washingtonpost.com
Life-Lengthening Hormone Found in Mouse Research

By Rob Stein
Washington Post Staff Writer
Friday, August 26, 2005; A01

Scientists have identified a hormone that significantly extends the
life span of mice, a discovery that could mark a crucial step toward
developing drugs that boost longevity in people.

The hormone is the first substance identified that is produced
naturally in mammals, including humans, and can extend life span -- a
long-sought goal in the intense effort to help people live longer.

Much more work is needed to study the substance, and investigate
whether the hormone or a similar compound would be effective and safe
in people, experts cautioned. But the discovery opens highly promising
avenues for research and provides tantalizing new clues toward
deciphering the basic biology of aging.

"This is a significant discovery. It's an exciting paper," said Anna
McCormick of the National Institute on Aging, which helped fund the
new research, published online yesterday by the journal Science. "It's
definitely the way you would go about designing molecules that would
promote healthy aging and longevity in people."

Makoto Kuro-o of the University of Texas's Southwestern Medical Center
at Dallas, who led the research, said, "This could provide a key to
understanding the molecular mechanisms of aging and opens up new areas
to the potential therapy for multiple age-related diseases in humans."

The discovery was triggered by a study Kuro-o and his colleagues
published in 1997. That study identified a gene in mice that, when
damaged, caused the animals to experience all the hallmarks of aging
in humans -- hardening of the arteries, thinning bones, withered skin,
weak lungs -- and to die prematurely. They dubbed the gene Klotho, for
the Greek goddess who spins the thread of life.

Suspecting the gene may play a role in regulating life span, Kuro-o
and his colleagues genetically engineered mice with overactive Klotho
genes. In the latest experiments, they found that these animals lived
an average of 20 to 30 percent longer than normal -- 2.4 to 2.6 years
vs. a normal life span of about two years -- without any signs of ill
effects, according to the new report.

"The extension of life span is widely accepted as a reliable marker
for the suppression of aging," Kuro-o said. "This shows the Klotho
gene regulates aging."

The researchers then identified a small protein component, called a
peptide, that the gene produces and found it circulating in the
animals' blood at double the normal level.

After isolating and purifying the substance and reproducing it through
genetic engineering techniques, the researchers injected the substance
into normal mice. Tests on those animals, combined with experiments
involving cells in the laboratory, indicate that the substance
modulates a crucial biological pathway involved in an array of basic
metabolic functions that has become the focus of aging research in
recent years.

"It's a pathway that has been conserved by evolution that has been
found to play a key role in regulating life span for flies, worms,
mice and probably humans," Kuro-o said.

Studies, for example, suggest that damping down this pathway -- known
as the insulin/insulin-like growth factor-1 signaling pathway -- may
be the mechanism that extends longevity in animals that are fed an
ultra-low-calorie diet.

The Klotho hormone appears to have a similar effect, Kuro-o said.

"Our work shows that the Klotho gene is an aging-suppressor gene," he
said.

Other researchers said the findings were remarkable because no one had
previously found a naturally occurring hormone capable of extending
the life span of a mammal.

"You have lots of ways to shorten the life of an animal, but it's hard
to get an animal to live longer," said George M. Martin of the
University of Washington, who is scientific director of the American
Federation for Aging Research. "You can kick a radio to make it not
work so well, but it's hard to make it work better. It's quite a
wonderful discovery."

Kuro-o and his colleagues plan to inject the substance into normal
mice to see whether it extends their life spans and to measure the
substance in humans to determine whether levels of the protein are
correlated with longevity. Previous research has shown that humans
have the protein in their blood, and that people with a certain
variation of the gene are prone to age-related diseases such as heart
attacks, strokes and osteoporosis.

Scientists will have to determine whether the protein can be produced
in sufficient quantities to use it as a drug. It may turn out that
other substances that mimic the protein's effects would also work or
be safer, Kuro-o said. "That might be more practical," he said.

Kuro-o and others cautioned, however, that agents that appear
effective and safe in mice often produce complications in humans. The
hormone, for example, appears to decrease the effectiveness of
insulin, which could limit its usefulness.

"It appears to play a role in the same pathway in people, but that
doesn't necessarily mean it's going to be as straightforward to extend
life span in people as it is in mice," said Valter Longo of the
University of Southern California. "But this adds a new component to
our picture and perhaps a component that could extend life span with
few ill effects."

Beyond the possible clinical applications, other researchers said the
finding underscores the growing understanding of the basic biology of
aging.

"Papers like this are filling in the pieces of the puzzle that will
explain the evolutionary biology of aging," said L. Stephen Coles of
the UCLA School of Medicine.
© 2005 The Washington Post Company




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