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Kynurenic acid and kynurenine aminotransferases in retinal aging and neurodegeneration

机译:尿酸和犬尿氨酸转氨酶在视网膜衰老和神经变性中的作用

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摘要

The kynurenine aminotransferases (KATs) KAT I and KAT II are pivotal to the synthesis of kynurenic acid (KYNA), the only known endogenous glutamate receptor antagonist and neuroprotectant. KAT I and II have been found in avian, rodent, and human retina. Expression of KAT I in Müller cell endfeet and KAT II in retinal ganglion cells has been documented. Developmental changes in KAT expression and KYNA concentration in the avian and rodent retina have also been found. Studies of retinal neurodegeneration have shown alterations in KYNA synthesis in the retina in response to retinal ganglion cell loss. In DBA/2J mice, a model of ocular hypertension, an age-dependent decrease of retinal KYNA and KATs was found. In the corpora amylacea in the human retina intensive KAT I and II immunoreactivity was demonstrated. In summary, these findings point to the potential involvement of KYNA in the mechanisms of retinal aging and neurodegeneration.
机译:犬尿氨酸转氨酶(KATs)KAT I和KAT II对于合成犬尿酸(KYNA)是至关重要的,后者是唯一已知的内源性谷氨酸受体拮抗剂和神经保护剂。已在鸟类,啮齿动物和人类视网膜中发现了KAT I和II。已有文献证明MAT-Müller细胞中KAT I的表达以及视网膜神经节细胞中KAT II的表达。还发现了鸟类和啮齿动物视网膜中KAT表达和KYNA浓度的发育变化。视网膜神经变性的研究表明响应视网膜神经节细胞丧失,视网膜中KYNA合成发生改变。在DBA / 2J小鼠中,发现了一种高眼压症模型,其视网膜KYNA和KATs的年龄依赖性降低。在人视网膜的淀粉体中,证实了高强度的KAT I和II的免疫反应性。总之,这些发现表明,KYNA可能参与了视网膜衰老和神经变性的机制。

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