首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Anxiety-like behavior in the elevated-plus maze tests and enhanced IL-1beta, IL-6, NADPH oxidase-1, and iNOS mRNAs in the hippocampus during early stage of adjuvant arthritis in rats.
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Anxiety-like behavior in the elevated-plus maze tests and enhanced IL-1beta, IL-6, NADPH oxidase-1, and iNOS mRNAs in the hippocampus during early stage of adjuvant arthritis in rats.

机译:在佐剂性关节炎的早期大鼠中,高架迷宫测试中的焦虑样行为以及海马中IL-1beta,IL-6,NADPH氧化酶-1和iNOS mRNA的增强。

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摘要

We studied anxiety-like behavior in the elevated plus-maze (EPM) tests in male Lewis rats on days 2 and 4 of adjuvant arthritis (AA). In plasma we analyzed C-reactive protein (CRP), albumin, ACTH, corticosterone, in the hippocampus the mRNA expression of interleukin-1beta (IL-1beta), interleukin-6 (IL-6), corticotrophin releasing factor (CRH), NADPH oxidases NOX1 and NOX2, and inducible NO-synthase (iNOS). EPM tests showed a higher anxiety index in AA rats on days 2 and 4 and reduction of total entries. On days 2 and 4 we found reduced plasma albumin, enhanced CRP, ACTH and corticosterone, and in the hippocampus enhanced mRNA for NOX1 and IL-1beta in AA rats, on day 4 we found enhanced mRNAs for iNOS and IL-6, and reduced mRNA for CRH. The mRNA for NOX2 did not change on any experimental day. These results suggest enhanced anxiety, as well as locomotor impairment during the early phase of AA that correlate with enhanced mRNA expressions of parameters of oxidative stress NOX1, iNOS, and inflammatory cytokines IL-1beta and IL-6 in the hippocampus.
机译:我们在佐剂性关节炎(AA)的第2天和第4天,在雄性Lewis大鼠的高架迷宫(EPM)测试中研究了焦虑样行为。在血浆中,我们分析了海马中的C反应蛋白(CRP),白蛋白,促肾上腺皮质激素,皮质酮,白细胞介素1β(IL-1beta),白细胞介素6(IL-6),促肾上腺皮质激素释放因子(CRH)的mRNA表达, NADPH氧化酶NOX1和NOX2,以及诱导型NO合酶(iNOS)。 EPM测试显示,在第2天和第4天,AA大鼠的焦虑指数更高,总入场次数减少。在第2天和第4天,我们发现血浆白蛋白降低,CRP,ACTH和皮质酮升高,在海马中,AA大鼠中NOX1和IL-1beta的mRNA升高;在第4天,我们发现iNOS和IL-6的mRNA升高,并且降低了CRH的mRNA。 NOX2的mRNA在任何实验日均未改变。这些结果表明,焦虑的增加以及AA早期的运动障碍与海马区氧化应激NOX1,iNOS和炎性细胞因子IL-1beta和IL-6参数的mRNA表达增强有关。

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