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高珀(Highper)的特征,一种ENU 诱导的具有异常精神兴奋剂和应激反应的小鼠突变体。

Characterization of Highper, an ENU-induced mouse mutant with abnormal psychostimulant and stress responses.

机构信息

Department of Psychiatry, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Psychopharmacology (Berl). 2013 Jan;225(2):407-19. doi: 10.1007/s00213-012-2827-5. Epub 2012 Sep 5.

Abstract

RATIONALE

Chemical mutagenesis in the mouse is a forward genetics approach that introduces random mutations into the genome, thereby providing an opportunity to annotate gene function and characterize phenotypes that have not been previously linked to a given gene.

OBJECTIVES

We report on the behavioral characterization of Highper, an N-ethyl-N-nitrosourea (ENU)-induced mutant mouse line.

METHODS

Highper and B6 control mice were assessed for locomotor activity in the open field and home cage environments. Basal and acute restraint stress-induced corticosterone levels were measured. Mice were tested for locomotor response to cocaine (5, 20, 30, and 45 mg/kg), methylphenidate (30 mg/kg), and ethanol (0.75, 1.25, and 1.75 g/kg). The rewarding and reinforcing effects of cocaine were assessed using conditioned place preference and self-administration paradigms.

RESULTS

Highper mice are hyperactive during behavioral tests but show normal home cage locomotor behavior. Highper mice also exhibit a twofold increase in locomotor response to cocaine, methylphenidate, and ethanol and prolonged activation of the hypothalamic-pituitary-adrenal axis in response to acute stress. Highper mice are more sensitive to the rewarding and reinforcing effects of cocaine, although place preference in Highper mice appears to be significantly influenced by the environment in which the drug is administered.

CONCLUSIONS

Altogether, our findings indicate that Highper mice may provide important insights into the genetic, molecular, and biological mechanisms underlying stress and the drug reward pathway.

摘要

原理

小鼠的化学诱变是一种正向遗传学方法,它将随机突变引入基因组,从而有机会注释基因功能并表征以前与特定基因没有关联的表型。

目的

我们报告了 N-乙基-N-亚硝脲(ENU)诱导的突变小鼠品系 Highper 的行为特征。

方法

在开放场和笼内环境中评估 Highper 和 B6 对照小鼠的运动活动。测量基础和急性束缚应激诱导的皮质酮水平。测试小鼠对可卡因(5、20、30 和 45mg/kg)、哌甲酯(30mg/kg)和乙醇(0.75、1.25 和 1.75g/kg)的运动反应。使用条件性位置偏爱和自我给药范式评估可卡因的奖赏和强化作用。

结果

Highper 小鼠在行为测试中表现出过度活跃,但在笼内运动行为正常。Highper 小鼠对可卡因、哌甲酯和乙醇的运动反应也增加了两倍,并且对急性应激的下丘脑-垂体-肾上腺轴的激活时间延长。Highper 小鼠对可卡因的奖赏和强化作用更为敏感,尽管 Highper 小鼠的位置偏好似乎受到给药环境的显著影响。

结论

总之,我们的发现表明,Highper 小鼠可能为应激和药物奖励途径的遗传、分子和生物学机制提供重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22aa/3536991/30c8f1d73758/213_2012_2827_Fig1_HTML.jpg

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