SBIR-STTR Award

Amyotrophic lateral sclerosis (ALS) is characterized by the progressive and selective loss of motor neurons (MNs) in the motor cortex, brainstem, and spinal cord, resulting in death of patients typically 2-5 years after diagnosis. Glutamate-mediated excitotoxicity in the CNS has been implicated as a major contributor to MN cell death in ALS. It is thought that the vulnerability of MNs to glutamate-mediated excitotoxicity is due to a combination of their high density of Ca2+ permeable ion channels, and their diminished capacity to handle excessive Ca2+ influx, which serves as a trigger for neurodegeneration. Why MNs of ALS patients are especially vulnerable to excitotoxicity remains unknown, but there is nearly universal acceptance that excitotoxicity contributes to selective death on MNs in ALS patients. Therefore, the development of drugs which lower Ca2+ influx during excitatory activity in the CNS, is a crucial focal point in the pursuit for therapeutics for ALS. Ionotropic AMPA receptors are glutamate-activated ion channels that are key mediators of Ca2+ influx in MNs. AMPA receptors are composed of four subunits termed GluR1-4. Two alternatively spliced variants of all four GluRs called ""flip"" and ""flop"" are normally expressed in the CNS and are known to modulate AMPA channel conductance. AMPA channels containing GluR-flip isoforms are 'higher gain'channels, which have greater current amplitudes and/or greater resistant to glutamate-desensitization than the 'lower gain'AMPA channels containing ""flop"" variants. Thus, when the flip/flop ratios of GluRs are elevated, AMPA receptors in MNs show enhanced excitatory activity, and greater Ca2+ influx. We recently developed several novel chemically-modified RNA oligonucleotides, called splice modulating oligomers (SMOs), which potently and specifically modulate GluR alternative splicing to reduce the flip/flop ratio of various GluR isoforms. Although SMOs do not cross the blood-brain-barrier, after direct delivery into the CSF they are broadly distributed throughout the CNS and have the extraordinary capacity to readily to cross the membrane and enter the nuclei of cells in the CNS, where their splice modulating activity persists for months. Here we propose a translational set of experiments to validate the potential of our SMOs as therapeutics for treating ALS. First, we will compare the efficacy of our lead SMO (LSP-GR3) in reducing GluR3-flip expression throughout the CNS, using (1) continuous ICV delivery, and (2) single bolus injection into the lumbar sac of the spinal column (Aim 1). We will then use the best delivery modality determined in Aim 1 and evaluate the efficacy of our two lead SMOs to improve motor function, and increase lifespan in ALS mice (Aim 2).

Public Health Relevance:
This proposal is designed to provide the 'proof of principle'that novel drug candidates developed by LifeSplice Pharma, LLC are efficacious at ameliorating pathology in ALS mice. These studies will lead to formal toxicology analysis, and ultimately an IND application and FDA approval for clinical trials in ALS patients.

