Phase II year
2017
(last award dollars: 2018)
More than 29 million people in the US and 422 million people world-wide are estimated to have diabetes mellitus. Peripheral neuropathy is the most common of the consequences of long term diabetes, affecting more than half of all diabetic patients. Diabetes also impacts the CNS leading to cognitive deficits associated with encephalopathy (loss of neurons) and myelopathy (myelin damage). Diabetes is a risk factor for Alzheimer's disease (AD) and increases risk of progression from mild cognitive impairment to AD. The only current recommendation for preventing or slowing progression of neuropathy is to maintain close glycemic control, which is not feasible for the majority of patients, while there is no recommendation for preventing or slowing encephalopathy. NSI-189 is a new chemical entity that when orally administered promotes endogenous neurogenesis in the adult hippocampus, increases hippocampal volume, enhances synaptic plasticity, and stimulates neuro-regeneration. In our preliminary studies with a mouse model of type 1 diabetes, it has shown the ability to prevent multiple indices of peripheral neuropathy, increase hippocampal volume, and protect long-term memory. In the proposed project, we aim to demonstrate that NSI-189 can prevent and/or reverse peripheral and/or central neuropathy in various animals models of both type 1 and type 2 diabetes.
Public Health Relevance Statement: Project Narrative NSI-189 is a novel, orally active agent that is being tested for clinical efficacy to treat major depressive disorder and in preliminary studies significantly prevented indices of peripheral neuropathy in a mouse model of type 1 diabetes. The proposed project aims to assess NSI-189's therapeutic potential to prevent/reverse diabetic neuropathy in various animal models of type 1 and type 2 diabetes. If successful, NSI-189 could be the first disease modifying therapy for diabetic neuropathy, a condition that will affect more than half of the 422 million diabetic patients world-wide.
Project Terms: Adjuvant; Adult; Affect; Alzheimer's Disease; Angiotensin-Converting Enzyme Inhibitors; Animal Model; Attention; Behavior; Chemicals; clinical efficacy; Clinical Research; Clinical Trials Design; clinically relevant; Cognitive deficits; Cornea; Data; Defect; density; Development; Diabetes Mellitus; diabetic; Diabetic Neuropathies; diabetic patient; Disease; Dose; Encephalopathies; Fiber; Formulation; Future; glycemic control; Hippocampus (Brain); Hyperglycemia; Hypoglycemic Agents; indexing; innovation; Insulin; Insulin-Dependent Diabetes Mellitus; Intervention; Learning; Light; long term memory; Major Depressive Disorder; Measures; Memory; Metabolic syndrome; Metformin; mild cognitive impairment; Modeling; Motor; mouse model; Myelin; Nerve; Nerve Regeneration; neurogenesis; neuron loss; Neurons; Neuropathy; neurotrophic factor; Non-Insulin-Dependent Diabetes Mellitus; novel; novel strategies; novel therapeutics; object recognition; Oral; Pathogenesis; Pathway interactions; Patients; Peripheral; Peripheral Nervous System Diseases; Pharmaceutical Preparations; polypeptide; Population; prevent; Property; Recommendation; response; Response Latencies; Risk; Risk Factors; Rodent; Sensory; Side; Site; Skin; small molecule; Spinal Cord Diseases; standard of care; stressor; Synapses; Synaptic plasticity; synergism; Target Populations; Testing; Therapeutic; Therapeutic Intervention; therapeutic target; therapy development; Touch sensation
