From: Subject: You Must Remember This :: Spring 2009 :: Washington State Magazine Date: Tue, 10 Mar 2009 10:52:18 -0700 MIME-Version: 1.0 Content-Type: multipart/related; type="text/html"; boundary="----=_NextPart_000_0000_01C9A16E.48562750" X-MimeOLE: Produced By Microsoft MimeOLE V6.00.2900.5579 This is a multi-part message in MIME format. ------=_NextPart_000_0000_01C9A16E.48562750 Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Content-Location: http://wsm.wsu.edu/2009/Spring/remember.php You Must = Remember This :: Spring 2009 :: Washington State Magazine

Spring 2009

Memory

Washington State Magazine

[+]

Features

What Is=20 Art For? :: Art, says = independent=20 scholar Ellen Dissanayake '57, is "making special." It is an act that = gives us a=20 sense of belonging and meaning. It is passed from mother to child. Its = origins=20 lie deep in our evolutionary past. It makes us human. by Tim = Steury

The Love=20 Letters :: In 1907, Othello had no high = school, so=20 Xerpha Mae McCulloch '30 traveled 50 miles to Ritzville to finish = school. There=20 she met, and fell in love with, Edward Gaines, a few years her senior. = The=20 recent gift to Washington State University of her steamer trunk reveals = the life=20 of a woman whose story is not only threaded through the University's, = but also=20 through the story of agriculture in Washington State. by Hannelore=20 Sudermann { WEB EXCLUSIVE=97GALLERY: Photos and = letters from=20 Xerpha's trunk }

You = Must=20 Remember This :: Having reached a certain = age, our=20 correspondent sets out to learn the latest from Washington State = University=20 researchers about memory. She learns that memory comes in different = forms, that=20 the human brain is made for problem-solving, and that the key to much of = brain=20 health is the "dendritic arbor." And then she sets out to create an = action plan.=20 by Cherie Winner
{ WEB EXCLUSIVE=97STORY: Maureen=20 Schmitter-Edgecombe's work to help people with memory loss=20 }
{ DISCOVERY: Te= sting 1 2=20 3, online tests for different aspects of memory = }

ESSAY

Privacy=20 and the Words of the Dead :: Do we violate = the=20 privacy of the dead when we read what they wrote for themselves? Maybe = it=20 depends on our purposes. by Will Hamlin { WEB=20 EXCLUSIVE=97GALLERY: Annotated = pages from=20 early English editions of Montaigne's Essays. = }

Panoramas

Space = chronicles :: Come = MapWith.Us=20 :: The webs=20 we weave :: Hunger for = justice=20 :: Great=20 promise in a nitrogen conundrum

Departments

FIRST = WORDS=20 :: LETTERS=20 :: Sports: = Coaching with=20 heart :: GREEN PAGES: Building = green=20 :: A = long-term biofuels=20 strategy for Washington :: A gift = toward fuel=20 research :: In season: = Lentils=20 :: LAST WORDS: = Hotel at the=20 top
{ WEB EXCLUSIVE=97STORY: Yucatecan = lentil soup=20 recipe }

Tracking

Jason = Ambrose =96=20 Counting beans in Costa Rica :: Roger = McClellan =96 A=20 suitable combination :: Robert Helm, 65 = =96=20 Acclaimed Northwest artist, teacher :: Wallis = Beasley, 92 =96=20 Sociologist, administrator, interim WSU president

Cover photo: Bryan Hall clock tower reflected in the = Abelson-Heald=20 skybridge windows on the Pullman campus. By Zach=20 Mazur.

Washington State Magazine :: Coordinates

Print :: Return to web = page

Features

Web exclusives:

{ Maureen=20 Schmitter-Edgecombe's work to help people with memory loss }

{ DI= SCOVERY=20 :: Testing 1 2 3, online tests for different aspects of = memory=20 }

by Cherie Winner | =A9 Washington State = University

It=92s been decades since I was asked, =93What do you want to be when = you grow=20 up?,=94 but now I=92m facing a mid-life version of the question, this = one tinged=20 more with fear than with hope. I just turned 53 and my current answer to = the=20 question of what I want to be in 20 or 30 years boils down to three = things:=20 healthy, solvent, and of sound mind.

