Dendrimer-conjugated nSMase2 inhibitor as a novel therapeutic approach for Alzheimer's Disease

树枝状聚合物结合的 nSMase2 抑制剂作为阿尔茨海默病的新型治疗方法

• 批准号: 10397570
• 负责人: Rana Rais
• 金额: $ 52.62万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-05-01 至 2025-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10397570
• 关键词: 3xTg-AD mouse; Abeta synthesis; Address; Adrenoleukodystrophy; Alzheimer' s Disease; Alzheimer' s disease brain; Alzheimer' s disease model; Alzheimer' s disease patient; Alzheimer' s disease therapeutic; American; Animal Model; Animals; Biochemical; Biodistribution; Biogenesis; Biological Assay; Biological Availability; Biological Markers; Blood Circulation; Body Weight; Brain; Brain Injuries; Brain imaging; Cells; Ceramides; Cerebrum; Chemicals; Chemistry; Childhood; Chronic; Clinical; Clinical Chemistry; Clinical Trials; Cognition; Cognitive; Collaborations; Data; Dendrimers; Disease; Disease Progression; Dose; Drug Kinetics; Enzymes; Etiology; Exhibits; Experimental Models; Fluorescence Spectroscopy; Future; Generations; Genetic; Half-Life; Histologic; Histology; Human; Hydrolysis; Hydroxyl Radical; In Vitro; Kinetics; Label; Ligands; Liquid substance; Mediating; Membrane; Metabolic; Methods; Microglia; Minor; Modification; Mus; N-Methylaspartate; National Center for Advancing Translational Sciences; Neuroglia; Oral; Oxidative Stress; Pathologic; Penetration; Persons; Pharmaceutical Preparations; Pharmacology; Phase I Clinical Trials; Phenols; Plasma; Play; Production; Property; Proteins; RNA; Radial; Role; Safety; Senile Plaques; Signaling Molecule; Slice; Source; Sphingomyelinase; Sphingomyelins; Stimulus; Stomach; Symptoms; Synapses; Testing; Therapeutic; Time; Up-Regulation; Western Blotting; Work; abeta accumulation; analog; arm; brain volume; chemical stability; clinical translation; cohort; cyanine dye 5; drug discovery; efficacy testing; esterase; exosome; experience; extracellular vesicles; high throughput analysis; high throughput screening; human old age (65+); improved; in vivo; inhibitor; liquid chromatography mass spectrometry; mouse model; multidisciplinary; nanoparticle; near infrared dye; neural network; neuroinflammation; neuron loss; novel; novel therapeutic intervention; response; tau Proteins; therapeutic target; treatment duration; uptake; vesicular release; water maze

The number of people suffering from Alzheimer's disease (AD) is steadily rising and current treatments only provide minor symptom amelioration. Results from recent clinical trials targeting amyloid-β (Aβ) production or clearance were disappointing, prompting a reexamination of approaches to AD treatment. Brains from AD patients exhibit accumulation of ceramide, a signaling molecule and an integral component of exosomal membranes. One major source of ceramide is through the hydrolysis of sphingomyelin catalyzed by neutral sphingomyelinase 2 (nSmase2). Even though transient increases in ceramide through nSMase2 upregulation are part of normal brain functioning, experimental evidence indicates that chronic nSMase2 upregulation results in negative effects including neuroinflammation and oxidative stress. Recent studies implicate nSMase2 in both Aβ aggregation and tau protein propagation through exosome secretion from glial cells. Moreover, inhibition of exosome synthesis by genetic or pharmacological inhibition of nSMase2 was shown to block Aβ aggregation and tau propagation in both in vitro and in vivo AD models, thus opening a new avenue for AD therapeutics. Unfortunately, there are no clinically useful nSMase2 inhibitors. Current inhibitors are weak (µM-mM) with poor physicochemical properties and/or limited brain penetration. In collaboration with NCATS we carried out a human nSMase2 high throughput screen (HTS) of >350,000 compounds. Filtering and analysis of HTS hits led to discovery of 2,6-dimethoxy-4-(5-phenyl-4-(thiophen-2-yl)-1H-imidazol -2-yl) phenol (DPTIP) the first nM inhibitor (IC50 = 30 nM). DPTIP was found to be selective and capable of dose-dependently inhibiting exosome release in glial cultures. Unfortunately, in vivo DPTIP exhibited rapid clearance resulting in a short half-life (t1/2< 0.5h) and had poor oral bioavailability (F<5%). Structural modifications (~200 analogs synthesized by our group) have not led to substantial improvements. Given its significant clinical potential, we propose to address the pharmacokinetic limitations by utilizing dendrimer nanoparticles to deliver DPTIP selectively to activated glial cells in the brain. Our team discovered that systemically-administered hydroxyl-terminated poly(amidoamine) (PAMAM) dendrimers (~4 nm in size) target activated glia in the injured brain, without the need for targeting ligands, showing minimal uptake in healthy brains. While the dendrimers are endocytosed and retained by activated glial cells in the brain maintaining exposure for >2 weeks, they are rapidly cleared from the periphery (plasma t1/2 ~ 6-24 h). We have validated the brain targeting, safety, and efficacy in multiple small and large animal models, and are in Phase 1 clinical trials with our first dendrimer product (D-NAC in childhood cerebral adrenoleukodystrophy). Herein, we propose to synthesize and evaluate the in vivo pharmacokinetics and target engagement of two differently sized dendrimers conjugated to DPTIP (D-DPTIP) following peroral administration. The optimal conjugate assessed by brain imaging, LC/MS bioanalysis, and functional inhibition of glial nSMase2 activity will be tested for efficacy and safety in two established mouse models of AD. We have assembled a highly experienced team with expertise in dendrimer nanoparticles (Rangaramanujam), pharmacokinetics, biomarkers and target engagement studies (Rais) and pharmacology, drug discovery and clinical translation (Slusher).

患有阿尔茨海默病（AD）的人数正在稳步上升，目前只有治疗方法