2019
DOI: 10.1111/jocd.12959
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Enzymatic hydrolysates obtained from Trametes versicolor polysaccharopeptides protect human skin keratinocyte against AAPH‑induced oxidative stress and inflammatory

Abstract: Background Polysaccharopeptides (PSPs) extracted from Trametes versicolor show antitumor, anti‐inflammatory, and immunomodulation effects. According to our previous report, the enzymatic hydrolysates obtained from T versicolor PSPs by 80 U/mL β‐1,3‐D‐glucanase (PSPs‐EH80) did not change the functional groups of PSPs but enhanced their antioxidative activities. However, the mechanism elevating the antioxidant and anti‐inflammatory effect of PSPs‐EH80 is not clear. Aims This research focused on the protective me… Show more

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Cited by 8 publications
(5 citation statements)
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“…The epidermis, and therefore keratinocites, have the potential risk of being exposed to traumatic damage; genotoxic stress, including chemical compounds; ionizing radiation; ultraviolet rays [6]; and inflammatory agents [7], or having severe cutaneous adverse reactions to drugs [8].…”
Section: Introductionmentioning
confidence: 99%
“…The epidermis, and therefore keratinocites, have the potential risk of being exposed to traumatic damage; genotoxic stress, including chemical compounds; ionizing radiation; ultraviolet rays [6]; and inflammatory agents [7], or having severe cutaneous adverse reactions to drugs [8].…”
Section: Introductionmentioning
confidence: 99%
“…Moreover, a study on the rabbit model of atherosclerosis indicated that derived PSK from T. versicolor significantly declined the stimulated oxidative damage [71]. In another study, the enzymatic hydrolysate of PSPs extracted from T. versicolor exhibited vigorous antioxidant activities in keratinocytes [72]. Furthermore, the results of a study on human lymphocytes suggested that T. versicolor might protect DNA against oxidizing damage [73].…”
Section: Discussionmentioning
confidence: 98%
“…Regarding the method of Ahmad et al [ 48 ] and Chou et al [ 49 ], we made few modifications. The HUVEC cells were inoculated in 96-well plates and exposed to F1, FD1 and FDS1 (125, 500 μg/mL) for 24 h. DMEM without fucoidan was used as blank.…”
Section: Methodsmentioning
confidence: 99%