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山东大学学报 (医学版) ›› 2020, Vol. 1 ›› Issue (7): 15-23.doi: 10.6040/j.issn.1671-7554.0.2019.1273

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Noggin蛋白对小鼠脑缺血再灌注损伤后学习和记忆能力与齿状回结构的影响

龙婷婷,谢明,周璐,朱俊德   

  1. 贵州医科大学基础医学院人体解剖学教研室, 贵州 贵安 550025
  • 出版日期:2020-07-20 发布日期:2020-07-10
  • 通讯作者: 朱俊德. E-mail:jdzhu73@126.com
  • 基金资助:
    国家自然科学基金(81660243);贵州省科技厅社会发展科技计划(黔科合SY字[2015]3041号)

Effect of Noggin protein on learning and memory abilities and the dentate gyrus structure after cerebral ischemia reperfusion injury in mice

LONG Tingting, XIE Ming, ZHOU Lu, ZHU Junde   

  1. Department of Human Anatomy, School of Basic Medical Science, Guizhou Medical University, Guian 550025, Guizhou, China
  • Online:2020-07-20 Published:2020-07-10

摘要: 目的 探讨侧脑室注射Noggin蛋白对小鼠脑缺血再灌注损伤(CIRI)后学习、记忆能力及齿状回(DG)结构的影响,以期为临床缺血性脑血管疾病的预防与治疗提供新思路。 方法 240只小鼠随机分为:假手术组(n=80)、缺血再灌注损伤组(I/R组,n=80)、缺血再灌注损伤+Noggin治疗组(Noggin组,n=80),每组再分为1、3、7、14 d共 4个亚组;取材前1天采用Y型迷宫检测小鼠学习记忆能力(n=5);然后比色法检测缺血侧脑组织超氧化物歧化酶(SOD)与丙二醛(MDA)含量(n=5);2,3,5-氯化三苯基四氮唑(TTC)染色检测脑梗死面积(n=5); 尼氏染色与免疫荧光检测DG神经元与胶质原纤维酸性蛋白(GFAP)阳性细胞变化(n=5);Western blotting法检测骨形态发生蛋白4(BMP4)蛋白表达(n=5)。 结果 随着损伤时间的增加,I/R组、Noggin组与假手术组相比,小鼠神经功能评分升高(F组别=21.19, P<0.001; F时间=25.13, P<0.001),学习记忆能力均下降[(F组别=216.10, P<0.001; F时间=260.10, P<0.001)、(F组别=114.40, P<0.001; F时间=184.60, P<0.001)],脑梗死面积增加(F组别=2374, P<0.001; F时间=3 292, P<0.001),SOD活性降低(F组别=1 426, P<0.001; F时间=1 723, P<0.001),MDA含量升高(F组别=2.22, P<0.001; F时间=6.33, P<0.001),神经元数量减少(F组别=148.90, P<0.001; F时间=485.50, P<0.001),GFAP阳性细胞和BMP4蛋白表达量增加[(F组别=40.18, P<0.001; F时间=141.90, P<0.001)、(F组别=426.70, P<0.001; F时间=1 329, P<0.001)]。在各个相同时间点,与I/R组相比,Noggin各组小鼠神经功能评分降低(P<0.001),学习记忆能力提高(P<0.001),脑梗死面积减小(P<0.001),SOD活性升高及MDA含量降低(P<0.001),神经元数量增加及染色变浅(P<0.001),GFAP阳性细胞和BMP4 蛋白表达量降低(P<0.001)。 结论 Noggin蛋白对小鼠脑缺血再灌注损伤后学习、记忆能力提高与DG组织损伤修复有改善作用,其作用机制可能与阻断BMP4蛋白表达和抑制胶质细胞的反应性增生有关。

