BIOUSIAN GLYCONEUROPEPTIDE AMPHIPATHS PENETRATE THE BBB

BIOUSIAN 糖欧洲肽两亲蛋白穿透血脑屏障

基本信息

批准号：
8056497
负责人：
ROBIN POLT
金额：
$ 30.43万
依托单位：
UNIVERSITY OF ARIZONA
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-04-10 至 2013-03-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8056497
关键词：
Adopted Adsorption Adverse effects Affinity Agonist Analgesics Anti-Anxiety Agents Antidepressive Agents Anxiety Area Behavioral Behavioral Assay Benchmarking Binding Biodistribution Biological Biological Assay Biological Availability Biological Models Biotechnology Blood - brain barrier anatomy Blood capillaries Brain Carbohydrate Conformation Chronic Circular Dichroism Clinical Collaborations Comorbidity Coupled Data Dependence Development Diffusion Disease Dose-Limiting Drug Administration Routes Drug Delivery Systems Drug Design Drug Kinetics Dynorphins Endocytosis Endorphins Enkephalins Equipment Evaluation Evaluation Studies Functional disorder Glycopeptides Glycosides Goals Grant Human In Situ In Vitro Laboratories Lead Measures Mediating Membrane Mental Depression Methodology Methods Micelles Modeling Molecular Conformation Morphine Mus Neuropeptides Nuclear Nuclear Magnetic Resonance Opioid Opioid Analgesics Opioid Receptor Outcome Oxycodone Paper Partition Coefficient Pathology Penetration Peptides Pharmaceutical Preparations Pharmacodynamics Pharmacologic Substance Pharmacology Pharmacopoeias Phase Physical Dependence Pre-Clinical Model Process Publishing Research Research Personnel Robin bird Rodent Model Role Running Sea Side Staging Structure Syndrome Techniques Technology Testing Therapeutic Toxic effect Ursidae Family Vertebral column Water addiction aqueous base capillary chronic pain delta opioid receptor design drug candidate drug development efficacy testing glycosylation improved in vivo inflammatory neuropathic pain interdisciplinary approach membrane model nervous system disorder neurochemistry non-cancer pain pre-clinical programs rapid growth solid solution tool

项目摘要

DESCRIPTION (provided by applicant): The penetration of the blood-brain barrier (BBB) by neurologically active peptides has remained an enigmatic problem for many decades. Studies have shown that glycosylation of small peptides (enkephalins) leads to glycopeptides that are more stable, and which penetrate the BBB in pharmacologically useful amounts. Mechanistic studies have shown that endocytosis at the endothelial layer of the brain capillaries is responsible for transport. Recent studies indicate that much larger peptides (endorphins) are capable of adopting helical conformations in the presence of membranes, and are also transported across the BBB. This proposal seeks to explore and exploit the transport and pharmacology of glycosylated dynorphin and endorphin peptides, and to evaluate them as candidates for the treatment of chronic pain. A unique group of investigators has been assembled in order to bring synthetic organic, biophysical, and pharmacological tools to bear on this problem. Solution and solid phase NMR techniques will examine the effects of glycopeptide adsorption to membrane models, seeking to understand the effects on glycopeptide conformation, as well perturbations of the membrane during adsorption. Data from these studies will be correlated with glycopeptide stability, transport rates, and binding affinities. Finally, behavioral studies in mice will be carried out to test the effects of systematic administration of these drugs in models of inflammatory and neuropathic pain, opioid-mediated side effect (Gl transit, tolerance/dependence, etc.) and anxiety/depression. Based on our previous research and published papers on delta receptors, we predict that some of the compounds will have better efficacy, reduced toxicity and/or improved side effect profiles compared to morphine-like analgesics. More importantly, the central hypothesis (that glycosylation strategies can be applied to larger peptides to increase CNS bioavailability) will be rigorously tested using a multidisciplinary approach. If the hypothesis is supported, the technology may lead to a sea-changing platform technology on which to base the clinical development of diverse pharmaceuticals based on endogenous neuropeptides.

描述（由申请人提供）：神经学活跃肽对血脑屏障（BBB）的渗透一直是数十年来的神秘问题。研究表明，小肽（Enkephalins）的糖基化导致更稳定的糖肽，并且在药理上有用的量中穿透了BBB。机械研究表明，脑毛细血管内皮层的内吞作用负责运输。最近的研究表明，较大的肽（内啡肽）能够在存在膜的情况下采用螺旋构象，并且也跨BBB运输。该提案旨在探索和利用糖基化强肽和内啡肽肽的运输和药理学，并评估它们作为治疗慢性疼痛的候选者。为了携带合成有机，生物物理和药理学工具来解决这个问题，已经组装了一组独特的研究者。溶液和固相NMR技术将检查糖肽吸附对膜模型的影响，以寻求了解对糖肽构象的影响，以及在吸附过程中膜的扰动。这些研究的数据将与糖肽稳定性，运输速率和结合亲和力相关。最后，将进行小鼠的行为研究，以测试这些药物在炎症和神经性疼痛，阿片类药物介导的副作用（GL Transit，耐受性/依赖性等）和焦虑/抑郁症模型中的系统施用的影响。根据我们先前的研究和关于三角洲受体的发表论文，我们预测，与吗啡样镇痛药相比，某些化合物将具有更好的功效，降低毒性和/或改善的副作用谱。更重要的是，将使用多学科方法严格测试中心假设（可以将糖基化策略应用于较大的肽以增加CNS生物利用度）。如果支持该假设，该技术可能会导致一种改变海上的平台技术，以基于内源性神经肽的各种药物的临床开发为基础。

项目成果

期刊论文数量（9）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Effects of the novel glycopeptide opioid agonist MMP-2200 in preclinical models of Parkinson's disease.

DOI：
10.1016/j.brainres.2011.07.038
发表时间：
2011-09-21
期刊：
Brain research
影响因子：
2.9
作者：
Yue X;Falk T;Zuniga LA;Szabò L;Porreca F;Polt R;Sherman SJ
通讯作者：
Sherman SJ

Preparation of S-glycoside surfactants and cysteine thioglycosides using minimally competent Lewis acid catalysis.

使用最低能力路易斯酸催化制备 S-糖苷表面活性剂和半胱氨酸硫代糖苷。

DOI：
10.1016/j.carres.2015.12.008
发表时间：
2016
期刊：
Carbohydrate research
影响因子：
3.1
作者：
Szabó,LajosZ;Hanrahan,DillonJ;Jones,EvanM;Martin,Erin;Pemberton,JeanneE;Polt,Robin
通讯作者：
Polt,Robin

Opioid glycopeptide analgesics derived from endogenous enkephalins and endorphins.

DOI：
10.4155/fmc.11.195
发表时间：
2012-02
期刊：
Future medicinal chemistry
影响因子：
4.2
作者：
Li Y;Lefever MR;Muthu D;Bidlack JM;Bilsky EJ;Polt R
通讯作者：
Polt R

CNS active O-linked glycopeptides.

DOI：
10.3389/fchem.2015.00040
发表时间：
2015
期刊：
Frontiers in chemistry
影响因子：
5.5
作者：
Jones EM;Polt R
通讯作者：
Polt R

Phosphorylation of enkephalins: NMR and CD studies in aqueous and membrane-mimicking environments.

DOI：
10.1111/j.1747-0285.2011.01203.x
发表时间：
2011-11
期刊：
Chemical biology & drug design
影响因子：
3
作者：
Yeomans L;Muthu D;Lowery JJ;Martinez HN;Abrell L;Lin G;Strom K;Knapp BI;Bidlack JM;Bilsky EJ;Polt R
通讯作者：
Polt R