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Glycation of Human Cortical and Cancellous Bone Captures Differences in the Formation of Maillard Reaction Products between Glucose and Ribose

机译:糖皮质激素和松质骨的糖化捕获葡萄糖和核糖之间的美拉德反应产物的形成差异。

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摘要

To better understand some aspects of bone matrix glycation, we used an in vitro glycation approach. Within two weeks, our glycation procedures led to the formation of advanced glycation end products (AGEs) at the levels that corresponded to approx. 25–30 years of the natural in vivo glycation. Cortical and cancellous bones from human tibias were glycated in vitro using either glucose (glucosylation) or ribose (ribosylation). Both glucosylation and ribosylation led to the formation of higher levels of AGEs and pentosidine (PEN) in cancellous than cortical bone dissected from all tested donors (young, middle-age and elderly men and women). More efficient glycation of bone matrix proteins in cancellous bone most likely depended on the higher porosity of this tissue, which facilitated better accessibility of the sugars to the matrix proteins. Notably, glycation of cortical bone from older donors led to much higher AGEs levels as compared to young donors. Such efficient in vitro glycation of older cortical bone could result from aging-related increase in porosity caused by the loss of mineral content. In addition, more pronounced glycation in vivo would be driven by elevated oxidation processes. Interestingly, the levels of PEN formation differed pronouncedly between glucosylation and ribosylation. Ribosylation generated very high levels of PEN (approx. 6- vs. 2.5-fold higher PEN level than in glucosylated samples). Kinetic studies of AGEs and PEN formation in human cortical and cancellous bone matrix confirmed higher accumulation of fluorescent crosslinks for ribosylation. Our results suggest that in vitro glycation of bone using glucose leads to the formation of lower levels of AGEs including PEN, whereas ribosylation appears to support a pathway toward PEN formation. Our studies may help to understand differences in the progression of bone pathologies related to protein glycation by different sugars, and raise awareness for excessive sugar supplementation in food and drinks.
机译:为了更好地了解骨基质糖化的某些方面,我们使用了体外糖化方法。在两周内,我们的糖化步骤导致形成了高级糖化终产物(AGEs),其水平相当于大约50%。 25-30年的天然体内糖化作用。使用葡萄糖(糖基化)或核糖(核糖基化)在体外对人胫骨的皮质和松质骨糖化。糖基化和核糖基化均导致在松质骨中形成的AGEs和戊糖苷(PEN)的水平高于从所有测试的供体(年轻,中年和老年男性和女性)解剖的皮质骨。松质骨中骨基质蛋白更有效的糖基化很可能取决于该组织的较高孔隙率,这有助于糖更好地接近基质蛋白。值得注意的是,与年轻的供体相比,年龄较大的供体的皮质骨糖基化导致更高的AGEs水平。老年皮质骨的这种有效的体外糖基化作用可能是由于矿物质含量减少引起的孔隙度的老化相关增加。另外,升高的氧化过程将驱动体内更明显的糖基化。有趣的是,在糖基化和核糖基化之间,PEN的形成水平明显不同。核糖基化产生非常高的PEN水平(比糖基化样品的PEN水平高约6倍至2.5倍)。在人类皮质和松质骨基质中AGEs和PEN形成的动力学研究证实,用于核糖基化的荧光交联剂的积累更多。我们的结果表明,使用葡萄糖对骨骼进行体外糖基化会导致形成较低水平的AGEs(包括PEN),而核糖基化似乎支持了通向PEN形成的途径。我们的研究可能有助于了解与不同糖分使蛋白质糖基化有关的骨病理学进展的差异,并提高人们对食品和饮料中过量补充糖分的认识。

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