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Updated clinical pharmacologic considerations for HIV-1 protease inhibitors.
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肽能神经传递和神经退行性疾病中的蛋白酶途径。

Protease pathways in peptide neurotransmission and neurodegenerative diseases.

作者信息

Hook Vivian Y H

机构信息

Department of Pharmacology, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, 9500 Gilman Drive MC 0744, La Jolla, CA 92093-0324, USA.

出版信息

Cell Mol Neurobiol. 2006 Jul-Aug;26(4-6):449-69. doi: 10.1007/s10571-006-9047-7. Epub 2006 May 25.

DOI:10.1007/s10571-006-9047-7
PMID:16724274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11520631/
Abstract
  1. Recent research demonstrates the critical importance of neuroproteases for the production of peptide neurotransmitters, and for the production of toxic peptides in major neurodegenerative diseases that include Alzheimer's (AD) and Huntington's diseases. This review describes the strategies utilized to identify the appropriate proteases responsible for producing active peptides for neurotransmission, with application of such approaches for defining protease mechanisms in neurodegenerative diseases. 2. Integration of multidisciplinary approaches in neurobiology, biochemistry, chemistry, proteomics, molecular biology, and genetics has been utilized for neuroprotease studies. These investigations have identified secretory vesicle cathepsin L for the production of the enkephalin opioid peptide neurotransmitter and other neuropeptides. Furthermore, new results using these strategies have identified secretory vesicle cathepsin B for the production of beta-amyloid (Abeta) in the major regulated secretory pathway that provides activity-dependent secretion of Abeta peptides, which accumulate in AD. 3. CNS neuroproteases that participate in peptide neurotransmission and in neurodegenerative diseases represent new candidate drug targets that may be explored in future research for the development of novel therapeutic agents for neurological conditions.
摘要
  1. 近期研究表明,神经蛋白酶对于肽类神经递质的产生,以及在包括阿尔茨海默病(AD)和亨廷顿舞蹈症在内的主要神经退行性疾病中有毒肽的产生至关重要。本综述描述了用于鉴定负责产生用于神经传递的活性肽的合适蛋白酶的策略,以及将此类方法应用于确定神经退行性疾病中的蛋白酶机制。2. 神经生物学、生物化学、化学、蛋白质组学、分子生物学和遗传学等多学科方法的整合已用于神经蛋白酶研究。这些研究已确定分泌性囊泡组织蛋白酶L参与脑啡肽阿片样肽神经递质和其他神经肽的产生。此外,使用这些策略的新结果已确定分泌性囊泡组织蛋白酶B在主要调节性分泌途径中参与β-淀粉样蛋白(Aβ)的产生,该途径提供Aβ肽的活性依赖性分泌,Aβ肽在AD中会积累。3. 参与肽类神经传递和神经退行性疾病的中枢神经系统神经蛋白酶代表了新的候选药物靶点,未来研究中可能会探索这些靶点以开发用于治疗神经疾病的新型治疗药物。