Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice
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Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice
Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice
中国结合医学杂志(英文版)2018年24卷第2期 页码:133-139
Affiliations:
1. Research Center for Pharmacology and Toxicology, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College,Beijing,China
2. Guang’anmen Hospital, China Academy of Chinese Medical Sciences,Beijing,China
3. Beijing Hospital of Traditional Chinese Medicine, Capital Medical University,Beijing,China
Author bio:
Funds:
Supported by the National Natureal Science Foundation of China (No. 30701121)
He, Xl., Zhao, Sh., You, W. et al. Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice., Chin. J. Integr. Med. 24, 133–139 (2018). https://doi.org/10.1007/s11655-016-2265-z
Xiao-li He, Shi-hui Zhao, Wei You, et al. Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice[J]. Chinese Journal of Integrative Medicine, 2018,24(2):133-139.
He, Xl., Zhao, Sh., You, W. et al. Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice., Chin. J. Integr. Med. 24, 133–139 (2018). https://doi.org/10.1007/s11655-016-2265-zDOI:
Xiao-li He, Shi-hui Zhao, Wei You, et al. Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice[J]. Chinese Journal of Integrative Medicine, 2018,24(2):133-139. DOI: 10.1007/s11655-016-2265-z.
Neuroprotective Effects of Electroacupuncture Preventive Treatment in Senescence-Accelerated Mouse Prone 8 Mice
摘要
To investigate the preventive treatment effects of electroacupuncture (EA) on cognitive changes and brain damage in senescence-accelerated mouse prone 8 (SAMP8) mice. The 5-month-old male SAMP8 and age-matched homologous normal aging mice (SAMR1) were adopted in this study. EA stimulation at Baihui (GV 20) and Yintang (EX-HN 3) was performed every other day for 12 weeks
4 weeks as a course. Morris water maze test and Nissl-stained with cresyl violet were used for cognitive impairments evaluation and brain morphometric analysis. Amyloid-β (A β) expression in hippocampus and parietal cortex was detected by immunohistochemistry
and apoptosis was observed by TUNEL staining. After 3 courses of EA preventive treatment
the escape latencies of 8-month-old SAMP8 mice in EA group were significantly shortened than those of un-pretreated SAMP8 mice. Compared with SAMR1 mice
extensive neuronal changes were visualized in the CA1 area of hippocampus in SAMP8 mice
while these pathological changes and attenuate cell loss in hippocampal CA1 area of SAMP8 mice markedly reduced after EA preventive treatment. Furthermore
A β expression in hippocampus and parietal cortex of SAMP8 mice decreased significantly after EA treatment
and neuronal apoptosis decreased as well. EA preventive treatment at GV 20 and EX-HN 3 might improve cognitive deficits and neuropathological changes in SAMP8 mice
which might be
at least in part
due to the effects of reducing brain neuronal damage
decreasing neuronal apoptosis and inhibiting A β-containing aggregates.
Abstract
To investigate the preventive treatment effects of electroacupuncture (EA) on cognitive changes and brain damage in senescence-accelerated mouse prone 8 (SAMP8) mice. The 5-month-old male SAMP8 and age-matched homologous normal aging mice (SAMR1) were adopted in this study. EA stimulation at Baihui (GV 20) and Yintang (EX-HN 3) was performed every other day for 12 weeks
4 weeks as a course. Morris water maze test and Nissl-stained with cresyl violet were used for cognitive impairments evaluation and brain morphometric analysis. Amyloid-β (A β) expression in hippocampus and parietal cortex was detected by immunohistochemistry
and apoptosis was observed by TUNEL staining. After 3 courses of EA preventive treatment
the escape latencies of 8-month-old SAMP8 mice in EA group were significantly shortened than those of un-pretreated SAMP8 mice. Compared with SAMR1 mice
extensive neuronal changes were visualized in the CA1 area of hippocampus in SAMP8 mice
while these pathological changes and attenuate cell loss in hippocampal CA1 area of SAMP8 mice markedly reduced after EA preventive treatment. Furthermore
A β expression in hippocampus and parietal cortex of SAMP8 mice decreased significantly after EA treatment
and neuronal apoptosis decreased as well. EA preventive treatment at GV 20 and EX-HN 3 might improve cognitive deficits and neuropathological changes in SAMP8 mice
which might be
at least in part
due to the effects of reducing brain neuronal damage
decreasing neuronal apoptosis and inhibiting A β-containing aggregates.
关键词
electroacupuncturesenescence-accelerated mouse prone 8 micepreventionlearning and memorycognitive impairmentbrain damage
Keywords
electroacupuncturesenescence-accelerated mouse prone 8 micepreventionlearning and memorycognitive impairmentbrain damage
references
Tanzi RE, Bertram L. Twenty years of the Alzheimer’s disease amyloid hypothesis: a genetic perspective. Cell 2005;120:545–555.
Huang Y, Mucke L. Alzheimer mechanisms and therapeutic strategies. Cell 2012;148:1204–1222.
Su D, Li L. Trends in the use of complementary and alternative medicine in the United States: 2002-2007. J Health Care Poor Underserved 2011;22:296–310.
