吕佳桐, 林海生, 秦小明, 章超桦, 曹文红, 高加龙, 郑慧娜. 牡蛎及其酶解产物抗皮肤光老化的初步研究[J]. 南方水产科学, 2021, 17(1): 91-100. DOI: 10.12131/20200141
引用本文: 吕佳桐, 林海生, 秦小明, 章超桦, 曹文红, 高加龙, 郑慧娜. 牡蛎及其酶解产物抗皮肤光老化的初步研究[J]. 南方水产科学, 2021, 17(1): 91-100. DOI: 10.12131/20200141
LÜ Jiatong, LIN Haisheng, QIN Xiaoming, ZHANG Chaohua, CAO Wenhong, GAO Jialong, ZHENG Huina. Preliminary study on resistance of oyster and its enzymatic hydrolysis products to skin photoaging[J]. South China Fisheries Science, 2021, 17(1): 91-100. DOI: 10.12131/20200141
Citation: LÜ Jiatong, LIN Haisheng, QIN Xiaoming, ZHANG Chaohua, CAO Wenhong, GAO Jialong, ZHENG Huina. Preliminary study on resistance of oyster and its enzymatic hydrolysis products to skin photoaging[J]. South China Fisheries Science, 2021, 17(1): 91-100. DOI: 10.12131/20200141

牡蛎及其酶解产物抗皮肤光老化的初步研究

Preliminary study on resistance of oyster and its enzymatic hydrolysis products to skin photoaging

  • 摘要: 文章探讨了香港牡蛎 (Crassostrea hongkongensis) 肉粉 (Oyster meat, OM) 及其酶解产物 (Oyster hydrolysis, OH) 对紫外线诱导的小鼠 (Mus musculus) 皮肤光老化的保护作用。紫外线 (UVA+UVB) 每天照射构建小鼠皮肤光老化模型并灌胃OM和OH,分为低、中、高三组 (30、90、180 mg·kg−1) 给药,持续8周。结果表明,OM和OH可减轻小鼠皮肤皱纹,提高皮肤弹性,减少皮下血管的萎缩,防止血管通透性增加;皮肤HE染色结果表明,中高剂量的OM和OH可显著减缓表皮层过度角化增厚 (P<0.05);Masson染色和醛品红染色结果表明,OM和OH可减少胶原纤维的卷曲和降解,避免弹性纤维的异常增生,恢复真皮细胞外基质网络的排列;与模型组相比,OM和OH可使皮肤中超氧化物歧化酶 (SOD) 和谷胱甘肽过氧化氢酶 (GSH-Px) 的活力显著提高,同时使丙二醛 (MDA) 和8-羟基脱氧鸟苷 (8-OHDG) 的浓度降低 (P<0.05);OM和OH可抑制基质金属蛋白酶 (MMP-3、MMP-9) 的表达,显著降低真皮中羟脯胺酸 (Hyp) 的降解;此外,高剂量的OH可显著降低皮肤中炎症因子细胞白介素6 (IL-6) 和肿瘤坏死因子 (TNF-α) 的表达,并通过提高转化生长因子 (TGF-β) 来提高皮肤抗炎能力。

     

    Abstract: To explore the protective effects of Hong Kong oyster (Crassostrea hongkongensis) meat (OM) and its enzymatic hydrolysis (OH) products on UV-induced photoaging of mouse (Mus musculus) skin. Ultraviolet rays (UVA+UVB) were irradiated every day to build a mouse skin photoaging model. The mice were given OM and OH daily and divided into low, medium and high dose groups (30, 90, 180 mg·kg−1) for eight weeks. The results show that OM and OH can reduce mice skin wrinkles, improve skin elasticity, reduce subcutaneous blood vessel atrophy, and prevent increase in vascular permeability. The results of skin HE staining show that medium and high doses of OM and OH can slow down hyperkeratosis and epidermis thickening significantly (P<0.05). Masson staining and aldehyde fuchsin staining results show that OM and OH can reduce the curling and degradation of collagen fibers, avoid abnormal proliferation of elastic fibers, and restore the arrangement of the dermal extracellular matrix network. Compared with the model group, OM and OH can increase the enzyme activity of superoxide dismutase (SOD) and glutathione catalase (GSH-Px) in skin, while malondialdehyde (MDA) and 8-hydroxydeoxyguanosine (8-OHDG) concentration decreased significantly (P<0.05). OM and OH can inhibit the expression of matrix metalloproteinases (MMP-3, MMP-9), and reduce the degradation of hydroxyproline (Hyp) in the dermis significantly. In addition, high doses of OH can reduce the expression of inflammatory factors, interleukin 6 (IL-6) and tumor necrosis factor (TNF-α) in the skin significantly, and increase the skin's anti-inflammatory ability by increasing transforming growth factor (TGF-β).

     

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