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一氧化氮供体在小鼠海马背侧对组胺诱导的类焦虑样效应的影响。

Influence of nitric oxide agents in the dorsal hippocampus of mice on anxiogenic-like effect induced by histamine.

机构信息

Department of Biology, Faculty of Basic Sciences, Islamic Azad University, Ardabil Branch, Ardabil, Iran.

出版信息

Pharmacol Biochem Behav. 2012 Sep;102(3):391-9. doi: 10.1016/j.pbb.2012.06.004. Epub 2012 Jun 9.

DOI:10.1016/j.pbb.2012.06.004
PMID:22687724
Abstract

Histaminergic receptors and neuronal nitric oxide synthase (nNOS) are co-expressed at high levels in the hippocampal neurons and alter anxiety-like behaviors in rodents. Since the dorsal hippocampus may be involved in modulation of anxiety-like behaviors, the aim of the present study was to assess whether the nitric oxide (NO) system in the dorsal hippocampus affects anxiety-like behaviors induced by histaminergic agents in mice. The effects of the NO precursor, L-arginine and NOS inhibitor, L-nitro-amino-methyl-ester (L-NAME) on histamine, pyrilamine and ranitidine responses in elevated plus maze (E.P.M.) in mice were investigated. Intra-CA1 microinjection of histamine (9 μg/mouse) or H1 receptor antagonist, pyrilamine (3, 6 and 9 μg/mouse), but not H2 receptor antagonist, ranitidine decreased the percentage of open arm time (%OAT) and open arm entries (%OAE), without affecting locomotor activity, suggesting an anxiogenic-like response. Both L-arginine (0.4 and 0.8 μg/mouse) and L-NAME (40 ng/mouse) when injected into the dorsal hippocampus induced anxiety-like behaviors, but the drugs reversed the anxiogenic response induced by the effective dose of histamine (9 μg/mouse) or pyrilamine (9 μg/mouse). Our results also indicated that intra-CA1 administration of L-arginine and L-NAME, in the presence or absence of ranitidine, exerted an anxiogenic effect. The results may indicate a modulatory role for NO in the dorsal hippocampus in the anxiogenic-like response induced by histamine or pyrilamine.

摘要

组氨酸能受体和神经元型一氧化氮合酶(nNOS)在海马神经元中高水平共表达,并改变啮齿动物的焦虑样行为。由于背侧海马可能参与调节焦虑样行为,因此本研究旨在评估背侧海马中的一氧化氮(NO)系统是否会影响组胺能药物诱导的小鼠焦虑样行为。研究了 NO 前体 L-精氨酸和 NOS 抑制剂 L-硝基-氨基-甲酯(L-NAME)对小鼠高架十字迷宫(E.P.M.)中组胺、吡拉明和雷尼替丁反应的影响。海马 CA1 内注射组胺(9μg/只)或 H1 受体拮抗剂吡拉明(3、6 和 9μg/只),但不是 H2 受体拮抗剂雷尼替丁,可降低开放臂时间百分比(%OAT)和开放臂进入次数百分比(%OAE),而不影响运动活动,表明具有焦虑样反应。当将 L-精氨酸(0.4 和 0.8μg/只)和 L-NAME(40ng/只)注射到背侧海马中时,均会引起焦虑样行为,但这些药物逆转了有效剂量的组胺(9μg/只)或吡拉明(9μg/只)引起的焦虑反应。我们的结果还表明,CA1 内注射 L-精氨酸和 L-NAME,无论是单独给药还是与雷尼替丁一起给药,都会产生焦虑样作用。结果可能表明,NO 在背侧海马中的调制作用可能参与了组胺或吡拉明诱导的焦虑样反应。

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