奥拉西坦对大鼠脑梗死的脑保护作用及机制
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(1.济南市第五人民医院神经内科,山东省济南市 250022;2.山东省济南市中医医院妇科,山东省济南市 250022)

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赵宗刚,硕士,主治医师,研究方向为神经内科中西医结合治疗,E-mail为zhaozg1976@163.com。

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Protective effect and mechanism of oxiracetam on rats with cerebral infarction
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1.Department of Neurology, the 5th People's Hospital of Ji'nan, Ji'nan, Shandong 250022, China;2.Department of Gynecology, Ji'nan Hospital of Traditional Chinese Medicine, Ji'nan, Shandong 250022, China)

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    摘要:

    目的 研究奥拉西坦对大鼠脑梗死的脑保护作用及缺氧诱导因子1α(HIF-1α)/AMP依赖的蛋白激酶(AMPK)/热休克蛋白70(HSP70)通路所起的作用。方法 选择成年雄性SD大鼠,随机分为假手术组、脑梗死组、奥拉西坦组、奥拉西坦+YC-1组、奥拉西坦+8-bAMP组、奥拉西坦+Que组。采用线栓法建立脑梗死模型,奥拉西坦组给予200 mg/kg奥拉西坦尾静脉注射,奥拉西坦+YC-1组、奥拉西坦+8-bAMP组、奥拉西坦+Que组在奥拉西坦尾静脉注射的基础上分别给予HIF-1α抑制剂YC-1、AMPK抑制剂8-bAMP、HSP70抑制剂Quercetin尾静脉注射。干预14天后,测定其脑梗死体积、行为学指标及脑组织中氧化应激指标的含量、HIF-1α/AMPK/HSP70通路分子的表达情况。结果 与脑梗死组比较,奥拉西坦组大鼠的脑梗死体积明显缩小,平衡木站立时间、平衡木行走时间明显延长,脑组织中活性氧簇(ROS)、丙二醛(MDA)、8-羟基脱氧鸟苷(8-OHdG)的含量明显减少,超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)的含量及核因子E2相关因子2(Nrf2)、HO-1、AMPK、HSP70的表达水平明显增多。与奥拉西坦组比较,奥拉西坦+YC-1组、奥拉西坦+8-bAMP组、奥拉西坦+Que组大鼠脑组织中ROS、MDA、8-OHdG的含量明显增多,SOD、GPx的含量及Nrf2、HO-1的表达水平均明显减少(P<0.05)。结论 奥拉西坦能够通过激活HIF-1α/AMPK/HSP70通路减轻大鼠脑梗死的脑损伤。

    Abstract:

    Aim To study the protective effect and oxiracetam on rats with cerebral infarction and the role of HIF-1α/AMPK/HSP70 signaling pathway. Methods Adult male SD rats were randomly divided into sham group, cerebral infarction group, oxiracetam group, oxiracetam+YC-1 group, oxiracetam+8-bAMP group and oxiracetam+Que group. The model of cerebral infarction was established by thread embolization. Oxiracetam group was given tail vein injection of 200 mg/kg oxiracetam, Oxiracetam+YC-1 group, Oxiracetam+8-bAMP group, Oxiracetam+Que group were given tail vein injection of HIF-1α inhibitor YC-1, AMPK inhibitor 8-bAMP, HSP70 inhibitor Quercetin separately on the basis of Oxiracetam tail vein injection. After 14 days of intervention, cerebral infarction volume, behavioral parameters, oxidative stress index and HIF-1α/AMPK/HSP70 pathway molecule in brain were measured. Results Compared with cerebral infarction group, the volume of cerebral infarction significantly reduced, the standing time of balance beam and walking time of balance beam significantly prolonged, the contents of ROS, MDA, 8-OHdG in brain tissue significantly decreased, the contents of SOD and GPx and the expressions of Nrf2, HO-1, AMPK and HSP70 in brain tissue significantly increased. Compared with the oxiracetam + YC-1 group, oxiracetam + 8-bAMP group and oxiracetam + Que group, the contents of ROS, MDA, 8-OHdG in brain tissue significantly increased, the contents of SOD, GPx and the expression of Nrf2, HO-1 significantly decreased(P<0.05). Conclusion Oxiracetam can alleviate cerebral infarction injury in rats by activating HIF-1α/AMPK/HSP70 pathway.

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赵宗刚,金辉,王胜男.奥拉西坦对大鼠脑梗死的脑保护作用及机制[J].中国动脉硬化杂志,2019,27(11):944~949.

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  • 收稿日期:2019-03-05
  • 最后修改日期:2019-06-11
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  • 在线发布日期: 2019-12-18