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L-蛋氨酸-S,R-亚砜亚胺对人谷氨酰胺合成酶的抑制作用——与神经疾病治疗的相关性

Inhibition of human glutamine synthetase by L-methionine-S,R-sulfoximine-relevance to the treatment of neurological diseases.

作者信息

Jeitner Thomas M, Cooper Arthur J L

机构信息

Neurosciences, Biomedical Research Core, Winthrop University Hospital, 222 Station Plaza North, Mineola, NY, 11501, USA,

出版信息

Metab Brain Dis. 2014 Dec;29(4):983-9. doi: 10.1007/s11011-013-9439-6. Epub 2013 Oct 18.

Abstract

At high concentrations, the glutamine synthetase inhibitor L-methionine-S,R-sulfoximine (MSO) is a convulsant, especially in dogs. Nevertheless, sub-convulsive doses of MSO are neuroprotective in rodent models of hyperammonemia, acute liver disease, and amyotrophic lateral sclerosis and suggest MSO may be clinically useful. Previous work has also shown that much lower doses of MSO are required to produce convulsions in dogs than in primates. Evidence from the mid-20th century suggests that humans are also less sensitive. In the present work, the inhibition of recombinant human glutamine synthetase by MSO is shown to be biphasic-an initial reversible competitive inhibition (K i 1.19 mM) is followed by rapid irreversible inactivation. This K i value for the human enzyme accounts, in part, for relative insensitivity of primates to MSO and suggests that this inhibitor could be used to safely inhibit glutamine synthetase activity in humans.

摘要

在高浓度时,谷氨酰胺合成酶抑制剂L-蛋氨酸-S,R-亚砜亚胺(MSO)是一种惊厥剂,对犬类尤其如此。然而,亚惊厥剂量的MSO在高氨血症、急性肝病和肌萎缩侧索硬化症的啮齿动物模型中具有神经保护作用,这表明MSO可能具有临床应用价值。先前的研究还表明,与灵长类动物相比,犬类产生惊厥所需的MSO剂量要低得多。20世纪中叶的证据表明,人类对MSO的敏感性也较低。在本研究中,MSO对重组人谷氨酰胺合成酶的抑制作用呈双相性——最初是可逆的竞争性抑制(Ki为1.19 mM),随后是快速的不可逆失活。这种人类酶的Ki值部分解释了灵长类动物对MSO相对不敏感的原因,并表明这种抑制剂可用于安全地抑制人类谷氨酰胺合成酶的活性。

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