首页> 外文期刊>Behavioural Brain Research: An International Journal >Comparison of the effects of PACAP-38 and its analog, acetyl-[Ala(15), Ala(20)] PACAP-38-propylamide, on spatial memory, post-learning BDNF expression and oxidative stress in rat
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Comparison of the effects of PACAP-38 and its analog, acetyl-[Ala(15), Ala(20)] PACAP-38-propylamide, on spatial memory, post-learning BDNF expression and oxidative stress in rat

机译:PACAP-38及其模拟,乙酰基[ALA(15),ALA(20)] PACAP-38-丙基酰胺对大鼠的空间记忆,后学习BDNF表达和氧化应激的影响的比较

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摘要

We compared the effects of single intraveinous injection of pituitary adenylate cyclase-activating polypeptide-38 (P38) to those of its analog, acetyl-[Ala(15),Ala(20)] PACAP-38-propylamide (P38-alg) on spatial memory in the Morris water maze (MWM) using a weak massed-learning procedure, post-training brain derived neurotrophic factor (BDNF) and post-training oxidative stress biomarker assays in male Wistar rats. Acquisition of the MWM task following P38 (30 mu g/kg) and P38-alg (30 mu g/kg) treatments was similar to control group (Saline: 0.9% NaCl) and there was no interaction between treatments and performance. However, in the probe test, P38treated group showed a specific interest for the target quadrant whereas the two other groups exhibited less focused place searching behavior. Moreover, P38 had an anxiogenic effect as measured by the distribution of swimming at the periphery of the pool. The swimming test resulted in a decrease in BDNF contents in the hippocampus. P38 but not P38-alg treatment restored BDNF expression. In terms of oxidative stress, both P38 and P38-alg treatments had antioxidative effects. The activity of antioxidative enzymes in the neocortex was increased. However only P38 reduced the levels of carbonylated proteins (CP). These data show that P38 and P38-alg have different behavioral and neurobiological effects. Thus, P38-alg and other analogs with specific functional profiles, inducing beneficial central effects (e.g. neuroprotection) while minimizing undesired peripheral effects may be useful for potential therapeutical use.
机译:比较了单一的腺苷酸腺苷酸环酶活化多肽-38(P38)对其模拟,乙酰基[ALA(15),ALA(20)] PACAP-38-丙基酰胺(P38-ALG)的影响的影响使用弱大规模学习程序,培训后脑源性脑源性因子(BDNF)和训练后氧化胁迫生物标志物在雄性Wistar大鼠中的训练后氧化应激生物标志物测定的空间记忆。采集P38(30μg/ kg)和P38-Alg(30μg/ kg)处理后的MWM任务类似于对照组(盐水:0.9%NaCl),并且在治疗和性能之间没有相互作用。然而,在探测试验中,P38treated基团对目标象限表现出特定的兴趣,而另外两个组呈现较少的聚焦地点搜索行为。此外,P38通过在游泳池周边的游泳分配来测量的焦躁效果。游泳测试导致海马BDNF内容物降低。 P38但不是P38-ALG治疗恢复了BDNF表达。就氧化应激而言,P38和P38-ALG治疗均具有抗氧化作用。促新生素中的抗氧化酶的活性增加。然而,只有P38降低了羰基化蛋白质(CP)的水平。这些数据显示P38和P38-ALG具有不同的行为和神经生物学效应。因此,P38-ALG和具有特异性功能性曲线的其他类似物,诱导有益的中枢效应(例如神经保护区),同时最小化不需要的外周效应可用于潜在的治疗用途。

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