Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Showing posts with label zileuton. Show all posts
Showing posts with label zileuton. Show all posts

Tuesday, July 10, 2018

A Decades-Old Asthma Drug Has Reversed Brain Damage From Dementia in Mice - zileuton

Did your stroke hospital do anything with this earlier one? If not you need to fire the whole staff.  They will do nothing with this new research.

Can An Anti-Asthma Drug Rejuvenate the Brain? Jan. 2016


A Decades-Old Asthma Drug Has Reversed Brain Damage From Dementia in Mice - zileuton 

Scientists have used a mice model to reverse some of the most severe damage done to the brain by dementia - and they did this with a surprisingly old medication typically used for asthma.
The discovery could open up the road for treatments that could restore memory and spatial impairment in people with conditions like Alzheimer's. While a human treatment is still some way off, the research shows one method we could use to retroactively treat the buildup of tau proteins, long thought to be a key factor in dementia.
Key to the improvement was an asthma drug called zileuton (or Zyflo) that's been in use for 22 years. The team from Temple University in Philadelphia is highly optimistic, claiming that their findings could eventually improve the lives of millions of people with dementia.
"We show that we can intervene after disease is established and pharmacologically rescue mice that have tau-induced memory deficits," says senior investigator Domenico Praticò.
There's still plenty we don't know about diseases like Alzheimer's, but the evidence points to tangles of tau proteins blocking connections between neurons. Another protein, amyloid precursor protein (APP), is also thought to be involved.
In this study the scientists targeted inflammatory molecules called leukotrienes. Having found that leukotrienes cause damage to nerve cells as dementia develops, the team wanted to try blocking the formation of these molecules.
That's where zileuton came in. It was given to one group of mice engineered to have similar dementia problems to 60-year-old humans with the condition, while another group of mice were given placebos instead.
After 16 weeks, treated mice were performing much better on maze tests than mice who hadn't received zileuton. The treated group was also found to have 90 percent fewer leukotrienes in their brains, and 50 percent fewer tau tangles.
"It's really dramatic what we observed," Praticò told Stacey Burling at The Inquirer. "For the first time, we are showing that we can do something after the disease is established."
In fact, the synapses of the mice given zileuton looked as healthy as normal mice after close analysis. It's almost as if this aspect of the dementia had been completely cleared up.
Before we get too excited, there are some limitations to consider. For example, these mice didn't have any beta-amyloid plaque build ups (caused by APP) in their brains, which are consistently found alongside tau plaques in human brains with dementia.
And while mice are often used in research for their genetic and biological similarity to humans, transferring treatments over from these animals can be difficult. Add to that the limits of our understanding about dementia, and there's still a lot of work to be done.
Nevertheless, the fact that researchers were able to actually reverse some of the damage of dementia after it had taken hold is cause for celebration, because the condition isn't usually diagnosed in humans until the effects have already started.
Another reason for optimism is that zileuton has already been approved as a safe drug, albeit with advisory warnings and potential side effects. But it should make it easier to set up a clinical trial, which the team of scientists wants to do next.
"This is an old drug for a new disease," says Praticò. "The research could soon be translated to the clinic, to human patients with Alzheimer's disease."
The research has been published in Molecular Neurobiology.

Monday, June 11, 2018

Asthma drug may reverse memory loss in dementia patients


No followup in humans will be done.
Our fucking failures of stroke associations will DO NOTHING. Your doctor will DO NOTHING. Your stroke hospital will DO NOTHING.  You're screwed. 


Are YOU going to allow your incompetent doctor and hospital to not contact researchers and follow this up with testing in humans?
Up to you. 

Your chances of getting dementia.

1. A documented 33% dementia chance post-stroke from an Australian study?   May 2012.
2. Then this study came out and seems to have a range from 17-66%. December 2013.
3. A 20% chance in this research.   July 2013.

Asthma drug may reverse memory loss in dementia patients

NEW YORK: A drug used for the treatment of asthma can help reverse the cognitive impairments like memory loss caused by abnormal accumulations of a protein in patients with Alzheimer's disease, breakthrough research on mice has shown.

Tau protein is the second-most important lesion in the brain causing memory deficits and impairments in spatial learning among patients with Alzheimer's, the first being abnormal levels of beta-amyloid proteins that clump together to form plaques that collect between neurons and disrupt cell function.

In the study, researchers from Temple University in Pennsylvania, US, engineered mice with abnormal levels of tau, which develop tau pathology -- characterised by neurofibrillary tangles, disrupted synapses (the junctions between neurons that allow them to communicate with one another), and declines in memory and learning ability -- as they age.

When the animals were 12 months old, the equivalent of age 60 in humans, they were treated with "zileuton" -- approved by the US Food and Drug Administration for the treatment of asthma.

The results, published in the journal Molecular Neurobiology, showed that mice treated with "zileuton" experienced a 90 per cent reduction in the formation of leukotrienes -- inflammatory molecules that are deregulated in Alzheimer's and related dementias.

In addition, levels of phosphorylated and insoluble tau, the form of protein that is known to directly damage synapses, were 50 per cent lower.

While untreated animals had severe synaptic deterioration, the synapses of treated tau animals were indistinguishable from those of ordinary mice without the disease.


"We show that we can intervene after the disease is established and pharmacologically rescue mice that have tau-induced memory deficits," said Domenico Pratico, Professor at the varsity.

After 16 weeks, the zileuton treated tau mice performed significantly better on maze tests, suggesting a successful reversal of memory deficiency.

"Inflammation was completely gone from tau mice treated with the drug. The therapy shut down inflammatory processes in the brain, allowing the tau damage to be reversed," Pratico said.

"This is an old drug for a new disease. The research could soon be translated to the clinic, to human patients with Alzheimer's disease," he noted.