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首页> 外文期刊>Behavioural Brain Research: An International Journal >Does long term potentiation in periacqueductal gray (PAG) mediate lasting changes in rodent anxiety-like behavior (ALB) produced by predator stress?--Effects of low frequency stimulation (LFS) of PAG on place preference and changes in ALB produced by
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Does long term potentiation in periacqueductal gray (PAG) mediate lasting changes in rodent anxiety-like behavior (ALB) produced by predator stress?--Effects of low frequency stimulation (LFS) of PAG on place preference and changes in ALB produced by

机译:导水管周围灰色(PAG)的长期增强作用是否介导了食肉动物应激引起的啮齿动物焦虑样行为(ALB)的持久变化?-PAG的低频刺激(LFS)对场所偏好和由其引起的ALB变化的影响

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摘要

The effects on rodent behavior of low frequency bilateral stimulation (LFS, 900 pulses at 1 Hz) of periacqueducatal gray (PAG) was investigated. The first experiment examined aversive qualities of LFS in a place preference paradigm. There was no evidence of a place preference after 1 or 7 applications of LFS. After the first LFS, rats showed longer latencies to leave the conditioned chamber, suggesting a positively reinforcing effect of LFS. Latency differences were not accounted for by freezing or immobility prior to leaving. Rats with electrodes outside the PAG did not show these effects. After repeated LFS, stimulated rats did not differ from controls in place preference or in anxiety-like behavior (ALB). Experiment 2 studied the effects of predator stress in unimplanted rats on an extended battery of measures of ALB in hole board, plus maze and light/dark box tests of rodent anxiety. Effects of electrode damage in the PAG on ALB was also examined. In addition, the effect of 7 applications of bilateral LFS of PAG on ALB following a 5 min unprotected exposure of rats to a cat (predator stress) was examined. Predator stress lastingly changed a wide variety of behaviors in the plus maze, [Rodgers, Behav. Pharmacol. 8 (1997) 477] replicating and extending previous reports. A new finding is an increase in light avoidance in the light/dark box test. Moreover, factor analysis revealed open arm avoidance, risk assessment, light avoidance and cautious exploration loaded on independent factors, replicating and extending previous findings. Bilateral, but not unilateral, damage specific to PAG was also found to be anxiolytic in plus maze measures of ALB. Bilateral implants in the PAG seemed to prevent many of the effects of predator stress on ALB measured 8 days later. Nevertheless, predator stress did decrease head dips in the open arm and LFS reversed this effect. Light avoidance also increased following predator stress and LFS reversed this increase. These findings suggest the PAG occupies an important position in the final common path of substrate changes mediating effects of predator stress on a range of behaviors in the rodent. The fact that LFS in the PAG can reverse stress induced changes in behavior supports the idea that LTP in PAG mediates stress induced increases in anxiety in rodents, as it does in the cat [Adamec, Neurosci. Biobevav. Rev. 21(6) (1997) 755; Adamec, J. Psychopharmacol. 2000 (in press); Adamec, J. Psychopharmacol. 2000 (in press); Adamec, J. Psychopharmacol. 12(2) (1998) 129; Adamec, J. Psychopharmacol. 12(13) (1998) 227].
机译:研究了尿道周围灰质(PAG)的低频双侧刺激(LFS,1 Hz下900脉冲)对啮齿动物行为的影响。第一个实验在场所偏好范式中研究了LFS的厌恶品质。没有证据表明LFS施用1或7次后会获得优先选择。在第一个LFS之后,大鼠表现出更长的潜伏时间离开条件腔,这表明LFS具有积极的增强作用。离职前的冻结或动静不能解决延迟差异。电极在PAG外部的大鼠未显示出这些作用。重复进行LFS后,受刺激的大鼠在位置偏爱或焦虑样行为(ALB)方面与对照组没有区别。实验2研究了未植入大鼠的捕食者应激对扩大的孔板ALB测度,迷宫和明/暗盒啮齿动物焦虑测试的影响。还检查了PAG中电极损坏对ALB的影响。另外,检查了大鼠在猫的无保护暴露5分钟(捕食者应激)后,PAG的双侧LFS的7次应用对ALB的影响。掠食者的压力最终改变了迷宫[Rodgers,Behav。 Pharmacol。 8(1997)477]复制并扩展了以前的报告。一个新发现是在明/暗盒测试中增加了避光性能。此外,因素分析还显示了对独立因素的开放式回避,风险评估,避光和谨慎探索,复制和扩展了先前的发现。在ALB的迷宫措施中,PAG的双侧但非单侧损害也被发现具有抗焦虑作用。 PAG中的双侧植入物似乎可以防止捕食者应激对8天后测量的ALB的许多影响。然而,捕食者的压力确实减少了张开双臂的头部跌落,而LFS扭转了这种影响。在捕食者应激之后,避光也增加了,LFS扭转了这种增加的趋势。这些发现表明,PAG在底物变化的最终共同路径中占据重要位置,该变化是食肉动物应激对啮齿动物行为的介导作用。 PAG中的LFS可以逆转压力引起的行为变化这一事实支持以下观点:PAG中的LTP可以像啮齿类动物一样,在啮齿类动物中引起压力引起的焦虑增加[Adamec,Neurosci。 Biobevav。 Rev.21(6)(1997)755; Adamec,J.Psychopharmacol。 2000(印刷中); Adamec,J.Psychopharmacol。 2000(印刷中); Adamec,J.Psychopharmacol。 12(2)(1998)129; Adamec,J.Psychopharmacol。 12(13)(1998)227]。

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