Venglustat 对过度表达α-突触核蛋白的小鼠行为和病理学的双重影响。
Double-Edged Effects of Venglustat on Behavior and Pathology in Mice Overexpressing α-Synuclein.
机构信息
Department of Pharmacology, Toxicology and Pharmacy, University of Veterinary Medicine Hannover, Hannover, Germany.
CNS Pharmacology and Drug Discovery, Idorsia Pharmaceuticals Ltd., Allschwil, Switzerland.
出版信息
Mov Disord. 2023 Jun;38(6):1044-1055. doi: 10.1002/mds.29398. Epub 2023 Apr 12.
BACKGROUND
Venglustat is a brain-penetrant, small molecule inhibitor of glucosylceramide synthase used in clinical testing for treatment of Parkinson's disease (PD). Despite beneficial effects in certain cellular and rodent models, patients with PD with mutations in GBA, the gene for lysosomal glucocerebrosidase, experienced worsening of their motor function under venglustat treatment (NCT02906020, MOVES-PD, phase 2 trial).
OBJECTIVE
The objective of this study was to evaluate venglustat in mouse models of PD with overexpression of wild-type α-synuclein.
METHODS
Mice overexpressing α-synuclein (Thy1-aSyn line 61) or Gba-mutated mice with viral vector-induced overexpression of α-synuclein in the substantia nigra were administered venglustat as food admixture. Motor and cognitive performance, α-synuclein-related pathology, and microgliosis were compared with untreated controls.
RESULTS
Venglustat worsened motor function in Thy1-aSyn transgenics on the challenging beam and the pole test. Although venglustat did not alter the cognitive deficit in the Y-maze test, it alleviated anxiety-related behavior in the novel object recognition test. Venglustat reduced soluble and membrane-bound α-synuclein in the striatum and phosphorylated α-synuclein in limbic brain regions. Although venglustat reversed the loss of parvalbumin immunoreactivity in the basolateral amygdala, it tended to increase microgliosis and phosphorylated α-synuclein in the substantia nigra. Furthermore, venglustat also partially worsened motor performance and tended to increase neurofilament light chain in the cerebrospinal fluid in the Gba-deficient model with nigral α-synuclein overexpression and neurodegeneration.
CONCLUSIONS
Venglustat treatment in two mouse models of α-synuclein overexpression showed that glucosylceramide synthase inhibition had differential detrimental or beneficial effects on behavior and neuropathology possibly related to brain region-specific effects. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
背景
Venglustat 是一种脑穿透性、小分子葡萄糖神经酰胺合酶抑制剂,用于治疗帕金森病(PD)的临床试验。尽管在某些细胞和啮齿动物模型中具有有益的效果,但在 GBA 基因突变的 PD 患者中,使用 venglustat 治疗会导致运动功能恶化(NCT02906020,MOVES-PD,二期试验)。
目的
本研究旨在评估 venglustat 在过表达野生型 α-突触核蛋白的 PD 小鼠模型中的作用。
方法
过表达 α-突触核蛋白的小鼠(Thy1-aSyn 线 61)或 Gba 突变小鼠通过病毒载体在黑质中过表达 α-突触核蛋白,并用 venglustat 作为食物混合物进行给药。比较未治疗对照组的运动和认知表现、α-突触核蛋白相关病理和小胶质细胞增生。
结果
Venglustat 加重了 Thy1-aSyn 转基因小鼠在挑战性横梁和杆测试中的运动功能障碍。尽管 venglustat 并未改变 Y 迷宫测试中的认知缺陷,但它减轻了新颖物体识别测试中的焦虑相关行为。Venglustat 降低了纹状体中的可溶性和膜结合 α-突触核蛋白以及边缘脑区中的磷酸化 α-突触核蛋白。尽管 venglustat 逆转了外侧杏仁核中 parvalbumin 免疫反应性的丧失,但它倾向于增加黑质中微胶质细胞增生和磷酸化 α-突触核蛋白。此外,venglustat 还部分加重了运动表现,并倾向于增加 Gba 缺陷型模型中黑质 α-突触核蛋白过表达和神经退行性变的脑脊液中的神经丝轻链。
结论
在两种过表达 α-突触核蛋白的小鼠模型中,venglustat 治疗表明葡萄糖神经酰胺合酶抑制对行为和神经病理学具有不同的有害或有益影响,这可能与脑区特异性效应有关。