Noise-Induced Hearing Loss Restored in Mice Through Increased NT3 Production

yonkapin

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Dec 23, 2012
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Melbourne, Australia
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March 2012
This popped up on my Facebook feed today:

http://www.medicalnewstoday.com/articles/284159.php

Researchers from the University of Michigan and Harvard Medical School in Boston, MA, may be well on the way to finding new therapies that restore noise-induced and age-related hearing loss in humans. In a new study, the team describes how they recovered hearing in mice partially deafened by noise.

In their study, the researchers explain how they were able to increase production of a protein called Neurotrophin-3 (NT3) in mice, which they found plays a key role in communication between the ears and the brain.

NT3 allows sound signals to be sent from the ear to the brain. The protein is crucial in establishing a super-fast connection between the ear's hair cells and nerve cells - a connection the researchers call the "ribbon synapse." But this ribbon synapse can become damaged as a result of noise exposure or normal aging, which can lead to hearing loss.

Boosting NT3 production in mice
In their study, the researchers identified supporting cells in the inner ear that produce NT3. They set out to see what would happen if they increased production of NT3 through these supporting cells.

They adopted a method called conditional gene recombination. This allows researchers to activate genes in particular cells by administering a drug that prompts the cells to "read" additional copies of a gene that have been inserted into them.

For this study, the team used the technique to activate additional NT3 genes that had been introduced to the supporting cells of the inner ear in mice that had been partially deafened by loud noise.

The drug tamoxifen was introduced to the supporting cells in the inner ear, which prompted them to produce extra NT3 protein. The researchers then tested the hearing of the mice through a test normally used in humans - the auditory brainstem response (ABR).

The researchers found the mice that had experienced boosted NT3 production regained their hearing over a 2-week period, compared with mice that had not had additional NT3 production.

According to the team, these findings indicate that NT3 production is important for making ribbon synapses, and that boosting production of this protein may restore noise-induced and age-related hearing loss.

The potential to restore hearing loss in humans
Corfas and his team say they now plan to investigate the role of NT3 in human ears and identify drugs that produce the same effect as the protein, offering the potential to restore hearing loss in humans.

The researchers note that the gene therapy technique used in this study has the potential to work in humans, but that a drug-based method would be "simpler" and a drug could be repeatedly administered for as long as it takes for hearing to be restored. Corfas says he already has some drug candidates in mind.

The researchers stress, however, that since the mice in this study were only partially deaf, it is unclear whether increased NT3 production would restore hearing in subjects that are fully deaf.

But the team believes their findings are promising. Corfas says:

"It has become apparent that hearing loss due to damaged ribbon synapses is a very common and challenging problem, whether it's due to noise or normal aging. We began this work 15 years ago to answer very basic questions about the inner ear, and now we have been able to restore hearing after partial deafening with noise, a common problem for people. It's very exciting."

Their findings may even reach further than hearing loss. The researchers say they may offer new strategies to treat neurodegenerative diseases, in which nerve cell connections are impaired.


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This is the first time I've read anything about this approach, so apologies if something related to this has already been posted. Exciting stuff though, hopefully they can figure out a way to trial this approach on humans soon!
 
hi guys

it might be good for the mice but it have several side effects :
one of them

Endometrial cancer
Tamoxifen is a selective estrogen receptor modulator.[41] Even though it is an antagonist in breast tissue it acts as partial agonist on the endometrium and has been linked to endometrial cancer in some women. Therefore endometrial changes, including cancer, are among tamoxifen's side effects.[42] With time, risk of endometrial cancer may be doubled to quadrupled, which is a reason tamoxifen is typically only used for 5 years.[43]

The American Cancer Society lists tamoxifen as a known carcinogen, stating that it increases the risk of some types of uterine cancer while lowering the risk of breast cancer recurrence.[44] The ACS states that its use should not be avoided in cases where the risk of breast cancer recurrence without the drug is higher than the risk of developing uterine cancer with the drug.

https://en.wikipedia.org/wiki/Tamoxifen
 
So why not start human trial immidietly?
Well although they have the most similarities they still have to adjust for humans.
This proves that it can be done in mammals now they need to find what chemical in Humans causes this.
Once they do the trials will start and hopefully we'll see people improving :)
 
Hello, I have been taking 6mg of astaxanthin for the last year but recently found out that 12mg is what has been found in clinical trials to help for many conditions and none of them mention T. I have started taking 12mg two days ago and just saw this info, I will update if any improvement is found as I was taking this when T started, but maybe the 12mg is what may show improvement.
 
Hello, I have been taking 6mg of astaxanthin for the last year but recently found out that 12mg is what has been found in clinical trials to help for many conditions and none of them mention T. I have started taking 12mg two days ago and just saw this info, I will update if any improvement is found as I was taking this when T started, but maybe the 12mg is what may show improvement.

Hi

the study is showing effect on mice while they use 80mg/kg.they said in average of 30mg/kg,it should have effects.

so basically your 6 or 12 mg /day doesnt make any sense.

You should have a dose of 1/2 g a day to see a difference.

are we agree on this?

below is the research i m talking about

http://academicjournals.org/article/article1380799074_Bai et al.pdf

Also i ve read that vitamin d3 can increase nt-3 anyone have tried it for t?
 
Also i ve read that vitamin d3 can increase nt-3 anyone have tried it for t?

