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Circadian genes Period 1 and Period 2 in the nucleus accumbens regulate anxiety-related behavior

机译:核心基因时期1和核中的2期核心调节焦虑相关的行为

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摘要

It has been suggested for some time that circadian rhythm abnormalities underlie the development of multiple psychiatric disorders. However, it is unclear how disruptions in individual circadian genes might regulate mood and anxiety. Here we found that mice lacking functional mPeriod 1 (mPer1) or mPeriod 2 (mPer2) individually did not have consistent behavioral abnormalities in measures of anxiety-related behavior. However, mice deficient in both mPer1 and mPer2 had an increase in levels of anxiety-like behavior in multiple measures. Moreover, we found that mPer1 and mPer2 expression was reduced in the nucleus accumbens (NAc) after exposure to chronic social defeat stress, a paradigm that led to increased anxiety-related behavior. Following social defeat, chronic treatment with fluoxetine normalized Per gene expression towards wild-type levels. Knockdown of both mPer1 and mPer2 expression via RNA interference specifically in the NAc led to a similar increase in anxiety-like behavior as seen in the mutant animals. Taken together, these results implicate the Per genes in the NAc in response to stress and the development of anxiety.
机译:一段时间以来,有人提出昼夜节律异常是多种精神病发展的基础。但是,尚不清楚单个生物钟基因的破坏如何调节情绪和焦虑。在这里,我们发现缺少功能性mPeriod 1(mPer1)或mPeriod 2(mPer2)的小鼠在焦虑相关行为的测量中没有一致的行为异常。但是,同时缺乏mPer1和mPer2的小鼠在多项措施中的焦虑样行为水平有所提高。此外,我们发现暴露于慢性社交衰竭压力后伏伏核(NAc)中mPer1和mPer2的表达降低,该范式导致与焦虑相关的行为增加。社交失利后,氟西汀的长期治疗使Per基因表达朝着野生型水平正常化。通过在RNA干扰中特异地通过RNA干扰抑制mPer1和mPer2表达,导致突变动物中类似的焦虑样行为增加。综上所述,这些结果暗示了NAc中的Per基因对压力和焦虑的反应。

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