Salinger Walter L, Ladrow Pamela, Wheeler Catherine
Department of Psychology, University of North Carolina at Greensboro, 27402-6170, USA.
Behav Neurosci. 2003 Dec;117(6):1257-75. doi: 10.1037/0735-7044.117.6.1257.
Reeler (rl/rl) and reeler/wild-type (+/rl) mice synthesize Reln at subnormal rates, as do patients with schizophrenia, bipolar disorder, and autism, thereby forming the basis for a Reln hypothesis for vulnerability to these psychopathologies and justifying attention to the behavioral phenotypes of Reln-deficient mice. Tests of gait, emotionality, social aggression, spatial working memory, novel-object detection, fear conditioning, and sensorimotor reflex modulation revealed the behavioral phenotype of rl/rl, but not +/rl, mice to be different from that of wild-type (+/+) mice. These results reveal no effect of Reln gene dosage and provide significant challenges to both the Reln and the neurodevelopmental hypotheses of the etiology of major psychopathologies.
瑞勒(rl/rl)和瑞勒/野生型(+/rl)小鼠合成Reln的速率低于正常水平,精神分裂症、双相情感障碍和自闭症患者也是如此,从而形成了一个关于易患这些精神病理学疾病的Reln假说的基础,并证明关注Reln基因缺陷小鼠的行为表型是合理的。对步态、情绪、社会攻击性、空间工作记忆、新物体检测、恐惧条件反射和感觉运动反射调节的测试表明,rl/rl小鼠而非+/rl小鼠的行为表型与野生型(+/+)小鼠不同。这些结果显示Reln基因剂量没有影响,并对主要精神病理学病因的Reln假说和神经发育假说都提出了重大挑战。