Galantamine clearance of amyloid-beta
A technology of amyloid and galantamine, which is applied in the directions of medical preparations containing active ingredients, drug combinations, active ingredients of heterocyclic compounds, etc.
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[0081] A method for determining an appropriate dose range for galantamine can be achieved by evaluating in vitro the concentration that improves Aβ oligomer clearance, and doing so with a concentration that protects the neurite network from residual oligomer damage. adjust. Galantamine or a pharmaceutically acceptable salt is then administered to experimental animals to determine plasma and brain concentrations, and to apply plasma concentrations related to effective brain concentrations to human subjects. To determine appropriate doses of galantamine for groups of subjects with varying degrees of cognitive impairment, counter-regulatory increases in CSF acetylcholinesterase can be determined. The dose of galantamine will be determined when the increase in CSF acetylcholinesterase does not exceed the increase in CSF acetylcholinesterase when 16 to 24 mg of galantamine is administered to a subject with Alzheimer's dementia Suitable, as demonstrated by Nordberg et al., 2009, su...
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