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2
Comparative Effectiveness and Safety of Cognitive Enhancers for Treating Alzheimer's Disease: Systematic Review and Network Metaanalysis.认知增强剂治疗阿尔茨海默病的有效性和安全性的比较:系统评价和网络荟萃分析。
J Am Geriatr Soc. 2018 Jan;66(1):170-178. doi: 10.1111/jgs.15069. Epub 2017 Sep 29.
3
Butyrylcholinesterase gene transfer in obese mice prevents postdieting body weight rebound by suppressing ghrelin signaling.肥胖小鼠中的丁酰胆碱酯酶基因转移通过抑制胃饥饿素信号来防止节食后的体重反弹。
Proc Natl Acad Sci U S A. 2017 Oct 10;114(41):10960-10965. doi: 10.1073/pnas.1706517114. Epub 2017 Sep 25.
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Evaluation of the Edrophonium Challenge Test for Cervical Dystonia.用于颈部肌张力障碍的依酚氯铵激发试验的评估
Intern Med. 2017 Sep 15;56(18):2415-2421. doi: 10.2169/internalmedicine.8555-16. Epub 2017 Aug 21.
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Efficacy and safety of sugammadex versus neostigmine in reversing neuromuscular blockade in adults.舒更葡糖钠与新斯的明在成人中逆转神经肌肉阻滞的疗效与安全性比较
Cochrane Database Syst Rev. 2017 Aug 14;8(8):CD012763. doi: 10.1002/14651858.CD012763.
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Design, synthesis and biological evaluation of novel coumarin-N-benzyl pyridinium hybrids as multi-target agents for the treatment of Alzheimer's disease.设计、合成及新型香豆素-N-苄基吡啶𬭩杂合体的生物学评价作为阿尔茨海默病治疗的多靶点药物。
Eur J Med Chem. 2017 Oct 20;139:48-59. doi: 10.1016/j.ejmech.2017.07.055. Epub 2017 Jul 24.
7
Polyionic complexes of butyrylcholinesterase and poly-l-lysine-g-poly(ethylene glycol): Comparative kinetics of catalysis and inhibition and in vitro inactivation by proteases and heat.丁酰胆碱酯酶与聚-L-赖氨酸-g-聚(乙二醇)的聚离子复合物:催化与抑制的比较动力学以及蛋白酶和热的体外失活作用
Chem Biol Interact. 2017 Sep 25;275:86-94. doi: 10.1016/j.cbi.2017.07.019. Epub 2017 Jul 27.
8
Assessment of Enzyme Inhibition: A Review with Examples from the Development of Monoamine Oxidase and Cholinesterase Inhibitory Drugs.酶抑制作用的评估:以单胺氧化酶和胆碱酯酶抑制药物开发为例的综述
Molecules. 2017 Jul 15;22(7):1192. doi: 10.3390/molecules22071192.
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Cell Mol Neurobiol. 2018 Jan;38(1):7-12. doi: 10.1007/s10571-017-0523-z. Epub 2017 Jul 15.
10
Therapeutic Delivery of Butyrylcholinesterase by Brain-Wide Viral Gene Transfer to Mice.通过全脑病毒基因转移向小鼠递送丁酰胆碱酯酶用于治疗
Molecules. 2017 Jul 8;22(7):1145. doi: 10.3390/molecules22071145.

胆碱酯酶与毒与药之间的微妙界限。

Cholinesterases and the fine line between poison and remedy.

机构信息

Department of Physiological Sciences, Interdisciplinary Toxicology Program, Oklahoma State University, Stillwater, OK 74078, USA.

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN 55902, USA.

出版信息

Biochem Pharmacol. 2018 Jul;153:205-216. doi: 10.1016/j.bcp.2018.01.044. Epub 2018 Jan 31.

DOI:10.1016/j.bcp.2018.01.044
PMID:29409903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5959757/
Abstract

Acetylcholinesterase (AChE, EC 3.1.1.7) and butyrylcholinesterase (BChE, EC 3.1.1.8) are related enzymes found across the animal kingdom. The critical role of acetylcholinesterase in neurotransmission has been known for almost a century, but a physiological role for butyrylcholinesterase is just now emerging. The cholinesterases have been deliberately targeted for both therapy and toxicity, with cholinesterase inhibitors being used in the clinic for a variety of disorders and conversely for their toxic potential as pesticides and chemical weapons. Non-catalytic functions of the cholinesterases (ChEs) participate in both neurodevelopment and disease. Manipulating either the catalytic activities or the structure of these enzymes can potentially shift the balance between beneficial and adverse effect in a wide number of physiological processes.

摘要

乙酰胆碱酯酶(AChE,EC 3.1.1.7)和丁酰胆碱酯酶(BChE,EC 3.1.1.8)是在动物界中发现的相关酶。乙酰胆碱酯酶在神经传递中的关键作用已经为人所知近一个世纪,但丁酰胆碱酯酶的生理作用才刚刚出现。人们故意针对胆碱酯酶进行治疗和毒性研究,临床上使用胆碱酯酶抑制剂治疗各种疾病,而胆碱酯酶抑制剂作为杀虫剂和化学武器也具有潜在毒性。胆碱酯酶(ChEs)的非催化功能参与神经发育和疾病。操纵这些酶的催化活性或结构可能会在许多生理过程中改变有益和有害影响之间的平衡。