Abstract

The structure–activity relationships and repair mechanism of six low-molecular-weight seaweed polysaccharides (SPSs) on oxalate-induced damaged human kidney proximal tubular epithelial cells (HK-2) were investigated. These SPSs included Laminaria japonica polysaccharide, degraded Porphyra yezoensis polysaccharide, degraded Gracilaria lemaneiformis polysaccharide, degraded Sargassum fusiforme polysaccharide, Eucheuma gelatinae polysaccharide, and degraded Undaria pinnatifida polysaccharide. These SPSs have a narrow difference of molecular weight (from 1968 to 4020 Da) after degradation by controlling H2O2 concentration. The sulfate group (–SO3H) content of the six SPSs was 21.7%, 17.9%, 13.3%, 8.2%, 7.0%, and 5.5%, respectively, and the –COOH contents varied between 1.0% to 1.7%. After degradation, no significant difference was observed in the contents of characteristic –SO3H and –COOH groups of polysaccharides. The repair effect of polysaccharides was determined using cell-viability test by CCK-8 assay and cell-morphology test by hematoxylin-eosin staining. The results revealed that these SPSs within 0.1–100 μg/mL did not express cytotoxicity in HK-2 cells, and each polysaccharide had a repair effect on oxalate-induced damaged HK-2 cells. Simultaneously, the content of polysaccharide –SO3H was positively correlated with repair ability. Furthermore, the low-molecular-weight degraded polysaccharides showed better repair activity on damaged HK-2 cells than their undegraded counterpart. Our results can provide reference for inhibiting the formation of kidney stones and for developing original anti-stone polysaccharide drugs.

Highlights

  • Kidney stone is a common disease which occurrence is closely related to the damage of renal tubular epithelial cells

  • We focused on studying the effect of –SO3 H content of seaweed polysaccharides (SPSs) on their ability to repair injured human kidney proximal tubular epithelial cells (HK-2)

  • Sulfated polysaccharides from different seaweeds were selected for this study and further degraded using H2 O2

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Summary

Introduction

Kidney stone is a common disease which occurrence is closely related to the damage of renal tubular epithelial cells. A high concentration of oxalate in the urine can damage renal tubular epithelial cells to trigger a series of oxidative stress reactions and eventually lead to the formation of kidney stones [1,2]. Urinary glycosaminoglycans (GAGs) can protect renal tubular epithelial cells against oxidative damage [3,4] and inhibit the formation of calcium oxalate stones. Seaweed polysaccharides (SPSs) comprise repeating disaccharide sugar chains, similar to GAGs. SPSs may be used to repair damaged renal tubular epithelial cells and inhibit the formation of stones. Polysaccharides from the seaweeds Fucus [5] and Sargassum [6] reportedly play significant protective roles in renal-tissue injury

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