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首页> 外文期刊>Behavioural Brain Research: An International Journal >Interfering effect and mechanism of neuregulin on experimental dementia model in rats.
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Interfering effect and mechanism of neuregulin on experimental dementia model in rats.

机译:神经调节蛋白对大鼠痴呆模型的干预作用及其机制。

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OBJECTIVE: To investigate the effect of neuregulin 1beta (NRG1beta) on the neuronal apoptosis and the expressions of Bcl-2 and Bax proteins in experimental dementia model rats. METHODS: Thirty adult healthy male Wistar rats were randomly divided into control group, model group and treated group consisting of 10 rats, respectively. The experimental dementia models were established by injecting beta-amyloid protein 1-40 (Abeta1-40) stereotactically into the left lateral ventricle, and treated by injecting NRG1beta into right lateral ventricle. The cognitive capacity of rats was evaluated with Y-electric maze. The neuronal apoptosis was counted by TUNEL assay. The expressions of Bcl-2 and Bax were determined with immunohistochemistry assay and double immunofluorescence labeling. RESULTS: The cognitive ability in model group rats decreased, along with the number of neuronal apoptosis and the expressions of Bcl-2 and Bax increased significantly than those in control group (P < 0.05). After treatment with NRG1beta, the cognitive ability of rats improved, the number of neuronal apoptosis reduced and the expression of Bcl-2 increased while Bax decreased significantly than those in model group (P < 0.05). CONCLUSION: NRG1beta could inhibit neuronal apoptosis by regulating the expressions of Bcl-2/Bax to improve the capacity of learning and memory in experimental dementia rats.
机译:目的:观察神经调节蛋白1β(NRG1β)对痴呆模型大鼠神经细胞凋亡及Bcl-2和Bax蛋白表达的影响。方法:将30只成年健康雄性Wistar大鼠随机分为对照组,模型组和治疗组,每组10只。通过立体定向将β-淀粉样蛋白1-40(Abeta1-40)注射到左心室中,并通过将NRG1beta注射到右心室中来建立实验性痴呆模型。用Y-电迷宫评估大鼠的认知能力。通过TUNEL测定对神经元凋亡进行计数。免疫组织化学法和双重免疫荧光标记法检测Bcl-2和Bax的表达。结果:模型组大鼠的认知能力下降,神经元凋亡数目明显增加,Bcl-2和Bax的表达明显高于对照组(P <0.05)。与模型组比较,NRG1β处理后,大鼠的认知能力提高,神经元凋亡数目减少,Bcl-2表达增加,而Bax表达则明显减少(P <0.05)。结论:NRG1β可以通过调节Bcl-2 / Bax的表达来抑制神经元凋亡,从而提高痴呆大鼠的学习记忆能力。

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