References
- Ballard, C. G. (2002) Advances in the treatment of Alzheimer's disease: benefits of dual cholinesterase inhibition. Eur. Neurol. 47, 64-70. https://doi.org/10.1159/000047952
- Bekinschtein, P., Cammarota, M., Izquierdo, I. and Medina, J. H. (2008) BDNF and memory formation and storage. Neuroscientist 14, 147-156. https://doi.org/10.1177/1073858407305850
- Blokland, A. (1995) Acetylcholine: A neurotransmitter for learning and memory? Brain Res. Brain Res. Rev. 21, 285-300. https://doi.org/10.1016/0165-0173(95)00016-X
- Bramham, C. R. and Messaoudi, E. (2005) BDNF function in adult synaptic plasticity: the synaptic consolidation hypothesis. Prog. Neurobiol. 76, 99-125. https://doi.org/10.1016/j.pneurobio.2005.06.003
- Chen, X., Luo, J. G. and Kong, L.Y. (2010) Two new triterpenoid saponins from Dianthus superbus L. J. Asian Nat. Prod. Res. 12, 458-463. https://doi.org/10.1080/10286020.2010.493326
- Collerton, D. (1986) Cholinergic function and intellectual decline in Alzheimer's disease. Neuroscience 19, 1-28. https://doi.org/10.1016/0306-4522(86)90002-3
- Coyle, J. T., Price, D. L. and DeLong, M. R. (1983) Alzheimer's disease: a disorder of cortical cholinergic innervation. Science 219, 1184-1190. https://doi.org/10.1126/science.6338589
- Crapper, D. R. and DeBoni, U. (1978) Brain aging and Alzheimer's disease. Can. Psychiatr. Assoc. J. 23, 229-233. https://doi.org/10.1177/070674377802300406
- Dahiya, R. (2008) Synthesis and biological activity of a cyclic hexapeptide from Dianthus superbus. Chem. Pap. 62, 527-535.
- Ding, C., Zhang, W., Li, J., Lei, J. and Yu, J. (2013) Cytotoxic constituents of ethyl acetate fraction from Dianthus superbus. Nat. Prod. Res. 27, 1691-1694. https://doi.org/10.1080/14786419.2012.763127
- Flood, J.F. and Cherkin, A. (1986) Scopolamine effects on memory retention in mice: a model of dementia? Behav. Neural. Biol. 45, 169-184. https://doi.org/10.1016/S0163-1047(86)90750-8
- Gou, J., Zou, Y. and Ahn, J. (2011) Enhancement of antioxidant and antimicrobial activities of Dianthus superbus, Polygonum aviculare, Sophora flavescens, and Lygodium japonicum by pressure-assisted water extraction. Food Sci. Biotechnol. 20, 283-287. https://doi.org/10.1007/s10068-011-0040-7
- Hsieh, P. W., Chang, F. R., Wu, C. C., Wu, K. Y., Li, C. M., Chen, S. L. and Wu, Y. C. (2004) New cytotoxic cyclic peptides and dianthramide from Dianthus superbus. J. Nat. Prod. 67, 1522-1527. https://doi.org/10.1021/np040036v
- Hsieh, P. W., Chang, F. R., Wu, C. C., Li, C. M., Wu, K. Y. and Chen, S. L. (2005) Longicalycinin A, a new cytotoxic cyclic peptide from Dianthus superbus var. longicalycinus (MAXIM.) WILL. Chem. Pharm. Bull. 53, 336-338. https://doi.org/10.1248/cpb.53.336
- Lewis, P. R., Shute, C. C. and Silver, A. (1967) Confirmation from choline acetylase analyses of a massive cholinergic innervation to the rat hippocampus. J. Physiol. 191, 215-224. https://doi.org/10.1113/jphysiol.1967.sp008246
- Lopez-Exposito, I., Castillo, A., Yang, N., Liang, B. and Li, X. M. (2011) Chinese herbal extracts of Rubia cordifolia and Dianthus superbus suppress IgE production and prevent peanut-induced anaphylaxis. Chin. Med. 16, 35-44.
- Luo, J. G., Chen, X. C. and Kong, L. Y. (2011) Three new triterpenoid saponins from Dianthus superbus. Chem. Pharm. Bull. 59, 518-521. https://doi.org/10.1248/cpb.59.518
- McGleenon, B. M., Dynan, K. B. and Passmore, A. P. (1999) Acetylcholinesterase inhibitors in Alzheimer's disease. Br. J. Clin. Pharmacol. 48, 471-480.
- Morris, R. (1984) Developments of a water-maze procedure for studying spatial learning in the rat. J. Neurosci. Methods 11, 47-60. https://doi.org/10.1016/0165-0270(84)90007-4
- O'Keefe, J. and Nadel, L. (1978) The hippocampus as a cognitive map. Clarendon Press., Oxford.
