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Adenylyl cyclase isoforms as novel therapeutic targets: an exciting example of excitotoxicity neuroprotection.

机译:腺苷酸环化酶同工型作为新型治疗靶标:兴奋性兴奋性神经保护的令人兴奋的例子。

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摘要

The use of transgenic animals lacking one or multiple adenylyl cyclase (AC) isoforms has provided significant information on the roles of AC-dependent signaling in the central nervous system. A recent study provides evidence that AC type 1 (AC1) might be important in glutamate-induced neuronal toxicity. However, the absolute AC specificity revealed in this study contrasts earlier work examining other forms of neurodegeneration. Nonetheless, these observations suggest that specific AC isoforms may represent novel targets for the treatment of central nervous system disorders. It is anticipated that such findings will help catalyze new drug discovery efforts to identify small-molecule modulators of individual AC isoforms.
机译:缺乏一种或多种腺苷酸环化酶(AC)同种型的转基因动物的使用提供了有关AC依赖性信号传导在中枢神经系统中的作用的重要信息。最近的一项研究提供了证据,表明AC 1型(AC1)在谷氨酸诱导的神经元毒性中可能很重要。但是,这项研究揭示的绝对AC特异性与检查其他形式的神经变性的早期工作形成了对比。尽管如此,这些观察结果表明,特定的AC同工型可能代表了中枢神经系统疾病治疗的新靶标。可以预料,这些发现将有助于催化新药的发现,以鉴定出各个AC同工型的小分子调节剂。

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