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基于BDNF/TrkB/CREB通路的参灵开心颗粒抗抑郁机制

[Antidepressant mechanism of Shenling Kaixin Granules based on BDNF/TrkB/CREB pathway].

作者信息

Xu Yan, Liu Dong-Guang, Ning Ting-Bo, Zhu Jian-Guo, Yao Ru, Meng Xue, Yao Jing-Chun, Zhao Wen-Xue

机构信息

New Drug Pharmacological Center of Lunan Pharmaceutical Group Corporation Linyi 276006, China State Key Laboratory of Generic Manufacture Technology of Chinese Traditional Medicine Linyi 276006, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2023 Apr;48(8):2184-2192. doi: 10.19540/j.cnki.cjcmm.20221114.402.

Abstract

To investigate the antidepressant mechanism of Shenling Kaixin Granules(SLKX) in treating chronic unpredictable mild stress(CUMS) model rats. Ninety male SD rats were randomly divided into control group, model group, Shugan Jieyu Capsules(110 mg·kg(-1)) group and SLKX low-(90 mg·kg(-1)), medium-(180 mg·kg(-1)), and high-dose(360 mg·kg(-1)) groups. Depression rat model was replicated by CUMS method. After treatment, the behavioral changes of rats were evaluated by sugar preference, open field, elevated cross maze and forced swimming experiments. The contents of interleukin 1 beta(IL-1β), tumor necrosis factor α(TNF-α), brain-derived neurotrophic factor(BDNF) and 5-hydroxytryptamine(5-HT) in serum were determined by enzyme linked immunosorbent assay(ELISA), and the activities of superoxide dismutase(SOD) and catalase(CAT) in hippocampal CA1 region were also detected. Pathological changes in hippocampal CA1 region were detected by hematoxylin-eosin(HE) staining, and Western blot was used to determine the expression of nerve growth factor(NGF), BDNF, phospho-tyrosine kinase receptor(p-TrkB)/TrkB, phospho-cAMP-response element binding protein(p-CREB)/CREB, nuclear factor E2 related factor 2(Nrf2), heme oxygenase 1(HO-1), B-cell lymphoma-2(Bcl-2)/Bcl-2 associated X protein(Bax) and caspase-3 in hippocampal CA1 region. RESULTS:: showed that compared with the control group, the model group had decreased sugar preference, reduced number of entries and time spent in the center of open field and shortened total distance of movement, reduced number of entries and proportion of time spent in open arm, and increased number and time of immobility in forced swimming experiment. Additionally, the serum contents of IL-1β and TNF-α and the expression of caspase-3 were higher, while the contents of BDNF and 5-HT, the activities of SOD and CAT in hippocampal CA1 region, the expressions of NGF, BDNF, p-TrkB/TrkB, p-CREB/CREB, HO-1 and Bcl-2/Bax, and the Nrf2 nuclear translocation were lower in model group than in control group. Compared with the conditions in model group, the sugar preference, the number of entries and time spent in the center of open, total distance of movement, and the number of entries and proportion of time spent in open arm in treatment groups were increased while the number and time of immobility in forced swimming experiment were decreased; the serum contents of IL-1β and TNF-α and the expression of caspase-3 were down regulated, while the contents of BDNF and 5-HT, the activities of SOD and CAT in hippocampal CA1 region, the expressions of NGF, BDNF, p-TrkB/TrkB, p-CREB/CREB, HO-1, Bcl-2/Bax, and Nrf2 nuclear translocation were enhanced. In conclusion, SLKX might regulate the Nrf2 nucleus translocation by activating BDNF/TrkB/CREB pathway, lower oxidative stress damage in hippocampus, inhibit caspase-3 activity, and reduce apoptosis of hippocampal nerve cells, thereby playing an antidepressant role.

摘要

探讨参灵开心颗粒(SLKX)对慢性不可预测性轻度应激(CUMS)模型大鼠的抗抑郁作用机制。将90只雄性SD大鼠随机分为对照组、模型组、疏肝解郁胶囊(110 mg·kg⁻¹)组及SLKX低剂量(90 mg·kg⁻¹)组、中剂量(180 mg·kg⁻¹)组、高剂量(360 mg·kg⁻¹)组。采用CUMS法复制抑郁大鼠模型。给药后,通过糖水偏好、旷场、高架十字迷宫和强迫游泳实验评价大鼠行为学变化。采用酶联免疫吸附测定(ELISA)法检测血清白细胞介素1β(IL-1β)、肿瘤坏死因子α(TNF-α)、脑源性神经营养因子(BDNF)和5-羟色胺(5-HT)含量,同时检测海马CA1区超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。采用苏木精-伊红(HE)染色检测海马CA1区病理变化,采用蛋白质免疫印迹法检测海马CA1区神经生长因子(NGF)、BDNF、磷酸化酪氨酸激酶受体(p-TrkB)/TrkB、磷酸化环磷腺苷反应元件结合蛋白(p-CREB)/CREB、核因子E2相关因子2(Nrf2)、血红素加氧酶1(HO-1)、B细胞淋巴瘤-2(Bcl-2)/Bcl-2相关X蛋白(Bax)及半胱天冬酶-3(caspase-3)的表达。结果显示,与对照组相比,模型组大鼠糖水偏好降低,旷场实验中进入中央格的次数和停留时间减少,总运动距离缩短,高架十字迷宫实验中进入开放臂的次数和在开放臂停留时间的比例降低,强迫游泳实验中不动时间和不动次数增加。此外,模型组大鼠血清IL-1β、TNF-α含量及caspase-3表达升高,而BDNF、5-HT含量,海马CA1区SOD、CAT活性,NGF、BDNF、p-TrkB/TrkB、p-CREB/CREB、HO-1、Bcl-2/Bax表达及Nrf2核转位均低于对照组。与模型组相比,各治疗组大鼠糖水偏好、旷场实验中进入中央格的次数和停留时间、总运动距离、高架十字迷宫实验中进入开放臂的次数和在开放臂停留时间的比例增加,强迫游泳实验中不动时间和不动次数减少;血清IL-1β、TNF-α含量及caspase-3表达下调,BDNF、5-HT含量,海马CA1区SOD、CAT活性,NGF、BDNF、p-TrkB/TrkB、p-CREB/CREB、HO-1、Bcl-2/Bax表达及Nrf2核转位增强。综上所述,SLKX可能通过激活BDNF/TrkB/CREB通路调节Nrf2核转位,降低海马氧化应激损伤,抑制caspase-3活性,减少海马神经细胞凋亡,从而发挥抗抑郁作用。

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