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Sevoflurane Impairs Short-Term Memory by Affecting PSD-95 and AMPA Receptor in the Hippocampus of a Mouse Model

机译:七氟烷通过影响小鼠模型的海马的PSD-95和AMPA受体来损害短期记忆

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Objective. To explore the effects of sevoflurane on the latency and error times of the passive avoidance and levels of PSD-95 and AMPA receptors in the hippocampus. We evaluated the effects of sevoflurane on short-term memory in adult mice and explored the possible mechanism. Methods. 144 Kunming mice (2-3 months, 30-35?g) were randomly divided into two groups A (n=64) and B (n=80) and received the dark-avoidance (DA) and step-down avoidance (SA) tests, respectively. The groups DA and SA were further divided into control (inhaled 40% O2 2?h) and sevoflurane (3.3% sevoflurane and 40% O2 2?h) subgroups. Before inhalation intervention, all mice were trained to be familiar with the Morris water maze (MWM). According to the test points of behavioral indicators, 8 mice were randomly selected from each subgroup at point 12?h (T1), 24?h (T2), 48?h (T3), and 72?h (T4) after inhalation intervention. The step-through latency and error times were measured in 5?min. After the behavioral test, the mice were killed and the tissues of the hippocampus were taken for hematoxylin and eosin (H&E) staining. The expression level of PSD-95 and AMPA receptors in the hippocampus was detected by immunohistochemistry and Western Blot. The changes of synaptic transmission were measured via electrophysiology analysis of hippocampal slices. Results. The mice in the control subgroups found the platform in a shorter pathway than those in the sevoflurane subgroups during an MWM test. The step-through latency of T1 and T2 in the sevoflurane subgroup was shorter than baseline time, and the error times were increased in 5?min and higher than baseline time when compared with the control subgroup (P0.05) in the A and B groups. Compared with the control subgroup, the expression level of PSD-95 and AMPA receptors in the hippocampus was decreased at T1 and T2 in the sevoflurane subgroup (P0.05). The nerve cells were partially swelling. Electrophysiology analysis showed that the levels of PSD-95 and AMPA receptor expression were associated with synaptic transmission. Conclusion. Sevoflurane impaired short-term memory in adult mice by inhibiting the expression of PSD-95 and AMPA receptors in the hippocampus, which led to the decrease in synaptic transmission.
机译:客观的。探讨七氟醚对海马中被动避免和PSD-95和AMPA受体的潜伏期和误差时间的影响。我们评估了七氟烷对成人小鼠短期记忆的影响,并探索了可能的机制。方法。 144昆明小鼠(2-3个月,30-35μg)随机分为两个(n = 64)和B(n = 80),并接收了暗避免(da)和降压避免(sa分别测试。将DA和SA群体进一步分为对照(吸入40%O 2 2→H)和七氟醚(3.3%七氟醚和40%O 2 2→H)亚组。在吸入干预之前,培训所有小鼠才熟悉莫里斯水迷宫(MWM)。根据行为指标的测试点,在吸入干预后,从点12Ω·H(t1),24Ω,48Ω,48Ω,48?H(t4)中,从每种亚组中随机选择8只小鼠。在5?min中测量级联延迟和错误时间。在行为试验之后,杀死小鼠,对海马的组织进行苏木精和曙红(H&E)染色。通过免疫组织化学和Western印迹检测PSD-95和海马中AMPA受体的表达水平。通过海马切片的电生理分析测量突触传递的变化。结果。对照组中的小鼠在MWM测试期间发现了比七氟醚亚组中的较短通路中的平台。七氟醚亚组中T1和T2的级联潜水短于基线时间短,并且在A和B中的对照亚组(P <0.05)比较时,误差时间增加5?min,高于基线时间(P <0.05)团体。与对照亚组相比,在七氟醚亚组的T1和T2下,海马PSD-95和AMPA受体的表达水平降低(P <0.05)。神经细胞部分溶胀。电生理学分析表明,PSD-95和AMPA受体表达的水平与突触传递相关。结论。通过抑制海马的PSD-95和AMPA受体的表达,七氟脲在成人小鼠中损害了成年小鼠的短期记忆,这导致突触传递的减少。

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