Kaptchuk TJ. Acupuncture: theory, efficacy, and practice. Ann Intern Med 2002;136:374–383.
Cady RK, Farmer K. Acupuncture in the treatment of headache: a traditional explanation of an ancient art. Headache 2015;55:457–464.
Zhou Y, Jin J. Effect of acupuncture given at the HT 7, ST 36, ST 40 and KI 3 acupoints on various parts of the brains of Alzheimer’s disease patients. Acupunct Electrother Res 2008;33:9–17.
Peng XW, Dong KL. Clinical observation on acupuncture combined with Yizhi Jiannao Granules for treatment of Alzheimer’s disease. Chin Acupunct Moxibust (Chin) 2009;29:269–271.
Zhu H, Dong KL, Wu Y, Zhang T, Li RM, Dai SS, et al. Influence of acupuncture on isoprostane in patients with Alzheimer’s disease. Chin Acupunct Moxibust (Chin) 2010;30:18–21.
Lee GJ, Yin CS, Choi SK, Choi S, Yang JS, Lee H, et al. Acupuncture attenuates extracellular glutamate level in global ischemia model of rat. Neurol Res 2010;32:79–83.
Chen Y, Zhou J, Li J, Yang SB, Mo LQ, Hu JH, et al. Electroacupuncture pretreatment prevents cognitive impairment induced by limb ischemia-reperfusion via inhibition of microglial activation and attenuation of oxidative stress in rats. Brain Res 2012;1432:36–45.
Chen GH, Wang YJ, Wang XM, Zhou JN. Accelerated senescence prone mouse-8 shows early onset of deficits in spatial learning and memory in the radial six-arm water maze. Physiol Behav 2004;82:883–890.
Morley JE. The SAMP8 mouse: a model of Alzheimer disease? Biogerontology 2002;3:57–60.
Gong Y, Liu L, Xie B, Liao Y, Yang E, Sun Z. Ameliorative effects of lotus seedpod proanthocyanidins on cognitive deficits and oxidative damage in senescence-accelerated mice. Behav Brain Res 2008;194:100–107.
Pallas M, Camins A, Smith MA, Perry G, Lee HG, Casadesus G. From aging to Alzheimer’s disease: unveiling "the switch" with the senescence-accelerated mouse model (SAMP8). J Alzheimers Dis 2008;15:615–624.
Butterfield DA, Poon HF. The senescence-accelerated prone mouse (SAMP8): a model of age-related cognitive decline with relevance to alterations of the gene expression and protein abnormalities in Alzheimer’s disease. Exp Gerontol 2005;40:774–783.
Gu W, Jin XX, Zhang YJ, Li ZJ, Kong Y. Clinical observation of Alzheimer’s disease treated with acupuncture. Chin Acupunct Moxibust (Chin) 2014;34: 1156–1160.
Lu J, Li KC. fMRI study of acupuncture mechanism underlying Alzheimer’s. J Med Imaging 2011;21:302–304.
Zeng BY, Salvage S, Jenner P. Effect and mechanism of acupuncture on Alzheimer’s disease. Int Rev Neurobiol 2013;111:181–195.
Hunter AJ, Mackay KB, Rogers DC. To what extent have functional studies of ischaemia in animals been useful in the assessment of potential neuroprotective agents? Trends Pharmacol Sci 1998;19:59–66.
Sheng JG, Zhou XQ, Mrak RE, Griffin WS. Progressive neuronal injury associated with amyloid plaque formation in Alzheimer disease. J Neuropathol Exp Neurol 1998;57:714–717.
Fifre A, Sponne I, Koziel V, Kriem B, Yen Potin FT, Bihain BE, et al. Microtubule-associated protein MAP1A, MAP1B, and MAP2 proteolysis during soluble amyloid beta-peptideinduced neuronal apoptosis. Synergistic involvement of calpain and caspase-3. J Biol Chem 2006;281:229–240.
Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer’s disease: progress and problems on the road to therapeutics. Science 2002;297:353–356.
Zhao L, Shen P, Han Y, Zhang X, Nie K, Cheng H, et al. Effects of acupuncture on glycometabolic enzymes in multiinfarct dementia rats. Neurochem Res 2011;36:693–700.
Wang T, Liu CZ, Yu JC, Jiang W, Han JX. Acupuncture protected cerebral multi-infarction rats from memory impairment by regulating the expression of apoptosis related genes Bcl-2 and Bax in hippocampus. Physiol Behav 2009;96:155–161.
The preventive effect of garlicin on a porcine model of myocardial infarction reperfusion no-reflow
Effects of 5-hydroxymethyl furfural extracted from Rehmannia glutinosa Libosch on the expression of signaling molecules relevant to learning and memory among hippocampal neurons exposed to high concentration of corticosterone
Improved mesenchymal stem cell survival in ischemic heart through electroacupuncture
Effect of electroacupuncture on the pathomorphology of the sciatic nerve and the sensitization of P2X3 receptors in the dorsal root ganglion in rats with chronic constrictive injury
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