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.

Monday, April 7, 2025

Stroke breakthrough takes aim at the gut

 You'll need your incompetent doctors and hospital to step up and ensure human testing gets done! But that won't occur, will it? 

Stroke breakthrough takes aim at the gut     

What does gut fermentation and stroke-induced brain inflammation have in common? Potentially a lot, according to new research looking into how the microbiome directly influences brain inflammation. It could make recovery faster, reduce cognitive impairment and protect the brain from secondary injuries following a stroke.

Scientists from The University of Texas Health Science Center at Houston (UTHealth Houston) have turned their attention to the gut – in particular, the ligands produced there. Ligands, produced in the gut as well as elsewhere in the body, are important molecules that bind to specific receptors – proteins on the surface of a cell – and play a crucial role in signaling and cell function. Some of these ligands serve as neurotransmitters and are essential for healthy neuronal activity.


The researchers were particularly interested in the gut-produced ligands that bind to the aryl hydrocarbon receptor (AhR) – AHR ligands – which impact immune response and inflammation in the body – including in the brain. Following a stroke, the gut's microbiota is compromised, resulting in an imbalance (dysbiosis) which in turn leads to a drop in gut-produced AHR ligands (dysbiosis). At the same time, there's an uptick in Kynuerine (Kyn) AHR ligands, not derived from the gut, and their overactivity results in neuroinflammation dysregulation. Ultimately, without the gut-sourced ligands binding to receptors of the microglia – the central nervous system's immune cells – in the brain, the imbalance can leave post-stroke neuroinflammation difficult to reduce, potentially leading to secondary brain injury and damage.

As such, the gut-derived ligands are essential in regulating and reducing inflammation. It's further evidence of the relationship between the gut and brain, particularly when it comes to inflammation. Late last year, research out of another Texan institute, Texas A&M University, also found that post-stroke gut health had a direct impact on the brain and recovery.

Bhanu Priya Ganesh led research revealing that changes in gut bacteria impact inflammation after stroke
Bhanu Priya Ganesh led research revealing that changes in gut bacteria impact inflammation after stroke

“This study looked at how substances from the body and gut bacteria called AHR ligands affect post-stroke inflammation,” said senior author Bhanu Priya Ganesh, associate professor of neurology with McGovern Medical School at UTHealth Houston. “They found that after a stroke, changes in gut bacteria lead to a drop in beneficial substances and an increase in harmful ones. This suggests that restoring these beneficial substances from gut bacteria could help reduce inflammation after a stroke.”

In an earlier preclinical animal study, the researchers showed how stroke and other neurodegenerative diseases disrupt the gut microbiota, which in turn affects brain function – and that dysbiosis worsened with age. It again underpinned the critical role of the microbiota-gut-brain-axis (MGBA).

Now, once again studying aged mice, the team has demonstrated how restoring the gut's balance following a stroke, in order to provide the right fermentation environment for those important ligand metabolites to be made, can ultimately reduce neuroinflammation.

“Our recent animal-model study points to new treatment options that could focus on the gut-brain connection, offering potential ways to improve recovery after a stroke and reduce brain damage,” Ganesh said.

While the team identified some limitations, such as a sex difference in beneficial outcomes (their research focused on aged male mice, which had the strongest cognitive response), it's nonetheless an important discovery into improving brain function and recovery for stroke patients.

"Restoring a balanced pool of host- and microbiota-derived AHR ligands may be beneficial after stroke and may represent a therapeutic target," the researchers wrote.

The study was published in the journal Nature Communications.

Source: UTHealth Houston

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