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中性内肽酶抑制会因低镁血症而增强P物质介导的炎症反应。

Neutral endopeptidase inhibition enhances substance P mediated inflammation due to hypomagnesemia.

作者信息

Weglicki William B, Chmielinska Joanna J, Tejero-Taldo Isabel, Kramer Jay H, Spurney Christopher F, Viswalingham Kandan, Lu Bao, Mak I Tong

机构信息

The Department of Biochemistry & Molecular Biology, 439 Ross Hall, The George Washington University Medical Center, 2300 Eye ST., N.W., Washington, DC 20037, USA.

出版信息

Magnes Res. 2009 Sep;22(3):167S-173S.

Abstract

During dietary deficiency of magnesium neurogenic inflammation is mediated, primarily, by elevated levels of substance P (SP). The enzyme most specific for degrading this neuropeptide is neutral endopeptidase (NEP). In recent studies we found that pharmacological inhibition of NEP by phosphoramidon resulted in elevated plasma levels of SP and greater oxidative stress. We also observed that hypomagnesemia reduced cardiac and intestinal expression of NEP. In these magnesium-deficient rats increased intestinal permeability and impaired cardiac contractility occurred. In our colony of genetically-engineered NEP knockout mice that have reduced ability to degrade SP, we found increased oxidative stress that was prevented by SP (neurokinin-1) receptor blockade. Thus, we submit that inhibition of NEP by pharmacological, genetic and dietary approaches (magnesium restriction), causes greater neurogenic inflammation that may result in increased intestinal and cardiac dysfunction.

摘要

在饮食缺镁期间,神经源性炎症主要由P物质(SP)水平升高介导。降解这种神经肽最具特异性的酶是中性内肽酶(NEP)。在最近的研究中,我们发现磷酰胺对NEP的药理抑制导致血浆SP水平升高和更大的氧化应激。我们还观察到低镁血症降低了心脏和肠道中NEP的表达。在这些缺镁大鼠中,出现了肠道通透性增加和心脏收缩功能受损。在我们的基因工程NEP基因敲除小鼠群体中,其降解SP的能力降低,我们发现氧化应激增加,而这种氧化应激可通过SP(神经激肽-1)受体阻断来预防。因此,我们认为通过药理、基因和饮食方法(限制镁摄入)抑制NEP会导致更大的神经源性炎症,这可能会导致肠道和心脏功能障碍增加。

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