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Phosphodiesterase 9A in Brain Regulates cGMP Signaling Independent of Nitric-Oxide

机译:脑中的磷酸二酯酶9A调节独立于一氧化氮的cGMP信号传导

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PDE9A is a cGMP-specific phosphodiesterase expressed in neurons throughout the brain that has attracted attention as a therapeutic target to treat cognitive disorders. Indeed, PDE9A inhibitors are under evaluation in clinical trials as a treatment for Alzheimer’s disease and schizophrenia. However, little is known about the cGMP signaling cascades regulated by PDE9A. Canonical cGMP signaling in brain follows the activation of neuronal nitric oxide synthase (nNOS) and the generation of nitric oxide, which activates soluble guanylyl cyclase and cGMP synthesis. However, we show that in mice, PDE9A regulates a pool of cGMP that is independent of nNOS, specifically, and nitric oxide signaling in general. This PDE9A-regulated cGMP pool appears to be highly compartmentalized and independent of cGMP pools regulated by several PDEs. These findings provide a new foundation for study of the upstream and downstream signaling elements regulated by PDE9A and its potential as a therapeutic target for brain disease.
机译:PDE9A是在整个大脑神经元中表达的cGMP特异性磷酸二酯酶,作为治疗认知障碍的治疗靶点已引起关注。确实,PDE9A抑制剂正在临床试验中评估作为阿尔茨海默氏病和精神分裂症的治疗方法。但是,关于由PDE9A调控的cGMP信号级联反应知之甚少。脑中的典型cGMP信号传导是神经元一氧化氮合酶(nNOS)的激活和一氧化氮的产生的,一氧化氮可激活可溶性鸟苷酸环化酶和cGMP的合成。但是,我们显示,在小鼠中,PDE9A调节cGMP库,该库独立于nNOS(具体而言)和一氧化氮信号传导。此PDE9A调节的cGMP池似乎是高度分隔的,并且独立于几个PDE所调节的cGMP池。这些发现为研究受PDE9A调控的上游和下游信号传导元件及其作为脑疾病治疗靶标的潜力提供了新的基础。

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