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Activating Prostaglandin E2 EP2 may reduce memory loss in a Huntington's disease mouse model by boosting brain growth factor and synapse strength
Updated
Abstract
Misoprostol treatment improves long-term memory deficits in R6/1 mice, a model of Huntington's disease.
- PGE2 EP2 receptor stimulation is linked to enhanced synaptic plasticity and memory formation.
- Misoprostol increases dendritic branching in hippocampal neurons, dependent on brain-derived neurotrophic factor (BDNF).
- Chronic administration of misoprostol from 14 to 18 weeks of age ameliorates long-term memory deficits in R6/1 mice.
- Misoprostol treatment increases BDNF expression in the hippocampus of treated R6/1 mice.
- The treatment prevents the reduction of PSD-95 and VGluT-1 positive particles in the hippocampus of vehicle-treated R6/1 mice.
- Misoprostol administration results in increased cAMP levels and a reduction in nuclear inclusions of mutant huntingtin in R6/1 mice.
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