张欣, 龙倩, 楚世峰, 王莎莎, 韦桂宁, 李冬梅, 陈乃宏. 拟黑多刺蚁石油醚部位对抑郁大鼠神经炎症反应的抑制作用J. 药学学报, 2018,53(7): 1042-1047. doi: 10.16438/j.0513-4870.2017-1010
引用本文: 张欣, 龙倩, 楚世峰, 王莎莎, 韦桂宁, 李冬梅, 陈乃宏. 拟黑多刺蚁石油醚部位对抑郁大鼠神经炎症反应的抑制作用J. 药学学报, 2018,53(7): 1042-1047. doi: 10.16438/j.0513-4870.2017-1010
ZHANG Xin, LONG Qian, CHU Shi-feng, WANG Sha-sha, WEI Gui-ning, LI Dong-mei, CHEN Nai-hong. Inhibitory effect of extratable petroleum ether of Polyrhachis vicina Roger on neuroinflammatory response in depressed ratsJ. Acta Pharmaceutica Sinica, 2018,53(7): 1042-1047. doi: 10.16438/j.0513-4870.2017-1010
Citation: ZHANG Xin, LONG Qian, CHU Shi-feng, WANG Sha-sha, WEI Gui-ning, LI Dong-mei, CHEN Nai-hong. Inhibitory effect of extratable petroleum ether of Polyrhachis vicina Roger on neuroinflammatory response in depressed ratsJ. Acta Pharmaceutica Sinica, 2018,53(7): 1042-1047. doi: 10.16438/j.0513-4870.2017-1010

拟黑多刺蚁石油醚部位对抑郁大鼠神经炎症反应的抑制作用

Inhibitory effect of extratable petroleum ether of Polyrhachis vicina Roger on neuroinflammatory response in depressed rats

  • 摘要: 拟黑多刺蚁石油醚部位(extratable petroleum ether of Polyrhachis vicina Roger,EPPR)主要成分为十八碳烯不饱和脂肪酸,有研究表明,N-3多不饱和脂肪酸可以改善神经炎症,降低氧化应激,保护神经元。为探究EPPR对抑郁大鼠炎性反应的影响,本实验运用慢性不可预见性温和刺激(chronic unpredictable mild stress,CUMS)建立大鼠抑郁模型,采用糖水偏好(sucrose preference test)、强迫游泳(forced swimming test)检测大鼠行为,免疫荧光观察EPPR对抑郁大鼠前额皮层小胶质细胞、星形胶质细胞激活的影响,运用实时荧光定量PCR (Quantitative Real-time PCR,qRT-PCR)对大鼠前额皮层炎症因子RNA水平进行检测,免疫印迹检测核因子κB (nuclear factor-κB,NF-κB)通路蛋白表达。结果表明,EPPR可以显著改善大鼠抑郁样行为,抑制抑郁大鼠小胶质细胞及星形胶质细胞激活,抑制NF-κB信号通路,下调前额皮层炎症因子白细胞介素1β(interleukin-1β,IL-1β)和肿瘤坏死因子α(tumor necrosis factor α,TNF-α),以及吲哚胺2,3-双加氧酶(indoleamine 2,3-dioxygenase,IDO)基因表达水平。以上结果提示,EPPR改善抑郁症状与改善脑内炎症反应相关。

     

    Abstract: The main ingredient of extractable petroleum ether of Polyrhachis vicina Roger (EPPR) is octadecene unsaturated fatty acids. Mounting evidence supports that N-3 polyunsaturated fatty acids can attenuate neuroinflammation, reduce oxidative stress, then protect neurons. In order to explore the effect of EPPR on the inflammatory response of depressed rats, the model of depression was established by chronic unpredictable mild stress (CUMS). Sucrose preference test, forced swimming test were employed to investigate the anti-depressive effect of EPPR in rat. The activation of glial cells and astrocytes in the prefrontal cortex of depressed rats was observed by immunofluorescence. The levels of inflammatory factors were measured by Quantitative Real-time PCR. NF-κB was detected by immunoblotting. EPPR could significantly improve the depressive behavior of rats, decrease NF-κB translocation to the compartment of nucleus, down-regulate the pro-inflammatory cytokines IL-1β, TNF-α and indoleamine 2,3-dioxygenase (IDO) gene expression levels, inhibit the activation of microglia and astrocytes in depressed rats. These results suggest that EPPR could notably ameliorate inflammation induced by chronic stress, and the protective effect might be linked to the regulation of NF-κB p65.

     

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