基于血清外泌体的芎麻药对对血管性认知障碍大鼠胆碱能突触信号通路的干预研究

    Exploration of Intervention in Xiongma Herb Pair on Cholinergic Synaptic Signal Pathway in Vascular Cognitive Impairment Rats Based on Serum Exosomes

    • 摘要:
      目的 探究芎麻药对对血管性认知障碍(vascular cognitive impairment,VCI)大鼠脑和血清中外泌体表达的影响及其干预作用机制。
      方法 选用SPF级8~10周龄雄性Wistar大鼠50只,利用双侧颈总动脉(2-vessel occlusion,2-VO)法复制大鼠VCI模型,依据脑血流量结果将2-VO组大鼠随机分为VCI模型组,盐酸多奈哌齐阳性药组,芎麻药对高、低剂量组,假手术组。于模型建立后3 d开始灌胃给药,每天2次。观察芎麻药对对大鼠脑血流量的干预作用;通过Morris水迷宫试验检验大鼠的学习记忆能力,社交试验考察大鼠社交能力;检测乙酰胆碱(acetylcholine,Ach)含量与乙酰胆碱酯酶(acetylcholinesterase,AChE)活性以及脑内、血清、血清外泌体中的AKT1、AChE和PKCβ1的表达水平及含量。
      结果 Morris水迷宫试验和社交试验结果显示,模型组大鼠从28 d开始到56 d持续发生学习记忆障碍以及社交障碍,给药组能够有效改善VCI大鼠学习记忆能力和社交行为障碍。各组大鼠脑内ACh含量与AChE活力值测试结果表明,与模型组相比,芎麻高剂量组及阳性药组大鼠脑内ACh含量显著升高,各给药组AChE活力值均显著降低。各组大鼠脑内相关蛋白表达结果显示,与模型组相比,各给药组大鼠脑内AKT1和AChE的表达显著上调;芎麻高剂量组及阳性药组大鼠脑内PKCβ1表达显著上调。各组大鼠血清外泌体中胆碱能突触信号通路中关键蛋白表达结果显示,与模型组相比,各给药组大鼠血清外泌体中PKCβ1及AChE表达水平显著上调。差异均具有统计学意义(P<0.05)。
      结论 芎麻药对通过抑制VCI大鼠脑内AChE活性并增加ACh的含量来达到治疗VCI的目的,胆碱能突触通路中的关键蛋白AChE与PKCβ1在脑中和血清外泌体中的变化基本一致,提示血清外泌体可能携带AChE和PKCβ1,在外周血液与脑组织之间传递疾病信息。

       

      Abstract:
      OBJECTIVE To investigate the effect of Xiongma herb pair on exosomes expression in the brain and serum of rats with vascular cognitive impairment(VCI) and its intervention mechanism.
      METHODS A total of 50 male Wistar rats, which were 8−10 weeks old and at the SPF grade, were chosen. Subsequently, the rat model of VCI was established by means of the 2-vessel occlusion(2-VO) method. According to the outcomes of cerebral blood flow, the rats in the 2-VO group were randomly allocated into several subgroups, namely the VCI model group, the donepezil hydrochloride positive drug group, the high-, low-dose group of the Xiongma herb pair, and the sham operation group. Starting three days after the successful establishment of the model, gastric gavage was carried out twice daily. The intervention effect of the Xiongma herb pair on the cerebral blood flow in rats was carefully observed. Meanwhile, the learning and memory capabilities of the rats were evaluated through the Morris water maze experiment, and their social abilities were explored via social interaction tests. Additionally, the content of acetylcholine(Ach) and the activity of acetylcholinesterase(AChE) were determined. Furthermore, the expression levels as well as the contents of AKT1, AChE, and PKCβ1 in the brain, serum, and serum exosomes were examined.
      RESULTS The outcomes of the Morris water maze experiment and the social interaction experiment manifested that the rats in the model group constantly exhibited learning and memory impairments along with social behavior disorders commencing from the 28th day and persisting until the 56th day. The groups that received drug administration effectively enhanced the learning and memory abilities and alleviated the social behavior disorders of the rats with VCI. According to the test results regarding the ACh content and the AChE activity within the brains of rats in each group, it was demonstrated that, in comparison to the model group, the ACh content in the high-dose Xiongma herb pair group and the positive drug group was notably elevated, while the AChE activity values in all the administration groups were significantly reduced. The results concerning the expression of relevant proteins in the brains of rats in each group indicated that, when contrasted with the model group, the expressions of AKT1 and AChE in all the administration groups were significantly enhanced, and the expression of PKCβ1 in the high-dose Xiongma herb pair group and the positive drug group was significantly increased. The results of the expression of key proteins in the cholinergic synapse signaling pathway within the serum exosomes of rats in each group disclosed that, compared to the model group, the expression levels of PKCβ1 and AChE in the serum exosomes of rats in all the administration groups were significantly boosted. All these differences were statistically significant(P<0.05).
      CONCLUSION The Xiongma herb pair accomplishes the treatment of VCI through inhibiting the activity of AChE within the brains of VCI rats and enhancing the content of ACh. The variations of the key proteins AChE and PKCβ1 in the cholinergic synapse pathway in the brain are largely in line with those in the serum exosomes, suggesting that serum exosomes might carry AChE and PKCβ1 and convey disease information between the peripheral blood and brain tissue.

       

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