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用于 N-甲基-D-天冬氨酸功能的人丝氨酸消旋酶调节剂的研发

The Development of a Regulator of Human Serine Racemase for N-Methyl-D-aspartate Function.

作者信息

Lu Lu-Ping, Chang Wei-Hua, Mao Yi-Wen, Cheng Min-Chi, Zhuang Xiao-Yi, Kuo Chi-Sheng, Lai Yi-An, Shih Tsai-Miao, Chou Teh-Ying, Tsai Guochuan Emil

机构信息

Department of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei 221416, Taiwan.

Institute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.

出版信息

Biomedicines. 2024 Apr 12;12(4):853. doi: 10.3390/biomedicines12040853.

Abstract

It is crucial to regulate N-methyl-D-aspartate (NMDA) function bivalently depending on the central nervous system (CNS) conditions. CNS disorders with NMDA hyperfunction are involved in the pathogenesis of neurotoxic and/or neurodegenerative disorders with elevated D-serine, one of the NMDA receptor co-agonists. On the contrary, NMDA-enhancing agents have been demonstrated to improve psychotic symptoms and cognition in CNS disorders with NMDA hypofunction. Serine racemase (SR), the enzyme regulating both D- and L-serine levels through both racemization (catalysis from L-serine to D-serine) and β-elimination (degradation of both D- and L-serine), emerges as a promising target for bidirectional regulation of NMDA function. In this study, we explored using dimethyl malonate (DMM), a pro-drug of the SR inhibitor malonate, to modulate NMDA activity in C57BL/6J male mice via intravenous administration. Unexpectedly, 400 mg/kg DMM significantly elevated, rather than decreased (as a racemization inhibitor), D-serine levels in the cerebral cortex and plasma. This outcome prompted us to investigate the regulatory effects of dodecagalloyl-α-D-xylose (α12G), a synthesized tannic acid analog, on SR activity. Our findings showed that α12G enhanced the racemization activity of human SR by about 8-fold. The simulated and fluorescent assay of binding affinity suggested a noncooperative binding close to the catalytic residues, Lys56 and Ser84. Moreover, α12G treatment can improve behaviors associated with major CNS disorders with NMDA hypofunction including hyperactivity, prepulse inhibition deficit, and memory impairment in animal models of positive symptoms and cognitive impairment of psychosis. In sum, our findings suggested α12G is a potential therapeutic for treating CNS disorders with NMDA hypofunction.

摘要

根据中枢神经系统(CNS)的状况对N-甲基-D-天冬氨酸(NMDA)功能进行双向调节至关重要。NMDA功能亢进的中枢神经系统疾病与神经毒性和/或神经退行性疾病的发病机制有关,这些疾病中NMDA受体共激动剂之一的D-丝氨酸水平升高。相反,在NMDA功能低下的中枢神经系统疾病中,已证明NMDA增强剂可改善精神病症状和认知。丝氨酸消旋酶(SR)通过消旋作用(从L-丝氨酸催化生成D-丝氨酸)和β-消除作用(D-丝氨酸和L-丝氨酸的降解)调节D-丝氨酸和L-丝氨酸水平,是NMDA功能双向调节的一个有前景的靶点。在本研究中,我们探索通过静脉注射丙二酸二甲酯(DMM,SR抑制剂丙二酸的前体药物)来调节C57BL/6J雄性小鼠的NMDA活性。出乎意料的是,400mg/kg的DMM显著提高了大脑皮层和血浆中D-丝氨酸的水平,而不是降低(作为消旋酶抑制剂)。这一结果促使我们研究合成的单宁酸类似物十二没食子酰-α-D-木糖(α12G)对SR活性的调节作用。我们的研究结果表明,α12G可将人SR的消旋酶活性提高约8倍。结合亲和力的模拟和荧光测定表明,其与催化残基Lys56和Ser84附近存在非协同结合。此外,α12G治疗可改善与NMDA功能低下的主要中枢神经系统疾病相关的行为,包括动物模型中精神病阳性症状和认知障碍的多动、前脉冲抑制缺陷和记忆损害。总之,我们的研究结果表明α12G是治疗NMDA功能低下的中枢神经系统疾病的潜在疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e7/11048566/475ddcb56d5a/biomedicines-12-00853-sch001.jpg

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