Study shows new evidence of age-related
decline in the brain's master circadian
clock
Research by UCLA's Gene Block, Christopher
Colwell provides new insights into sleep
difficulties among older people
By Stuart Wolpert
July 21, 2011--A
new study of the brain's master circadian
clock — known as the suprachiasmatic
nucleus, or SCN — reveals that a key pattern
of rhythmic neural activity begins to
decline by middle age. The study, whose
senior author is UCLA Chancellor Gene Block,
may have implications for the large number
of older people who have difficulty sleeping
and adjusting to time changes.
"Aging has a profound effect on circadian
timing," said Block, a professor of
psychiatry and biobehavioral sciences and of
physiological science.
"It is very clear that animals' circadian
systems begin to deteriorate as they age,
and humans have enormous problems with the
quality of their sleep as they age,
difficulty adjusting to time-zone changes
and difficulty performing shift-work, as
well as less alertness when awake. There is
a real change in the sleep–wake cycle.
"The question is, what changes in the
nervous system underlie all of that? This
paper suggests a primary cause of at least
some of these changes is a reduction in the
amplitude of the rhythmic signals from the
SCN."
The SCN, located in the hypothalamus, is the
central circadian clock in humans and other
mammals and controls not only the timing of
the sleep–wake cycle but also many other
rhythmic and non-rhythmic processes in the
body.
The UCLA research team examined the SCN in
mice and found that while critical neural
activity rhythms were already disrupted in
middle age, the molecular mechanisms that
generate these rhythms were not
significantly altered.
"These results indicate that the outputs of
the central circadian clock start to decline
in middle age and suggest that the same may
be true in humans," said study co-author
Christopher Colwell, a UCLA professor of
psychiatry and biobehavioral sciences who
has conducted research with Block for many
years. "Before this study, we did not know
that the SCN was the site where the decline
occurs."
In a technical tour de force, the
research team successfully recorded
electrical activity from the brain's SCN —
not in a Petri dish but in living animals.
The research marks the first time this has
been achieved in middle-aged animals and the
first time scientists have watched the
central biological clock of aging animals in
action. The study was published July 13 in
the Journal of Neuroscience, the journal of
the Society for Neuroscience.
The scientists studied young mice, which
were just a few months old, and middle-aged
mice, which were more than a year old. SCN
brain cells are electrically active during
the day and electrically silent during the
night in younger animals and younger people,
the researchers said, but that difference is
reduced with aging.
"The changes we observed in the electrical
rhythm between the young and middle-aged
animals, which are quite dramatic, occur
even though we do not see significant
changes in the underlying molecular rhythm,"
Block said.
"Our hypothesis is that the age-related
changes in the circadian timing system are
primarily occurring, at least initially, at
the level of the electrical output
signaling, perhaps mediated by changes in
the cell-membrane properties of SCN clock
cells. This is good news, because it points
where in the cell to look for the
age-related 'lesion' and thus helps inform
what type of measures may be available to
reduce these age-related deficits."
Block and Colwell suspect the process is
similar in humans.
The SCN keeps the system of multiple
distributed circadian oscillators in
synchrony, but disruptions in the SCN lead
to disrupted sleep, as well as dysfunction
in memory, the cardiovascular system, and
the body's immune response and metabolism.
The SCN, Block said, can be imagined as a
heavy pendulum that controls many light
pendulums (oscillators), with rubber bands
between them.
"If the central clock weakens, it's
effectively like making those rubber bands
thinner and weaker," Block said. "When the
SCN ages and those rubber bands become
weaker, it becomes hard for the SCN to
synchronize all of these other oscillators."
In the young mice, the scientists found high
levels of activity during the day and much
lower activity levels during the night. In
middle-aged mice, there was not nearly as
large a difference in activity between the
day and the night.
"In the middle-aged mice, they still have a
circadian rhythm, but the amplitude is
reduced," Block said. "During the nighttime,
when electrical impulse activity levels are
usually fairly low, the levels have
increased. Thus, the difference between the
highest levels of activity during the
daytime and the lowest levels of activity
during the nighttime is much smaller in the
middle-aged mice."
