CNDAP is developing a new class of drugs, acting through a unique mechanism of action, to reverse early pathophysiological and cognitive alterations in Alzheimer's disease (AD). Recent studies indicate that network dysfunction, which includes network hyperactivity, altered oscillatory rhythms, and hyper- synchronized networks, is an early pathogenic event found in preclinical models of AD and in patients with early stages of AD. Network dysfunction contributes to cognitive abnormalities, Ab and tau accumulation, and neurodegeneration. In animal models, network dysfunction can be restored by enhancing inhibitory (GABAergic) interneuron-dependent gamma rhythms via optogenetic/sensory stimulation or genetic overexpression of Nav1.1. This restoration of gamma rhythms in the AD models leads to reduced amyloid and tau deposition, neurodegeneration, microglia and astrocytic activation, inflammation, neurovascular alterations, AD-induced genome-wide transcriptomics changes, altered oscillatory activity, and cognitive decline. Because overexpression of the sodium channel Nav1.1 by as little as 25% restores gamma rhythms to normal levels in AD models, we are developing small molecule therapeutics designed to safely increase Nav1.1 activity in the brain to treat AD. We have identified several small molecule chemotypes that effectively enhance human Nav1.1 currents in cell lines and interneuron-dependent gamma oscillations in brain slices. Systemic intraperitoneal administration of high doses of a Nav1.1 enhancer in vivo in mice produced no overt toxicity or behavioural side effects but significantly increased endogenous gamma oscillatory activity in wildtype mice, suggesting that our compounds are brain penetrant and may have beneficial effects following systemic administration. In this fast-track SBIR grant, we propose to further develop Nav1.1 enhancers to treat AD. In Phase 1 studies, we will employ medicinal chemistry and SAR analysis to identify structurally unique, potent and selective Nav1.1 enhancers to expand our chemical composition of matter. Pharmacokinetics and brain bioavailability analyses will be used to select the most active compounds with optimal pharmaceutical properties. Our milestone to achieve to move to Phase 2 studies is the identification of at least one structurally novel Nav1.1 enhancer that selectively and significantly increases gamma oscillations ex vivo in brain. Phase 2 studies are designed to establish the ex vivo and in vivo efficacy of our Nav1.1 enhancers to restore network dysfunction in preclinical AD mouse models by their ability to prevent network hypersynchrony and abnormal oscillatory activity, restore genome-wide transcriptomic changes and to reduce cognitive impairment, neuropathology and improve survival to support their future development to treat AD patients.
Public Health Relevance Statement: PROJECT NARRATIVE CNDAP is developing a new class of drugs for Alzheimer's disease (AD) by enhancing the activity of the voltage-gated sodium channel Nav1.1 and subsequently reversing brain network dysfunction and early pathological changes that are prevalent in early stages of AD and that are linked to rapid cognitive decline. CNDAP identified several small molecule compounds that effectively enhance human Nav1.1 currents in cell lines and consequently increase inhibitory-dependent gamma oscillations in wildtype mouse brains, while producing no overt toxicity, side effects, or other behavioural alterations. In this fast-track SBIR grant, we propose to further develop our Nav1.1 enhancers to treat AD by establishing their efficacy and selectivity ex vivo, optimizing their pharmaceutical properties using medicinal chemistry, and then establishing their efficacy in AD mouse models, resulting in the selection of drug candidate(s) for further drug development.
