Fig. 1. COE ameliorates EtOH-induced memory deficit in the passive avoidance test.
Fig. 2. COE ameliorates EtOH-induced memory deficit in the Y-maze test.
Fig. 3. COE reduces ethanol-induced LTP impairment.
Fig. 4. COE improves ethanol-induced NMDAmediated fEPSP.
참고문헌
- Bauer, E. P., Schafe, G. E. and LeDoux, J. E. 2002. NMDA receptors and L-type voltage-gated calcium channels contribute to long-term potentiation and different components of fear memory formation in the lateral amygdala. J. Neurosci. 22, 5239-5249. https://doi.org/10.1523/JNEUROSCI.22-12-05239.2002
- Bito, H., Deisseroth, K. and Tsien, R. W. 1996. CREB phosphorylation and dephosphorylation: a Ca2+-and stimulus duration-dependent switch for hippocampal gene expression. Cell 87, 1203-1214. https://doi.org/10.1016/S0092-8674(00)81816-4
- Chen, C. and Tonegawa, S. 1997. Molecular genetic analysis of synaptic plasticity, activity-dependent neural development, learning, and memory in the mammalian brain. Annu. Rev. Neurosci. 20, 157-184. https://doi.org/10.1146/annurev.neuro.20.1.157
- Citri, A. and Malenka, R. C. 2008. Synaptic plasticity: multiple forms, functions, and mechanisms. Neuropsychopharmacology 33, 18-41. https://doi.org/10.1038/sj.npp.1301559
- Curtin, J. J., Patrick, C. J., Lang, A. R., Cacioppo, J. T. and Birbaume, N. 2001. Alcohol affects emotion through cognition. Psychol. Sci. 6, 527-531.
- Deisseroth, K., Bito, H. and Tsien, R. W. 1996. Signaling from synapse to nucleus: postsynaptic CREB phosphorylation during multiple forms of hippocampal synaptic plasticity. Neuron 16, 89-101. https://doi.org/10.1016/S0896-6273(00)80026-4
- Dodd, P. R., Beckmann, A. M., Davidson, M. S. and Wilce, P. A. 2000. Glutamate-mediated transmission, alcohol, and alcoholism. Neurochem. Int. 37, 509-533. https://doi.org/10.1016/S0197-0186(00)00061-9
- Gerson, L. W. and Donald, A. P. 1979. Alcohol consumption and the incidence of violent crime. J. Stud. Alcohol. 3, 307-312. https://doi.org/10.15288/jsa.1979.40.307
- Joe, K. H., Kim, Y. K., Kim, T. S., Roh, S. W., Choi, S. W., Kim, Y. B., Lee, H. J. and Kim, D. J. 2007. Decreased plasma brain-derived neurotrophic factor levelsin patients with alcohol dependence. Alcohol Clin. Exp. Res. 31, 1833-1838. https://doi.org/10.1111/j.1530-0277.2007.00507.x
- Kim, D. H., Park, H. J., Jung, J. W. and Lee, S. 2017. Effect of the extract of Hydrangea Ducis Folium on alcohol-induced psychiatric deficits. J. Life Sci. 27, 355-360. https://doi.org/10.5352/JLS.2017.27.3.355
- Kranzler, H. R. and Jeffrey, V. K. 2001. Efficacy of naltrexone and acamprosate for alcoholism treatment: a meta-analysis. Alcohol Clin. Exp. Res. 25, 1335-1341. https://doi.org/10.1111/j.1530-0277.2001.tb02356.x
- Kril, J. J. and Glenda, M. H. 1999. Brain shrinkage in alcoholics:a decade on and what have we learned? Prog. Neurobiol. 58, 381-387. https://doi.org/10.1016/S0301-0082(98)00091-4
- Malenka, R. C. 1994. Synaptic plasticity in the hippocampus:LTP and LTD. Cell 78, 535-538. https://doi.org/10.1016/0092-8674(94)90517-7
- Nikaido, T., Ohmoto, T., Sankawa, U., Kitanaka, S. and Takido, M. 1984. Inhibitors of adenosine 3', 5'-cyclicmonophosphate phosphodiesterase in Cassia seed. Chem. Pharm. Bull. (Tokyo) 32, 3075-3078. https://doi.org/10.1248/cpb.32.3075
- Park, H. J., Lee, S., Jung, J. W., Lee, Y. C., Choi, S. M. and Kim, D. H. 2016. Salvia miltiorrhiza Bunge blocks ethanol-induced synaptic dysfunction through regulation of NMDA receptor-dependent synaptic transmission. Biomol. Ther. (Seoul). 24, 433-437. https://doi.org/10.4062/biomolther.2015.184
- Ramachandran, B., Ahmed, S., Zafar, N. and Dean, C. 2015. Ethanol inhibits long-term potentiation in hippocampal CA1 neurons, irrespective of lamina and stimulus strength, through neurosteroidogenesis. Hippocampus 25, 106-118. https://doi.org/10.1002/hipo.22356
- Rodriguez-Duran, L. F. and Escobar, M. L. 2014. NMDA receptor activation and PKC but not PKA lead to the modification of the long-term potentiation in the insular cortex induced by conditioned taste aversion: differential role of kinases in metaplasticity. Behav. Brain Res. 266, 58-62. https://doi.org/10.1016/j.bbr.2014.02.049
- Stuchlik, A. 2014. Dynamic learning and memory, synaptic plasticity and neurogenesis: an update. Front. Behav. Neurosci. 8, 106.
- Tizabi, Y., Getachew, B., Ferguson, C. L., Csoka, A. B., Thompson, K. M., Gomez-Paz, A., Ruda-Kucerova, J. and Taylor, R. E. 2018. Low vs. high alcohol: central benefits vs. detriments. Neurotox. Res. 34, 860-869 https://doi.org/10.1007/s12640-017-9859-x
- Tokuda, K., Izumi, Y. and Zorumski, C. F. 2011. Ethanol enhances neurosteroidogenesis in hippocampal pyramidal neurons by paradoxical NMDA receptor activation. J. Neurosci. 31, 9905-9909. https://doi.org/10.1523/JNEUROSCI.1660-11.2011
- Tsai, G., Gastfriend, D. R. and Coyle, J. T. 1995. The glutamatergic basis of human alcoholism. Am. J. Psychiatry 152, 332-340. https://doi.org/10.1176/ajp.152.3.332
- White, A. M. 2003. What happened? Alcohol, memory blackouts, and the brain. Alcohol Res. Health 2, 186-196.
- Wong, S. T., Athos, J., Figueroa, X. A., Pineda, V. V., Schaefer, M. L., Chavkin, C. C., Muglia, L. J. and Storm, D. R. Calcium-stimulated adenylyl cyclase activity is critical for hippocampus-dependent long-term memory and late phase LTP. Neuron 23, 787-798. https://doi.org/10.1016/S0896-6273(01)80036-2
- Yamin, G. 2009. NMDA receptor-dependent signaling pathways that underlie amyloid beta-protein disruption of LTP in the hippocampus. J. Neurosci. Res. 87, 1729-1736. https://doi.org/10.1002/jnr.21998
- Zhang, J., Li, Y., Xu, J. and Yang, Z. 2014. The role of Nmethyl-D-aspartate receptor in Alzheimer's disease. J. Neurol. Sci. 339, 123-129. https://doi.org/10.1016/j.jns.2014.01.041