The mountingevidence for age genes that influence the aging process is by no means conclusive , but it is quite impressive, coming from a variety of independent research from aging in worms and fruit flies to antioxidants and gene repair mechanisms, and human mutations. Still, the connections are circumstantial.
Christopher Wills, professor of biology at the University of California in San Diego, thinks that by 2025 science will likely isolate the mammalian age genes in mice. We share roughly 75 percent of our genes with mice and have much the same body chemistry; this is a strong reason to believe that an age gene found in mice could also be at work in humans. If such genes are located, the next step would be to find out if these age genes have their counterparts in humans. Wills believes that if they are found in humans, they may extend the human life span perhaps to 150 years.
But by 2020, when personalized DNA sequencing becomes widespread, a secondtactic may prove fruitful as well. By analyzing populations of healthy individuals in their nineties and beyond, scientists will find it possible to use computers to compare their genetic backgrounds and cross-check for similarities in key genes that are suspected of influencing aging. A combination of studies on the DNA of long-lived animals and on the personalized DNA sequences of elderly individuals may considerably narrow down the search for the age gene.
As yet, none of these methods can prove that we can increase the human life span. Indeed, the only theory with a proven trackrecord of extending the life span of animals is the caloric restriction theory, which states that animals which consume calories just above starvation levels live significantly longer than the average. Although this theory flies in the face of commonsense (a well-fed animal is well nourished and healthy, and should have greater resistance to disease and aging), it has held up under repeated testing among a wide range of animals. Scientists have consistently increased the life span of rats and mice in the laboratory by 50 to 100 percent. It is the only laboratory-tested theory of age extension for animals that has held up under decades of careful scrutiny. Why?
Across the animal kingdom, the life span of animals is roughly inversely correlated to the metabolismrate. The slower their normal metabolismrate, the longer their normal life span. In 1996, in a study that reduced the calorie intake of 200 monkeys by 30 percent, the monkeys were shown to have a slower metabolismrate, a longer life span, and reduced rates of cancer, heart disease, and diabetes. “We have known for 70 years that if you feed laboratorymice less food, they age slower, they live longer, and they get diseases less frequently. We find that monkeys respond in the same way as rodents and that the same biological changes may be in play here,” says George Roth of the National Institute of Aging.
There is still room for scientificdebate on the question “why?” Ron Hart, a scientist at the National Center for Toxicological Research, believes that the answer may tie in the high body temperature of mammals, and humans in particular. “Heat causes pieces of the DNA molecule to split off randomly, and it must be repaired,” Hart says. “Under calorie restriction, though, the engine runs cooler and there’s less damage. Merely reducing caloric intake by 40 percent reduced this form of spontaneous DNA damage almost 24 percent!” Furthermore, at a higher internal body temperature, oxygen is being burned at a greater rate, creating more free radicals, which also speed up the aging process. Cooling the body, on the other hand, increases the amount of antioxidants in the body. Hart found a fourfold increase in the enzyme catalase and a threefold increase in superoxidedismutase in animals on a restricteddiet. “What’s fascinating," Hart concludes, “is that reduced food intake is the only experimental paradigm ever found that enhances DNA repair.” Hart is so convinced of the importance of this work that in 1993 he began the first systematic studies of caloric restrictions in humans.
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