26 June 2007

Getting rid of glutamate to prevent brain injury

Vivian Teichberg has hit upon a novel way to prevent neuronal death following an insult to the brain. Glutamate is an excitatory amino acid, which is necessary for normal brain function. However, it becomes excito-toxic when released in large amounts, which is exactly what happens during an injury. How to stop this? Well, you could interfere with the actions of glutamate; or you can remove excess glutamate from the brain via the bloodstream.
"Normally the brain recognizes the fact that the glutamate is extremely toxic and has an inherent defense mechanism which pumps it back into the brain cells," says Teichberg. However, with trauma or disease, the brain's normal mechanisms don't function properly. They need a helping hand. Teichberg's idea was to move the excess glutamate from the brain into the blood, which would then carry it safely away and prevent its destructive effects. [snip] There is an enzyme present in blood, known as GOT, which is able to break down glutamate in the presence of a chemical called oxaloacetate (O). Teichberg figured that by injecting large amounts of O into the bloodstream, this would "drive" more glutamate from the brain into the bloodstream. "After a head injury, you give one injection of O for a short, intense time of thirty minutes, and this drains excess glutamate from the brain into the blood and protects the brain."
Sounds good. Of course, one of the problems with trying to affect glutamate levels in the brain is that brain function is so dependent on glutamate (I think the number of glutamatergic neurons in the brain approaches 50%, but don't quote me on that) that decreasing levels all around runs the danger of placing the patient into a coma. However, perhaps this method, though systemic, would only be functional near the injury site (due to the high concentration) and not really affect non-injury sites.

17 comments:

Doofi said...

huh

Lorena's Blogbilingüe said...

Sounds interesting, but is there any research to show the efficacy of this? Or is it just theoretical?

katiewil said...

Interesting - does this have anything to do with what causes Alzheimers?

L.RabbitGirl said...

Does the brain always respond by releasing too much glutamate in a crisis?

Then is it always unable to deal with the levels of glutamate it has released? Would it be hard to differentiate between those that are suffering from a "glutamate overdose" and those who aren't quickly enough?

I'm just wondering how we can know what exactly is going on in the short amount of time available when someone is injured without doing further harm like, as you said, possibly inducing coma.

Interesting stuff.

LOVE AND IMMIGRATION CRIER said...

Nice concept but i am aware everything ends up in theory for now.Hoping for a better future

toothdigger said...

Actually, after injury, the brain will 're-wire' itself even after many many years. Brain scans have shown remarkable evidence of new growth in or beyond damaged areas which have 'taken over' functions.

The brain is 'plastic,' after all.

jude1023 said...
This comment has been removed by a blog administrator.
someGirl said...

I found you through Blogs of Note (congrats by the way) and I've read almost every one of your posts (I'm spastic that way) and I must say you are GREAT!! I don’t pretend to understand half the stuff you write about, but I enjoy reading what intelligent people have to say and this place appeals to my spastic practical side....Enough said.

lucus said...

Yeah!

lucus said...
This comment has been removed by the author.
David Huang said...

whether inoculationof oxaloacetate will not have an effect
to blood pressure.
According me, have to be performed a research to see is there any relation between
oxaloacetate with blood pressure

david

http://dvdhuanghealthcare.blogspot.com

Anonymous said...

Sounds interesting, but is there any research to show the efficacy of this? Or is it just theoretical?

Anonymous said...

thats gr8

dj said...

second one

Hypnosis said...

I thought that your post was interesting and somewhat educational.

http://www.smokeveil.blogspot.com

Tantalus Prime said...

Lorena's Blogbilingüe said...
"Sounds interesting, but is there any research to show the efficacy of this? Or is it just theoretical?"

Only in lab animals so far, as I understand.

katiewil said...
"Interesting - does this have anything to do with what causes Alzheimers?"

No, the injury mechanism in Alsheimers is the accumulation of beta-amyloid plaques. So, no direct connection as I see it.

L.RabbitGirl said...
"Does the brain always respond by releasing too much glutamate in a crisis?"

With injuries that create cell death (a blood clot, car accident). When cells die, they rupture and release their glutamate stores to levels far beyond what is physiologically normal. But under normal situations, the brain can handle glutamate quite well.

toothdigger said...
"Actually, after injury, the brain will 're-wire' itself even after many many years."

True, but this is also a function of the age of the individual and size of the injured area. Even if re-wiring works it does take time (years). But, if scientists could find a way to exploit, enhance, and speed up that mechanism, it would be a good treatment.

someGirl said...
"...I must say you are GREAT!! I don’t pretend to understand half the stuff you write about, but I enjoy reading what intelligent people have to say ..."

Oh stop, flattery will get you no where. Oh wait, yes it will. :)

Anonymous said...

I'm also in grad school for neuroscience--I've just finished reading an article (Volterra & Meldolesi in Nature Neuroscience Reviews) that discusses the release of gliotransmitter sites may upregulate glutamate receptors after TBI (sort of a compensatory measure). What would be interesting would be to 'somehow' chemically increase the uptake of glutamate via astrocytic activity. Perhaps, lowering glutamate levels via blood would be effective and I think this research is starting to turn away from looking at neurons themselves to reduce neurotoxic process of glutamate and rather look at glial cells or some other mechanism. The future should prove interesting in reducting neurotoxic activity.