Of the three, the one I worry about most is the last. I=92ll have = support=20 networks to help me work around the others, if need be, but if my mind = goes=96

The fear, of course, is of the big A: Alzheimer=92s disease. The most = common=20 cause of dementia, Alzheimer=92s already afflicts more than four million = Americans. By 2050, with the aging of my fellow boomers, that number is = expected=20 to triple. And there=92s not much we can do about it. A few drugs are = available=20 that help in the early stages of the disease; but for the foreseeable = future, to=20 come down with Alzheimer=92s is to step into an abyss.

Several scientists at Washington State University are exploring how = memory=20 works and what=92s gone wrong when it doesn=92t. I set out to talk with = them about=20 their research and, I hope, pick up tips about what I can do now to = improve the=20 odds that when I=92m 80 my brain will still be healthy enough to let me = cook my=20 own meals, pay my own bills, enjoy my friends and family, and understand = what=92s=20 going on in the world.

My first visit is with psychologist Maureen Schmitter-Edgecombe, who = explores=20 the borderland between normal functioning and the beginnings of = dementia.=20 Doctors call it MCI, for Mild Cognitive Impairment. She says MCI is not = the same=20 thing as early-stage Alzheimer=92s, although the term is sometimes used = that way.=20 It=92s just a label assigned to people who do poorly on certain tests of = memory=20 and routine thinking.

=93Some would argue that people in this category really are early = stage=20 dementia,=94 she says, =93but depending on how you get your sample, some = of the=20 people that fall into this stage actually revert back to looking like = normal=20 older adults the next time you test them a couple of years later.=94

In her lab, simply failing a word-recall test doesn=92t land you in = the MCI=20 category. Schmitter-Edgecombe is working to develop better ways to = assess memory=20 problems. Are a client=92s memory lapses normal age-related glitches, or = signs of=20 an irrevocable slide into neverland?

=93[People] can=92t get in that category just because they had one = poor test,=94=20 she says. =93They have to be reporting a history of difficulties, the = significant=20 other has to be reporting a history of difficulties, and then all that=20 information has to make sense with what we=92re seeing in the testing = data.=94

In one test, she asks each client to do eight memory-related tasks = over the=20 course of an hour. The client is also asked to remember that after each = task, he=20 should remind a third person to take medication. At the end of the hour, = Schmitter-Edgecombe asks the client to describe the eight tasks (not in = detail,=20 just well enough for her to recognize each one)=96and to tell = what order=20 they came in.

I can imagine getting the first one and maybe the last two in the = right order=20 (assuming I could even recall all eight), but the ones in the middle? = That=20 sounds hard.

She says it=92s not hard at all for young adults, =93but as we get = older, we do=20 start to see changes.=94 Recalling the order in which events happened, = or=20 temporal order memory, is distinct from recalling the events = themselves,=20 which is called content memory. It=92s possible to remember an = event=20 clearly but forget when it occurred, says Schmitter-Edgecombe. So far, = most=20 tests for Alzheimer=92s focus on content memory: You=92re asked to = recall a list of=20 words, who=92s President, or what you ate for breakfast. But such tests = miss=20 non-content aspects of memory that may be even more important to = everyday=20 functioning than content memory.

=93We=92ve got a group [of clients] who are not having content memory = problems,=20 yet they=92re reporting, or their significant others are reporting, just = as many=20 difficulties in their everyday lives,=94 says Schmitter-Edgecombe. = =93These other=20 aspects of memory may actually have greater contributions to what people = are=20 reporting as causing problems.=94

In addition to temporal order memory, there=92s source = memory, which=20 records where you got the information. When you tell a story to the = person you=20 first heard it from, that=92s a failure of source memory. Your content = memory is=20 fine=96you remember the story perfectly=96but you=92ve forgotten who = told it to=20 you.

Finally, there=92s prospective memory, the ability to = remember to do=20 things in the future. Prospective memory involves long-term goals, like = vacation=20 plans, and daily details, like remembering to take medications at = specific=20 times.

It makes perfect sense, but I=92ve never thought about memory like = this before.=20 Schmitter-Edgecombe says I=92m not alone; there=92s been very little = research on=20 non-content memory, especially in the context of dementia. That=92s = beginning to=20 change. She and other researchers have found that serious problems often = show up=20 first with non-content processes. Temporal-order memory, especially, = starts=20 declining years before significant losses of content memory.

