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一种基因型依赖性海马强啡肽能机制控制小鼠探索行为。

A genotype-dependent hippocampal dynorphinergic mechanism controls mouse exploration.

作者信息

Van Daal J H, De Kok Y J, Jenks B G, Wendelaar Bonga S E, Van Abeelen J H

机构信息

Department of Animal Physiology, University of Nijmegen, The Netherlands.

出版信息

Pharmacol Biochem Behav. 1987 Dec;28(4):465-8. doi: 10.1016/0091-3057(87)90507-7.

Abstract

Following microinjections with two dilutions of anti-dynorphin B antiserum into the hippocampal CA3 region, adult male mice from the inbred strains DBA/2 and C57BL/6 were individually tested for various exploratory behaviors in a novel environment and compared to preimmune serum control animals. Treatment augmented vertically-oriented exploratory acts in strain DBA/2 and reduced the scores in strain C57BL/6 so that strain differences originally present between the controls were reversed or eliminated after antiserum. These opposite effects indicate that a hippocampal dynorphinergic mechanism is involved in the regulation of novelty-induced behavior in mice and that its modulatory function depends on the genotype. It is concluded that DBA/2 animals exposed to novelty, as compared to C57BL/6, are characterized by an over-release of hippocampal dynorphin B which is neutralized in part by small amounts of antibody.

摘要

在用两种稀释度的抗强啡肽B抗血清微量注射到海马CA3区后,对近交系DBA/2和C57BL/6的成年雄性小鼠在新环境中进行各种探索行为的个体测试,并与免疫前血清对照动物进行比较。处理增加了DBA/2品系垂直方向的探索行为,降低了C57BL/6品系的得分,使得对照组原本存在的品系差异在注射抗血清后被逆转或消除。这些相反的效应表明,海马强啡肽能机制参与了小鼠新奇诱导行为的调节,并且其调节功能取决于基因型。得出的结论是,与C57BL/6相比,暴露于新奇环境的DBA/2动物的特征是海马强啡肽B过度释放,而少量抗体可部分中和这种过度释放。

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