Senkowska Anna, Ossowska Krystyna
Faculty of Biotechnology, Jagiellonian University, Gronostajowa 7, PL 30-387 Kraków, Poland.
Pol J Pharmacol. 2003 Nov-Dec;55(6):935-50.
The efficacy of the majority of drugs currently used for treatment of Parkinson's disease is insufficient. Moreover, such therapeutics are not devoid of serious side effects. Multiple studies on animal models of parkinsonism have shown that new class of drugs, acting selectively on metabotropic glutamate receptors (mGluRs) might be very promising for the future therapy of Parkinson's disease. This review briefly describes changes in glutamatergic transmission in the neuronal circuitry of the extrapyramidal system that occur in parkinsonian patients, contains background information on structure, function and distribution of mGluRs throughout the basal ganglia and concentrates on discussion of the results obtained from numerous animal model studies aimed to establish potential antiparkinsonian properties of various mGluR ligands. The reviewed literature data indicate that among these compounds group I mGluR antagonists and group II mGluR agonists might be beneficial to the treatment of parkinsonian akinesia and muscle rigidity.
目前用于治疗帕金森病的大多数药物疗效不足。此外,这类疗法并非没有严重的副作用。多项针对帕金森病动物模型的研究表明,一类新型药物,即选择性作用于代谢型谷氨酸受体(mGluRs)的药物,可能对帕金森病的未来治疗非常有前景。本综述简要描述了帕金森病患者锥体外系神经回路中谷氨酸能传递的变化,包含了mGluRs在整个基底神经节的结构、功能和分布的背景信息,并着重讨论了众多动物模型研究的结果,这些研究旨在确定各种mGluR配体的潜在抗帕金森病特性。综述的文献数据表明,在这些化合物中,I组mGluR拮抗剂和II组mGluR激动剂可能对治疗帕金森病性运动不能和肌肉强直有益。