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Reduction of iron/zinc interactions using metal bound to the caseinophosphopeptide 1-25 of beta-casein

机译:使用与β-酪蛋白酪蛋白磷酸肽1-25结合的金属减少铁/锌相互作用

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The isolated, perfused rat duodenal loop system was used to assess the influence of binding Fe to soluble 1-25 caseinophosphopeptide (beta-CN (1-25)), produced by the hydrolysis of beta-casein, against the inhibition of its absorption by Zn. Fe (100鎊250LM) was perfused as Fe gluconate (FeGluc) or bound to the beta-CN (1-25) (Fe-CN), alone (controls) or in the presence of Zn as ZnSO4 or as (Zn-CN) at Fe:Zn ratios ranging from 2:1 to 1:5. ZnSO4 significantly reduced disappearance from the lumen (Q1) andnet Fe absorption at Fe:Zn ratios from 1:1.5 to 1:5 (P<0.001). Fe mucosal retention (Q2) did not change significantly. When Zn was provided as Zn-CN, Q1, Q2 and Fe absorption did not significantly differ from control group for FeGluc. ZnSO4 and Zn-CN did not reduce significantly Q1, Q2 or Fe absorption for Fe-CN whatever ratios considered. It is concluded that binding Fe to beta-CN (1-25) prevented Zn from inhibiting its absorption and this could have therapeutic applications in dietary supplementationof trace-elements.
机译:分离的灌注大鼠十二指肠环系统用于评估Fe与可溶的1-25酪蛋白磷酸肽(β-CN(1-25))结合所产生的抑制作用,该作用是由β-酪蛋白水解产生的,抑制了铁的吸收锌单独(对照)或在存在Zn的情况下,以葡萄糖酸铁(FeGluc)或结合到β-CN(1-25)(Fe-CN)或在Zn的存在下以ZnSO4或(Zn-CN )的Fe:Zn比率范围为2:1至1:5。 ZnSO4在Fe:Zn比从1:1.5至1:5时显着减少了管腔(Q1)的消失和净铁吸收(P <0.001)。铁黏膜保留(Q2)没有明显变化。当提供Zn作为Zn-CN时,FeGluc的Q1,Q2和Fe吸收与对照组无显着差异。无论考虑哪种比率,ZnSO4和Zn-CN均不会显着降低Fe-CN的Q1,Q2或Fe吸收。结论是,Fe与β-CN(1-25)的结合阻止了Zn抑制其吸收,在膳食中微量元素的补充中可能具有治疗应用。

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