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Interactions between APP secretases and inflammatory mediators

机译:APP分泌​​酶与炎症介质之间的相互作用

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There is now a large body of evidence linking inflammation to Alzheimer's disease (AD). This association manifests itself neuropathologically in the presence of activated microglia and astrocytes around neuritic plaques and increased levels of inflammatory mediators in the brains of AD patients. It is considered that amyloid-β peptide (Aβ), which is derived from the processing of the longer amyloid precursor protein (APP), could be the most important stimulator of this response, and therefore determining the role of the different secretases involved in its generation is essential for a better understanding of the regulation of inflammation in AD. The finding that certain non-steroidal anti-inflammatory drugs (NSAIDs) can affect the processing of APP by inhibiting β- and γ-secretases, together with recent revelations that these enzymes may be regulated by inflammation, suggest that they could be an interesting target for anti-inflammatory drugs. In this review we will discuss some of these issues and the role of the secretases in inflammation, independent of their effect on Aβ formation.
机译:现在有大量证据将炎症与阿尔茨海默氏病(AD)联系起来。这种关联在神经病理学上表现为神经胶质斑周围存在活化的小胶质细胞和星形胶质细胞,并在AD患者的大脑中增加了炎症介质的水平。人们认为,淀粉样蛋白-β肽(Aβ)源自更长的淀粉样蛋白前体蛋白(APP)的加工过程,可能是该反应的最重要刺激因素,因此确定了参与其反应的不同分泌酶的作用。产生对于更好地了解AD炎症的调节至关重要。某些非甾体类抗炎药(NSAIDs)可以通过抑制β-和γ-分泌酶来影响APP的加工,以及最近发现这些酶可能受炎症调节的发现,表明它们可能是一个有趣的靶标用于消炎药。在这篇综述中,我们将讨论其中的一些问题以及分泌酶在炎症中的作用,而与它们对Aβ形成的影响无关。

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