Wisniecki Anna, Correa Merce, Arizzi Maria N, Ishiwari Keitha, Salamone John D
Department of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.
Psychopharmacology (Berl). 2003 Nov;170(2):140-9. doi: 10.1007/s00213-003-1521-z. Epub 2003 Jun 24.
Although most rodent studies related to parkinsonian symptoms have focused on locomotion, tremulous jaw movements also have been used as a rodent model of tremor for investigating the circuitry of the basal ganglia.
There are multiple pathways involved in the generation of parkinsonian symptoms. The globus pallidus is a basal ganglia relay nucleus, and the present study was conducted to investigate the effect of pallidal GABA antagonism on locomotion and tremulous jaw movements.
Suppression of locomotion and induction of tremulous jaw movements were produced by repeated (i.e., 14 day) systemic administration of the dopamine D2 antagonist haloperidol, and by acute systemic injection of the muscarinic agonist pilocarpine. The GABA(A) antagonist bicuculline was injected into the globus pallidus, and its effects on locomotion in haloperidol- and pilocarpine-treated rats were assessed in the first group of experiments. In the second group of experiments, the effects of intrapallidal infusions of bicuculline on haloperidol- and pilocarpine-induced jaw movements were observed.
Pallidal GABA antagonism stimulated locomotion when no other treatment was present, and also when animals were coadministered haloperidol or pilocarpine. Bicuculline suppressed haloperidol-induced jaw movements in a dose-related manner, and had no effect on pilocarpine-induced jaw movements.
These results support the notion that there are distinct pathways conveying basal ganglia outflow and demonstrate that the striatopallidal pathway is involved in the generation of the haloperidol-induced tremulous jaw movements. These findings are consistent with some features of current models of basal ganglia function and may lead to an understanding of the specific mechanisms that generate parkinsonian symptoms.
尽管大多数与帕金森症状相关的啮齿动物研究都集中在运动方面,但颤抖的下颌运动也已被用作震颤的啮齿动物模型,用于研究基底神经节的神经回路。
帕金森症状的产生涉及多种途径。苍白球是基底神经节的中继核,本研究旨在探讨苍白球γ-氨基丁酸(GABA)拮抗作用对运动和颤抖下颌运动的影响。
通过重复(即14天)全身给予多巴胺D2拮抗剂氟哌啶醇以及急性全身注射毒蕈碱激动剂毛果芸香碱来抑制运动并诱导颤抖的下颌运动。将GABA(A)拮抗剂荷包牡丹碱注入苍白球,并在第一组实验中评估其对氟哌啶醇和毛果芸香碱处理的大鼠运动的影响。在第二组实验中,观察苍白球内注入荷包牡丹碱对氟哌啶醇和毛果芸香碱诱导的下颌运动的影响。
在没有其他处理时,以及动物同时接受氟哌啶醇或毛果芸香碱处理时,苍白球GABA拮抗作用均刺激运动。荷包牡丹碱以剂量相关的方式抑制氟哌啶醇诱导的下颌运动,而对毛果芸香碱诱导的下颌运动没有影响。
这些结果支持这样的观点,即存在不同的途径传递基底神经节的输出,并表明纹状体-苍白球通路参与氟哌啶醇诱导的颤抖下颌运动的产生。这些发现与当前基底神经节功能模型的一些特征一致,可能有助于理解产生帕金森症状的具体机制。