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反应时间和运动时间的缺陷与MPTP诱导的纹状体多巴胺耗竭的猴子运动减少的相关性。

Deficits in reaction times and movement times as correlates of hypokinesia in monkeys with MPTP-induced striatal dopamine depletion.

作者信息

Schultz W, Studer A, Romo R, Sundström E, Jonsson G, Scarnati E

机构信息

Institut de Physiologie, Université de Fribourg, Switzerland.

出版信息

J Neurophysiol. 1989 Mar;61(3):651-68. doi: 10.1152/jn.1989.61.3.651.

Abstract
  1. We quantitatively assessed deficits in the initiation and execution of arm movements occurring after destruction of nigrostriatal dopamine neurons by systemic administration of MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) (Sigma). Three monkeys performed a reaction time task in which they reached toward a single and constant target for food reward. 2. After administration of MPTP, all three monkeys showed hypokinesia necessitating dopamine precursor or receptor agonist treatment. The partial recovery of one animal from initial akinesia after 19 days permitted discontinuation of dopaminergic drug therapy, although marked hypokinesia remained present. The two other animals displayed additional, intermittent phases of rigidity and activation tremor and needed continuous dopaminergic drug therapy for most of the postlesion period. 3. Administration of MPTP significantly prolonged EMG reaction time in prime mover muscles and arm movement reaction time by 47-225% and 18-129%, respectively, on the six sides of the three animals, compared with control measurements before the lesion. EMG and arm movement reaction time increased over consecutive trials in most sessions comprising 110-130 movements, the first 20 movements showing almost normal values. The delay time between onsets of EMG and arm movement showed unsystematic changes. These deficits in movement initiation were observed both with and without dopamine precursor therapy. They lasted during the whole testing period of several months. 4. Linear correlations between arm movement onset and EMG onset in the two prime mover muscles, the extensor digitorum communis and the biceps, showed coefficients of mostly 0.7-0.9, both before and after MPTP. These data suggest that the temporal relationship between onsets of arm movement and EMG were not substantially affected by MPTP. 5. Arm movement time was divided into two phases. The duration of movement between the resting key and the target, a small food-containing box located ahead of the animal, was denoted as reaching movement time. The following hand manipulation inside the food box was measured as box movement time. After MPTP, both measures were significantly prolonged by 10-103% and 12-251%, respectively, on the six sides of the three monkeys. These deficits in movement execution were observed both with and without dopaminergic drug therapy and during the whole testing period. 6. Task performance after MPTP treatment was studied in one monkey in the absence of dopaminergic drug therapy. EMG and arm movement reaction times recovered partially over several weeks, while the prolongations in reaching and box movement times remained unchanged.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 我们通过全身注射MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)(西格玛公司)定量评估了黑质纹状体多巴胺神经元破坏后出现的手臂运动起始和执行缺陷。三只猴子执行了一项反应时间任务,即它们朝着一个单一且固定的目标伸手以获取食物奖励。

  2. 注射MPTP后,所有三只猴子均出现运动迟缓,需要多巴胺前体或受体激动剂治疗。一只动物在19天后从最初的运动不能中部分恢复,从而可以停止多巴胺能药物治疗,尽管仍存在明显的运动迟缓。另外两只动物表现出额外的、间歇性的强直和激活震颤阶段,并且在损伤后的大部分时间里都需要持续的多巴胺能药物治疗。

  3. 与损伤前的对照测量相比,在三只动物的六个肢体上,注射MPTP后,原动肌的肌电图反应时间和手臂运动反应时间分别显著延长了47%-225%和18%-129%。在大多数包含110-至130次运动的试验中,肌电图和手臂运动反应时间在连续试验中增加,前20次运动显示几乎正常的值。肌电图和手臂运动起始之间的延迟时间显示出无规律的变化。无论有无多巴胺前体治疗,均观察到这些运动起始缺陷。它们在几个月的整个测试期间持续存在。

  4. 在注射MPTP前后,两块原动肌(指总伸肌和二头肌)的手臂运动起始和肌电图起始之间的线性相关性显示系数大多为0.7-0.9。这些数据表明,MPTP对手臂运动起始和肌电图起始之间的时间关系没有实质性影响。

  5. 手臂运动时间分为两个阶段。从静止按键到目标(位于动物前方的一个装有少量食物的小盒子)之间的运动持续时间被记为伸手运动时间。在食物盒内接下来的手部操作被测量为盒子运动时间。注射MPTP后,在三只猴子的六个肢体上,这两个测量值分别显著延长了10%-103%和12%-251%。无论有无多巴胺能药物治疗,在整个测试期间均观察到这些运动执行缺陷。

  6. 在一只猴子身上,在没有多巴胺能药物治疗的情况下研究了MPTP治疗后的任务表现。肌电图和手臂运动反应时间在几周内部分恢复,而伸手和盒子运动时间的延长保持不变。(摘要截断于400字)

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