Schmitter-Edgecombe says that while the various forms of memory = interact with=20 each other, they largely reside in different regions of the brain. = Content=20 memory relies most heavily on the hippocampus, which lies fairly deep in = the=20 brain. Temporal ordering, source, and prospective memory involve higher = circuits=20 in the frontal lobes (behind your forehead), the parts of the brain = responsible=20 for decision-making or =93executive ability.=94 She thinks that if we = can understand=20 how the different aspects of memory are related and how they affect = people=92s=20 ability to get along in everyday life, we=92ll have a better shot at = developing=20 strategies to compensate for memory deficits, and perhaps even delay the = onset=20 of memory-related problems.

She=92s especially intrigued by =93cognitive reserve,=94 the notion = that staying=20 mentally active gives us some degree of protection against dementia. = People with=20 lots of cognitive reserve still get Alzheimer=92s, but they have excess = capacity,=20 a cushion, so they can still function well even with moderate = deterioration in=20 the brain. Eventually, the disease progresses so far that the reserve = can=92t=20 help, and then the person declines with stunning speed. Still, delaying = the=20 onset of symptoms by a couple of years sounds good.

So, how can we tell if we have a sizeable reserve? Can we do anything = to=20 boost it?

To some extent, the die is already cast, she says. How much education = you=20 had, your language skills in early adulthood, and your genetic history = all=20 contribute. But there are some things we can do to improve it. Being = socially=20 active helps. So does aerobic exercise, keeping a healthy flow of oxygen = to the=20 brain. Mainly, we need to keep learning. More and more evidence suggests = that we=20 can pad our cognitive cushion through mental activity.

That=92s what I was hoping to hear. My job requires plenty of mental = heavy=20 lifting, and at home I read challenging books, recently took up a = musical=20 instrument, and enjoy doing word and number puzzles. Is there merit in = the=20 suggestion I=92ve read that working crosswords or Sudoku keeps the brain = cells in=20 shape?

Schmitter-Edgecombe thinks puzzles may help, as long as they require = you to=20 actively search for and integrate new information. Her colleague, = biochemical=20 psychologist Jay Wright, agrees, =93but only if you=92re really = interested in doing=20 it. Pick something that=92s stimulating mentally, that you want = to do. It=20 could be reading, it could be solving things, it could be learning = anything new=20 that keeps you processing. You really need new experiences in order to = keep=20 things rolling.=94

The human brain is made for problem-solving, says Wright. =93We=92ve = got this=20 cortex that requires us to use it. I think that=92s the key to aging. I = think it=92s=20 anything that continues you problem-solving and trying to make sense out = of=20 something that challenges you.=94

He says mental activity strengthens the brain=92s ability to work = around=20 damaged areas and keeps brain cells alive longer, enhancing cognitive = reserve.=20 In Alzheimer=92s disease, wads of protein gum up the neural connections = and lots=20 of brain cells simply die. We all lose brain cells as we age; people = with=20 Alzheimer=92s lose more.

In particular, they lose cholinergic neurons, those that communicate = via a=20 neurotransmitter called acetylcholine. The drugs now used to treat = early-stage=20 Alzheimer=92s all boost the amount or longevity of acetylcholine, which = enables=20 the neurons to keep talking to each other longer.
That=92s OK as far = as it=20 goes, says Wright, but it ignores other chemical pathways that play a = role in=20 memory formation. Several years ago he and biochemist Joe Harding = discovered one=20 such pathway while researching how the body regulates its blood = pressure. They=20 were testing potential drugs that targeted molecules called angiotensin=20 receptors and came across a receptor (AT4) that just wouldn=92t = cooperate. Turns=20 out it=92s absent from parts of the brain that control blood pressure = but is=20 abundant in parts that deal with memory.

Wright and Harding took a closer look at AT4 and found that it is, in = fact,=20 involved in memory formation. Their discovery helped explain a reported=20 side-effect of certain blood-pressure medications. People who had taken = the meds=20 for several months had told their doctors, =91oh, by the way, I feel a = bit sharper=20 mentally than I was before.=92 That made sense, since maintaining a = healthy blood=20 pressure was known to be good for brain health. However, not all blood = pressure=20 medications had the same effect=96only those that worked via the = brain=92s=20 angiotensin receptors and activated AT4.

