
together,
these
results
demonstrate
in neuroendocrine-gonadal
function
in the Djungarian
function
depend
upon
the phase-relationship
between
INTRODUCTION
day,
many
early
on
free-
observed
phase-shift
pulses
of light
were
locomotor
activity
and/or
hamsters
in the rhythm
that
in the
period
of darkness)
while other animals
showed
a long-day
entrainment
pattern
(i.e.,
to the short
period
of darkness).
Importantly,
the stimulatory
effects
of light
activity
were clearly
dependent
on the phase-relationship
between
the light pulses
locomotor
activity.
While exposure
to two 10-mm
pulses
of light per day induced
hamsters
shifts
to
or no
of
during
the night
in animals
otherwise
weight.
Daily
exposure
to two 1-b
increases.
When
entrainment
activity
Exposure
phase-dependent
“phase-response
the
to 1-mm
FSH and
on
male
of light
were
pulses
for 7 days
of serum
in
1-h pulse
shape
light
in duration)
investigated
to a single
while
rhythm.
resulted
mm
was
general
The
respectively,
not
(1-60
axis
demonstrated
the active
bight
cycles,
hamster
a!., 1972;
Eskes
and
Using
a
Elliott
cycle
of the
golden
hamster,
stimulation
neuroendocrine-gonadab
axis
occurs.
This
inducible
phase”
begins
at about
the time
327
and
that
when
light
phase
of the activity/rest
his
is
of the
“photoof the
ABSTRACT
328
MILETTE
onset
of
locomotor
activity
and
lasts
for
AND
about
TUREK
transferred
to
of
h)
the
about
3 wk exposure
to 6L:18D,
and each
animal
was
categorized
into
one
of four
stages
according
to the
method
of Hoffmann
(1978).
Only
those
animals
with
testes
in the smallest
class
(Stage
N,
direct
methods
of the
clock
are
available
itself.
The
be an excellent
model
perties
of the circadian
difficulty
release
in daylength
(Berndtson
In
for examining
clock involved
a robust
change
and/or
gonadal
is usually
not
and
contrast,
the
has
phase
proved
to
the formal
in photoperiodic
pro-
nonpabpabbe)
However,
use of this species
for inneural
and cellular
events
underlying
time
measurement
presents
a major
in that
tropin
measuring
hamster
in pituitary
activity
Desjardins,
1974;
photostimulation
for
the
a change
many
Turek
of
gonado-
after
observed
size
weeks
et ab., 1975).
juvenile
Djung-
induces
a clear
Activity
To
was
were
assessed
used
by
in these
regression.
palpation
experiments.
Recording
record
locomotor
activity,
animals
were
the running
wheel
an Esterline-Angus
activated
a microswitch
that led to
(Indianapolis,
IN) event
recorder.
records
for individual
animals
and pasted
onto
a board
to
rise in serum
FSH levels within
3 days and an increase
in testicular
weight
within
5 days
(Simpson
et ab.,
1982).
Furthermore,
as it can in the golden
hamster
visualization
of
(Rudeen
activity
hamster
1984;
and
Ellis
during
the
photoperiod
activity
1982).
Reiter,
and
1980;
Foblett,
night
can
Earnest
1983),
of an
stimulate
Turek,
pulse
1983,
of light
was
5-10
Djungarian
hamster
an excellent
model
the relationship
between
the circadian
systems.
The present
study
examines
for
and
the
state
of light
as well
testicular
MATERIALS
on the circadian
as on pituitary
weight
AND
in the
rhythm
gonadoDjungarian
Animals
Djungarian
hamsters
(Phodo
pus sungorus
sungorus)
were
born
and
raised
in our
laboratory
breeding
colony
under
a 16L:8D
photoperiod
(bights
on from
0500-02100
h).
The
colony
was
derived
from
animals
(Worcester
Shrewsbury,
hamster
received
kindly
provided
Foundation
MA).
The
by
for
Dr.
Bruce
Experimental
animals
chow
(Winfield,
IA)
a weekly
supplement
were
Goldman
Biology,
fed
and water
ad
of sunflower
The
young
remained
with
their
parents
unti (...truncated)