丰富环境通过抑制NOD样受体蛋白3炎性小体活化缓解脂多糖小鼠的认知障碍

牛磊 罗诗诗 李威 罗丹 刘志文 曹文宇 徐杨 刘政海

解剖学报 ›› 2020, Vol. 51 ›› Issue (2) : 172-177.

PDF(5490 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(5490 KB)
解剖学报 ›› 2020, Vol. 51 ›› Issue (2) : 172-177. DOI: 10.16098/j.issn.0529-1356.2020.02.004
神经生物学

丰富环境通过抑制NOD样受体蛋白3炎性小体活化缓解脂多糖小鼠的认知障碍

  • 牛磊1 罗诗诗1 李威1 罗丹2 刘志文3 曹文宇1 徐杨4* 刘政海1*
作者信息 +

Environmental enrichment ameliorates lipopolysaccharide-induced cognitive impairment by  inhibiting NOD-like recepter protein 3 in fla mmasome activation in mice

  • NIU Lei1  LUO Shi-shi1  Li Wei1  Luo Dan2  LIU Zhi-wen CAO Wen-yu1  XU Yang4*  LIU Zheng-hai1*
Author information +
文章历史 +

摘要

目的 探讨丰富环境(EE)对脂多糖(LPS)诱导的小鼠认知功能障碍的影响及其可能机制。 方法 36只3周龄昆明小鼠进行8周的EE刺激或者标准环境(SE)饲养后分为以下3组:标准环境+生理盐水(SE+NS)组、标准环境+脂多糖(SE+LPS)组及丰富环境+脂多糖(EE+LPS)组。采用旷场实验检测小鼠的活动度;新旧事物识别实验检测小鼠认知功能;免疫组织化学方法检测小胶质细胞标记物离子钙接头蛋白分子1(IBA1)表达;Western blotting方法检测海马组织小胶质细胞激活标记物CD68及NOD样受体蛋白3(NOD-like receptor protein3, NLRP3)炎性小体相关蛋白的表达。 结果 旷场实验中,各组小鼠穿越的总格数无明显差异。在新旧事物识别实验中,与SE+NS组相比,SE+LPS组新事物辨别指数明显下降(P<0.05);与SE+NS组相比,小胶质细胞标记物IBA1表达上调(P<0.05);SE+LPS组海马CD68及NLRP3炎性小体相关蛋白的表达明显上调(P<0.05);而丰富环境可以逆转上述改变(P<0.05)。 结论 丰富环境可缓解脂多糖诱导的认知功能损伤,其机制可能与抑制海马小胶质细胞激活及NLRP3炎性小体的产生有关。

Abstract

Objective  To investigate the effect of environmental enrichment (EE) on lipopolysaccharide (LPS) induced cognitive dysfunction in mice.  Methods A total of thirty six 3 weeks old Kunming mice experienced 8 weeks of EE or standard environment (SE) feeding. After 8 weeks, they were divided into three groups: standard environment+normal saline (SE+NS) group, standard environment+lipopolysaccharide (SE+LPS) group, environmental enrichment+lipopolysaccharide (EE+LPS) group. The open field test was used to measure the locomotive of mice, and the cognitive function was determined by novelty object recognition test. The expression of microglial marker ionized calcium binding adaptor molecule-1 (IBA-1) in hippocampus was determined by immunohistochemical staining. The expression of microglial activation marker CD68 and NOD-like receptor protein 3 (NLRP3) inflammasome related protein in the hippocampus was detected by Western blotting.  Results  In the open field test, there was no difference in the activity among the three groups. Compared with the SE+NS group, SE+LPS group showed decreased discrimination ratio in novelty object recognition task, with remarkably up-regulated expression of CD68 in the hippocampus (P<0.01). In addition, SE+LPS group exhibited significantly enhanced expression of NLRP3, apoptosis associated speck-like protein (ASC), Caspase-1 and interleukin-1β(IL-1β) in the hippocampus compared with SE+NS group (P<0.05). Compared with the SE+LPS group, EE+LPS group showed enhanced discrimination ratio in the object recognition task, with down-regulated expression of CD68, NLRP3, ASC, Caspase-1, IL-1β and IL-18 in the hippocampus (P<0.01).   Conclusion  Environmental enrichment can alleviate LPS induced cognitive dysfunction, which might be attributed to the inhibiting of microglia and NLRP3 activation in the hippocampus.

关键词

炎性小体 / 脂多糖 / 认知功能障碍 / 小胶质细胞 / 海马 / 免疫印迹法 / 小鼠

Key words

Inflammasome / Lipopolysaccharide / Cognitive dysfunction / Microglia / Hippocampus / Western blotting / Mouse

引用本文

导出引用
牛磊 罗诗诗 李威 罗丹 刘志文 曹文宇 徐杨 刘政海. 丰富环境通过抑制NOD样受体蛋白3炎性小体活化缓解脂多糖小鼠的认知障碍[J]. 解剖学报. 2020, 51(2): 172-177 https://doi.org/10.16098/j.issn.0529-1356.2020.02.004
NIU Lei LUO Shi-shi Li Wei Luo Dan LIU Zhi-wen CAO Wen-yu XU Yang LIU Zheng-hai. Environmental enrichment ameliorates lipopolysaccharide-induced cognitive impairment by  inhibiting NOD-like recepter protein 3 in fla mmasome activation in mice[J]. Acta Anatomica Sinica. 2020, 51(2): 172-177 https://doi.org/10.16098/j.issn.0529-1356.2020.02.004
中图分类号: R749.93    R322.81    