Project Terms: Acceleration; Oral Administration; Oral Drug Administration; intraoral drug delivery; Alzheimer's Disease; AD dementia; Alzheimer; Alzheimer Type Dementia; Alzheimer disease; Alzheimer sclerosis; Alzheimer syndrome; Alzheimer's; Alzheimer's disease dementia; Alzheimers Dementia; Alzheimers disease; Primary Senile Degenerative Dementia; dementia of the Alzheimer type; primary degenerative dementia; senile dementia of the Alzheimer type; Amyloid; Amyloid Substance; Astrocytes; Astrocytus; Astroglia; astrocytic glia; Biological Assay; Assay; Bioassay; Biologic Assays; Biological Availability; Bioavailability; Biologic Availability; Physiologic Availability; Brain; Brain Nervous System; Encephalon; Cell Line; CellLine; Strains Cell Lines; cultured cell line; Cells; Cell Body; Central Nervous System Diseases; CNS Diseases; CNS disorder; Central Nervous System Disorders; Pharmaceutical Chemistry; Medicinal Chemistry; Pharmaceutic Chemistry; Clinical Trials; Disease; Disorder; Drug Design; Pharmaceutical Preparations; Drugs; Medication; Pharmaceutic Preparations; drug/agent; Electrocardiogram; ECG; EKG; Electrocardiography; Electroencephalography; EEG; Future; Grant; Heart; Human; Modern Man; In Vitro; Inflammation; Interneurons; Connector Neuron; Intercalary Neuron; Intercalated Neurons; Internuncial Cell; Internuncial Neuron; Liver Microsomes; mortality; Mus; Mice; Mice Mammals; Murine; Nerve Degeneration; Neuron Degeneration; neural degeneration; neurodegeneration; neurodegenerative; neurological degeneration; neuronal degeneration; Neurons; Nerve Cells; Nerve Unit; Neural Cell; Neurocyte; neuronal; Pathology; Patients; Drug Kinetics; Pharmacokinetics; Role; social role; Sodium Channel; Sodium Ion Channels; Specificity; Transplantation; transplant; tau Proteins; MT-bound tau; microtubule bound tau; microtubule-bound tau; tau; tau factor; Ï Proteins; Enhancers; base; improved; Acute; Phase; Physiological; Physiologic; Series; Microglia; Hortega cell; gitter cell; mesoglia; microglial cell; microgliocyte; perivascular glial cell; Link; Chemicals; heart function; cardiac function; function of the heart; Functional disorder; Dysfunction; Physiopathology; pathophysiology; Genetic; Deposit; Deposition; Cognitive Disturbance; Cognitive Impairment; Cognitive decline; Cognitive function abnormal; Disturbance in cognition; cognitive dysfunction; cognitive loss; Impaired cognition; programs; cognitive function; Event; intraperitoneal; Sensory; System; restoration; magnetic; Magnetism; voltage; Animal Models and Related Studies; model of animal; model organism; Animal Model; Toxicities; Toxic effect; Structure; novel; Reporting; Property; drug development; neuropathology; Intervention Strategies; interventional strategy; Intervention; BAC clone; BACs; Bacterial Artificial Chromosomes; patch clamp; Pathogenicity; Pharmaceutical Agent; Pharmaceuticals; Pharmacological Substance; Pharmacologic Substance; preventing; prevent; small molecule; Mediator; Mediator of Activation; Mediator of activation protein; Dose; Molecular Target; Preclinical Models; Pre-Clinical Model; in vivo; Cognitive; Slice; Small Business Innovation Research Grant; SBIR; Small Business Innovation Research; Wild Type Mouse; wildtype mouse; Pathologic; Monitor; Molecular; Cardiac; Development; developmental; Behavioral; pre-clinical; preclinical; APP-PS1; APP/PS1; tau aggregation; abnormally aggregated tau protein; filamentous tau inclusion; microtubule associated protein tau aggregation; microtubule associated protein tau deposit; paired helical filament of tau; self-aggregate tau; tau PHF; tau accumulation; tau aggregate; tau fibrillization; tau filament; tau neurofibrillary tangle; tau oligomer; tau paired helical filament; tau polymerization; tau-tau interaction; Ï aggregation; design; designing; network dysfunction; transcriptomics; human disease; novel therapeutics; new drug treatments; new drugs; new therapeutics; new therapy; next generation therapeutics; novel drug treatments; novel drugs; novel therapy; mouse model; murine model; Alzheimer's disease model; AD model; alzheimer model; therapeutic target; overexpression; overexpress; genome-wide; genome scale; genomewide; efficacy testing; stability testing; drug candidate; phase 1 study; Phase I Study; phase 2 study; phase II study; optogenetics; screening; mild cognitive impairment; mild cognitive disorder; Alzheimer's disease pathology; AD pathology; Alzheimer's pathology; transcriptome; global gene expression; global transcription profile; neurovascular; neuro-vascular; small molecule therapeutics; novel drug class; new drug class; in vivo evaluation; in vivo testing; J20 mouse; J20; side effect; Alzheimer's disease patient; Alzheimer's patient; Hyperactivity
