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用于神经元型戈谢病底物还原疗法的可进入中枢神经系统的葡糖神经酰胺合酶抑制剂

CNS-accessible Inhibitor of Glucosylceramide Synthase for Substrate Reduction Therapy of Neuronopathic Gaucher Disease.

作者信息

Marshall John, Sun Ying, Bangari Dinesh S, Budman Eva, Park Hyejung, Nietupski Jennifer B, Allaire Amy, Cromwell Mary A, Wang Bing, Grabowski Gregory A, Leonard John P, Cheng Seng H

机构信息

Sanofi Genzyme, Framingham, Massachusetts, USA.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA; Department of Pediatrics, University of Cincinnati School of Medicine, Cincinnati, Ohio, USA.

出版信息

Mol Ther. 2016 Jun;24(6):1019-1029. doi: 10.1038/mt.2016.53. Epub 2016 Mar 7.

Abstract

Gaucher disease (GD) is caused by a deficiency of glucocerebrosidase and the consequent lysosomal accumulation of unmetabolized glycolipid substrates. Enzyme-replacement therapy adequately manages the visceral manifestations of nonneuronopathic type-1 Gaucher patients, but not the brain disease in neuronopathic types 2 and 3 GD. Substrate reduction therapy through inhibition of glucosylceramide synthase (GCS) has also been shown to effectively treat the visceral disease. Here, we evaluated the efficacy of a novel small molecule inhibitor of GCS with central nervous system (CNS) access (Genz-682452) to treat the brain disease. Treatment of the conduritol β epoxide-induced mouse model of neuronopathic GD with Genz-682452 reduced the accumulation of liver and brain glycolipids (>70% and >20% respectively), extent of gliosis, and severity of ataxia. In the genetic 4L;C* mouse model, Genz-682452 reduced the levels of substrate in the brain by >40%, the extent of gliosis, and paresis. Importantly, Genz-682452-treated 4L;C* mice also exhibited an ~30% increase in lifespan. Together, these data indicate that an orally available antagonist of GCS that has CNS access is effective at attenuating several of the neuropathologic and behavioral manifestations associated with mouse models of neuronopathic GD. Therefore, Genz-682452 holds promise as a potential therapeutic approach for patients with type-3 GD.

摘要

戈谢病(GD)是由葡糖脑苷脂酶缺乏以及由此导致的未代谢糖脂底物在溶酶体中蓄积所致。酶替代疗法可有效控制非神经病变型1型戈谢病患者的内脏表现,但对神经病变型2型和3型戈谢病的脑部疾病无效。通过抑制葡糖神经酰胺合酶(GCS)进行底物减少疗法也已被证明可有效治疗内脏疾病。在此,我们评估了一种新型的具有中枢神经系统(CNS)通透性的GCS小分子抑制剂(Genz-682452)治疗脑部疾病的疗效。用Genz-682452治疗conduritolβ环氧化物诱导的神经病变型戈谢病小鼠模型,可减少肝脏和脑部糖脂的蓄积(分别减少>70%和>20%)、胶质增生程度以及共济失调的严重程度。在遗传性4L;C小鼠模型中,Genz-682452可使脑部底物水平降低>40%、胶质增生程度减轻以及轻瘫症状改善。重要的是,经Genz-682452治疗的4L;C小鼠寿命也延长了约30%。总之,这些数据表明,一种具有CNS通透性的口服可用GCS拮抗剂可有效减轻与神经病变型戈谢病小鼠模型相关的几种神经病理和行为表现。因此,Genz-682452有望成为治疗3型戈谢病患者的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d582/4923322/c2c70ec59292/mt201653f1.jpg

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