Principal Investigators



    National Institute on Drug Abuse

    Contact information of lead PI



    Title of project or programme

    Medicinal Chemistry of Drugs Acting on CRH Receptors

    Source of funding information

    NIH (NIA)

    Total sum awarded (Euro)


    Start date of award

    Total duration of award in years



    Acquired Cognitive Impairment... Aging... Alzheimer's Disease... Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)... Behavioral and Social Science... Brain Disorders... Dementia... Drug Abuse (NIDA only)... Neurodegenerative... Neurosciences... Prevention... Substance Abuse... Translational Research... Women's Health for IC Use

    Research Abstract

    The stress system is well known to play an important role in relapse to drug abuse and excessive eating and is largely controlled by corticotropin releasing hormone receptors (CRHR) and their endogenous ligands. Recent work has shown that stress and corticotropin-releasing hormone (CRH) are involved in the pathogenesis of Alzheimer’s disease (AD), but agents that impact CRF signaling have not been carefully tested for therapeutic efficacy or long-term safety in animal models. We have examined the question of whether antagonism of the type-1 corticotropin-releasing hormone receptor (CRHR1) could be used as a disease-modifying treatment for AD, we used a preclinical prevention paradigm and treated 30-day-old AD transgenic mice with the small-molecule, CRHR1-selective antagonist, R121919, (2,5-dimethyl-3-(6-dimethyl-4-methylpyridin-3-yl)-7 dipropylaminopyrazolo1,5-apyrimidine) for 5 months, and examined AD pathologic and behavioral end points. We found that R121919 significantly prevented the onset of cognitive impairment in female mice and reduced cellular and synaptic deficits and beta amyloid and C-terminal fragment- levels in both genders. We observed no tolerability or toxicity issues in mice treated with R121919. We conclude that CRHR1 antagonism may present a viable disease-modifying therapy for AD, and that appropriate CRHR1 antagonists should be considered for human studies.

    Further information available at:

Types: Investments < €500k
Member States: United States of America
Diseases: N/A
Years: 2016
Database Categories: N/A
Database Tags: N/A

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