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Modulation of Calcium Oxalate Crystal Growth and Protection from Oxidatively Damaged Renal Epithelial Cells of Corn Silk Polysaccharides with Different Molecular Weights

机译:用不同分子量的玉米丝多糖氧化损伤肾上皮细胞的氧化钙晶体生长和保护的调节

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Corn silk polysaccharide (CSP0; molecular?weight=124?kDa) was degraded by ultrasonication to obtain five degraded polysaccharides, namely, CSP1, CSP2, CSP3, CSP4, and CSP5, with molecular weights of 26.1, 12.2, 6.0, 3.5, and 2.0?kDa, respectively. The structures of these polysaccharides were characterized by FT-IR, 1H NMR, and 13C NMR analyses. The antioxidant activities, including scavenging ability for hydroxyl radicals and DPPH free radicals, chelation ability for Fe2+ ions, and reducing ability of CSP increased with decreased molecular weight of CSPs within 6.0 to 124?kDa. However, antioxidant activity weakened when the molecular weight of CSPs reached 3.5 and 2?kDa. CSP3 with a molecular weight of 6.0?kDa exhibited the strongest antioxidant activity. After protection with 60?μg/mL CSPs, the viability of human renal proximal tubular epithelial cells (HK-2) damaged by nano-COM crystals increased, the level of reactive oxygen species decreased, and the amount of COM crystal adhered onto the cell surface decreased. The ability of CSPs to protect cells from CaOx crystal damage was consistent with their antioxidant activity. CSPs can specifically combine with CaOx crystal to inhibit the conversion of calcium oxalate dihydrate crystal to calcium oxalate monohydrate crystal. All these results showed that the activity of CSPs was closely correlated with molecular weight. A very high or low molecular weight of CSPs was not conducive to their activity. CSPs, especially CSP3 with a molecular weight of 6.0?kDa, can be used as a potential antistone drug.
机译:通过超声波降解玉米丝多糖(CSP0;分子量= 124 kda),以获得五种降解的多糖,即CSP1,CSP2,CSP3,CSP4和CSP5,分子量为26.1,12.2,6.0,3.5和2.0?KDA分别。通过FT-IR,1H NMR和13C NMR分析表征这些多糖的结构。抗氧化活性,包括羟基自由基的清除能力和DPPH自由基,Fe2 +离子的螯合能力,以及CSP的降低能力随6.0至124 kda内的CSP分子量的降低而增加。然而,当CSP的分子量达到3.5和2?KDA时,抗氧化活性削弱。 CSP3分子量为6.0?KDA表现出最强的抗氧化活性。在用60Ω克/ mL CSP进行保护后,通过纳米 - COM晶体损坏的人肾近端上皮细胞(HK-2)的可行性增加,反应性氧物种的水平降低,并且粘附在细胞上的COM晶体的量表面降低。 CSP保护来自CAOX晶体损伤细胞的能力与其抗氧化活性一致。 CSP可以与CAOX晶体特别合并,以抑制草酸钙的二水合物晶体转化为草酸钙一水合物晶体。所有这些结果表明,CSP的活性与分子量密切相关。非常高或低分子量的CSP不利于它们的活性。 CSP,尤其是分子量为6.0?KDA的CSP3,可用作潜在的抗静电药物。

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