コンテンツへスキップ
Merck
  • Glycation of human cortical and cancellous bone captures differences in the formation of Maillard reaction products between glucose and ribose.

Glycation of human cortical and cancellous bone captures differences in the formation of Maillard reaction products between glucose and ribose.

PloS one (2015-02-14)
Grażyna E Sroga, Alankrita Siddula, Deepak Vashishth
要旨

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.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
アセトニトリル, suitable for HPLC, gradient grade, ≥99.9%
Sigma-Aldrich
硫酸, ACS reagent, 95.0-98.0%
Sigma-Aldrich
酢酸, glacial, ACS reagent, ≥99.7%
Sigma-Aldrich
酢酸, glacial, ReagentPlus®, ≥99%
Sigma-Aldrich
アセトニトリル, ACS reagent, ≥99.5%
Sigma-Aldrich
アセトニトリル, for HPLC, for UV, ≥99.9% (GC)
Sigma-Aldrich
アセトニトリル, suitable for HPLC, gradient grade, ≥99.9%
Sigma-Aldrich
硫酸, 99.999%
Sigma-Aldrich
酢酸, glacial, ≥99.99% trace metals basis
Sigma-Aldrich
酢酸 溶液, suitable for HPLC
Sigma-Aldrich
パーフルオロ酪酸, 98%
Sigma-Aldrich
酢酸, glacial, puriss., meets analytical specification of Ph. Eur., BP, USP, FCC, 99.8-100.5%
Sigma-Aldrich
硫酸, puriss. p.a., for determination of Hg, ACS reagent, reag. ISO, reag. Ph. Eur., 95.0-97.0%
Sigma-Aldrich
アセトニトリル, suitable for HPLC-GC, ≥99.8% (GC)
Sigma-Aldrich
硫酸, SAJ first grade, ≥95.0%
Sigma-Aldrich
硫酸, JIS special grade, ≥95.0%
Sigma-Aldrich
酢酸, for luminescence, BioUltra, ≥99.5% (GC)
Sigma-Aldrich
アセトニトリル, biotech. grade, ≥99.93%
Sigma-Aldrich
硫酸, puriss., meets analytical specification of Ph. Eur., BP, 95-97%
Sigma-Aldrich
ヘプタフルオロ酪酸, ≥99.0% (GC)
USP
氷酢酸, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
酢酸, ≥99.5%, FCC, FG
Sigma-Aldrich
酢酸, natural, ≥99.5%, FG
Sigma-Aldrich
5α-アンドロスタン-17β-オール-3-オン, ≥97.5%
Sigma-Aldrich
アセトニトリル, anhydrous, 99.8%
Sigma-Aldrich
硫酸 溶液, puriss. p.a., ≥25% (T)
Sigma-Aldrich
キニーネ, 90%
Sigma-Aldrich
キニーネ, suitable for fluorescence, anhydrous, ≥98.0% (dried material, NT)
Sigma-Aldrich
酢酸, ≥99.7%
Sigma-Aldrich
酢酸, JIS special grade, ≥99.7%