关键词: Noggin蛋白, 脑缺血再灌注损伤, 齿状回, 骨形态发生蛋白4, 胶质原纤维酸性蛋白, 小鼠, zw

Abstract: Objective To investigate the effect of injection of Noggin protein into the lateral ventricle on the learning and memory abilities and the structure of dentate gyrus after cerebral ischemia reperfusion injury(CIRI)in mice, in order to provide new ideas for the prevention and treatment of clinical ischemic cerebrovascular diseases. Methods A total of 240 health mice were randomly divided into the sham group(n=80), the ischemia-reperfusion group(I/R group, n=80), and the Noggin treatment group(Noggin group, n=80). Each group was subdivided into the 1days, 3 days, 7 days and 14 days subgroups. The learning and memory abilities were detected by Y-maze at 1 day before execution. Infarct size was detected by triphenyltetrazolium chloride staining(n=5). The colorimetric method was used to detect the superoxide dismutase(SOD)and malondialdehyde(MDA)activity after the behavior capability determined(n=5). Infarct size was detected by 2,3,5-triphenyl tetrazolium chloride staining(n=5). Glial fibrillary acidic protein(GFAP)immunopositive cells in the DG were observed under a light microscopy and quantitative analysis were performed by cell morphometric technique(n=5). The BMP4 protein expression was detected by Western blotting(n=5). Results Compared with the sham group, the neurological function score of mice in the I/R group and Noggin group increased(Fgroup=21.19, P<0.001; Ftime=25.13, P<0.001), learning and memory abilities declined(Fgroup=216.10, P<0.001; Ftime=260.10, P<0.001)(Fgroup=114.40, P<0.001; Ftime=184.60, P<0.001), and area of cerebral infarction increased(Fgroup=2 374, P<0.001; Ftime=3 292, P<0.001), SOD activity reduced(Fgroup=1 426, P<0.001; Ftime=1 723, P<0.001)and MDA content increased(Fgroup=2.22, P<0.001; Ftime=6.33, P<0.001), number of neurons reduced(Fgroup=148.90, P<0.001; Ftime=485.50, P<0.001), and expression of GFAP positive cells and BMP4 protein increased(Fgroup=40.18, P<0.001; Ftime=141.90, P<0.001)(Fgroup=426.70, P<0.001; Ftime=1 329, P<0.001)with the increase of injury time. At each same time point, compared with the I/R group, the Noggin groups neurological function score decreased(P<0.001), learning and memory abilities increased(P<0.001), and cerebral infarction area decreased(P<0.001), SOD activity increased and MDA content decreased(P<0.001), number of neurons increased and staining was lightened (P<0.001), expression of GFAP positive cells and BMP4 protein decreased(P<0.001). Conclusion Noggin can efficiently improve the learning and memory abilities and decrease the pathological lesion of DG after cerebral ischemia reperfusion injury in mice, and its mechanism may closely related to BMP4 protein expression and glial cells activation.

Key words: Noggin protein, Cerebral ischemia reperfusion injury, Dentate gyrus, Bone morphogenetic protein 4, Glial fibrillary acidic protein, Mouse, zw

中图分类号: 

