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.

Thursday, February 22, 2024

Drug-Activated Protein Boosts Memory

 Did your competent? doctor and hospital do anything with this earlier research on rapamycin?

rapamycin (5 posts to May 2017)

Or anything with these 26 posts on memory loss?

Or are you dealing with total incompetence in your stroke medical 'professionals'?

Drug-Activated Protein Boosts Memory

Summary: Researchers made a breakthrough in memory research by genetically modifying the LIMK1 protein, crucial for memory, to be controlled by the drug rapamycin.

This study demonstrates the ability to enhance memory functions by manipulating synaptic plasticity in the brain.

The engineered protein showed significant memory improvement in animal models with age-related cognitive decline, offering potential for innovative treatments for neuropsychiatric diseases like dementia. This ‘chemogenetic’ approach, blending genetics and chemistry, opens new avenues in neurological research and therapy.

Key Facts:

  1. The LIMK1 protein, essential for memory formation, was genetically modified to be activated by rapamycin.
  2. The modification improved memory in animal models, suggesting potential for treating memory-related neurodegenerative diseases.
  3. The study represents a pioneering ‘chemogenetic’ strategy, offering a new method to control synaptic plasticity and memory functions.

Source: Universita Cattolica del Sacro Cuore

Neuroscientists at the Faculty of Medicine and Surgery of the Catholic University, Rome, and the Fondazione Policlinico Universitario Agostino Gemelli IRCCS have genetically modified a molecule, the protein LIMK1, which is normally active in the brain, with a key role in memory.

They added a “molecular switch” that is activated by administering a drug, rapamycin, known for its several anti-aging effects on the brain.

Credit: Neuroscience News

This is the result of a study published in the journal Science Advances, which involves the Catholic University, Rome, and the Fondazione Policlinico Universitario Agostino Gemelli IRCCS. The study was coordinated by Claudio Grassi, Full Professor of Physiology and Director of the Department of Neuroscience.

The research, supported by the Italian Ministry of Education, University and Research, the American Alzheimer’s Association Foundation, and the Italian Ministry of Health, has great potential applications, by improving our understanding of memory function and facilitating the identification of innovative solutions for neuropsychiatric diseases like dementia.

The LIMK1 protein plays a crucial role in determining structural changes in neurons, namely the formation of dendritic spines, which enhance information transmission in neural networks and are crucial in learning and memory processes.

Prof. Claudio Grassi, senior author of the study, explains: “Memory is a complex process that involves modifications in synapses, which are the connections between neurons, in specific brain areas such as the hippocampus, which is a neural structure playing a critical role in memory formation.

“This phenomenon, known as synaptic plasticity, involves changes in the structure and function of synapses that occur when a neural circuit is activated, for example, by sensory experiences. These experiences promote the activation of complex signaling pathways involving numerous proteins” Prof. Grassi adds.

“Some of these proteins are particularly important for memory, in fact reduced expression or modifications of these proteins are associated with alterations in cognitive functions.

“One of these proteins is LIMK1. The goal of our study was to regulate the activity of this protein, as it plays a key role in the maturation of dendritic spines between neurons. Controlling LIMK1 with a drug means being able to promote synaptic plasticity and, therefore, the physiological processes that depend on it,” Prof. Grassi emphasizes.

Cristian Ripoli, Associate Professor of Physiology at the Catholic University, and first author of the study, adds: “the key to this innovative ‘chemogenetic’ strategy, which combines genetics and chemistry, is precisely linked to the use of rapamycin”, an immunosuppressive drug known to increase life expectancy and for its beneficial effects on the brain, in preclinical models.

“We have therefore modified the sequence of the LIMK1 protein by inserting a molecular switch that allowed us to activate it, on command, through the administration of rapamycin” Prof. Ripoli emphasizes.

“In animals with age-related cognitive decline, using this gene therapy to modify the LIMK1 protein and activate it with the drug resulted in a significant memory improvement. This approach allows us to manipulate synaptic plasticity processes and memory in physiological and pathological conditions.

“Furthermore, it paves the way for the development of further ‘engineered’ proteins that could revolutionize research and therapy in the field of neurology,” the expert emphasizes.

“The next step will be to verify the effectiveness of this treatment in experimental models of neurodegenerative diseases exhibiting memory deficits, such as Alzheimer’s disease. Further studies will also be necessary to validate the use of this technology in humans” Prof. Grassi concludes.

About this memory research news

Author: Nicola Cerbino
Source: Universita Cattolica del Sacro Cuore
Contact: Nicola Cerbino – Universita Cattolica del Sacro Cuore
Image: The image is credited to Neuroscience News

Original Research: The findings will appear in Science Advances

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