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.

Friday, August 12, 2016

Can a Common Anti-Inflammatory Drug Reverse Alzheimer's?

And if we had any leadership at all in our stroke associations they would be teaming up with the Alzheimers Foundations to get clinical trials run on this. You need this for these reasons and I almost guarantee that your doctor hasn't told you about this. Not to be done on your own
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.

Can a Common Anti-Inflammatory Drug Reverse Alzheimer's? 

Can a common anti-inflammatory drug reverse Alzheimer's? Researchers from The University of Manchester found that mefenamic acid, a common non-steroidal anti-inflammatory drug (NSAID) that's used for period pain, completely reversed memory loss and brain inflammation in mice.

Mefenamic acid, an oral capsule available by prescription to treat moderate pain and menstrual pain, is sold under the brand name Ponstel, but is also available in a generic version. It works by reducing hormones that cause inflammation in the body.

The study is the first time a drug has been shown to target this inflammatory pathway, but team leader David Brough cautions that more research is necessary to determine its impact on humans, and the long-term implications of its use.

In the study, mice were used whose genes had been altered to develop symptoms of Alzheimer's, and they had already developed symptoms of the disease. One group of 10 mice was treated with mefenamic acid, which was given to them by a mini-pump implanted under the skin for one month, and 10 mice were treated with a placebo.

In mice given the drug, memory loss was completely reversed to the levels seen in mice without the disease.
Latest News Update

"There is experimental evidence now to strongly suggest that inflammation in the brain makes Alzheimer's disease worse," said Brough.

"Our research shows for the first time that mefenamic acid, a simple non-steroidal anti-inflammatory drug, can target an important inflammatory pathway called the NLRP3 inflammasome, which damages brain cells."

"Until now, no drug has been available to target this pathway, so we are very excited by this result.

"However, much more work needs to be done until we can say with certainty that it will tackle the disease in humans as mouse models don't always faithfully replicate the human disease.

"Because this drug is already available and the toxicity and pharmacokinetics of the drug is known, the time for it to reach patients should, in theory, be shorter than if we were developing completely new drugs.

Brough is preparing early phase II trials to test the drug in humans.

"We are now preparing applications to perform early phase II trials to determine a proof-of-concept that the molecules have an effect on neuroinflammation in humans."

According to the Alzheimer's Association, an estimated 5.4 million Americans have Alzheimer's, and it's the sixth leading cause of death. Experts expect the number of seniors with Alzheimer's to triple by 2050.

Study results were published in the journal Nature Communications.

No comments:

Post a Comment