基础医学与临床 ›› 2024, Vol. 44 ›› Issue (8): 1126-1132.doi: 10.16352/j.issn.1001-6325.2024.08.1126

• 研究论文 • 上一篇    下一篇

青蒿琥酯调节cGAS-STING信号通路对抑郁症模型小鼠神经炎性反应的影响

高超1*, 张润菡1, 王伟2, 赵曼婷1, 焦艳3, 李喆3   

  1. 沧州市中心医院 1.儿童保健科;2.急诊医学部,河北 沧州 061000;
    3.沧州医学高等专科学校 药学系,河北 沧州 061000
  • 收稿日期:2024-01-23 修回日期:2024-04-02 出版日期:2024-08-05 发布日期:2024-07-24
  • 通讯作者: *goub2004404@163.com
  • 基金资助:
    沧州市重点研发计划指导项目(222106097)

Effect of artesunate on neuroinflammation in depressed mouse model by regulating cGAS-STING signaling pathway

GAO Chao1*, ZHANG Runhan1, WANG Wei2, ZHAO Manting1, JIAO Yan3, LI Zhe3   

  1. 1. Department of Child Health; 2. Department of Emergency Medicine, Cangzhou Central Hospital, Cangzhou 061000;
    3. Department of Pharmacy, Cangzhou Medical College, Cangzhou 061000, China
  • Received:2024-01-23 Revised:2024-04-02 Online:2024-08-05 Published:2024-07-24
  • Contact: *goub2004404@163.com

摘要: 目的 探讨青蒿琥酯(ART)调节环磷酸鸟苷-腺苷酸合成酶(cGAS)-干扰素基因刺激因子(STING)通路对抑郁症小鼠神经炎性反应的影响。方法 小鼠分为模型组、对照组、ART低剂量组、ART高剂量组、氟西汀组、ART高剂量+ RocA(cGAS-STING通路激活剂)组。糖水消耗实验、强迫游泳实验评估小鼠的抑郁行为;HE染色检测海马组织病理变化;ELISA检测白细胞介素(IL)-6、肿瘤坏死因子-α(TNF-α)、五羟色胺(5-HT)、多巴胺(DA)水平;TUNEL染色检测神经元凋亡;Western blot检测Bcl-2相关X蛋白(Bax)、p53、cGAS、STING蛋白。结果 与对照组相比,模型组小鼠表现出神经元性脓疱变性,糖水消耗率、5-HT、DA水平降低,强迫游泳静止时间延长,IL-6、TNF-α水平、神经元凋亡率及Bax、p53、cGAS、STING蛋白表达升高(P<0.05);与模型组相比,ART低剂量组、ART高剂量组、氟西汀组小鼠海马神经元损伤有所缓解,糖水消耗率、5-HT、DA水平升高,强迫游泳静止时间缩短,IL-6、TNF-α水平、神经元凋亡率及Bax、p53、cGAS、STING蛋白表达降低(P<0.05);RocA逆转了高剂量ART对小鼠抑郁症的改善作用。结论 ART抑制抑郁症小鼠神经炎性反应及神经元凋亡,上调胺类神经递质水平的机制可能与阻断cGAS-STING通路有关。

关键词: 青蒿琥酯, 环磷酸鸟苷-腺苷酸合成酶-干扰素基因刺激因子通路, 抑郁症, 炎性反应, 凋亡

Abstract: Objective To investigate the effect of artesunate (ART) on neuroinflammation in depressed mice by regulating the cyclic guanosine monophosphate-adenosine monophosphate synthase (cGAS)-stimulator of interferon gene (STING) pathway. Methods Mice were divided into model group, control group, low-dose ART group, high-dose ART group, fluoxetine group, and high-dose ART+RocA (cGAS-STING pathway activator) group. Sugar solution consumption experiment and forced swimming experiment were applied to evaluate the depressive behavior of mice; HE staining microscopy was applied to detect pathological changes in hippocampal tissue; ELISA method was applied to detect the level of interleukin-6(IL-6), tumor necrosis factor-α(TNF-α), serotonin(5-HT) and dopamine (DA); TUNEL staining microscopy was applied to detect neuronal apoptosis; Western blot was applied to detect Bcl-2 associated X protein (Bax), p53, cGAS, and STING proteins. Results Compared to the control group, the mice in the model group exhibited neuronal pustule degeneration, the sugar water consumption rate, level of 5-HT and DA decreased, the rest time of forced swimming increased. The level of IL-6 and TNF-α, neuronal apoptosis rate, expression of Bax, p53, cGAS, and STING proteins all elevated (P<0.05); Compared with model group, the damage to hippocampus neurons in the ART low-dose group, ART high-dose group and fluoxetine group neuronal pustular degeneration was alleviated, while sugar water consumption rate, 5-HT, and DA levels increased, the rest time of forced swimming reduced, the level of IL-6 and TNF-α, neuronal apoptosis rate and the expression of Bax, p53, cGAS, and STING proteins reduced (P<0.05); RocA reversed the improvement effect of high-dose ART on depression in mice. Conclusions ART inhibits neuroinflammation and neuronal apoptosis in depressed mice, and up-regulates amine neurotransmitters expression. The mechanism is potentially related to the blocking of cGAS-STING pathway.

Key words: artesunate, cyclic guanosine monophosphate-adenosine monophosphate synthase- stimulator of interferon gene pathway, depression, inflammation, apoptosis

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