Phase II year
2017
(last award dollars: 2023)
Phase II Amount
$3,662,684
Glycosaminoglycan-Interacting Small Molecule (GISMO) as Alzheimer's Therapeutics ABSTRACT The aim of this project is to develop a novel, disease-modifying oral therapeutic agent for the treatment of Alzheimer's Disease. In the first phase of this project, we identified promising lead compounds via proprietary Glycosaminoglycan-Interacting Small Molecule (GISMO) drug discovery platform. GISMOs are based on a novel hypothesis for the cause of Alzheimer's Disease and provide a new therapeutic principle for the treatment of this devastating neurodegenerative disease. Alzheimer's Disease is associated with the pathological aggregation (i.e., amyloidosis) of amyloid-beta peptides (Abeta peptides). According to GISMO hypothesis, Abeta aggregation is necessary but not sufficient to cause Alzheimer's Disease. Rather, excessive accumulation and storage of a class of complex polysaccharides, glycosaminoglycans (GAGs), in the lysosomes of nerve cells is another essential component of the pathological process leading to Alzheimer's Disease. In our current work we show that GISMOs directly target heparan sulfate GAGs (HS-GAGs), inhibit Abeta42 binding to HS-GAGs, and have potent biological activity in at several assays relevant to amyloidosis in nerve cell cultures. Specifically, we identified GISMO lead compounds that inhibit uptake of Abeta by neuronal cells, and display potent neuroprotective properties against Abeta peptides, Abeta40 and Abeta42. This is the first report of Abeta/HS-GAG inhibitors (GISMOs) having potent neuroprotective properties against toxic Abeta peptides. In addition to reducing the toxic accumulation of amyloid aggregates inside nerve cells, GISMOs may also slow the progression of Alzheimers disease by inhibiting the spread of amyloid proteopathic seeds in brain tissue. The identified lead compounds conform to Lipinski rules and display selectivity and other drug-like properties. These results provide in vitro target validation as well as justification for further development of GISMO compounds as Alzheimer's Disease therapeutics. In Specific Aim 1, we will assess the lead compounds for their pharmacokinetic profiles, oral bioavailability, blood-brain-barrier penetration, and establish their maximum tolerated dose (MTD). In Specific Aim 2, we will test the two best lead compounds (selected from Aim 1) for their efficacy in two transgenic mouse models of AD. We will treat transgenic AD mice with two compounds at three doses for each compound and evaluate the effectiveness of treatment using standard tests for learning and memory, as well as biochemical, histopathological, and immunochemical methods. In Specific Aim 3, we will perform further preclinical testing of the selected development candidate. The successful completion of these studies will allow us to select a development candidate for preclinical development, towards an IND, and clinical trials.
Public Health Relevance Statement: PROJECT NARRATIVE Alzheimers disease is a progressive neurological disease of the brain leading to the irreversible loss memory and cognitive performance which become severe enough to impede social or occupational functioning. This chronic, debilitating disorder results in a devastating burden on the families and caregivers of patients, with the rising costs of care in the United States exceeding $170 billion a year. The goal of this proposal is to develop an effective small molecule for the treatment of Alzheimers disease with an improved efficacy and minimized safety risk compared to the current standard of care.
Project Terms: abeta accumulation; abeta toxicity; acute toxicity; AD transgenic mice; Aging; Alzheimer's Disease; Alzheimer's disease model; Ames Assay; Amyloid; Amyloid beta-Protein; Amyloidosis; Animal Model; Area Under Curve; base; Binding; Binding Proteins; Bioavailable; Biochemical; Biological; Biological Assay; Biological Availability; Blood - brain barrier anatomy; Blood Chemical Analysis; Brain; Brain Diseases; brain tissue; Caring; Cell Culture Techniques; Cells; Characteristics; Chronic; Clinical Trials; Cognition; Cognitive; cognitive performance; Collaborations; Complex; Contractor; cost; cytotoxicity; Development; Disease; Dose; drug discovery; Drug Kinetics; efficacy study; Evaluation; Family Caregiver; Glycosaminoglycans; Goals; Half-Life; Heparitin Sulfate; Hepatocyte; Histopathology; Human; improved; In Vitro; in vivo; inhibitor/antagonist; Kentucky; Knowledge; Lead; Learning; Lysosomes; Maximum Tolerated Dose; Measures; Mediating; Memory; Memory Loss; Methods; micronucleus; mouse model; Mus; Mutagenicity Tests; nervous system disorder; Neurodegenerative Disorders; Neurons; Neurosciences; novel; novel therapeutics; Occupational; Oral; Pathologic; Pathologic Processes; Pathology; Patients; Penetration; Peptides; Pharmaceutical Preparations; Pharmacy (field); Phase; Plasma; Plasma Proteins; Polysaccharides; polysulfated glycosaminoglycan; preclinical development; Preclinical Testing; prevent; Property; Reporting; Research; Risk; Rodent; Safety; screening; Seeds; small molecule; social; standard of care; Testing; Therapeutic; Therapeutic Agents; Therapeutic Effect; Toxic effect; Toxicology; Transgenic Mice; Transgenic Model; Treatment Effectiveness; United States; Universities; uptake; Use Effectiveness; Validation; Work
