Chen C, Rainnie D G, Greene R W, Tonegawa S
Howard Hughes Medical Institute, Center for Cancer Research, Cambridge, MA.
Science. 1994 Oct 14;266(5183):291-4. doi: 10.1126/science.7939668.
Mice deficient for the gene encoding alpha-calcium-calmodulin-dependent kinase II (alpha-CaMKII knockout mice) provide a promising tool to link behavioral and cellular abnormalities with a specific molecular lesion. The heterozygous mouse exhibited a well-circumscribed syndrome of behavioral abnormalities, consisting primarily of a decreased fear response and an increase in defensive aggression, in the absence of any measured cognitive deficits. Unlike the heterozygote, the homozygote displayed abnormal behavior in all paradigms tested. At the cellular level, both extracellular and whole-cell patch clamp recordings indicated that serotonin release in putative serotonergic neurons of the dorsal raphe was reduced. Thus, alpha-CaMKII knockout mice, in particular the heterozygote, may provide a model for studying the molecular and cellular basis underlying emotional disorders involving fear and aggression.
缺乏编码α-钙调蛋白依赖性蛋白激酶II基因的小鼠(α-钙调蛋白依赖性蛋白激酶II基因敲除小鼠)为将行为和细胞异常与特定分子损伤联系起来提供了一个很有前景的工具。杂合子小鼠表现出一种明确界定的行为异常综合征,主要包括恐惧反应降低和防御性攻击增加,且未检测到任何认知缺陷。与杂合子不同,纯合子在所有测试范式中均表现出异常行为。在细胞水平上,细胞外和全细胞膜片钳记录均表明,中缝背核假定的5-羟色胺能神经元中的5-羟色胺释放减少。因此,α-钙调蛋白依赖性蛋白激酶II基因敲除小鼠,尤其是杂合子,可能为研究涉及恐惧和攻击的情绪障碍的分子和细胞基础提供一个模型。