BCI-838
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July 31, 2024
Beneficial effects of physical exercise and an orally active mGluR2/3 antagonist pro-drug on neurogenesis and behavior in an Alzheimer's amyloidosis model.
(PubMed, Front Dement)
- "Here we show that (i) administration of BCI-838 and a combination of BCI-838 and PE enhanced AHN in a 4-month old mouse model of AD amyloid pathology (APP KM670/671NL /PSEN1 Δexon9= APP/PS1), (ii) administration of BCI-838 alone or with PE led to stimulation of AHN and improvement in recognition memory, (iii) the hippocampal dentate gyrus transcriptome of APP/PS1 mice following BCI-838 treatment showed up-regulation of brain-derived neurotrophic factor (BDNF), PIK3C2A of the PI3K-mTOR pathway, and metabotropic glutamate receptors, and down-regulation of EIF5A involved in modulation of mTOR activity by ketamine, and (iv) validation by qPCR of an association between increased BDNF levels and BCI-838 treatment. Our study points to BCI-838 as a safe and orally active compound capable of mimicking the beneficial effect of PE on AHN and recognition memory in a mouse model of AD amyloid pathology."
Journal • Alzheimer's Disease • Amyloidosis • CNS Disorders • Cognitive Disorders • Dementia • Mood Disorders • Psychiatry • BDNF
June 24, 2022
BCI-838, an orally active mGluR2/3 antagonist pro-drug, mimics the beneficial effects of physical exercise on neurogenesis, behavior and exercise-related molecular pathways in an Alzheimer’s disease mouse model
(AAIC 2022)
- No abstract available
Preclinical • Alzheimer's Disease • CNS Disorders
January 20, 2023
BCI-838, an orally active mGluR2/3 receptor antagonist pro-drug, rescues learning behavior deficits in the PS19 MAPT mouse model of tauopathy.
(PubMed, Neurosci Lett)
- "These studies extend the potential utility of BCI-838 to neurodegenerative conditions that have tauopathy as their underlying basis. They also suggest an mGluR2/3 dependent mechanism as a basis for the behavioral deficits in PS19 mice."
Journal • Preclinical • Alzheimer's Disease • CNS Disorders • Cognitive Disorders • Dementia • Frontotemporal Lobar Degeneration • Immunology • Mood Disorders • Psychiatry • MAPT
February 03, 2018
PTSD-Related Behavioral Traits in a Rat Model of Blast-Induced mTBI Are Reversed by the mGluR2/3 Receptor Antagonist BCI-838.
(PubMed, eNeuro)
- "Treatment with BCI-838 also increased neurogenesis in the dentate gyrus (DG) of blast-exposed rats. The safety profile of BCI-838 together with the therapeutic activities reported here, make BCI-838 a promising drug for the treatment of former battlefield Warfighters suffering from PTSD-related symptoms following blast-induced mTBI."
Journal • Preclinical • Biosimilar • CNS Disorders • Depression • Mood Disorders • Post-traumatic Stress Disorder
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