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首页> 外文期刊>Neuropharmacology >Withdrawal from chronic amphetamine produces persistent anxiety-like behavior but temporally-limited reductions in monoamines and neurogenesis in the adult rat dentate gyrus.
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Withdrawal from chronic amphetamine produces persistent anxiety-like behavior but temporally-limited reductions in monoamines and neurogenesis in the adult rat dentate gyrus.

机译:从慢性苯丙胺中退出会产生持续的焦虑样行为,但在成年大鼠齿状回中单胺和神经发生的时间有限的减少。

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Acute amphetamine administration activates monoaminergic pathways and increases systemic corticosterone, both of which influence anxiety states and adult dentate gyrus neurogenesis. Chronic amphetamine increases anxiety states in rats when measured at 24 h and at 2 weeks of withdrawal. However, the effects of chronic amphetamine exposure and withdrawal on long term anxiety-like behavior and adult neurogenesis in the dentate gyrus are unknown. Adult male rats were administered amphetamine (2.5 mg/kg, ip.) daily for two weeks. Anxiety-like behaviors were increased markedly in amphetamine-treated rats following four weeks of withdrawal from amphetamine. Plasma corticosterone level was unaltered by amphetamine treatment or withdrawal. However, norepinephrine and serotonin concentrations were selectively reduced in the dentate gyrus 20 h following amphetamine treatment. This effect did not persist through the four week withdrawal period. In separate experiments, rats received bromodeoxyuridine to label cells in S-phase, prior to or immediately following amphetamine treatment. Newly generated cells were quantified to measure extent of progenitor cell proliferation and neurogenesis following treatment or withdrawal. Progenitor cell proliferation and neurogenesis were not significantly affected by amphetamine exposure when measured 20 h following the last amphetamine treatment. However, neurogenesis in the dentate gyrus was reduced after four weeks of withdrawal when compared to saline-pretreated rats. Overall, our findings indicate that withdrawal from chronic amphetamine leads to persistent anxiety-like behavior which may be maintained by reduced neurogenesis in the dentate gyrus at this protracted withdrawal time point. However, neurogenesis is unaffected at earlier withdrawal time points where anxiety states emerge, suggesting different mechanisms may underlie the emergence of anxiety states during amphetamine withdrawal.
机译:急性苯丙胺给药可激活单胺能途径并增加全身性皮质酮,两者均会影响焦虑状态和成年齿状回神经发生。在停药后24小时和停药2周时,慢性苯丙胺会增加大鼠的焦虑状态。然而,慢性苯丙胺暴露和戒断对齿状回的长期焦虑样行为和成年神经发生的影响尚不清楚。成年雄性大鼠每天服用苯丙胺(2.5 mg / kg,腹腔注射),持续两周。从苯丙胺戒断四周后,苯丙胺治疗的大鼠的焦虑样行为明显增加。苯丙胺治疗或停药后血浆皮质类固醇水平未改变。然而,苯丙胺治疗20小时后,齿状回中去甲肾上腺素和5-羟色胺的浓度选择性降低。在四周的戒断期内,这种效果并未持续。在单独的实验中,大鼠在苯丙胺治疗之前或之后立即接受溴脱氧尿苷标记S期细胞。量化新产生的细胞,以测量治疗或停药后祖细胞增殖和神经发生的程度。在最后一次安非他明治疗后20小时进行测量时,安非他明暴露不会显着影响祖细胞的增殖和神经发生。然而,与盐水预处理的大鼠相比,戒断4周后齿状回的神经发生减少。总体而言,我们的研究结果表明,从慢性苯丙胺戒断会导致持续的焦虑样行为,这可以通过在这个延长的戒断时间点减少齿状回中的神经发生来维持。然而,神经发生在焦虑状态出现的较早戒断时间点上不受影响,表明苯丙胺戒断期间焦虑状态的出现可能是不同的机制。

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