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.

Tuesday, January 10, 2023

Parkinson’s Disease, It Takes Guts: The Correlation between Intestinal Microbiome and Cytokine Network with Neurodegeneration

Your doctor should already have protocols available on fixing the gut microbiome due to your stroke. With that your doctor probably doesn't have to worry about your chances of Parkinsons from your stroke. And if you believe your doctor is prepared on fixing your gut microbiome, then the Brooklyn bridge is for sale at a minimal price. 

 

Your risk of Parkinsons here:

Parkinson’s Disease May Have Link to Stroke March 2017 

The latest here:

Parkinson’s Disease, It Takes Guts: The Correlation between Intestinal Microbiome and Cytokine Network with Neurodegeneration

1
Department of Medicine, Faculty of Life Sciences, University of Thessaly, 41500 Larisa, Greece
2
Department of Biochemistry and Biotechnology, Faculty of Life Sciences, University of Thessaly, 41500 Larisa, Greece
*
Author to whom correspondence should be addressed.
Biology 2023, 12(1), 93; https://doi.org/10.3390/biology12010093
Received: 26 September 2022 / Revised: 3 January 2023 / Accepted: 5 January 2023 / Published: 7 January 2023

Simple Summary

Parkinson’s disease is a neurodegenerative disease of the central nervous system, characterized by movement problems and accompanied by behavioral changes such as depression and anxiety. It is a multifactorial condition that is affected by genetic alterations and environmental factors that progressively lead to the death of specialized neurons. This systematic review discusses the attractive hypothesis that gut intestinal dysbiosis is an initial step of a process that leads to Parkinson’s. Gut microbiota alterations and their metabolites can cause intestinal inflammation, but they can also alter gut-brain communication and the brain barrier. This can lead to brain inflammation and the deterioration of brain cells, a process called neurodegeneration. Understanding the role of gut microbiota in the progression of Parkinson’s could be a key element for research toward therapeutic approaches that could delay and even cure the disease.

Abstract

Parkinson’s disease is a progressive neurodegenerative disorder with motor, physical and behavioral symptoms that can have a profound impact on the patient’s quality of life. Most cases are idiopathic, and the exact mechanism of the disease’s cause is unknown. The current hypothesis focuses on the gut-brain axis and states that gut microbiota dysbiosis can trigger inflammation and advances the development of Parkinson’s disease. This systematic review presents the current knowledge of gut microbiota analysis and inflammation based on selected studies on Parkinson’s patients and experimental animal models. Changes in gut microbiota correlate with Parkinson’s disease, but only a few studies have considered inflammatory modulators as important triggers of the disease. Nevertheless, it is evident that proinflammatory cytokines and chemokines are induced in the gut, the circulation, and the brain before the development of the disease’s neurological symptoms and exacerbate the disease. Increased levels of tumor necrosis factor, interleukin-1β, interleukin-6, interleukin-17A and interferon-γ can correlate with altered gut microbiota. Instead, treatment of gut dysbiosis is accompanied by reduced levels of inflammatory mediators in specific tissues, such as the colon, brain and serum and/or cerebrospinal fluid. Deciphering the role of the immune responses and the mechanisms of the PD-associated gut microbiota will assist the interpretation of the pathogenesis of Parkinson’s and will elucidate appropriate therapeutic strategies.

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