Thesaurus Terms:
Ampa Receptors;Age;Alternate Splicing;Alternative Rna Splicing;Alternative Splicing;Amyotrophic Lateral Sclerosis;Amyotrophic Lateral Sclerosis Motor Neuron Disease;Blood - Brain Barrier Anatomy;Blood-Brain Barrier;Bolus;Bolus Infusion;Brain;Brain Nervous System;Brain Stem;Brainstem;Candida;Cannulas;Cell Nucleus;Cessation Of Life;Clinical Trials;Death;Diagnosis;Dose;Drugs;Encephalon;Familial Amyotrophic Lateral Sclerosis;Gehrig's Disease;Glutamates;Hemato-Encephalic Barrier;Infusion;Infusion Procedures;Injection Of Therapeutic Agent;Injections;Intraspinal Injections;Intrathecal Injections;Ion Channel;Ionic Channels;Isoforms;L-Glutamate;Loinc Axis 4 System;Lead;Length;Length Of Life;Longevity;Lou Gehrig Disease;Measures;Mediating;Mediator;Mediator Of Activation;Mediator Of Activation Protein;Medication;Medulla Spinalis;Membrane;Membrane Channels;Mice;Mice Mammals;Modality;Monilia;Motor;Motor Cell;Motor Cortex;Motor Neurons;Murine;Mus;Nerve Degeneration;Neuron Degeneration;Non-Polyadenylated Rna;Nucleus;Oligo;Oligonucleotides;Onset Of Illness;Pathology;Patients;Pb Element;Pharmaceutic Preparations;Pharmaceutical Preparations;Phase;Protein Isoforms;Rna;Rna Gene Products;Rna Splicing;Resistance;Ribonucleic Acid;Spinal;Spinal Canal;Spinal Column;Spinal Cord;Spinal Injections;Spine;Splicing;System;Therapeutic;Time;Toxicology;Transcript;Variant;Variation;Vertebral Column;Backbone;Base;Clinical Investigation;Comparative Efficacy;Compare Efficacy;Density;Desensitization;Design;Designing;Disease Onset;Disorder Onset;Drug Candidate;Drug Development;Drug/Agent;Excitotoxicity;Experiment;Experimental Research;Experimental Study;Glutamatergic;Heavy Metal Pb;Heavy Metal Lead;Improved;Life Span;Lifespan;Membrane Structure;Motoneuron;Neural Degeneration;Neurodegeneration;Neurodegenerative;Neuron Cell Death;Neuron Loss;Neuronal Cell Death;Neuronal Degeneration;Neuronal Loss;Novel;Product Development;Research Study;Resistant;Response;Vertebral Canal

Amyotrophic lateral sclerosis (ALS) is characterized by the progressive and selective loss of motor neurons (MNs) in the motor cortex, brainstem, and spinal cord, resulting in death of patients typically 2-5 years after diagnosis. Glutamate-mediated excitotoxicity in the CNS has been implicated as a major contributor to MN cell death in ALS. It is thought that the vulnerability of MNs to glutamate-mediated excitotoxicity is due to a combination of their high density of Ca2+ permeable ion channels, and their diminished capacity to handle excessive Ca2+ influx, which serves as a trigger for neurodegeneration. Why MNs of ALS patients are especially vulnerable to excitotoxicity remains unknown, but there is nearly universal acceptance that excitotoxicity contributes to selective death on MNs in ALS patients. Therefore, the development of drugs which lower Ca2+ influx during excitatory activity in the CNS, is a crucial focal point in the pursuit for therapeutics for ALS. Ionotropic AMPA receptors are glutamate-activated ion channels that are key mediators of Ca2+ influx in MNs. AMPA receptors are composed of four subunits termed GluR1-4. Two alternatively spliced variants of all four GluRs called ""flip"" and ""flop"" are normally expressed in the CNS and are known to modulate AMPA channel conductance. AMPA channels containing GluR-flip isoforms are 'higher gain'channels, which have greater current amplitudes and/or greater resistant to glutamate-desensitization than the 'lower gain'AMPA channels containing ""flop"" variants. Thus, when the flip/flop ratios of GluRs are elevated, AMPA receptors in MNs show enhanced excitatory activity, and greater Ca2+ influx. We recently developed several novel chemically-modified RNA oligonucleotides, called splice modulating oligomers (SMOs), which potently and specifically modulate GluR alternative splicing to reduce the flip/flop ratio of various GluR isoforms. Although SMOs do not cross the blood-brain-barrier, after direct delivery into the CSF they are broadly distributed throughout the CNS and have the extraordinary capacity to readily to cross the membrane and enter the nuclei of cells in the CNS, where their splice modulating activity persists for months. Here we propose a translational set of experiments to validate the potential of our SMOs as therapeutics for treating ALS. First, we will compare the efficacy of our lead SMO (LSP-GR3) in reducing GluR3-flip expression throughout the CNS, using (1) continuous ICV delivery, and (2) single bolus injection into the lumbar sac of the spinal column (Aim 1). We will then use the best delivery modality determined in Aim 1 and evaluate the efficacy of our two lead SMOs to improve motor function, and increase lifespan in ALS mice (Aim 2).