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中国精品科技期刊2020
史云静,李玉霞. 茯苓多糖通过NF-κB和NLRP3信号通路调节脂多糖引起的焦虑和抑郁样行为[J]. 食品工业科技,2023,44(12):371−377. doi: 10.13386/j.issn1002-0306.2022080276.
引用本文: 史云静,李玉霞. 茯苓多糖通过NF-κB和NLRP3信号通路调节脂多糖引起的焦虑和抑郁样行为[J]. 食品工业科技,2023,44(12):371−377. doi: 10.13386/j.issn1002-0306.2022080276.
SHI Yunjing, LI Yuxia. Poria cocos Polysaccharides Regulate Anxiety and Depression-like Behaviors Induced by Lipopolysaccharide through NF-κB and NLRP3 Signaling Pathways[J]. Science and Technology of Food Industry, 2023, 44(12): 371−377. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080276.
Citation: SHI Yunjing, LI Yuxia. Poria cocos Polysaccharides Regulate Anxiety and Depression-like Behaviors Induced by Lipopolysaccharide through NF-κB and NLRP3 Signaling Pathways[J]. Science and Technology of Food Industry, 2023, 44(12): 371−377. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080276.

茯苓多糖通过NF-κB和NLRP3信号通路调节脂多糖引起的焦虑和抑郁样行为

Poria cocos Polysaccharides Regulate Anxiety and Depression-like Behaviors Induced by Lipopolysaccharide through NF-κB and NLRP3 Signaling Pathways

  • 摘要: 目的:探讨茯苓多糖(Poria cocos polysaccharide,PPS)对脂多糖(LPS)引起的焦虑和抑郁样行为的影响,并分析其机制。方法:BV-2细胞分成对照组、LPS组、LPS+氟西汀组、LPS+PPS(PPS分别为4、8、16 μmol/L),处理24 h,二氯二氢荧光素二氢乙酸酯(DCFH-DA)荧光探针检测细胞内活性氧(ROS)水平,Griess法检测培养上清液NO水平,酶联免疫吸附试验(ELISA)检测培养上清液中TNF-α、IL-1β水平,Western blot实验检测CD206、CD16/32、NF-κB p65水平。动物实验将小鼠分为对照组、模型组、LPS+氟西汀组、LPS+PPS低剂量组(20 mg/kg)、LPS+PPS高剂量组(80 mg/kg),每组10只,测试抑郁样行为,检测海马组织TNF-α、IL-1β、IL-18的浓度,分析海马组织CD206、CD16/32、NF-κB p65、NLRP3、ASC、Cleaved caspase-1蛋白水平。结果:与LPS组比较,4、8、16 μmol/L PPS能极显著降低ROS荧光相对强度(P<0.01),下调NO、TNF-α、IL-1β水平,降低CD16/32、NF-κB p65水平,增加CD206水平(P<0.05);与模型组比较,LPS+PPS低剂量组、LPS+PPS高剂量组蔗糖偏爱率极显著增加(P<0.01),旷场穿越次数、修饰次数极显著上调(P<0.01),悬尾不动时间、强迫游泳不动时间极显著降低(P<0.01);与模型组比较,LPS+PPS低剂量组、LPS+PPS高剂量组IL-1β、IL-18、TNF-α水平极显著降低(P<0.01),CD16/32、NF-κB p65水平显著下调(P<0.05),CD206显著上调(P<0.05),NLRP3、ASC、Cleaved caspase-1水平极显著降低(P<0.01)。结论:茯苓多糖能通过抑制NF-κB和NLRP3信号通路减轻LPS诱导的焦虑和抑郁样行为。

     

    Abstract: Objective: To explore the effect of Poria cocos polysaccharides (Poria cocos polysaccharide, PPS) on anxiety and depression-like behaviors induced by lipopolysaccharide (LPS) and analyze its mechanism. Methods: BV-2 cells were divided into control group, LPS group, LPS+fluoxetine group and LPS+PPS (PPS of 4, 8, 16 μmol/L, respectively). After 24 h treatment, the level of intracellular reactive oxygen species (ROS) was detected by dichlorodihydrofluorescein dihydroacetate (DCFH-DA) fluorescence probe, the level of NO in culture supernatant was detected by griess method, and the levels of TNF-α and IL-1β in cell supernatant were detected by enzyme linked immunosorbent assay (ELISA). The levels of CD206, CD16/32 and NF-κB p65 were detected by western blot. In animal experiment, mice were divided into control group, model group, LPS+fluoxetine group, LPS+PPS low dose group (20 mg/kg) and LPS+PPS high dose group (80 mg/kg). Depression-like behavior test was performed, and the concentration of TNF-α, IL-1β and IL-18 in hippocampus was detected. The protein levels of CD206, CD16/32, NF-κB p65, NLRP3, ASC and Cleaved caspase-1 in hippocampus were analyzed. Results: Compared with LPS group, 4,8,16 μmol/L PPS significantly decreased the relative fluorescence intensity of ROS (P<0.01), decreased the levels of NO, TNF-α and IL-1β (P<0.01), decreased the levels of CD16/32 and NF-κB p65 (P<0.05), and increased the level of CD206 (P<0.05). Compared with the model group, the preference rate, crossing times and modification times in LPS+PPS low dose group and high dose LPS+PPS group significantly increased (P<0.01), while the tail suspension time and forced swimming immobility time significantly decreased (P<0.01). Compared with the model group, the levels of IL-1β, IL-18 and TNF-α in LPS+PPS low dose group and LPS+PPS high dose group significantly decreased (P<0.01), CD16/32 and NF-κB p65 level were significantly down-regulated, CD206 was significantly up-regulated, and the levels of NLRP3, ASC and Cleaved caspase-1 significantly decreased. Conclusion: Poria cocos polysaccharide can alleviate LPS-induced anxiety and depression-like behavior by inhibiting NF-κB and NLRP3 signal pathways.

     

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