Effect of Xingyo-tang on Learning and Memory Performances in Mice

  • Kim, Ki-Bong (Department of Pediatrics, College of Oriental Medicine, Dongguk University) ;
  • Chang, Gyu-Tae (Department of Pediatrics, College of Oriental Medicine, Dongguk University) ;
  • Kim, Jang-Hyun (Department of Pediatrics, College of Oriental Medicine, Dongguk University)
  • Published : 2005.02.25

Abstract

The effects on memory and learning ability of the Korean herbal medicine, Xingyo-tang(XGT, 神交湯), which consists of Ginseng Radix(人蔘) 4 g, Liriopis Tuber(麥門冬) 40 g, Morindae Officinalis Radix(巴戟天) 40 g, Biotae Semen(柏子仁) 20 g, Dioscoreae Rhizoma(山藥) 40 g, Euryales Semen(?實) 20 g, Scrophulariae Radix(玄蔘) 40 g, Salviae Miltiorrhizae Radix(丹蔘) 12 g, Poria(茯神) 12 g, Cuscutae Semen(免絲子) 40 g, was investigated. The effects of XGT on learning and memory performance were examined in normal or memory impaired mice by using avoidance tests, Pentobarbital -induced sleep test, fear conditioning task, novel object recognition task, and water maze task. Hot water extract from XGT was used for the studies. Learning ability and memory are based on modifications of synaptic strength among neurons that are simultaneously active. Enhanced synaptic coincidence detection leads to better learning and memory. The XGT-treated (30 mg/100 g and 60 mg/100 g, p.o.) mice exhibit superior ability in learning and memorizing when performing various behavioral tasks. XGT did not affect the passive avoidance responses of normal mice in the step through and step down tests, the conditioned and unconditioned avoidance responses of normal mice in the shuttle box, lever press performance tests, and the ambulatory activity of normal mice in normal condition. In contrast, XGT produced ameliorating effects on the memory retrieval impairment induced by ethanol. XGT also improved the memory consolidation disability induced by electric convulsive shock (ECS). XGT extended the sleeping time induced by pentobarbital dose-dependently, suggesting its transquilizing or antianxiety action. These results suggest that XGT has an improving effect on the impaired learning through the effects on memory registration and retrieval.

Keywords

References

  1. Qian Song (錢松), Bian-Zheng-Ji-Wen (辨證奇聞, in chinese). A book concern of gande (甘地出版社), Taibei, p.106. 1963.
  2. Kyeung-Sun Kim, Gyu-Mahn Jeong. A Literature Study of the reason of Amnesia. The Journal of Korean Oriental Pediatrics 7(1):45-49, 1993.
  3. Woo-Yeoun Kim, Deog-Kon Kim. A Literature Study of medical treatment and prescription for Amnesia. The Journal of Korean Oriental Pediatrics 7(1):63-75, 1993.
  4. Segawa, M., Saito, N. and Nishiyama, N. Biogenic Amines, Jpn. J. Pharmacol. 7: 191-196, 1990.
  5. Mumby, D.G. Ischemia-induced object-recognition defects in rats are attenuated by hippocampal ablation before or soon after ischemia. Behav Neurosci. 110:266-281, 1996.
  6. Zhou, Y., Saito, H. and Nishiyama, N. Effects of Acorus gramineus Soland on learning and memory performances in mice, Shoyakugaku. 46:103-108, 1992.
  7. Nishiyama, N., Wang Y-L. and Saito, H. Effects of Biota (Bai-Zi-Ren), a traditional chinese medicine, on learning performances in mice. Shoyakugaku Zasshi. 46:62-70, 1992.
  8. Creese, I., Schneider, R. and Snyder, S.H. [3H]-spiperone labels dopamine receptors in pituitary and brain. Eur. J. Pharmacol. 46:377-381, 1977.
  9. Blozovski, D. and Buser P. Passive avoidance memory consolidation and reinstatement in the young rat. Neurosci. Lett. Jun. 17:89, 114-119, 1988.
  10. Reed, J.M. and Squire, R.L. Impaired recognition memory in patients with lesions limited to the hippocampal formation. Behav Neurosci. 111:667-675, 1997.
  11. Jang-Hyun Kim Methodological Research in Development of Intelligence, The Journal of Korean Oriental Pediatrics 13(2):93-107, 1999.
  12. Saito, S., Lee, C-H. and Soella, M.: Annu Anim. Psychol. 21:19-23, 1971.
  13. Kucharski, D. and Hall, W.G. New routes to early memories. Science, Nov. 6:238, 786-788, 1987.
  14. Hock, F. J. Drug influences on learning and memory in aged animals and human, Neuropsychobiology. 17:145-152, 1987.
  15. Schaeffer, K.W. Parson, O.A. Int. J. Neurosci. 38:311-316, 1988.
  16. Scheema-Dhadli, S., Halperin, F. A., Sonnenberg, K., MacMillan, V. and Haplerin, M.L. Biochem. Cell. Biol, 65:458-463, 1987.
  17. Crawford, A. Drug Alcohol Depend. 10:279-285, 1978.
  18. Phillips, R.G. and LeDoux, J.E. Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. Behav Neurosci. 106:274-285, 1992.
  19. Myhrer, T. Exploratory behavior and reaction to novelty in rats with hippocampal perforant path systems disrupted. Behav Neurosci. Jun. 102:356-362, 1988.