磷酸盐活化谷氨酰胺酶抑制剂在精神分裂症药物治疗中的作用

Andra Mihali, C. Sorrento, Francine S Katz, Genevieve J. Kaunitz, J. Macdonald, S. Subramani, S. Rayport
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引用次数: 0

摘要

在大脑中,磷酸盐激活的谷氨酰胺酶催化谷氨酰胺再循环为谷氨酸,用于兴奋性神经传递。在小鼠实验中,磷酸盐激活谷氨酰胺酶的基因敲低已被证明对精神分裂症样症状具有恢复力,这表明抑制谷氨酰胺酶可能对精神分裂症的药物治疗具有治疗潜力。由于没有已知的谷氨酰胺酶的神经活性抑制剂,即进入大脑的抑制剂,因此使用基于荧光的测定法对58000种神经化合物进行了高通量筛选;该筛选确定了320个潜在的谷氨酰胺酶抑制剂。进行二次筛选以获得特异性;这产生了10个点击。通过动力学分析,发现了两个低微摩尔活性的引线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Inhibitors of Phosphate-activated Glutaminase for the Pharmacotherapy of Schizophrenia
In the brain, phosphate-activated glutaminase catalyzes the recycling of glutamine back to glutamate for excitatory neurotransmission. In mice, genetic knockdown of phosphate-activated glutaminase has been shown to confer resilience to schizophrenia-like symptoms, suggesting that inhibition of glutaminase may have therapeutic potential for the pharmacotherapy of schizophrenia. As there are no known neuroactive inhibitors of glutaminase, i.e. inhibitors that get into the brain, high-throughput screening of a library of 58,000 neuroative compounds was conducted using a fluorescence-based assay; this screen identified 320 potential glutaminase inhibitors. A secondary screen was carried out to access specificity; this yielded 10 hits. Using a kinetic analysis, two leads with low micromolar activity were found.
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