Wright and Harding ended up switching their research program from = blood=20 pressure to memory, which meant learning an entirely new literature and = new=20 experimental approaches. They found that the AT4 pathway works = independently of=20 the cholinergic system, and while its exact role isn=92t yet known, they = think it=20 offers another possible target for drug therapy to reduce the symptoms = of=20 Alzheimer=92s.

In one series of experiments, they are working to develop drugs that = aid=20 memory by =93revving up=94 the AT4 pathway. To test their potential = drugs, they have=20 developed an animal model of dementia. (No naturally-occurring model = exists.)=20 They treat rats with a drug called scopalomine, which interferes with = neurons=20 that use acetylcholine. For the next few hours the treated rats behave = in ways=20 that look familiar to anyone who deals with dementia patients. In = particular,=20 they have trouble retaining new information. It=92s not a permanent, = progressive=20 disease state, but a short-term, drug-induced inability to make new = memories.=20

Wright and Harding test each rat by putting it into a round horse = trough=20 filled with water. There=92s a small platform the rat can rest on, but = it=92s=20 slightly submerged and not visible from the surface. Until the rat finds = it, he=20 has to keep swimming. Wright and Harding time how long it takes the rat = to find=20 the platform on successive days. Each rat gets one try a day, for eight = days.=20 =93Demented=94 rats get scopalomine before each trial.
On the first = day, not=20 knowing the platform is there, the rats swim around for 90 to 100 = seconds before=20 finding it. Rats whose brains are functioning normally quickly learn = where the=20 platform is. Within a few days they swim more-or-less straight to it, = reaching=20 it in 15 to 20 seconds. A rat with drug-induced dementia, on the other = hand,=20 takes up to 75 seconds even after eight days of learning, and some never = find=20 it.

=93That=92s kind of what you see with people [who have dementia],=94 = says Wright.=20 =93They can learn things, but they=92ve got to rehearse it and = you=92ve got=20 to go over it and over it with them, and even then the progress is = really=20 slow.=94

In the key test of their potential drug, Wright and Harding gave the = rats=20 scopalomine to create dementia, and a new compound that enhances the AT4 = system.=20 After eight days of training, those rats found the platform in about 25=20 seconds=96almost as fast as the untreated controls. It was a major = finding:=20 boosting AT4 largely compensated for the problems in the cholinergic=20 pathway.

=93Our hope is that maybe the drugs we=92re developing would keep = people alert=20 and mentally active for another year, another two years, when they = normally=20 would be sliding,=94 says Wright. With one hand he sketches a sloping = line in the=20 air, indicating the decline in mental sharpness over time in dementia = patients.=20 =93We=92re not asking to stop the thing. I don=92t think that=92s = possible. But to make=20 the slope a little less [steep], so that they can still store new = memories,=20 retrieve those and old memories a little bit better.=94

For some reason I=92ve always thought of Alzheimer=92s in terms of = losing=20 existing memories. Yet people with the disease generally retain their = oldest=20 memories the longest. Like Wright=92s and Harding=92s rats, it=92s new = memories they=20 have the most trouble with, or integrating new ones with the old. And = that means=20 learning.

Wright says long-term memories are permanent in the sense that they = last a=20 long time, but they are not permanent in the sense of never changing. = When you=20 learn something new=96create a new memory=96you don=92t simply add new = information to=20 old, like stacking books on a shelf. The brain actually remodels itself, = its=20 internal wiring, all the time. If new information contradicts an = existing=20 circuit, for instance, your brain must weaken those previous connections = to=20 accommodate the new stuff.

The mysterious part is that the remodeling happens right where you = need it,=20 right in the brain cells involved with that prior memory. If you=92ve = just learned=20 a new route to the ballpark, you don=92t want your brain changing the = circuits=20 that store the knowledge of how to cook spaghetti. How does your brain = =91know=92=20 which connections to alter, which ones to strengthen, and which to do = away with=20 altogether?

Gary Wayman is working on those questions. He gets into the = nitty-gritty=20 biochemical details of how a signal from one nerve cell affects the = growth and=20 function of other nerve cells. =93I=92m a signal transductionist,=94 he = says, using a=20 term his mama surely never imagined for him. =93I absolutely love = dissecting these=20 puzzles out.=94

He also loves looking at nerve cells, or neurons, through the = microscope.=20 Healthy neurons are graceful things, with a roundish cell body that = houses the=20 nucleus, a long, sturdy axon that carries impulses toward other neurons, = and an=20 array of delicate branches called the dendritic arbor. Each dendrite, or = branch,=20 of the arbor has tiny hair-like spines that can meet up with an axon = from=20 another neuron to form a synapse. The synapse is the center of action in = neural=20 communication. A nerve impulse from one neuron travels down its axon to = a=20 synapse, where it crosses to a dendritic spine on another neuron. From = there the=20 impulse travels to the cell body, which determines whether to send the = signal=20 out through its own axon, or dampen the signal by not responding.

