Abstract

BackgroundCAD-31 is an Alzheimer’s disease (AD) drug candidate that was selected on the basis of its ability to stimulate the replication of human embryonic stem cell-derived neural precursor cells as well as in APPswe/PS1ΔE9 AD mice. To move CAD-31 toward the clinic, experiments were undertaken to determine its neuroprotective and pharmacological properties, as well as to assay its therapeutic efficacy in a rigorous mouse model of AD.ResultsCAD-31 has potent neuroprotective properties in six distinct nerve cell assays that mimic toxicities observed in the old brain. Pharmacological and preliminary toxicological studies show that CAD-31 is brain-penetrant and likely safe. When fed to old, symptomatic APPswe/PS1ΔE9 AD mice starting at 10 months of age for 3 additional months in a therapeutic model of the disease, there was a reduction in the memory deficit and brain inflammation, as well as an increase in the expression of synaptic proteins. Small-molecule metabolic data from the brain and plasma showed that the major effect of CAD-31 is centered on fatty acid metabolism and inflammation. Pathway analysis of gene expression data showed that CAD-31 had major effects on synapse formation and AD energy metabolic pathways.ConclusionsAll of the multiple physiological effects of CAD-31 were favorable in the context of preventing some of the toxic events in old age-associated neurodegenerative diseases.

Highlights

  • CAD-31 is an Alzheimer’s disease (AD) drug candidate that was selected on the basis of its ability to stimulate the replication of human embryonic stem cell-derived neural precursor cells as well as in APPswe/PS1ΔE9 AD mice

  • We made a large number of structures related to CNB-023, and J147 was identified on the basis of exceptional potency [1]

  • CAD-31 is broadly neuroprotective Because J147 was selected on the basis of its broad neuroprotective activity [1] and CAD-31 was selected on the basis of its neurogenic properties in human cells [4], we asked if CAD-31 maintained all of the neuroprotective activities of J147

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Summary

Introduction

CAD-31 is an Alzheimer’s disease (AD) drug candidate that was selected on the basis of its ability to stimulate the replication of human embryonic stem cell-derived neural precursor cells as well as in APPswe/PS1ΔE9 AD mice. J147 facilitates memory in normal rodents, and it prevents the loss of synaptic proteins and cognitive decline when administered to 3-month-old APPswe/PS1ΔE9 mice for 7 months [1, 2, 4], as well as in rapidly aging senescence-accelerated mouse-prone 8 (SAMP8) mice, a model of sporadic AD [5]. It reverses memory deficits and some AD pathology when fed to very old transgenic AD mice [2]

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