Been taking 44,000 IU (500 IU/kg loading doses) every so often and 10,000-20,000 IU most days for the past week or two after seeing an article about nerve growth factors. It's done diddly squat apart from making me twitch every so often and probably putting me close to having hypercalcemia. Been taking it with fatty food like milk and yoghurt as it's apparently fat soluble.

If you have noise induced T, it probably doesn't matter if your nerves endings extend - the hair cells are gone. There's nothing for them to connect to. The rats and a lot of these other nerve related treatments only seem to work if you get to it within a day or two.
 
Hello, I have been taking 6mg of astaxanthin for the last year but recently found out that 12mg is what has been found in clinical trials to help for many conditions and none of them mention T. I have started taking 12mg two days ago and just saw this info, I will update if any improvement is found as I was taking this when T started, but maybe the 12mg is what may show improvement.
Hi, what is your progress? Has astaxanthin helped you at all?
 
Hello, no my hearing is fine, the T just appeared one morning out of the blue. I had been on it at the 6mg level for at least a year and started the 12mg several months ago. It has made no change to the T. Hope that this info is of some use to you.
 
Re astaxanthin, just tried it last night. After first two 6mg pills noticed a couple of micro dropouts in my high pitched T in right ear. Thought, Hmmmm... I'll take a couple more. Each "couple more" seemed to produce a very slight reduction, and after taking 10, the constant high pitch seemed to have changed to 'cycling' between lound and quiet. Was a bit excited, but we all know not to get our hopes up. This morning have roughly %30 reduction in volume, and was not effected by the sounds of the kettle boiling (my H is pretty bad too). Luckily I was taking coconut oil at the same time (to fight mouth fungus), because after reading up on astx this morning, it needs to be taken with fats. Will keep trying over the next few days and see what happens, and post some more.
 
Re astaxanthin, just tried it last night. After first two 6mg pills noticed a couple of micro dropouts in my high pitched T in right ear. Thought, Hmmmm... I'll take a couple more. Each "couple more" seemed to produce a very slight reduction, and after taking 10, the constant high pitch seemed to have changed to 'cycling' between lound and quiet. Was a bit excited, but we all know not to get our hopes up. This morning have roughly %30 reduction in volume, and was not effected by the sounds of the kettle boiling (my H is pretty bad too). Luckily I was taking coconut oil at the same time (to fight mouth fungus), because after reading up on astx this morning, it needs to be taken with fats. Will keep trying over the next few days and see what happens, and post some more.
So you tried 60mg at once pretty much? Or you poped one 6mg pill each hour or half an hour? whats your body weight? I might check this out because of pure deseration :)
 
Took 10 over a period of a couple of hours, in the middle of the night. Started slow in case I had a reaction to it. I weigh 70kg. It was on an empty stomach, apart from some coconut oil I had been taking for an outbreak of fungus on my tongue. I took it because my T and H had ramped up by %50 or so since coming off Lyrica. I could barely listen to the TV/radio or the beep my car does when I put it in reverse. Will take less tonight, maybe 5 or so, and .... see what happens.
 
Took 5 x 6mg Astax straight after dinner, then 3 more at bed time with some coconut oil. Total of 48 mg. T reduced to 4 or 5 out of 10. In the morning now, T is 3 at most. Was sitting at 8 before started Astax. H is no question improved, but still there. Hard to put 'number out of 10' on it. Currently listening to bedside radio without usual ear plugs or trauma. Will take same dosage tonight. Side effects: huge mood lift, brain feels switched on, BPH symptoms diminished.
 
Took 5 x 6mg Astax straight after dinner, then 3 more at bed time with some coconut oil. Total of 48 mg. T reduced to 4 or 5 out of 10. In the morning now, T is 3 at most. Was sitting at 8 before started Astax. H is no question improved, but still there. Hard to put 'number out of 10' on it. Currently listening to bedside radio without usual ear plugs or trauma. Will take same dosage tonight. Side effects: huge mood lift, brain feels switched on, BPH symptoms diminished.
I can only find astax with other stuff in tabs like vitamins and lutein for example. Can you tell me brand name of astaxin you take? Link to amazon or someething?
 
I'm in Australia, the brand is MicrOrganics, it's 6mg astax, vit E 10 mg, Linseed oil 400 mg, Oleic, Linoleic, Linolenic acid. It sort of sounds like you get most of this from the extraction process, rather than all added seperately. Or maybe they are added to help absorbtion, cos astax is fat-soluble? It is the only brand I can buy at health stores here, so I wasn't too fussed. I had a quick look at it seems available online. T currently 3, H maybe %20 better. I would like H to be even less, but it was so bad, any improvement is fantastic. Just buy some and try it dude!
 
Still going strong, after 10 days. Take 7 * 6mg astax at 5pm with coconut oil. Take a few good nips of tart cherry concentrate at bed time, and I am falling to sleep, and staying asleep better than I have in many years. T drops off to 3 or 4 at night, and is similar in the morning. Starts to pick up again in the afternoon, before next hit of astax. The unknown long term side effects, or unknown long term efficacy is just something I live with. It would be great to know that astax will keep working long term with no ill effects, but what can we do? If I start to turn pink like a Flamingo or a Salmon than I may need to take a break :) (astaxanthin is what makes them pink)
 

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