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Yijing Yang

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Open access Aug 2026

Dietary Lycium barbarum Polysaccharides Support Retinal Redox Homeostasis Through Gut Microbiota–Associated Metabolic Modulation

ABSTRACT Dietary polysaccharides are important bioactive components of functional foods and play a key role in modulating host metabolism through interactions with the gut microbiota. Lycium barbarum polysaccharides (LBP) are widely consumed as dietary supplements; however, their nutritional relevance in linking gut microbiota–associated metabolic regulation to extra‐intestinal tissue homeostasis remains incompletely understood. In this study, we investigated the effects of dietary LBP intake on gut microbiota composition, metabolic profiles, and retinal redox status using oxidatively stressed 661W photoreceptor cells and rd10 mice. In vitro, LBP exposure was associated with reduced intracellular reactive oxygen species accumulation and enhanced cellular antioxidant capacity under oxidative stress conditions. In vivo, dietary LBP intake was associated with partial preservation of retinal structural parameters, including outer nuclear layer thickness and retinal vascular features. Integrated 16S rRNA gene sequencing and untargeted metabolomics analyses demonstrated that dietary LBP intake was associated with coordinated modulation of gut microbiota composition and microbial‐derived metabolic pathways, particularly those related to pantothenate and coenzyme A biosynthesis, aromatic amino acid metabolism, and aminoacyl‐tRNA biosynthesis. These metabolic alterations were reflected in retinal metabolic profiles and accompanied by improved redox balance. Overall, this study highlights the nutritional significance of LBP as a functional polysaccharide and supports the concept that dietary modulation of gut microbiota–associated metabolism may contribute to maintaining retinal metabolic homeostasis. These findings provide a nutritional and food science perspective on the potential role of dietary polysaccharides in supporting tissue function beyond the gastrointestinal tract.

Yi-Jing Yang, Jun Peng, Danyang Li et al. · 0 citations
Open access Aug 2026

A Structurally Characterized Lycium barbarum Polysaccharide Protects Against Retinal Degeneration Through Nrf2 Activation and NF-κB/NLRP3 Suppression

Retinal degeneration is characterized by progressive photoreceptor loss driven by oxidative stress and chronic inflammation, yet effective mutation-independent therapeutic strategies remain limited. Lycium barbarum polysaccharides (LBPs) possess antioxidant and anti-inflammatory activities; however, the structural features responsible for their retinal protective effects remain poorly defined. In this study, crude LBP was fractionated by DEAE-cellulose ion-exchange chromatography, and the most bioactive fraction, LBPF2, was identified using H2O2-injured 661W cone photoreceptor-like cells. LBPF2 was subsequently characterized by high-performance anion-exchange chromatography, SEC-MALLS-RI, GC–MS methylation analysis, and one- and two-dimensional NMR spectroscopy, and its protective effects were evaluated in H2O2-treated 661W cells and rd10 mice. LBPF2 was identified as a homogeneous glucose-rich polysaccharide with an average molecular weight of approximately 41 kDa and a backbone mainly composed of →4)-α-D-Glcp-(1→ and →4,6)-α-D-Glcp-(1→ residues. LBPF2 reduced oxidative stress, inflammation, and apoptosis in H2O2-treated 661W cells, preserved retinal morphology, improved electroretinographic responses and partial retention of rhodopsin immunoreactivity relative to untreated rd10 mice, and restored redox homeostasis in rd10 mice. Pharmacological inhibition of Nrf2 using ML385 attenuated these protective effects, supporting the involvement of Nrf2/HO-1 signaling. Collectively, these findings identify LBPF2 as a structurally characterized neuroprotective polysaccharide that mitigates retinal degeneration through coordinated regulation of oxidative stress and inflammation and highlight its therapeutic potential for retinal degenerative diseases.

Yijing Yang, Shu-Ting Yin, Ying Deng et al. · 0 citations

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