X-Message-Number: 25624
Date: Tue, 25 Jan 2005 02:54:42 -0800
Subject: Fwd: The Biology of . . . Cryogenics (take 3)
From: Kennita Watson <>

Grf.  One more try, with stuff I think confused the mailer elided.

Kennita

The Biology of . . . Cryogenics
Waking From a Dead Sleep
Wood frogs survive long periods in a deep freeze. Can people do the 
same?
By Elizabeth Svoboda
DISCOVER Vol. 26 No. 02 | February 2005 | Biology & Medicine

As far as Ken and Janet Storey are concerned, the most interesting frog 
is one that doesn t move or breathe and has no heartbeat or brain 
activity. In the Storeys  biochemistry lab 
atCarletonUniversityinOttawa, the typical study subject is

thrown into an industrial freezer. They call them frogsicles, though 
they re partially liquid inside.  Basically, the body turns into a 
syrupy mass,  Ken Storey says. As far as the frog is concerned, this is 
nothing out of the ordinary. Like a handful of other creatures, the 
common wood frog, Rana sylvatica, is a biological conundrum. It spends 
its winters interned in subzero sleep, its tissues steel-rigid, and 
revives in the spring raring to go. It s the Rip van Winkle of the 
animal world.

The Storeys have spent more than 20 years identifying the genetic 
switches and biochemical processes that make this reanimation possible. 
Their work has been avidly followed by biologists in the field of organ 
transplantation: If a donor s heart or kidney could be frozen and 
stored without damage, physicians could dramatically increase the 
number of transplants they perform. The fact that a wood frog can 
nearly come back from the dead has also fanned the futuristic fantasies 
peddled by commercial cryonics labs, where human corpses are kept on 
ice in the vain hope that medical science might one day restore them to 
life.

Warm-blooded animals are designed to stay at a near-constant 
temperature 98.6 degrees Fahrenheit in the case of humans. When they 
start to get cold, their metabolism revs up, generating internal heat. 
Once this system breaks down and the animals freeze solid, the ice 
tears up their insides: The water in their cells expands as it freezes, 
shredding membranes and dislodging organelles.

Wood frogs and a few other animals such as box turtles do exactly the 
opposite. When temperatures drop below freezing, the frog s metabolism 
eases to a near halt, so its cells can survive on negligible amounts of 
oxygen and energy. Meanwhile, the liver begins to pump out glucose, 
raising concentrations in the bloodstream to more than 50 times those 
found in a human diabetic. Ice crystallizing in the frog s body 
cavities draws some of the water from the cells in the flesh and 
organs. This further concentrates glucose inside the cells, turning it 
into an antifreeze that keeps the remaining water from solidifying. 
(Commercial antifreeze is made of a sugar alcohol similar to glucose, 
called ethylene glycol.) With the antifreeze in its cells, a frog can 
remain in a torpid state until spring, when its metabolism whirs back 
to life.  It goes brain dead for a few months, then has little froggy 
thoughts again,  Ken says.

The ability of wood frogs to freeze and thaw probably evolved during an 
ice age about 15,000 years ago, the Storeys say. The cells in the 
frog s moist, delicate skin were already optimized to prevent 
dehydration; glacial conditions just kicked the process up a notch. 
Ordinarily, high blood-sugar levels trigger a process known as 
glycation, in which glucose molecules bind to the body s structural 
proteins, among other things, causing cellular damage. Not so in wood 
frogs. The Storeys recently isolated a gene that short-circuits 
glycation. Other DNA tests have allowed them to identify genes that 
turn off metabolic processes, control cellular volume during freezing, 
and limit the damage that oxygen can do to cells when it flows into 
them again in the spring.

When the Storeys compared the livers of frozen wood frogs to those of 
control frogs in a normal state, they also found unusually high levels 
of messenger RNA molecules that code for fibrinogen, a clot-enhancing 
protein. Once activated by an enzyme in the bloodstream, fragments of 
fibrinogen bind together into a sturdy lattice, sealing any leaks that 
have formed in blood vessel walls due to the stress of the freeze-thaw 
cycle.

Boris Rubinsky, an engineer at theUniversityofCaliforniaatBerkeley, has 
worked with a number of scientists to apply the Storeys  findings to 
other animals, including humans. In 1999 Rubinsky and his colleagues 
used a computer-controlled pump to infuse rat livers with a cocktail of 
cryoprotective chemicals. He froze the livers at 29.3 degrees F for 
about two hours, then thawed and transplanted them into other rats. Of 
the nine transplantees, eight survived for several hours after 
receiving the donor organs, and one survived for five days, suggesting 
that the livers were at least partially functioning. Since that 
landmark trial, Rubinsky and researchers at theShebaMedicalCenterin Tel 
Hashomer,Israel, have applied similar freezing techniques to frozen rat 
hearts. In a 2003 experiment, the hearts remained viable and pumping 
for more than an hour after being thawed and transplanted.

Cryopreserving organs could one day revolutionize transplantation, but 
some scientists have their eyes on an even larger prize: freezing 
entire human bodies. The Alcor Life Extension Foundation 
inScottsdale,Arizona, made news in 2002 when it wrangled with some 
relatives of baseball player Ted Williams. Alcor officials say Williams 
paid them to freeze his body after he died, but his nephews John and 
Samuel Williams recently filed suit against the company, alleging it 
didn t have proper legal permission to do so. Alcor continues to hold 
the remains, pending future legal action.

Alcor s goal, trumpeted on its Web site, is to keep deceased customers 
 in a state that will be regarded as viable and treatable by future 
medicine.  Most cryobiologists deride this as a pie-in-the-sky 
enterprise.  They re trying to take a thousand steps at once,  Ken 
Storey says.  The temperatures they re dealing with are lower than 
anything in nature, so there s extensive tissue damage and cell 
dehydration.  Yet Alcor has never guaranteed that its patients will 
receive a return on their $150,000 investment.  This is an 
experiment it s speculative science at best,  the company s CEO, Joe 
Waynick, says.

Alcor is banking on the proposition, Waynick adds, that  survival of 
structure means survival of the person.  The company s scientists are 
trying to figure out how to cool corpses to temperatures that cause 
total metabolic arrest around  321degrees F with minimal tissue damage, 
so the bodies can remain perfectly intact for thousands of years. To 
that end, they infuse clients with a proprietary mixture of 
carbohydrate-based antifreezes similar to those naturally produced by 
the frogs in the Storeys  lab. Waynick thinks some of the first 
patients who signed up for Alcor preservation in the 1970s and 1980s 
were too damaged by freezing to be revived, but current techniques are 
less likely to cause  cracking,  he says. The tissues are pumped so 
full of cryoprotectant that they never completely solidify. Significant 
obstacles remain, however, including the toxic effects of antifreeze on 
tissue and its imperfect dispersal throughout the body.  Different 
organs absorb the cryoprotectant at varying rates, and some don t do as 
well as others,  Waynick says.

 
To the Storeys, there isn t that much difference between institutions 
like Alcor and most organized religions.  The promise of eternal life 
is something that s appealing to just about everybody,  Ken Storey 
says. Still, they don t entirely dismiss cryobiology s grander goals. 
 It s possible in decades that we might be able to freeze astronauts 
for long missions and

things like that,  Janet Storey says.  But our focus is not how to 
apply these techniques to humans down the line. We want to figure out 
how the biological systems work. Other people can take it from there. 

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