ACTA NEUROPHARMACOLOGICA ›› 2011, Vol. 1 ›› Issue (3): 16-22.

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The Effects of Tenuigenin on Expression of nAChRα4 and PSD95 in Alzheimer’s Disease Model Rats

Li Xiao-feng1,Zhao Da-peng1,Chen Shu-sha1,Jing Wei2,Li Xin-yi2   

  1. 1. Department of Neurology,The First Clinical Medical School,Shanxi Medical University,Taiyuan Shanxi, 030001,China   2. Shanxi Academy of Medical Science,Taiyuan, 030031,China
  • Online:2011-06-26 Published:2012-06-28

Abstract: Objective: To investigate the effects and the underlying mechanisms of Tenuigenin on Alzheimer’s disease by observing the effects of Tenuigenin(TEN) on expression of nicotinic acetylcholine receptor subunit alpha-4 (nAChRα4) and postsynaptic density 95(PSD-95) in Alzheimer’s disease model rat. Methods: 32 male Wistar rats were divided randomly into four groups: control group,model group,12.5 mg·mL-1 dose TEN group and 37.5 mg·mL-1 dose TEN group. The rat model with Alzheimer’s disease was made by injecting ibotenic acid into Meynert basal nuclei of aging rat induced by D-gal.The expressions of nAChRα4 and PSD-95 in the hippocampus CA1 were measured by immunohistochemistry method. Results: Compared with the control group,the average gray-scale values of hippocampus CA1 nAChRα4 and PSD-95 in the model group were increased significantly and the average optical density was decreased obviously (P<0.01). Compared with the model group,the average gray-scale values in the hippocampus CA1 of 37.5 mg·mL-1 dose TEN group and 12.5 mg·mL-1 dose TEN group were obviously decreased and the average optical density was increased significantly (P<0.05). Meanwhile,the average gray-scale value within the hippocampus CA1 of 37.5 mg·mL-1 dose TEN group was significantly less than that in 12.5 mg·mL-1 dose TEN group,but more distinct than that on the average optical density aspect (P<0.01). Conclusion: TEN can dose-dependently increase the expression of CA1 area nAChRα4 and PSD-95 in Alzheimer’s disease model rats,which may partly explain the beneficial effects of TEN on cognitive function.

Key words: Tenuigenin, Alzheimer&, rsquo, s disease, hippocampus, nAChR&, alpha, 4, PSD-95

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