电针刺激神门(HT7)、百会(GV20)、三阴交(SP6)对对氯苯丙氨酸诱导的失眠大鼠空间学习和记忆缺陷的疗效:单穴合穴。

Qiao Lina, Shi Yinan, Tan Lianhong, Jiang Yanshu, Yang Yongsheng
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引用次数: 0

摘要

目的研究电针神门(HT7)、百会(GV20)、三阴交(SP6)单穴及神门(HT7)、百会(GV20)、三阴交(SP6)合穴对海马PKA/CREB、BDNF/TrkB信号转导以及神经凋亡和神经发生的影响,并阐明单穴和合穴改善海马空间学习和记忆障碍的内在机制、以及海马神经凋亡和神经发生的影响,并阐明单穴和合穴改善原发性失眠大鼠模型空间学习和记忆缺陷的内在机制。研究方法神门穴(HT7)、百会穴(GV20)、三阴交穴(SP6)或神门穴(HT7)+百会穴(GV20)+三阴交穴(SP6)(联合)贴敷30 min,连续4 d。海马cAMP依赖性蛋白激酶(PKA)-Cβ、磷酸化cAMP反应元件结合蛋白(p-CREB)、脑源性神经营养因子(BDNF)和酪氨酸激酶受体B(TrkB)的蛋白表达采用Western印迹法进行评估。用转移酶介导的 dUTP-X 缺口标记法检测海马中神经元的凋亡。溴脱氧尿苷染色法检测内源性神经发生。在服用 PKA 选择性抑制剂(H89)后,对联合穴位组的 MWM 测试和海马 p-CREB、BDNF 和 TrkB 蛋白水平进行了评估:结果:失眠大鼠的空间学习和记忆能力明显受损。神门穴(HT7)、百会穴(GV20)、三阴交穴(SP6)和综合穴位组的空间学习障碍均有所改善;综合穴位组的改善程度明显高于单一穴位组。联合组、百会(GV20)组和神门(HT7)组的空间记忆障碍有所改善,而三阴交(SP6)组则没有。失眠大鼠体内PKA-Cβ、p-CREB、BDNF和TrkB的表达均下降。所有这些蛋白质在联合组中都明显上调。PKA/p-CREB蛋白水平在百会(GV20)组和神门(HT7)组中升高,而BDNF/TrkB表达在三阴交(SP6)组中上调。染色结果显示,联合组的海马细胞凋亡明显减少,增殖细胞数量增加,而单穴组只有凋亡细胞数量减少。在联合组中,PKA抑制剂逆转了EA对空间记忆的改善和p-CREB表达的上调,但并未影响其对BDNF/TrkB信号的激活:结论:单穴位EA治疗百会穴(GV20)、神门穴(HT7)或三阴交穴(SP6)对失眠引起的空间学习和记忆障碍有改善作用。联合穴位EA通过上调海马PKA/CREB和BDNF/TrkB信号传导、促进神经元生成和抑制神经元凋亡,对改善失眠大鼠的空间学习和记忆障碍具有协同作用。这些研究结果表明,与单一穴位EA相比,联合穴位EA[(百会(GV20)、神门(HT7)和三阴交(SP6)]对海马神经可塑性的调节作用更明显,这可能部分解释了联合穴位EA对失眠引起的认知功能障碍具有更好的改善作用的内在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of electroacupuncture stimulating Shenmen (HT7), Baihui (GV20), Sanyinjiao (SP6) on spatial learning and memory deficits in rats with insomnia induced by para-chlorophenylalanine: a single acupoint combined acupoints.

Objective: To investiage the effect of electroacupuncture (EA) at a single acupoint of Shenmen (HT7), Baihui (GV20), Sanyinjiao (SP6) and at combined acupoints of Shenmen (HT7) and Baihui (GV20) and Sanyinjiao (SP6) on the PKA/CREB and BDNF/TrkB signaling, as well as neuroapoptosis and neurogenesis in hippocampus and elucidate the underlying mechanism of single and combined acupoints on ameliorating spatial learning and memory deficits in a rat model of primary insomnia.

Methods: Primary insomnia was modeled by intraperitoneal injection of para-chlorophenylalanine (PCPA) once daily for 2 d. EA was applied at Shenmen (HT7), Baihui (GV20), Sanyinjiao (SP6), or Shenmen (HT7) + Baihui (GV20) + Sanyinjiao (SP6) (combined) for 30 min daily for 4 d. Spatial learning and memory function was evaluated by the Morris water maze (MWM) test. Protein expressions of hippocampal cAMP-dependent protein kinase (PKA)-Cβ, phosphorylated cAMP-responsive element-binding protein (p-CREB), brain-derived neurotrophic factor (BDNF), and tyrosine kinase receptor B (TrkB) were evaluated by Western blotting. Neuronal apoptosis in the hippocampus was detected with the transferase-mediated dUTP-X nick end labeling assay. Endogenous neurogenesis was examined with bromodeoxyuridine staining. The MWM test and hippocampal p-CREB, BDNF, and TrkB protein levels in the combined acupoints group were evaluated after the administration of a PKA-selective inhibitor (H89).

Results: Spatial learning and memory were significantly impaired in rats with insomnia. The spatial learning deficits were ameliorated in the Shenmen (HT7), Baihui (GV20), Sanyinjiao (SP6), and combined groups; this improvement was significantly greater in the combined group than the single acupoint groups. The spatial memory impairment was improved in the combined, Baihui (GV20), and Shenmen (HT7) groups, but not the Sanyinjiao (SP6) group. The expressions of PKA-Cβ, p-CREB, BDNF, and TrkB were decreased in rats with insomnia. All these proteins were significantly upregulated in the combined group. PKA/p-CREB protein levels were elevated in the Baihui (GV20) and Shenmen (HT7) groups, whereas BDNF/TrkB expression was upregulated in the Sanyinjiao (SP6) group. The staining results showed significant attenuation of hippocampal cell apoptosis and increased numbers of proliferating cells in the combined group, whereas the single acupoint groups only showed decreased numbers of apoptotic cells. In the combined group, the PKA inhibitor reversed the improvement of spatial memory and upregulation of p-CREB expression caused by EA, but did not affect its activation of BDNF/TrkB signaling.

Conclusions: EA at the single acupoints Baihui (GV20), Shenmen (HT7), or Sanyinjiao (SP6) had an ameliorating effect on the spatial learning and memory deficits induced by insomnia. EA at combined acupoints exerted a synergistic effect on the improvements in spatial learning and memory impairment in rats with insomnia by upregulating the hippocampal PKA/CREB and BDNF/TrkB signaling, facilitating neurogenesis, and inhibiting neuronal apoptosis. These findings indicate that EA at combined acupoints [(Baihui (GV20), Shenmen (HT7), and Sanyinjiao (SP6)] achieves a more pronounced regulation of hippocampal neuroplasticity than EA at single acupoints, which may partly explain the underlying mechanisms by which EA at combined acupoints exerts a better ameliorative effect on the cognitive dysfunction caused by insomnia.

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