参考文献

[1] Jansen WJ, Wilson RS, Visser PJ, et al. Age and the association of dementia-related pathology with trajectories of cognitive decline[J]. Neurobiol Aging, 2018,61:138-145.
[2] Tang YJ, Ouyang W. Inflammation-relevant mechanisms for postoperative cognitive dysfunction and the preventive strategy [J]. Journal of Central South University (Medical Sciences), 2017,42(11):1321-1326.(in Chinese)
唐玉洁,欧阳文.术后认知功能障碍炎症相关机制及其防治 [J]. 中南大学学报(医学版), 2017,42(11):1321-1326.
[3] Valero J, Bernardino L, Cardoso FL, et al. Impact of neuroinflammation on hippocampal neurogenesis: relevance to aging and Alzheimer’s disease[J]. J Alzheimers Dis, 2017, 60 (s1): S161-S168.
[4] Maier SF, Watkins LR. Cytokines for psychologists: implications of bidirectional immunetobrain communication for understanding behavior, mood, and cognition[J]. Psychol Rev, 1998, 105 (1): 83-107.
[5] Fu Q, Wu J, Zhou XY, et al. NLRP3/Caspase-1 pathway-induced pyroptosis mediated cognitive deficits in a mouse model of sepsis-associated encephalopathy[J]. Inflammation, 2019,42(1):306-318.
[6] Miura K, Yang L, van Rooijen N, et al. Toll-like receptor 2 and palmitic acid cooperatively contribute to the development of nonalcoholic steatohepatitis through inflammasome activation in mice[J]. Hepatology, 2013,57(2):577-589.
[7] Zhou R, Yazdi AS, Menu P, et al. A role for mitochondria in NLRP3 inflammasome activation[J]. Nature, 2011,469(7329):221-225.
[8] Marmol F, Sanchez J, Torres MN, et al. Environmental enrichment in the absence of wheel running produces beneficial behavioural and anti-oxidative effects in rats[J]. Behav Processes, 2017,144:66-71.
[9] Kokiko-Cochran ON, Godbout JP. The inflammatory continuum of traumatic brain injury and Alzheimer’s disease[J]. Front Immunol, 2018,9:672.
[10] Li N, Xu H, Ou Y, et al. LPS-induced CXCR7 expression promotes gastric cancer proliferation and migration via the TLR4/MD-2 pathway[J]. Diagn Pathol, 2019,14(1):3.
[11] Frank MG, Baratta MV, Sprunger DB, et al. Microglia serve as a neuroimmune substrate for stress-induced potentiation of CNS pro-inflammatory cytokine responses[J]. Brain Behav Immun, 2007,21(1):47-59.
[12] Ji MH, Tang H, Luo D, et al. Environmental conditions differentially affect neurobehavioral outcomes in a mouse model of sepsis-associated encephalopathy[J]. Oncotarget, 2017, 8(47): 82376-82389.
[13] Xu H, Gelyana E, Rajsombath M, et al. Environmental enrichment potently prevents microglia-mediated neuroinflammation by human amyloid beta-protein oligomers[J]. J Neurosci, 2016,36(35):9041-9056.
[14] Chen S, Yao L, Huang P, et al. Blockade of the NLRP3/Caspase-1 axis ameliorates airway neutrophilic inflammation in a toluene diisocyanate-induced murine asthma model[J]. Toxicol Sci, 2019,170(2):462-475.
[15] Patil T, More Ⅴ, Rane D, et al. Pro-inflammatory cytokine interleukin-1beta (IL-1beta) controls leishmania infection[J]. Cytokine, 2018,112:27-31.
[16] Fu Q, Wu J, Zhou XY, et al. NLRP3/Caspase-1 pathway-induced pyroptosis mediated cognitive deficits in a mouse model of  sepsis-associated encephalopathy[J]. Inflammation, 2018,42(1):306-318.
[17] Li Q, Chen L, Liu X, et al. Pterostilbene inhibits amyloid-beta-induced neuroinflammation in a microglia cell line by inactivating the NLRP3/Caspase-1 inflammasome pathway[J]. J Cell Biochem, 2018,119(8):7053-7062.
[18] Costa DA, Cracchiolo JR, Bachstetter AD, et al. Enrichment improves cognition in AD mice by amyloid-related and unrelated mechanisms[J]. Neurobiol Aging, 2007,28(6):831-844.
[19] Jurgens HA, Johnson RW. Environmental enrichment attenuates hippocampal neuroinflammation and improves cognitive function during influenza infection[J]. Brain Behav Immun, 2012, 26(6): 1006-1016.
[20] Arendash GW, Garcia MF, Costa DA, et al. Environmental enrichment improves cognition in aged Alzheimer’s transgenic mice despite stable beta-amyloid deposition[J].Neuroreport, 2004, 15(11): 1751-1754.

基金

湖南省自然科学基金青年基金项目;湖南省自然科学基金青年基金项目;湖南省自然科学基金省市联合基金项目;湖南省教育厅优秀青年项目;大学生研究性学习和创新实验设计计划项目

PDF(5490 KB)

Accesses

Citation

Detail

段落导航
相关文章

/