具有活性氧清除和抗炎活性的羧甲基壳聚糖低聚糖酶水解物,用于皮肤光损伤的局部治疗

Ziming Zhu , Hui Li , Xiansen Lv , Yan Yang , Baoqin Han , Zhiwen Jiang
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引用次数: 0

摘要

紫外线(UV)辐射造成的皮肤光损伤是一个主要的公共健康问题。紫外线穿透表皮,诱发氧化应激,损害细胞的基本成分。为了应对光损伤对皮肤的影响,人们对具有保湿、抗炎、抗氧化和兼容性等特性的天然成分的需求与日俱增。本文首次将羧甲基壳聚糖寡糖(CM-COS)酶羟化物用于皮肤光损伤的局部治疗。CM-COS 是羧甲基壳聚糖的降解产物,具有高水溶性和多种生物活性。研究结果表明,CM-COS 可促进人类表皮细胞(HaCaT)迁移,且不会产生细胞毒性。在光损伤的 HaCaT 细胞中,CM-COS 可维持细胞活力和细胞骨架完整性,同时抑制活性氧积累、细胞凋亡和细胞周期停滞。根据转录组和 qPCR 数据,CM-COS 可调节 UVB 辐射 HaCaT 细胞中与细胞周期、氧化应激和炎症有关的基因表达。在暴露于 UVB 的小鼠中,CM-COS 的局部治疗可明显减轻红肿和痂皮的形成,并增加光损伤皮肤的含水量。组织学分析表明,CM-COS 治疗后,光损伤皮肤的表皮厚度减少,胶原 I 和胶原 III 沉积增加。此外,根据转录组和 qPCR 数据,与细胞周期、细胞外基质和炎症有关的基因表达也被 CM-COS 显著激活。CM-COS 调节了胶原蛋白和炎症相关蛋白的水平。总之,这些数据证实了 CM-COS 对皮肤光损伤的治疗效果,并凸显了天然海洋寡糖在治疗皮肤疾病(如老化、伤口和烧伤)方面的潜力。
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Carboxymethyl chitosan oligosaccharide enzymatic hydroxylates with reactive oxygen species scavenging and anti-inflammatory activity for topical treatment of skin photodamage
Skin photodamage caused by ultraviolet (UV) radiation is a major public health concern. UVB rays penetrate the epidermis, inducing oxidative stress and compromising essential cellular components. The demand for natural ingredients with properties such as moisturization, anti-inflammatory effects, antioxidant protection, and compatibility is increasing to combat the impact of photodamage on the skin. Herein, the carboxymethyl chitosan oligosaccharide (CM-COS) enzymatic hydroxylates were used on the topical application of skin photodamage for the first time. CM-COS, the degradation product of carboxymethyl chitosan, has high water solubility and multiple biological activities. Results showed that CM-COS promoted human epidermal cell (HaCaT) migration without causing cytotoxicity. In photodamaged HaCaT cells, CM-COS maintained cell viability and cytoskeletal integrity while inhibiting reactive oxygen species accumulation, apoptosis, and cell cycle arrest. CM-COS regulates gene expression related to cell cycle, oxidative stress, and inflammation in UVB-radiated HaCaT based on transcriptomic and qPCR data. In UVB-exposed mice, topical treatment of CM-COS significantly alleviated redness and scab formation and increased the moisture content of photodamaged skin. Histological analyses revealed reduced epidermal thickness and increased collagen I and collagen III deposition in photodamaged skin following CM-COS treatment. Additionally, gene expression related to the cell cycle, extracellular matrix, and inflammation were significantly activated by CM-COS based on transcriptomic and qPCR data. CM-COS modulated the levels of collagen and inflammation-related proteins. Collectively, the data confirm the therapeutic effect of CM-COS against skin photodamage and highlight the potential of natural marine oligosaccharides for treating skin diseases such as aging, wounds, and burns.
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