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As Andrew Tobin points out, "In our four-year work, we have used mice whose brain
cells, in a manner similar to that of alzheimer's disease, died progressively. And what
our project has done is to focus on a specific brain protein that appears to be involved in
Alzheimer's disease and therefore could be a potential target for new drugs. "
Our work opens the door to the design of new drugs that treat the symptoms of
Alzheimer's disease and slow its progression.
Specifically, the protein in which the study focused is the M1 muscarinic receptor, one
of the five human receptors for the neurotransmitter acetylcholine and which is already
known to be involved in central nervous system functions related to memory and
learning. Thus, the authors administered to mice a new type of drugs, dubbed as
'allosteric ligands', specifically to activate the M1 muscarinic receptor. And what
they observed was that animals not only experienced an improvement in their cognitive
symptoms, but also lived longer - including those that, given the cumulative effects of
neurodegeneration, were already in a terminal phase.
As the research director points out, "what we have found is a new class of drugs that act
on a protein in the brain called the M1 muscarinic receptor. And the activation of this
protein receptor improves cognitive function in mice with progressive cerebral
neurodegeneration. Moreover, when the drug is given daily can also increase life
expectancy.
In conclusion, and in the opinion of the authors, the new results open the door to the
design of new drugs to improve cognition and increase the life expectancy of patients
with Alzheimer's disease. Not surprisingly, our research describes molecules that can
reverse memory loss and slow the progression of neurodegeneration in a way that
confirms the potential of these drugs in Alzheimer's disease in humans, because the new
'allosteric ligands' are much more selective than previous drugs, so did not cause
any adverse effects in the treated mice in the study.