- Reid-Adam, J., Yang, N., Song, Y., Cravedi, P., Li, X. M. and Heeger, P. (2013) Immunosuppressive effects of the traditional Chinese herb qu mai on human alloreactive T cells. Am. J. Transplant. 13, 1159-1167. https://doi.org/10.1111/ajt.12180
- Panja, D. and Bramham, C. R. (2014) BDNF mechanisms in late LTP formation: A synthesis and breakdown. Neuropharmacology 76, 664-676. https://doi.org/10.1016/j.neuropharm.2013.06.024
- Shimizu, M., Hayashi, T., Shimizu, K. and Morita, N. (1982) A pyrantype glycoside from Dianthus superbus var. longicalycinus. Phytochemistry 21, 245-247. https://doi.org/10.1016/0031-9422(82)80063-0
- Shin, I. S., Lee, M. Y., Ha, H., Jeon, W. Y., Seo, C. S. and Shin, H. K. (2012) Dianthus superbus fructus suppresses airway inflammation by downregulating of inducible nitric oxide synthase in an ovalbumin- induced murine model of asthma. J. Inflamm. (Lond) 9, 41-49. https://doi.org/10.1186/1476-9255-9-41
- Tong, Y., Luo, J. G., Wang, R., Wang, X. B. and Kong, L. Y. (2012) New cyclic peptides with osteoblastic proliferative activity from Dianthus superbus. Bioorg. Med. Chem. Lett. 22, 1908-1911. https://doi.org/10.1016/j.bmcl.2012.01.058
- Wang, Y. C., Tan, N. H., Zhou, J. and Wu, H. (1998) Cyclopeptides from Dianthus superbus. Phytochemistry 49, 1453-1456. https://doi.org/10.1016/S0031-9422(97)00857-1
- Yu, J. O., Liao, Z. X., Lei, J. C. and Hu, X. M. (2007) Antioxidant and cytotoxic activities of various fractions of ethanol extract of Dianthus superbus. Food Chem. 104, 1215-1219. https://doi.org/10.1016/j.foodchem.2007.01.039
- Yu, J. Q., Yin, Y., Lei, J. C., Zhang, X. Q., Chen, W., Ding, C. L., Wu, S., He, X. Y., Liu, Y. W. and Zou, G. L. (2012) Activation of apoptosis by ethyl acetate fraction of ethanol extract of Dianthus superbus in HepG2 cell line. Cancer Epidemiol. 36, e40-e45. https://doi.org/10.1016/j.canep.2011.09.004
Cited by
- Liquiritigenin ameliorates memory and cognitive impairment through cholinergic and BDNF pathways in the mouse hippocampus 2017, https://doi.org/10.1007/s12272-017-0954-6
- Organosulfur compound protects against memory decline induced by scopolamine through modulation of oxidative stress and Na+/K+ ATPase activity in mice 2017, https://doi.org/10.1007/s11011-017-0067-4
- Phytochemical and Pharmacological Role of Liquiritigenin and Isoliquiritigenin From Radix Glycyrrhizae in Human Health and Disease Models vol.10, pp.1663-4365, 2018, https://doi.org/10.3389/fnagi.2018.00348
- Ameliorates Cognitive Dysfunction Induced by Cholinergic Blockade in Mice vol.21, pp.10, 2018, https://doi.org/10.1089/jmf.2017.4131
- Cognitive enhancing and antioxidant effects of tetrahydroxystilbene glucoside in A β 1 - 42 -induced neurodegeneration in mice vol.17, pp.3-4, 2018, https://doi.org/10.3233/JIN-170059
- Butterbur Leaves Attenuate Memory Impairment and Neuronal Cell Damage in Amyloid Beta-Induced Alzheimer’s Disease Models vol.19, pp.6, 2018, https://doi.org/10.3390/ijms19061644
- Studies of the Anti-amnesic Effects and Mechanisms of Single and Combined Use of Donepezil and Ginkgo Ketoester Tablet on Scopolamine-Induced Memory Impairment in Mice vol.2019, pp.1942-0994, 2019, https://doi.org/10.1155/2019/8636835
- Therapeutic potential of selanyl amide derivatives in the in vitro anticholinesterase activity and in in vivo antiamnesic action vol.98, pp.5, 2016, https://doi.org/10.1139/cjpp-2019-0291
- Cancer Treatment by Caryophyllaceae-Type Cyclopeptides vol.11, pp.None, 2021, https://doi.org/10.3389/fendo.2020.600856
- Trichoderma reesei fungal degradation boosted the potentiality of date pit extract in fighting scopolamine-induced neurotoxicity in male rats vol.11, pp.1, 2016, https://doi.org/10.1038/s41598-021-94058-y