
AbstractIntroductionIntermittent fasting (IF) has been suggested to have neuroprotective effects through the activation of multiple signaling pathways. Rodents fasted intermittently exhibit enhanced hippocampal neurogenesis and long‐term potentiation (LTP) at hippocampal synapses compared with sedentary animals fed an ad libitum (AL) diet. However, the underlying mechanisms have not been studied. In this study, we evaluated the mechanistic gap in understanding IF‐induced neurogenesis.MethodsWe evaluated the impact of 3 months of IF (12, 16, and 24 hr of food deprivation on a daily basis) on hippocampal neurogenesis in C57BL/6NTac mice using immunoblot analysis.ResultsThree‐month IF significantly increased activation of the Notch signaling pathway (Notch 1, NICD1, and HES5), neurotrophic factor BDNF, and downstream cellular transcription factor, cAMP response element‐binding protein (p‐CREB). The expression of postsynaptic marker, PSD95, and neuronal stem cell marker, Nestin, was also increased in the hippocampus in response to 3‐month IF.ConclusionsThese findings suggest that IF may increase hippocampal neurogenesis involving the Notch 1 pathway.
Male, brain‐derived neurotrophic factor, Notch, Receptors, Notch, hippocampus, intermittent fasting, Brain-Derived Neurotrophic Factor, Neurogenesis, brain-derived neurotrophic factor, Neurosciences. Biological psychiatry. Neuropsychiatry, Fasting, Hippocampus, Mice, Inbred C57BL, neurogenesis, Mice, Synapses, Animals, Cyclic AMP Response Element-Binding Protein, RC321-571, Original Research, Signal Transduction
Male, brain‐derived neurotrophic factor, Notch, Receptors, Notch, hippocampus, intermittent fasting, Brain-Derived Neurotrophic Factor, Neurogenesis, brain-derived neurotrophic factor, Neurosciences. Biological psychiatry. Neuropsychiatry, Fasting, Hippocampus, Mice, Inbred C57BL, neurogenesis, Mice, Synapses, Animals, Cyclic AMP Response Element-Binding Protein, RC321-571, Original Research, Signal Transduction
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