Turski L, Schwarz M, Sontag K H
Behav Brain Res. 1984 Apr;12(1):29-37. doi: 10.1016/0166-4328(84)90200-6.
The mutant strain of Wistar rats carrying an autosomal recessive gene defect is characterized by a sequence of progressively developing behavioural alterations including hyperexcitability, tremor, olfactory and gustatory automatisms, bradykinesia, ataxia, rigidity, paresis and cachexia. The stereotypy and locomotor responses to increasing doses of apomorphine hydrochloride and D-amphetamine sulphate, and the catalepsy response to increasing doses of haloperidol were studied in mutant rats at the age of 6-7 weeks. In the mutants, both the stereotypy and locomotor responses to amphetamine were enhanced, while stereotypy and locomotor effects induced by apomorphine were unaltered. The cataleptic response to haloperidol was significantly diminished compared to controls. These findings indicate a derangement in the function of basal ganglia in the mutants.
携带常染色体隐性基因缺陷的Wistar大鼠突变株具有一系列逐渐发展的行为改变特征,包括过度兴奋、震颤、嗅觉和味觉自动症、运动迟缓、共济失调、僵硬、轻瘫和恶病质。在6 - 7周龄的突变大鼠中研究了对递增剂量盐酸阿扑吗啡和硫酸D - 苯丙胺的刻板行为和运动反应,以及对递增剂量氟哌啶醇的僵住反应。在突变体中,对苯丙胺的刻板行为和运动反应均增强,而阿扑吗啡诱导的刻板行为和运动效应未改变。与对照组相比,对氟哌啶醇的僵住反应显著减弱。这些发现表明突变体中基底神经节功能紊乱。