  • R743.31
[1] Lu H, Liu X, Zhang N, et al. Neuroprotective effects of brain-derived neurotrophic factor and noggin-modified bone mesenchymal stem cells in focal cerebral ischemia in rats[J]. J Stroke Cerebrovasc Dis, 2016, 25(2): 410-418.
[2] Xu H, Liu W, Liu T, et al. Synergistic neuroprotective effects of Danshensu and hydroxysafflor yellow A on cerebral ischemia-reperfusion injury in rats[J]. Oncotarget, 2017, 8(70): 115434-115443.
[3] Wang C, Jiang J, Zhang X, et al. Inhibiting HMGB1 reduces cerebral ischemia reperfusion injury in diabetic mice[J]. Inflammation, 2016, 39(6): 1862-1870.
[4] Young JJ, Kjolby RAS, Wu G, et al. Noggin is required for first pharyngeal arch differentiation in the frog Xenopus tropicalis[J]. Dev Biol, 2017, 426(2): 245-254.
[5] Smith WC, Harland RM. Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos[J]. Cell, 1992, 70(5): 829-840.
[6] 李伟. 阿尔茨海默病的影响因素和生物标志物研究[D]. 上海:上海交通大学,2017.
[7] Díaz-Moreno M, Armenteros T, Gradari S, et al. Noggin rescues age-related stem cell loss in the brain of senescent mice with neurodegenerative pathology[J]. Proc Natl Acad Sci U S A, 2018, 115(45): 11625-11630.
[8] Zimmerman LB, De Jesús-Escobar JM, Harland RM, et al. The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4[J]. Cell, 1996, 86(4): 599-606.
[9] 王俊婕,张先虎,朱俊德,等. DAPT对脑缺血再灌注损伤小鼠学习记忆的影响以及Notch信号通路的调节作用[J].解剖学报,2018,49(2):151-157. WANG Jun Jie, ZHANG Xian Hu, ZHU Jun De, et al. Effects of DAPT on learning and memory abilities and the regulation of Notch signaling pathway in cerebral ischemia-reperfusion injury mice[J]. Acta Anatomica Sinica, 2018, 49(2): 151-157.
[10] Mikawa S, Sato K. Noggin expression in the adult rat brain[J]. Neuroscience, 2011, 184: 38-53. doi: 10.1016/j.neuroscience.2011.03.036.
[11] Zhu JD, Wang JJ, Ge G, et al. Effects of noggin-transfected neural stem cells on neural functional recovery and underlying mechanism in rats with cerebral ischemia reperfusion injury[J]. J Stroke Cerebrovasc Dis, 2017, 26(7): 1547-1559.
[12] Shin JA, Kim YA, Kim HW, et al. Iron released from reactive microglia by noggin improves myelin repair in the ischemic brain[J]. Neuropharmacology, 2018, 133: 202-215. doi: 10.1016/j.neuropharm.2018.01.038.
[13] Wang JJ, Zhu JD, Zhang XH, et al. Neuroprotective effect of Notch pathway inhibitor DAPT against focal cerebral ischemia/reperfusion 3 hours before model establishment[J]. Neural Regen Res, 2019, 14(3): 452-461.
[14] Li S, Bian L, Fu X, et al. Gastrodin pretreatment alleviates rat brain injury caused by cerebral ischemic-reperfusion[J]. Brain Res, 2019, 1712: 207-216. doi: 10.1016/j.brainres.2019.02.006.
[15] Su Q, Zhang H, Dang S, et al. Hippocampal protein kinase C gamma signaling mediates the impairment of spatial learning and memory in prenatally stressed offspring rats[J]. Neuroscience, 2019, 414: 186-199. doi: 10.1016/j.neuroscience.2019.06.030.
[16] Bak J, Pyeon HI, Seok JI, et al. Effect of rotation preference on spontaneous alternation behavior on Y maze and introduction of a new analytical method, entropy of spontaneous alternation[J]. Behav Brain Res, 2017, 320: 219-224. doi: 10.1016/j.bbr.2016.12.011.
[17] He F, Dai R, Zhou X, et al. Protective effect of 4-Methoxy benzyl alcohol on the neurovascular unit after cerebral ischemia reperfusion injury[J]. Biomed Pharmacother, 2019, 118: 109260. doi: 10.1016/j.biopha.2019.109260.
[18] Zhang B, Zhang HX, Shi ST, et al. Interleukin-11 treatment protected against cerebral ischemia/reperfusion injury[J]. Biomed Pharmacother, 2019, 115: 108816. doi: 10.1016/j.biopha.2019.108816.
[19] Meyers EA, Gobeske KT, Bond AM, et al. Increased bone morphogenetic protein signaling contributes to age-related declines in neurogenesis and cognition[J]. Neurobiol Aging, 2016, 38: 164-175. doi: 10.1016/j.neurobiolaging.2015.10.035.
[20] 朱俊德,余资江,康朝胜,等. noggin蛋白对D-半乳糖致衰老小鼠学习记忆及海马齿状回神经发生的影响[J].山东大学学报(医学版),2009,30(8):72-74. ZHU Jun De, YU Zi Jiang, KANG Chao Sheng, et al. Effect of intracerebroventricular injection of noggin on learning and memory and neurogenesis in hippocampal dentate gyrus of D-galactose induced aging mice[J]. Journal of Shandong University(Health Sciences), 2009, 30(8): 72-74.
[21] 吴嶛,孙颖,孙波,等. 辛醇对大鼠脑缺血再灌注后星形胶质细胞和胶质原纤维酸性蛋白的影响[J].中国医药,2019,14(5):706-709. WU Liao, SUN Ying, SUN Bo, et al. Effect of octanol on astrocytes and glial fibrillary acidic protein in rats after cerebral ischemia-reperfusion[J]. China Medicine, 2019, 14(5): 706-709.
[22] 欧阳波,陈勇军,唐小容,等. 小RAN干扰Trx1促进大鼠缺血再灌注损伤的星形胶质细胞凋亡、抑制其增殖及作用机制[J].中国老年学杂志,2019,39(9):192-195.
[23] Watanabe T, Nagai A, Sheikh AM, et al. A human neural stem cell line provides neuroprotection and improves neurological performance by early intervention of neuroinflammatory system[J]. Brain Res, 2016, 1631: 194-203. doi: 10.1016/j.brainres.2015.11.031.
[24] Hamada-Kanazawa M, Ogawa D, Takano M, et al. Sox6 suppression induces RA-dependent apoptosis mediated by BMP-4 expression during neuronal differentiation in P19 cells[J]. Mol Cell Biochem, 2016, 412(1-2): 49-57.
[25] 姜明宇,任明永,刘海春,等. BMP4和拮抗剂Noggin在显性脊柱裂胎鼠发病中的作用[J].中国妇幼保健杂志,2017,32(20):5122-5123.
[26] Janowska J, Gargas J, Ziemka-Nalecz M, et al. Directed glial differentiation and transdifferentiation for neural tissue regeneration[J]. Exp Neurol, 2018, 319: 112813. doi: 10.1016/j.expneurol.2018.08.010.
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