Ferguson S A, Cada A M, Gray E P, Paule M G
Neurobehavioral Teratology Laboratory, Division of Neurotoxicology, National Center for Toxicological Research/FDA, HFT-132, 3900 NCTR Road, Jefferson, AR 72079, USA.
Behav Brain Res. 2001 Nov 29;126(1-2):135-46. doi: 10.1016/s0166-4328(01)00259-5.
The cerebellum is critically involved in temporal processes in the millisecond range and may be involved in longer time estimations (i.e. in the seconds range). Estimates in the millisecond range are impaired after developmentally induced cerebellar alterations, however, little is known about the effects of similar alterations on longer timing performance. Appropriately timed DFMO treatment reliably causes cerebellar stunting in rats, however, its effects on temporal estimation performance are unknown. Here, male and female Sprague-Dawley rats were treated with subcutaneous injections of 500 mg/kg DFMO on postnatal days 5-12, causing a 10% cerebellar weight reduction at adulthood. As adults, subjects were tested under one of two paradigms - a differential reinforcement of low response rate (DRL) task requiring that subjects withhold a lever press response for 10-14 s or a temporal response differentiation (TRD) task requiring that subjects maintain a lever press response for 10-14 s. Training and steady-state performance of the DRL and TRD tasks were not significantly altered by DFMO treatment. Performance after acute challenges with two dopaminergic agonists (2.00-7.50 mg/kg methylphenidate and 0.10-1.00 mg/kg d-amphetamine) was measured after which all subjects underwent behavioral extinction. Generally, performance after methylphenidate and d-amphetamine was similar in control and DFMO-treated rats and DFMO treatment had no differential effects on performance during extinction. These results support findings from an earlier study [Ferguson SA, Paule MG, Holson RR. Neonatal dexamethasoneon day 7 in rats causes behavioral alterations reflective of hippocampal, but not cerebellar, deficits. Neurotoxicol Teratol, 2001; 23:57-69] indicating that developmental cerebellar stunting has few effects on time estimation within the range of seconds.
小脑在毫秒级的时间进程中起着关键作用,并且可能参与更长时间的估计(即秒级范围)。发育诱导的小脑改变后,毫秒级范围内的估计会受损,然而,关于类似改变对更长时间计时表现的影响知之甚少。适当定时给予二氟甲基鸟氨酸(DFMO)治疗可可靠地导致大鼠小脑发育迟缓,但其对时间估计表现的影响尚不清楚。在此,对雄性和雌性斯普拉格-道利大鼠在出生后第5至12天皮下注射500mg/kg的DFMO进行治疗,导致成年时小脑重量减轻10%。成年后,对实验对象在两种范式之一进行测试——一种是低反应率差异强化(DRL)任务,要求实验对象在10至14秒内不按压杠杆;另一种是时间反应区分(TRD)任务,要求实验对象在10至14秒内持续按压杠杆。DFMO治疗并未显著改变DRL和TRD任务的训练及稳态表现。在用两种多巴胺能激动剂(2.00至7.50mg/kg哌甲酯和0.10至1.00mg/kg右旋苯丙胺)进行急性激发后测量表现,之后所有实验对象都经历行为消退。一般来说,哌甲酯和右旋苯丙胺给药后的表现在对照组和DFMO治疗组大鼠中相似,且DFMO治疗对消退期间的表现没有差异影响。这些结果支持了早期一项研究[弗格森SA、保勒MG、霍尔森RR。大鼠出生后第7天给予新生地塞米松会导致反映海马而非小脑缺陷的行为改变。神经毒理学与致畸学,2001;23:57 - 69]的发现,表明发育性小脑发育迟缓对秒级范围内的时间估计影响很小。