Researchers at the University of Sydney claim they have identified the trigger for the Alzheimer degeneration. The discovery could open up new vistas of treatment.
The groundbreaking new study led by Professor Jürgen Götz and Dr Lars Ittner, based at the University's Brain and Mind Research Institute (BMRI), is published in the prestigious international scientific journal Cell.
Alzheimers Disease
Alzheimer''s disease is a progressive neurodegenerative disease affecting memory and thinking and making the person increasingly dependent on others.
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The researchers have discovered how a protein called TAU affects and mediates the toxicity of amyloid-b, which together with TAU causes the symptoms of Alzheimer's disease.
The brain of all Alzheimer's patients is characterized by two types of insoluble deposits; amyloid-b plaques and neurofibrillary tangles, the latter formed by the protein TAU.
![Know Your Nervous System]( "Know Your Nervous System")
The Central nervous system consists of the brain, the spinal cord, and the body's nerve network. This complex system is based on one kind of cell the neurons.
In a milestone work published in Science in 2001, Professor Götz had already showed that the two hallmark proteins amyloid-b and TAU act together in disease, but their exact connection remained unexplained.
"It was always clear to me that finding this link could be the key to understanding the disease," Professor Götz said.
Dr Ittner said they focused on the relationship between the two, which produced a finding that challenges the accepted research paradigm.
"TAU was always thought to be a protein exclusively localised to the axons of neurons, but at the same time amyloid-b exerts its toxic effects at the dendritic site of the synapse, which is at the other end of the neuron," he said.
"The more data we obtained the clearer it became to us that TAU must have an as yet unrecognised function in the dendrite, so finally we had to break with the dogma of TAU being an exclusively axonal protein."
It was this thinking that achieved the major breakthrough.
The researchers found that TAU is essential for the positioning of yet another protein, the kinase FYN, at the dendritic site of the synapse, which then renders the neuron vulnerable to amyloid-b.
"By genetically deleting TAU or introducing a non-functional variant of TAU, we found we could prevent the development of symptoms in mouse models of Alzheimer's disease."
"These mice showed normal survival and their memory appeared to be perfectly fine."
In the second part of the study, Professor Götz and Dr Ittner explored the potential of their discovery for a treatment of Alzheimer's disease.
"We translated our findings into a novel therapeutic approach by using a small peptide that mimics the effects of removing TAU from the synapse, and we were thrilled to see that this not only fully prevented the pathology in our Alzheimer's disease models but cleared their memory deficits," Dr Ittner said.
"Although there is still a long way to go we believe we may have found a way of treating Alzheimer's disease," adds Professor Götz.
"We show that a protein which forms insoluble clumps outside of the nerve cells in the brain interacts with another protein inside the nerve cells," he said.
Professor Gotz says his team then used that knowledge to interrupt the interaction in mice developing the disease.
"We are basically able to prevent, at an early stage, Alzheimer's disease," he said.
"So when we interfere early enough in the mouse model which would eventually develop Alzheimer's disease - because it has been genetically modified - then we can prevent Alzheimer's disease in this mouse model."
"We can completely rescue all Alzheimer's effects, the seizures, the reduced lifespan."
Alzheimer's disease is a major health threat to Australia's aging population. More than 250,000 Australians are currently diagnosed with dementia, with numbers reaching epidemic proportions. Of all diseases with a memory loss, Alzheimer's is the most prevalent, predicted to affect one in 85 people globally by 2050.
To date Alzheimer's disease is incurable. "A handful of approved drugs provide if at all only very modest symptomatic relief, without curing the disease. Therefore, to develop effective treatments, it is absolutely necessary that the basic mechanisms underlying these disorders be understood. This was our challenge, " said Prof. Gotz, but they seem to have risen up to the challenge.
He believes development of a treatment for humans might be just five years away.
Source: Medindia
Know Your Nervous System
The Central nervous system consists of the brain, the spinal cord, and the body's nerve network. This complex system is based on one kind of cell the neurons.
Advertisement
In a milestone work published in Science in 2001, Professor Götz had already showed that the two hallmark proteins amyloid-b and TAU act together in disease, but their exact connection remained unexplained.
"It was always clear to me that finding this link could be the key to understanding the disease," Professor Götz said.
Dr Ittner said they focused on the relationship between the two, which produced a finding that challenges the accepted research paradigm.
"TAU was always thought to be a protein exclusively localised to the axons of neurons, but at the same time amyloid-b exerts its toxic effects at the dendritic site of the synapse, which is at the other end of the neuron," he said.
"The more data we obtained the clearer it became to us that TAU must have an as yet unrecognised function in the dendrite, so finally we had to break with the dogma of TAU being an exclusively axonal protein."
It was this thinking that achieved the major breakthrough.
The researchers found that TAU is essential for the positioning of yet another protein, the kinase FYN, at the dendritic site of the synapse, which then renders the neuron vulnerable to amyloid-b.
"By genetically deleting TAU or introducing a non-functional variant of TAU, we found we could prevent the development of symptoms in mouse models of Alzheimer's disease."
"These mice showed normal survival and their memory appeared to be perfectly fine."
In the second part of the study, Professor Götz and Dr Ittner explored the potential of their discovery for a treatment of Alzheimer's disease.
"We translated our findings into a novel therapeutic approach by using a small peptide that mimics the effects of removing TAU from the synapse, and we were thrilled to see that this not only fully prevented the pathology in our Alzheimer's disease models but cleared their memory deficits," Dr Ittner said.
"Although there is still a long way to go we believe we may have found a way of treating Alzheimer's disease," adds Professor Götz.
"We show that a protein which forms insoluble clumps outside of the nerve cells in the brain interacts with another protein inside the nerve cells," he said.
Professor Gotz says his team then used that knowledge to interrupt the interaction in mice developing the disease.
"We are basically able to prevent, at an early stage, Alzheimer's disease," he said.
"So when we interfere early enough in the mouse model which would eventually develop Alzheimer's disease - because it has been genetically modified - then we can prevent Alzheimer's disease in this mouse model."
"We can completely rescue all Alzheimer's effects, the seizures, the reduced lifespan."
Alzheimer's disease is a major health threat to Australia's aging population. More than 250,000 Australians are currently diagnosed with dementia, with numbers reaching epidemic proportions. Of all diseases with a memory loss, Alzheimer's is the most prevalent, predicted to affect one in 85 people globally by 2050.
To date Alzheimer's disease is incurable. "A handful of approved drugs provide if at all only very modest symptomatic relief, without curing the disease. Therefore, to develop effective treatments, it is absolutely necessary that the basic mechanisms underlying these disorders be understood. This was our challenge, " said Prof. Gotz, but they seem to have risen up to the challenge.
He believes development of a treatment for humans might be just five years away.
Source: Medindia
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