Wayman says the arbor is the key to much of brain health, including a = robust=20 memory. During infancy and childhood, as a child explores her = environment, a=20 flood of new information stimulates her neurons and the dendritic arbors = grow.=20 Dendrites that are used a lot branch more; dendrites that don=92t carry = many=20 signals get pruned back, as the neuron focuses its effort on the = connections=20 that are used most often.

Wayman starts with an experimental setup that shows clear links = between how=20 active neurons are and how connected and healthy they are. He puts = neurons from=20 a young rat brain into a culture dish and lets them grow a while to = establish=20 connections with each other. Then he adds the drug bicuculline, which = prompts=20 the neurons to transmit signals to each other as they would normally do = in=20 response to touch, sight, or whatever else the rat was experiencing. =

The arbors of neurons that receive signals from other neurons grow. = Some=20 dendrites get longer; others branch more. They also establish more = synapses with=20 neighboring neurons. It=92s exactly what you see in a young brain as the = animal it=20 belongs to learns about the world around it.
That much has been known = for=20 years, but the molecular mechanism for it has been a mystery.

=93They knew that if you increase synaptic activity, you modulate the = dendritic=20 arbor, you affect the formation of synapses,=94 says Wayman, =93but = nobody knows=20 what=92s going on inside the cell. That=92s where we came in.=94

He and his colleagues at the Oregon Health and Science University = have traced=20 much of what happens inside a neuron as a result of incoming signals. A = welter=20 of chemical details boils down to this: Dendrites contain a protein that = inhibits their further growth. Synaptic activity blocks the protein and = moves it=20 away from the active site. Synaptic activity also prompts the neuron to = make a=20 tiny RNA molecule called micro RNA 132 (miR132), which suppresses the = production=20 of more inhibitor. When miR132 production goes up, there=92s less = inhibitor and=20 the dendrites grow more in areas with active synapses. When Wayman = blocks=20 miR132, more inhibitor protein is made and dendrite growth stops or = slows down=20 (see an illustration).

My head is spinning. Boosting growth by inhibiting an inhibitor seems = overly=20 complicated, I say.

=93Is it complicated?=94 asks Wayman. =93Or is it giving the = cell a means=20 of fine tuning?=94 He reminds me that the conventional view of how cells = work=20 holds that a signal turns on genes in the nucleus, which leads to the = production=20 of messenger RNA and, eventually, of protein. That works for many = cellular=20 functions, but for the delicate job of making highly specific = connections with=20 other cells, it won=92t do. If a neuron=92s nucleus pumped out RNAs that = directly=20 promoted growth, all of its dendrites would grow, not just the = ones at=20 the site where the synaptic activity occurred.

And that=92s the key part of the system. When we learn something new, = we=20 don=92t get a wholesale activation of neurons throughout the = brain. Or we=20 shouldn=92t, at any rate. The last thing we want is general sprouting = throughout=20 the brain, says Wayman; that way lies madness, almost literally. = Indiscriminate=20 nerve firing causes seizures and has been linked to some forms of = retardation=20 and to loss of memory.

By having the molecular machinery for dendrite growth already in the=20 dendrites, but in an idle form, a signal at that site can activate the = machinery=20 in that locale alone, not throughout the neuron or brain as a whole.

The final piece clicks into place. It fits what Wright told me about=20 remodeling, it fits what he and Schmitter-Edgecombe said about giving = our brain=20 cells new problems to chew on, it fits what=92s known about more active = brains=20 suffering less neuron loss. Doing a hard mental task stimulates neural = activity,=20 which encourages neuron growth and connection. As Wayman says, =93an = active nerve=20 cell is a cell that=92s going to live another day.=94

So I=92m all set with an action plan for brain health. After work = today I=92ll=20 practice a new song, call my best friend, and go for a brisk walk with = the dogs.=20

Oh, and where did I leave that new Sudoku book?

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