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纸质出版日期:2021,
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异丙酚缓解大鼠脑缺血再灌注损伤及其机制研究[J]. 重庆医科大学学报, 2021,46(10):1153-1157.
Remission of propofol on cerebral ischemia-reperfusion injury in rats and its mechanism[J]. Journal of Chongqing Medical University, 2021,46(10):1153-1157.
异丙酚缓解大鼠脑缺血再灌注损伤及其机制研究[J]. 重庆医科大学学报, 2021,46(10):1153-1157. DOI: 10.13406/j.cnki.cyxb.002662.
Remission of propofol on cerebral ischemia-reperfusion injury in rats and its mechanism[J]. Journal of Chongqing Medical University, 2021,46(10):1153-1157. DOI: 10.13406/j.cnki.cyxb.002662.
目的: 探究麻醉药物异丙酚缓解大鼠脑缺血再灌注损伤(ischemia reperfusion,IR)的作用及机制。方法: 健康雄性SD大鼠72只,随机分为假手术组、模型组、异丙酚(Pro)组、Pro+DPCPX组、Pro+LY294002组、Pro+DPCPX+LY294002组,每组12只。血管内线栓法阻断大脑中动脉,建立局灶性IR损伤模型,再灌注24 h后进行大鼠神经功能评分,ELISA检测血浆肿瘤坏死因子α(tumor necrosis factor-α,TNF-α)和白介素-1β(interleukin-1β,IL-1β)含量,TTC染色检测脑梗死体积,免疫组织化学法检测Bcl-2阳性细胞表达情况,Western blot检测Akt、p-Akt表达量。结果: 与模型组大鼠相比,异丙酚能够有效降低IR大鼠神经功能评分,缩小脑梗死体积,提高脑组织Bcl-2阳性细胞表达率,有效降低IR大鼠血浆炎性因子TNF-α和IL-1β的表达水平(P<0.05)。与此同时,异丙酚能够明显升高大脑皮质区p-Akt表达(P<0.05),异丙酚干预的IR大鼠体内PI3K/Akt信号通路呈高度激活状态。当实验大鼠加PI3K抑制剂LY294002处理时,异丙酚的神经保护作用被明显抑制,失去治疗效果。其抑制作用与A1R受体拮抗剂DPCPX效果相当。结论: 异丙酚能够在IR大鼠模型中激活A1R,通过抑制兴奋性氨基酸的毒性,促进p-Akt表达,进一步激活PI3K/Akt信号通路,上调脑组织Bcl-2表达水平,发挥抗神经细胞凋亡作用,同时下调炎性因子TNF-α和IL-1β表达,减轻机体的炎症反应,发挥良好的脑缺血再灌注损伤缓解作用。
Objective: To investigate the effect and mechanism of anesthesia drug propofol on cerebral ischemia-reperfusion (IR) injury in rats. Methods: Seventy-two healthy male SD rats were randomly divided into sham operation group
model group
propofol (Pro) group
Pro+DPCPX group
Pro+LY294002 group
Pro+DPCPX+LY294002 group
with 12 rats in each group. The middle cerebral artery was blocked by the intravascular endothelial method
and a focal cerebral IR injury model was established. Rats were scored for neurological function 24 hours after reperfusion. Plasma levels of tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were measured by Enzyme-linked immunosorbent assay (ELISA). The brain was detected by Triphenyl tetrazolium chloride (TTC) staining infarct volume
the expression of Bcl-2 positive cells was detected by immunohistochemistry
and the expression of Akt and p-Akt was detected by Western blot. Results: Compared with the model group
propofol effectively reduced the neurological score of IR rats and the volume of cerebral infarction
increased the expression rate of Bcl-2 positive cells in brain tissue
and effectively reduced the expression levels of plasma inflammatory factor TNF-α and IL-1β in IR rats (P<0.05). At the same time
propofol significantly increased the level of p-Akt expression in the cerebral cortex (P<0.05)
and the PI3K/Akt signaling pathway in IR rats interfered with by propofol was highly activated. When the experimental rats were treated with the PI3K in-hibitor LY294002
the neuroprotective effect of propofol was significantly inhibited and the therapy was ineffective. Its in-hibitory effect was comparable to that of A1R receptor antagonist DPCPX. Conclusion: Propofol can activate A1R in IR rat models by inhibiting the excitatory amino acid toxicity
promote the expression of p-Akt
further activate the PI3K/Akt signaling pathway
up-regulate the expression level of Bcl-2 in brain tissue
and exert anti-apoptotic effects. At the same time
it can down-regulate the expression of inflammatory factors TNF-α and IL-1β
reduce the body’s inflammatory response
and thus exerts a good therapeutic effect.
异丙酚脑缺血再灌注损伤分子机制PI3K/Akt信号通路
propofolcerebral ischemia-reperfusion injurymolecular mechanismPI3K/Akt signaling pathway
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