Wang Hu-Ping, Hu Yun-Yun, Lyu Yu-Jie, Meng Zhi-Peng, Chen Yi-Qin, Yang Jiao
Gansu University of Chinese Medicine Lanzhou 730000, China Gansu Key Laboratory of Traditional Chinese Medicine Excavation and Innovative Transformation Gansu Engineering Laboratory for New Products of Traditional Chinese Medicine (TCM) Lanzhou 730000, China.
Gansu University of Chinese Medicine Lanzhou 730000, China.
Zhongguo Zhong Yao Za Zhi. 2024 Jun;49(12):3348-3355. doi: 10.19540/j.cnki.cjcmm.20240216.101.
To explore the effect of Hei Xiaoyaosan on autophagy levels in Alzheimer's disease(AD). A total of 100 4-month-old Wistar male rats were randomly selected as a blank group, and 10 rats were taken as a sham operation group and injected with 1 μL of normal saline on both sides of the hippocampus. The other rats were injected with Aβ_(1-42) solution in the hippocampus to replicate the AD model. Fifty successfully modeled rats were selected and randomly divided into the model group, Aricatio group(0.5 mg·kg(-1)), and high, medium, and low dose groups of Hei Xiaoyaosan(15.30, 7.65, and 3.82 g·kg(-1)), with 10 rats in each group. The rats were administered by continuous gavage for 42 days. Morris water maze was used to detect the learning and memory ability of rats, and Hoechst staining was used to observe the pathological changes of nerve cells in the hippocampal CA1 region. The mRNA expression of p38MAPK, Beclin-1, and Bcl-2 was detected by RT-qPCR.Western blot was used to detect the expressions of p38MAPK, Beclin-1, Bcl-2, APP, and related proteins. The level of Aβ_(1-42) in the hippocampus was detected by ELISA, and the expression level of LC3Ⅱ in the hippocampus was detected by immunohistochemistry. The experimental results showed that compared with the blank group, the learning and memory ability of rats in the model group decreased(P<0.01). The nuclei in the CA1 region of the hippocampus showed blue bright spots and were closely arranged. The mRNA expression of p38MAPK was up-regulated, and the mRNA expressions of Beclin-1 and Bcl-2 were down-regulated(P<0.01). The expressions of p38MAPK, p-p38MAPK, and APP were increased, while those of Beclin-1, Bcl-2, and p-Bcl-2 were decreased(P<0.01). The expression of Aβ_(1-42) was increased(P<0.01). The relative expression of LC3Ⅱ decreased(P<0.01). Compared with the model group, the learning and memory ability of rats in each administration group was improved(P<0.05 or P<0.01). The nuclei in the CA1 region of the hippocampus gradually became clear, showing light blue. The mRNA expression of p38MAPK was down-regulated(P<0.01), and that of Beclin-1 and Bcl-2 was increased(P<0.05 or P<0.01). The expressions of p38MAPK, p-p38MAPK, and APP were down-regulated, while those of Beclin-1, Bcl-2, and p-Bcl-2 were up-regulated(P<0.05 or P<0.01). The expression of Aβ_(1-42) was decreased(P<0.01). The relative expression of LC3Ⅱ was increased(P<0.01). It can be concluded that Hei Xiaoyaosan can improve the cognitive ability of AD model rats, and its potential mechanism may be related to regulating the p38MAPK/Beclin-1/Bcl-2 signaling pathway, increasing the level of autophagy, and reducing the accumulation of Aβ_(1-42).
探讨黑逍遥散对阿尔茨海默病(AD)自噬水平的影响。选取100只4月龄雄性Wistar大鼠,随机选取10只作为空白组,另选10只作为假手术组,在海马双侧注射1 μL生理盐水。其余大鼠海马注射Aβ₁₋₄₂溶液复制AD模型。选取50只造模成功的大鼠,随机分为模型组、阿立哌唑组(0.5 mg·kg⁻¹)、黑逍遥散高、中、低剂量组(15.30、7.65、3.82 g·kg⁻¹),每组10只。大鼠连续灌胃给药42天,采用Morris水迷宫检测大鼠学习记忆能力,采用Hoechst染色观察海马CA1区神经细胞病理变化。采用RT-qPCR检测p38MAPK、Beclin-1、Bcl-2的mRNA表达。采用Western blot检测p38MAPK、Beclin-1、Bcl-2、APP及相关蛋白表达。采用ELISA检测海马Aβ₁₋₄₂水平,采用免疫组化检测海马LC3Ⅱ表达水平。实验结果显示,与空白组比较,模型组大鼠学习记忆能力下降(P<0.01),海马CA1区细胞核呈蓝色亮点且排列紧密,p38MAPK的mRNA表达上调,Beclin-1、Bcl-2的mRNA表达下调(P<0.01);p38MAPK、p-p38MAPK、APP表达增加,Beclin-1、Bcl-2、p-Bcl-2表达降低(P<0.01);Aβ₁₋₄₂表达增加(P<0.01);LC3Ⅱ相对表达降低(P<0.01)。与模型组比较,各给药组大鼠学习记忆能力均有改善(P<0.05或P<0.01),海马CA1区细胞核逐渐清晰,呈浅蓝色;p38MAPK的mRNA表达下调(P<0.01),Beclin-1、Bcl-2的mRNA表达上调(P<0.05或P<0.01);p38MAPK、p-p38MAPK、APP表达下调,Beclin-1、Bcl-2、p-Bcl-2表达上调(P<0.05或P<0.01);Aβ₁₋₄₂表达降低(P<0.01);LC3Ⅱ相对表达增加(P<0.01)。结论:黑逍遥散可改善AD模型大鼠认知能力,其潜在机制可能与调控p38MAPK/Beclin-1/Bcl-2信号通路、提高自噬水平、减少Aβ₁₋₄₂蓄积有关。