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首页> 外文期刊>Biology of Mood & Anxiety Disorders >Caveats of chronic exogenous corticosterone treatments in adolescent rats and effects on anxiety-like and depressive behavior and hypothalamic-pituitary-adrenal (HPA) axis function
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Caveats of chronic exogenous corticosterone treatments in adolescent rats and effects on anxiety-like and depressive behavior and hypothalamic-pituitary-adrenal (HPA) axis function

机译:青春期大鼠慢性外源性皮质酮治疗的注意事项及其对焦虑样,抑郁行为和下丘脑-垂体-肾上腺(HPA)轴功能的影响

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Background Administration of exogenous corticosterone is an effective preclinical model of depression, but its use has involved primarily adult rodents. Using two different procedures of administration drawn from the literature, we explored the possibility of exogenous corticosterone models in adolescence, a time of heightened risk for mood disorders in humans. Methods In experiment 1, rats were injected with 40 mg/kg corticosterone or vehicle from postnatal days 30 to 45 and compared with no injection controls on behavior in the elevated plus maze (EPM) and the forced swim test (FST). Experiment 2 consisted of three treatments administered to rats from postnatal days 30 to 45 or as adults (days 70 to 85): either corticosterone (400 μg/ml) administered in the drinking water along with 2.5% ethanol, 2.5% ethanol or water only. In addition to testing on EPM, blood samples after the FST were obtained to measure plasma corticosterone. Analysis of variance (ANOVA) and alpha level of P Results In experiment 1, corticosterone treatment of adolescent rats increased anxiety in the EPM and decreased immobility in the FST compared to no injection control rats. However, vehicle injected rats were similar to corticosterone injected rats, suggesting that adolescent rats may be highly vulnerable to stress of injection. In experiment 2, the intake of treated water, and thus doses delivered, differed for adolescents and adults, but there were no effects of treatment on behavior in the EPM or FST. Rats that had ingested corticosterone had reduced corticosterone release after the FST. Ethanol vehicle also affected corticosterone release compared to those ingesting water only, but differently for adolescents than for adults. Conclusions The results indicate that several challenges must be overcome before the exogenous corticosterone model can be used effectively in adolescents.
机译:背景外源皮质酮的给药是有效的抑郁症临床前模型,但其使用主要涉及成年啮齿动物。使用从文献中得出的两种不同的给药方法,我们探索了青春期外源皮质酮模型的可能性,青春期是人类情绪失调风险增加的时期。方法在实验1中,从出生后30至45天给大鼠注射40 mg / kg皮质酮或媒介物,并与未注射对照组在高架迷宫(EPM)和强迫游泳试验(FST)中的行为进行比较。实验2由出生后30至45天或成年(70至85天)对大鼠给药的三种治疗方法组成:在饮用水中与2.5%乙醇,2.5%乙醇或仅与水一起使用皮质酮(400μg/ ml) 。除了对EPM进行测试外,还需在FST之后获取血样以测量血浆皮质酮。 P结果的方差分析(ANOVA)和α水平在实验1中,与没有注射对照组的大鼠相比,皮质类固醇治疗青春期大鼠增加了EPM的焦虑,并降低了FST的不动。然而,媒介物注射的大鼠类似于皮质酮注射的大鼠,这表明青春期大鼠可能极易受到注射压力的影响。在实验2中,青少年和成年人的处理水摄入量以及所输送的剂量有所不同,但在EPM或FST中,处理对行为的影响没有影响。 FST后,摄入皮质酮的大鼠皮质酮释放减少。与仅摄入水的人相比,乙醇媒介物还影响皮质酮的释放,但青少年与成年人不同。结论结果表明,在青少年中有效使用外源性皮质酮模型之前,必须克服几个挑战。

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