首页> 美国卫生研究院文献>Oncotarget >cAMP/PKA-CREB-BDNF signaling pathway in hippocampus mediates cyclooxygenase 2-induced learning/memory deficits of rats subjected to chronic unpredictable mild stress
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cAMP/PKA-CREB-BDNF signaling pathway in hippocampus mediates cyclooxygenase 2-induced learning/memory deficits of rats subjected to chronic unpredictable mild stress

机译:海马中的cAMP / PKA-CREB-BDNF信号传导通路介导环氧合酶2诱导的慢性不可预测轻度应激大鼠的学习/记忆缺陷

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摘要

To investigate the mechanism of cyclooxygenase 2 (COX2) in learning and memory impairments in rats subjected to chronic unpredictable mild stress (CUMS), meloxicam was used intragastrically to inhibit the activity of cyclooxygenase 2. Moreover, cyclooxygenase 2 over-expressing or RNA interfere lentivirus was injected intraventricularly to increase or decrease the enzyme's expression, respectively. The body weights and sucrose consumption were used to analyze depressive behaviors, while the Morris water maze and step-down-type passive avoidance tests were carried out to evaluate the learning-memory functions. The levels of inflammatory cytokines were measured to estimate inflammation and the contents of cyclic adenosine monophosphate (cAMP) were used to measure the levels of the second messenger. Changes in cyclooxygenase 2 mRNA levels were analyzed using reverse transcription polymerase chain reaction. Moreover, the expression of cyclooxygenase 2, brain-derived neurotrophic factor (BDNF), prostaglandins receptor 3 (EP3), protein kinase A (PKA), cAMP response element binding protein (CREB), and phosphorylated CREB were estimated using immunohistochemical staining or western blotting. The results showed that CUMS led to significant depressive-like behaviors and learning and memory dysfunctions. Also, the cAMP levels decreased significantly, while levels of inflammatory cytokines and prostaglandins E2 increased significantly. The expressions of PKA, BDNF, phosphorylated CREB/CREB declined and cyclooxygenase 2 was increased. Meloxicam and cyclooxygenase 2 RNA interfere lentivirus reversed the changes caused by CUMS while cyclooxygenase 2-overexpressing lentivirus worsened these abnormalities. The findings also showed that CUMS increased cyclooxygenase 2 expression, which can cause learning and memory impairments, mainly through activating the hippocampal neuronal cAMP/PKA-CREB-BDNF signaling pathways.
机译:为了研究环氧合酶2(COX2)在遭受慢性不可预测轻度应激(CUMS)的大鼠的学习和记忆障碍中的机制,在胃内使用美洛昔康抑制环氧合酶2的活性。此外,环氧合酶2的过表达或RNA干扰慢病毒。脑室内注射分别增加或减少酶的表达。体重和蔗糖消耗量用于分析抑郁行为,而莫里斯水迷宫和降压型被动回避测试用于评估学习记忆功能。测量炎性细胞因子的水平以估计炎症,并使用环状单磷酸腺苷(cAMP)的含量测量第二信使的水平。使用逆转录聚合酶链反应分析了环氧合酶2 mRNA水平的变化。此外,使用免疫组织化学染色或Western blot评估了环氧合酶2,脑源性神经营养因子(BDNF),前列腺素受体3(EP3),蛋白激酶A(PKA),cAMP反应元件结合蛋白(CREB)和磷酸化CREB的表达。印迹。结果表明,CUMS导致了明显的抑郁样行为以及学习和记忆功能障碍。同样,cAMP水平显着降低,而炎症细胞因子和前列腺素E2的水平显着提高。 PKA,BDNF,磷酸化的CREB ​​/ CREB的表达下降,环氧合酶2升高。 Meloxicam和环氧合酶2 RNA干扰慢病毒逆转了CUMS引起的变化,而环氧合酶2过表达的慢病毒使这些异常恶化。研究结果还表明,CUMS增加了环氧合酶2的表达,这可能导致学习和记忆障碍,主要是通过激活海马神经元cAMP / PKA-CREB-BDNF信号通路。

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