基于PI3K/AKT/mTOR信号通路探讨化瘀通络灸促血管性痴呆大鼠髓鞘再生的作用机制 |
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引用本文: | 梁嘉琪,樊吟秋,石海平,乔晓迪,邓 倩,郑紧紧,张庆萍. 基于PI3K/AKT/mTOR信号通路探讨化瘀通络灸促血管性痴呆大鼠髓鞘再生的作用机制[J]. 安徽中医药大学学报, 2024, 43(2): 61-66 |
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作者姓名: | 梁嘉琪 樊吟秋 石海平 乔晓迪 邓 倩 郑紧紧 张庆萍 |
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作者单位: | 1.安徽中医药大学研究生院,安徽 合肥 230012;2.安徽中医药大学第一附属医院,安徽 合肥 230012;3.安徽中医药大学针灸推拿学院,安徽 合肥 230012 |
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基金项目: | 国家自然科学基金项目(82104994);安徽省高校自然科学研究项目(KJ2021A0559);安徽中医药大学科研基金项目(2021yfylc15) |
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摘 要: | 目的 观察化瘀通络灸对血管性痴呆(vascular dementia, VD)大鼠胼胝体磷脂酰肌醇3激酶(phosphatidylinositol 3 kinase, PI3K)/蛋白激酶B(protein kinase B,AKT)/哺乳动物雷帕霉素靶蛋白(mammalian target of rapamycin, mTOR)信号通路的影响,探讨化瘀通络灸促VD大鼠髓鞘再生的作用机制。方法 经Morris水迷宫筛选后,随机选取12只大鼠纳入假手术组,剩余大鼠复制VD模型成功后,随机分为模型组、艾灸组、艾灸+LY294002组,每组12只。艾灸组予以化瘀通络灸干预,艾灸+LY294002组在化瘀通络灸干预的基础上予以PI3K抑制剂LY294002腹腔注射,采用Longa评分法评价各组大鼠神经功能损伤程度,Morris水迷宫实验检测各组大鼠学习记忆能力,Western blot法检测各组大鼠PI3K/AKT/mTOR信号通路相关蛋白的表达水平,神经髓鞘固蓝染色法观察各组大鼠胼胝体髓鞘的形态,透射电子显微镜观察各组大鼠髓鞘超微结构。结果 与假手术组比较,模型组和艾灸+LY294002组大...
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关 键 词: | 血管性痴呆 化瘀通络灸 PI3K/AKT/mTOR信号通路 髓鞘再生 |
Mechanism of Action of Stasis-resolving and Collateral-dredging Moxibustion in Promoting Myelin Regeneration in Rats with Vascular Dementia: A Study Based on the Phosphoinositide 3 Kinase/Protein Kinase B/Mammalian Target of Rapamycin Signaling Pathway |
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Affiliation: | 1.Graduate School of Anhui University of Chinese Medicine,Anhui Hefei 230012,China;2.The First Affiliated Hospital of Anhui University of Chinese Medicine,Anhui Hefei 230012,China;3.College of Acupuncture and Moxibustion,Anhui University of Chinese Medicine,Anhui Hefei 230012,China |
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Abstract: | Objective To investigate the mechanism of action of stasis-resolving and collateral-dredging moxibustion in promoting myelin regeneration in rats with vascular dementia (VD) by observing its effect on the phosphoinositide 3 kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) signaling pathway.Methods After screening by the Morris water maze test, 12 rats were randomly selected as sham-operation group,and the remaining rats were randomly divided into model group,moxibustion group,and moxibustion+LY294002 group after successful modeling of VD,with 12 rats in each group.The rats in the moxibustion group were given stasis-resolving and collateral-dredging moxibustion,and those in the moxibustion+LY294002 group were given intraperitoneal injection of the PI3K inhibitor LY294002 in addition to stasis-resolving and collateral-dredging moxibustion.The Longa scoring system was used to evaluate the degree of neurovascular injury in rats;the Morris water maze test was used to evaluate the learning and memory abilities of rats;Western blot was used to measure the expression of proteins associated with the PI3K/AKT/mTOR signaling pathway;LFB myelin staining was used to observe the morphology of myelin in the corpus callosum of rats; transmission electron microscopy was used to observe the myelin ultrastructure of rats.Results Compared with the sham-operation group,the model group and the moxibustion+LY294002 group had significant increases in Longa score (P<0.05) and escape latency (P<0.05) and significant reductions in the expression levels of the proteins associated with the PI3K/AKT/mTOR signaling pathway (P<0.05);the myelin in the corpus callosum showed unclear texture,disordered arrangement,vacuolar changes at the edge,and fragmentation with partial protrusions and disintegration,as well as a significant reduction in the number of myelinated nerve axons (P<0.05). Compared with the model group and the moxibustion+LY294002 group,the moxibustion group had significant reductions in Longa score (P<0.05) and escape latency (P<0.05) and significant increases in the expression levels of the proteins associated with the PI3K/AKT/mTOR signaling pathway (P<0.05),with certain recovery of the structure of myelin in the corpus callosum,ordered arrangement,dense structure at the edge,and a significant increase in the number of myelinated nerve axons (P<0.05). Conclusion Stasis-resolving and collateral-dredging moxibustion can repair myelin damage,promote myelin remodeling,and restore white matter function by activating the PI3K/AKT/mTOR signaling pathway. |
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Keywords: | Vascular dementia Stasis-resolving and collateral-dredging moxibustion Phosphoinositide 3 kinase/protein kinase B/mammalian target of rapamycin signaling pathway Myelin regeneration |
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