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.

Wednesday, April 27, 2022

Bacteria in the Nose May Increase Risk of Alzheimer’s Disease

So what is the prevention protocol? Don't know, then useless research. I'd have you all fired.

Bacteria in the Nose May Increase Risk of Alzheimer’s Disease

The bacterium Chlamydia pneumoniae (green) in the olfactory bulb region of the front of the brain. Beta amyloid peptide (red) accumulates around the bacteria. Blue indicates nuclei of cells of the brain.
Associate Professor Jenny Ekberg, Clem Jones Centre for Neurobiology and Stem Cell Research

New research from Griffith University has shown that a bacterium commonly present in the nose can sneak into the brain and set off a cascade of events that may lead to Alzheimer’s disease.  

Associate Professor Jenny Ekberg and colleagues from the Clem Jones Centre for Neurobiology and Stem Cell Research at Menzies Health Institute Queensland and Griffith Institute for Drug Discovery, in collaboration with Queensland University of Technology, have discovered that the bacterium Chlamydia pneumoniae can invade the brain via the nerves of the nasal cavity.  

While this bacterium often causes respiratory tract infections, it has also been found in the brain which has raised the question of whether it causes damage to the central nervous system.  

The research team has performed extensive research in animal models to show not only how the bacteria gets into the brain, but also how it leads to Alzheimer disease pathologies.    

“Our work has previously shown that that several different species of bacteria can rapidly, within 24 hours, enter the central nervous system via peripheral nerves extending between the nasal cavity and the brain,” Associate Professor Ekberg said.  

“With this background knowledge we were able to track how this new bacterium, Chlamydia pneumoniae can also sneak past the blood-brain barrier and quickly enter the brain.” 

 The new study shows that once the bacteria are in the central nervous system, the cells of the brain react within days by depositing beta amyloid peptide, the hallmark plaque of Alzheimer’s disease.  

 After several weeks, numerous gene pathways that are known to be involved in Alzheimer’s disease are also dramatically activated.  

 The research also showed that when the bacteria invade the olfactory nerve, peripheral nerve cells (glial cells), become infected and these cells may be how the bacteria can persist within the nervous system.  

 “These cells are usually important defenders against bacteria, but in this case, they become infected and can help the bacteria to spread,’’ Associate Professor Ekberg said. 

 “We have suspected for a long time that bacteria, and even viruses, can lead to neuroinflammation and contribute to initiation of Alzheimer’s disease, however, the bacteria alone may not be enough to cause disease in someone. Perhaps it requires the combination of a genetic susceptibility plus the bacteria to lead to Alzheimer’s disease in the long term. 

 “Now that we have this new evidence, it gives us the drive to urgently find treatments to stop this contributing factor to Alzheimer’s disease. 

 While the studies were conducted in mice, humans have the same nerves and can be infected by the same bacteria, so the researchers believe the results are translatable to humans. 

 “We are already working on treatment options. With the Griffith Institute for Drug Discovery, we are identifying potential drugs that can help the glial cells to destroy the bacteria which are already in the brain.  

 “In addition, Professor Ken Beagley at QUT is working on a vaccine against Chlamydia which may reduce the ability of the pathogen to enter the brain”. 

The study, published in the journal, Scientific Reports, was funded by the Clem Jones Foundation, the Goda Foundation, the Australian Research Council and the Menzies Health Institute Queensland.

 

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