Migdalska-Richards Anna, Ko Wai Kin D, Li Qin, Bezard Erwan, Schapira Anthony H V
Department of Clinical Neurosciences, Institute of Neurology, University College London, NW3 2PF, United Kingdom.
Motac Neuroscience, Manchester, United Kingdom.
Synapse. 2017 Jul;71(7). doi: 10.1002/syn.21967. Epub 2017 Mar 17.
Mutations in the glucocerebrosidase 1 (GBA1) gene are related to both Parkinson disease (PD) and Gaucher disease (GD). In both cases, the condition is associated with deficiency of glucocerebrosidase (GCase), the enzyme encoded by GBA1. Ambroxol is a small molecule chaperone that has been shown in mice to cross the blood-brain barrier, increase GCase activity and reduce alpha-synuclein protein levels. In this study, we analyze the effect of ambroxol treatment on GCase activity in healthy nonhuman primates. We show that daily administration of ambroxol results in increased brain GCase activity. Our work further indicates that ambroxol should be investigated as a novel therapy for both PD and neuronopathic GD in humans.
葡萄糖脑苷脂酶1(GBA1)基因的突变与帕金森病(PD)和戈谢病(GD)均相关。在这两种情况下,病情都与GBA1编码的酶——葡萄糖脑苷脂酶(GCase)缺乏有关。氨溴索是一种小分子伴侣,在小鼠实验中已表明它能穿过血脑屏障,提高GCase活性并降低α-突触核蛋白水平。在本研究中,我们分析了氨溴索治疗对健康非人灵长类动物GCase活性的影响。我们发现,每日给予氨溴索可使脑内GCase活性增加。我们的工作进一步表明,应将氨溴索作为治疗人类PD和神经病变型GD的一种新疗法进行研究。