Panorama Research Incorporated — Department of Health and Human Services SBIR Phase I: 200

Description

DESCRIPTION provided by applicant Novel NMDA Receptor Antagonists for Beta Cell Rescue Abstract Type diabetes mellitus T DM is rapidly becoming the most common chronic disease in the US with more than of the adult population affected and million new cases per year Fundamentally T DM involves beta cell dysfunction and poor control of blood glucose levels resulting in hyperglycemia Impaired insulin secretion is accompanied by a decrease in beta cell mass an increase in apoptosis of beta cells and a reduced functional capacity of the remaining cells A disease modifying treatment would not only promote insulin secretion but also reduce apoptosis and increase proliferation of beta cells Recent data from animal models and Phase clinical studies in humans suggest that NMDA receptors NMDAR inhibit insulin release and promote beta cell death and that NMDAR antagonists act as insulin secretagogues and can increase beta cell mass Although further mechanistic studies are required to fully understand the function of NMDARs in beta cells NMDARs may act as part of a negative feedback loop in pancreatic islets to ensure that insulin is not released in an excessive manner at high blood glucose concentrations The lack of extreme blood glucose lowering effects with high dose and long term exposure to NMDAR antagonists suggests that such treatment is unlikely to lead to life threatening hypoglycemia such as is seen with sulfonylurea treatment The larger islet cell mass observed in diabetic mice upon long term treatment with a high dose versus a low dose of NMDAR antagonists also indicates that inhibition of NMDARs could maintain the number of beta cells in diabetes These data suggest that NMDAR antagonists may be useful to reduce or even reverse progression of human diabetes Memantine an aminoadamantane selectively inhibits abnormally active NMDAR channels while preserving normal activity and physiological neuronal function Memantine has been approved for the treatment of moderate to severe Alzheimerandapos s disease for over years Pathological NMDA receptor activity is further down regulated by S nitrosylation of specific cysteine residues Taking advantage of these insights PRI has developed a proprietary series of bifunctional antagonists called nitromemantines that not only preferentially bind to the open channel state but also selectively target NO to a second modulatory site on the NMDAR using the memantine pharmacophore as a homing motif During this Phase I study we will evaluate our lead nitromemantine YQW for its activity in vitro and in an animal model of T DM Successful achievement of these milestones will provide a proprietary first in class disease modifying drug for T DM PUBLIC HEALTH RELEVANCE Type diabetes mellitus T DM affects over million people worldwide and its incidence is increasing T DM is associated with an increased risk of disease of the eye kidney and cardiovascular system Current treatments do not alter the long term course of the disease We have developed a new class of drugs that bind to a receptor that is critical for normal function and maintenance of normal numbers of pancreatic beta cells the cells that secrete insulin We will evaluate these new compounds as potential treatments for T DM