Large numbers of people over the age of 65
regularly take sleeping pills, but the
effects of taking such pills over many years
is not known, said Colwell, who hopes the
new research will lead to other options for
getting a good night's sleep.
Colwell, Block and their team plan to pursue
follow-up research on treatment options that
could enhance the function of the circadian
system with aging. They are studying the
specific membrane channel changes in the SCN
that are responsible for the electrical
rhythm and also are looking at the circadian
regulation of the heart and the mechanisms
underlying neural activity rhythms in the
SCN.
Their research could potentially lead to new
ways of boosting the circadian output. It is
possible, Colwell and Block said, that
relatively simple approaches could be
beneficial, such as exercising early in the
morning, getting regular exposure to bright
light, eating meals at consistent times and,
when traveling, eating meals at the
appropriate local time, regardless of
whether one is hungry then.
Possible interventions may involve
discovering ways to improve the sleep cycle
of aging people and their ability to better
handle time-zone changes, perhaps by
boosting the amplitude of the SCN. New
pharmaceutical approaches may be developed,
the scientists said. Future research may
reveal which approaches are likely to be
most effective.
Co-authors of the study included lead
scientist Takahiro Nakamura, a former UCLA
postdoctoral scholar in Colwell and Block's
laboratory, who is currently on the faculty
of Japan's Teikyo Heisei University; Takashi
Kudo, a UCLA postdoctoral scholar; and
Tamara Cutler, a UCLA undergraduate student
who works in Colwell and Block's lab.
The research was funded by the National
Institutes of Health and by UCLA.
Implications for patients with neurological
disorders such as Parkinson's
In related research, Colwell and his
colleagues have documented that changes
similar to those that occur as we age also
occur in mouse models of neurodegenerative
disorders like Huntington's disease and
Parkinson's disease.
"With many neurological disorders, patients
have a hard time sleeping during the night
and staying awake during the day," said
Colwell, who was a postdoctoral fellow in
Block's lab in the early 1990s at the
University of Virginia.
"One
of the main clinical complaints of patients
with Huntington's disease and Parkinson's
disease is they cannot sleep and do not
respond well to sleeping pills. We think the
same dysfunction we see with normal aging
occurs much earlier and more severely with
these patients, and we hope that the
treatment strategies we develop for aging
can be applied to help patients with
neurodegenerative diseases as well. If we
learn what is going wrong, then we may be
able to develop treatments."
Colwell's research on Huntington's disease
was published earlier this year in the
journal Experimental Neurology, and his
research on Parkinson's has been accepted
for publication in the same journal.
Undergraduate works in laboratory of Colwell
and Block
Tamara Cutler, a UCLA senior majoring in
neuroscience and physiological science,
co-authored the new SCN research. So what is
it like for an undergraduate to conduct
research with distinguished scientists,
including the university's chancellor?
"Working in the laboratory of Professor
Colwell and Chancellor Block has been
rewarding, demanding and priceless," Cutler
said. "I joined the lab with the usual book
knowledge of a life sciences student, a
nearly boundless enthusiasm for research and
a love for solving puzzles of every kind.
Professor Colwell, Chancellor Block, the
postdocs (Dawn Loh and Takshi Kudo) and the
graduate students all invested time in my
training and provided me with many fantastic
opportunities to develop a strong set of
skills.
"Since joining the lab, I have learned
numerous techniques and been allowed to
perform my own experiments from start to
finish while working on my honors thesis. I
have been treated as a valuable member of
the lab and have been encouraged to make
intellectual contributions to our research,
which I am certain has greatly accelerated
my growth as a scientist. Being granted a
co-authorship on this manuscript as an
undergraduate is very meaningful to me
because it is not handed out lightly here.
"Dr. Colwell and Chancellor Block are really
extraordinary scientists and renowned
figures in the circadian research community,
and it has been my great privilege to learn
from them. I know my time here in the
Colwell–Block lab has transformed me from
someone who merely learns science
into someone who can actually do science.
I still have years of training ahead, but
the journey thus far has been priceless."
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