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铁不饱和人乳铁蛋白对过氧化氢诱导的肠上皮细胞氧化损伤的影响。

Effects of iron-unsaturated human lactoferrin on hydrogen peroxide-induced oxidative damage in intestinal epithelial cells.

作者信息

Shoji Hiromichi, Oguchi Satoshi, Shinohara Koichi, Shimizu Toshiaki, Yamashiro Yuichiro

机构信息

Department of Pediatrics and Adolescent Medicine, Juntendo University School of Medicine, 113-0033 Tokyo, Japan.

出版信息

Pediatr Res. 2007 Jan;61(1):89-92. doi: 10.1203/01.pdr.0000250198.22735.20.

Abstract

Human milk (HM) contains various bioactive antioxidants. Lactoferrin (Lf) has been assumed to be one of the major antioxidants in HM. We examined the antioxidative properties of iron-unsaturated human Lf (apo-hLf, the major form of Lf in HM) in two intestinal epithelial cell lines: (1) An intestinal epithelial cell line (IEC-6) were preincubated for 24 h with either 50 microg/mL of apo-hLf, iron-saturated human Lf (holo-hLf), iron-unsaturated bovine transferrin (apo-bTf), or 800 ng/mL of the iron-chelating compound deferoxamine (DFX), followed by hydrogen peroxide (H2O2) challenge to induce oxidative stress. Survival rates were significantly higher in the cells preincubated with apo-hLf and DFX than those preincubated with holo-hLf. (2) Caco-2 cells were preincubated with or without apo-hLf for 24 h, followed by an H2O2 challenge. Intracellular oxidative stress was assessed by a fluorescent probe, 2',7'-dichlorodihydrofluorescein diacetate (DCF-DA). Fluorescent intensity of cell images and cell homogenates was significantly lower in the cells preincubated with apo-hLF than those preincubated without apo-hLF. Our study indicates that apo-hLf alleviates H2O2-induced oxidative damage in intestinal cells due to the iron-chelating capacity. Therefore, Lf in HM may act as an antioxidant in the gastrointestinal tract (GIT).

摘要

人乳(HM)含有多种生物活性抗氧化剂。乳铁蛋白(Lf)被认为是人乳中的主要抗氧化剂之一。我们在两种肠上皮细胞系中检测了铁不饱和人Lf(脱铁人乳铁蛋白,是人乳中Lf的主要形式)的抗氧化特性:(1)将一种肠上皮细胞系(IEC-6)分别用50μg/mL的脱铁人Lf、铁饱和人Lf(全铁人乳铁蛋白)、铁不饱和牛转铁蛋白(脱铁牛转铁蛋白)或800 ng/mL的铁螯合化合物去铁胺(DFX)预孵育24小时,随后用过氧化氢(H2O2)激发以诱导氧化应激。用脱铁人Lf和DFX预孵育的细胞的存活率显著高于用全铁人乳铁蛋白预孵育的细胞。(2)将Caco-2细胞在有或无脱铁人Lf的情况下预孵育24小时,随后进行H2O2激发。通过荧光探针2',7'-二氯二氢荧光素二乙酸酯(DCF-DA)评估细胞内氧化应激。用脱铁人Lf预孵育的细胞的细胞图像和细胞匀浆的荧光强度显著低于未用脱铁人Lf预孵育的细胞。我们的研究表明,脱铁人Lf由于其铁螯合能力减轻了H2O2诱导的肠细胞氧化损伤。因此,人乳中的Lf可能在胃肠道(GIT)中作为一种抗氧化剂发挥作用。

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