Learning and memory impairment induced by 1,4-butanediol is regulated by ERK1/2-CREB-BDNF signaling pathways in PC12 cells
- 29 March 2022
- journal article
- research article
- Published by Springer Nature in Metabolic Brain Disease
- Vol. 37 (5) , 1451-1463
Abstract
1,4-butanediol (1,4-BD) is a known γ-hydroxybutyric acid (GHB) precursor which affects the nervous system after ingestion, leading to uncontrolled behavioral consequences. In the present study, we investigated whether 1,4-BD induces oxidative stress and inflammation in PC12 cells and evaluated the toxic effects of 1,4-BD associates with learning and memory. CCK-8 results revealed a dose–effect relationship between the cell viability of PC12 cells and 1,4-BD when the duration of action was 2 h or 4 h. Assay kits results showed that 1,4-BD decreased the levels of Glutathione (GSH), Glutathione peroxidase (GSH-px), Superoxide dismutase (SOD), Acetylcholine (Ach) and increased the levels of Malondialdehyde (MDA), Nitric oxide (NO) and Acetylcholinesterase (AchE). Elisa kits results indicated that 1,4-BD decreased the levels of synaptophysin I (SYN-1), Postsynaptic density protein-95 (PSD-95), Growth associated protein-43 (GAP-43) and increased the levels of Tumor necrosis factor alpha (TNF-α) and Interleukin- 6 (IL-6). RT-PCR results showed that the mRNA levels of PSD-95, SYN-1 and GAP-43 were significantly decreased. The expression of phosphorylation extracellular signal-regulated protein kinase 1/2 (p-ERK1/2), phosphorylation cAMP response element binding protein (p-CREB) and brain-derived neurotrophic factor (BDNF) proteins were significantly decreased in PC12 cells by protein blotting. Overall, these results suggest that 1,4-BD may affect synaptic plasticity via the ERK1/2-CREB-BDNF pathway, leading to Ach release reduction and ultimately to learning and memory impairment. Furthermore, oxidative stress and inflammation induced by 1,4-BD may also result in learning and memory deficits. These findings will enrich the toxicity data of 1.4-BD associated with learning and memory impairment.Keywords
Funding Information
- Guangdong Key R&D Program, Department of Science and Technology of Guangdong Province (2019B020210002)
- Natural Science Foundation of Guangdong Province (2021A1515010825)
- Guangdong Provincial Key Laboratory of Food Quality and Safety (2020B1212060059)
This publication has 73 references indexed in Scilit:
- Long-term Relationships between Cholinergic Tone, Synchronous Bursting and Synaptic RemodelingPLOS ONE, 2012
- Synthesis, Characterization, X-ray Crystallography, Acetyl Cholinesterase Inhibition and Antioxidant Activities of Some Novel Ketone Derivatives of Gallic Hydrazide-Derived Schiff BasesMolecules, 2012
- Synaptic activity-responsive element in the Arc / Arg3.1 promoter essential for synapse-to-nucleus signaling in activated neuronsProceedings of the National Academy of Sciences, 2009
- Behavioral analyses of GHB: Receptor mechanismsPharmacology & Therapeutics, 2009
- Molecular and cellular mechanisms of memory allocation in neuronetworksNeurobiology of Learning and Memory, 2008
- GAP-43 gene expression regulates information storageLearning & Memory, 2007
- Increase in Neurite Formation and Acetylene line Release by Transfection of Growth-Associated Protein-43 cDNA into NG108-15 CellsJournal of Neurochemistry, 2006
- Resuscitative Treatments on 1,4-Butanediol Mortality in MiceAnnals of Emergency Medicine, 2006
- ??-Butyrolactone and 1,4-ButanediolToxicological Reviews, 2004
- GABAB Receptors: A New Paradigm in G Protein SignalingMolecular and Cellular Neuroscience, 2000