Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC 20007, USA.
J Neurosci. 2012 Sep 19;32(38):13326-32. doi: 10.1523/JNEUROSCI.2295-12.2012.
Cervical dystonia (CD; spasmodic torticollis) can be evoked by inhibition of substantia nigra pars reticulata (SNpr) in the nonhuman primate (Burbaud et al., 1998; Dybdal et al., 2012). Suppression of GABAergic neurons that project from SNpr results in the disinhibition of the targets to which these neurons project. It therefore should be possible to prevent CD by inhibition of the appropriate nigral target region(s). Here we tested the hypothesis that the deep and intermediate layers of the superior colliculus (DLSC), a key target of nigral projections, are required for the emergence of CD. To test this hypothesis, we pretreated the DLSC of four macaques with the GABA(A) agonist muscimol to determine whether this treatment would prevent CD evoked by muscimol infusions in SNpr. Our data supported this hypothesis: inhibition of DLSC attenuated CD evoked by muscimol in SNpr in all four animals. In two of the four subjects, quadrupedal rotations were evoked by muscimol application into SNpr sites that were distinct from those that induced dystonia. We found that inhibition of DLSC did not significantly alter quadrupedal rotations, suggesting that this response is dissociable from the SNpr-evoked CD. Our results are the first to demonstrate a role of DLSC in mediating the expression of CD. Furthermore, these data reveal a functional relationship between SNpr and DLSC in regulating posture and movement in the nonhuman primate, raising the possibility that the nigrotectal pathway has potential as a target for therapeutic interventions for CD.
颈部肌张力障碍 (CD; 痉挛性斜颈) 可通过抑制非人灵长类动物的黑质网状部 (SNpr) 诱发 (Burbaud 等人, 1998; Dybdal 等人, 2012)。抑制从 SNpr 投射的 GABA 能神经元会导致这些神经元投射的靶区去抑制。因此,通过抑制适当的黑质靶区,应该可以预防 CD。在这里,我们检验了一个假设,即黑质投射的关键靶区——上丘的深层和中层 (DLSC),是 CD 出现所必需的。为了验证这一假设,我们用 GABA(A) 激动剂 muscimol 预处理了四只猕猴的 DLSC,以确定这种处理是否会防止 SNpr 中 muscimol 输注引起的 CD。我们的数据支持这一假设:在所有四只动物中,DLSC 的抑制减轻了 SNpr 中 muscimol 诱发的 CD。在四只动物中的两只中,四肢旋转是由 SNpr 部位的 muscimol 应用引起的,这些部位与引起肌张力障碍的部位不同。我们发现,DLSC 的抑制并没有显著改变四肢旋转,这表明这种反应与 SNpr 诱发的 CD 是可分离的。我们的结果首次证明了 DLSC 在介导 CD 表达中的作用。此外,这些数据揭示了 SNpr 和 DLSC 之间在调节非人灵长类动物姿势和运动方面的功能关系,这表明黑质网状通路有可能成为治疗 CD 的靶点。