{"title":"对莼菜伤口愈合的体外和体内评估","authors":"Chien-Hsing Wang, Zih-Ting Huang, Kuo-Feng Tai","doi":"10.1101/2024.09.13.612816","DOIUrl":null,"url":null,"abstract":"Ulva lactuca (U. lactuca) is an important seaweed species. Some ingredients in these seaweeds are thought to accelerate wound healing. However, limited data on the use of seaweed for wound healing exists. This study examined whether ethanol or aqueous extracts of U. lactuca promote antioxidant and anti-inflammatory properties in vitro and wound healing in vitro and in vivo. Cell proliferation, antioxidation, and migration were observed in NIH3T3 cells treated with U. lactuca extract in vitro. Both U. lactuca extracts were examined for their ability to inhibit inflammatory cytokine synthesis in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. In vivo experiments involved four groups of albino mice (BALB/c; 10 mice per group). One 1.0 cm2 wound was created via excision of full-thickness skin on the back of all mice. Mice in Group I mice were treated topically with the ethanol extract of U. lactuca (25 mg/mL) for 10 d. group II mice were treated topically with an aqueous extract of U. lactuca (12.5 mg/mL) for 10 d. Group III received topical application of phosphate-buffered saline solution. Group IV wounds were maintained without treatment. Both extracts significantly increased fibroblast proliferation. The antioxidant activity of the U. lactuca extract was determined using a total antioxidant capacity assay. Both extracts inhibited the release of tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-?? from LPS-mediated inflammation in RAW 264.7 cells. These extracts also upregulated the expression of Th2 cytokines such as transforming growth factor beta 1 (TGF-β1) and interleukin 10 (IL-10) in RAW 264.7 cells under pro-inflammatory conditions. Both extracts enhanced the migratory ability of NIH3T3 cells. U. lactuca ethanol extract enhances wound healing properties in vivo. These results suggest that bioactive compounds derived from U. lactuca extract are beneficial for wound healing and anti-inflammatory therapies.","PeriodicalId":501518,"journal":{"name":"bioRxiv - Pharmacology and Toxicology","volume":"214 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In vitro and in vivo evaluation of Ulva lactuca for wound healing\",\"authors\":\"Chien-Hsing Wang, Zih-Ting Huang, Kuo-Feng Tai\",\"doi\":\"10.1101/2024.09.13.612816\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ulva lactuca (U. lactuca) is an important seaweed species. Some ingredients in these seaweeds are thought to accelerate wound healing. However, limited data on the use of seaweed for wound healing exists. This study examined whether ethanol or aqueous extracts of U. lactuca promote antioxidant and anti-inflammatory properties in vitro and wound healing in vitro and in vivo. Cell proliferation, antioxidation, and migration were observed in NIH3T3 cells treated with U. lactuca extract in vitro. Both U. lactuca extracts were examined for their ability to inhibit inflammatory cytokine synthesis in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. In vivo experiments involved four groups of albino mice (BALB/c; 10 mice per group). One 1.0 cm2 wound was created via excision of full-thickness skin on the back of all mice. Mice in Group I mice were treated topically with the ethanol extract of U. lactuca (25 mg/mL) for 10 d. group II mice were treated topically with an aqueous extract of U. lactuca (12.5 mg/mL) for 10 d. Group III received topical application of phosphate-buffered saline solution. Group IV wounds were maintained without treatment. Both extracts significantly increased fibroblast proliferation. The antioxidant activity of the U. lactuca extract was determined using a total antioxidant capacity assay. Both extracts inhibited the release of tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-?? from LPS-mediated inflammation in RAW 264.7 cells. These extracts also upregulated the expression of Th2 cytokines such as transforming growth factor beta 1 (TGF-β1) and interleukin 10 (IL-10) in RAW 264.7 cells under pro-inflammatory conditions. Both extracts enhanced the migratory ability of NIH3T3 cells. U. lactuca ethanol extract enhances wound healing properties in vivo. 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引用次数: 0
摘要
乳莼(U. lactuca)是一种重要的海藻品种。这些海藻中的一些成分被认为可以加速伤口愈合。然而,利用海藻促进伤口愈合的数据还很有限。本研究考察了乳芥菜的乙醇或水提取物是否在体外促进抗氧化和抗炎特性,以及在体外和体内促进伤口愈合。体外观察发现,经乳丁香提取物处理的 NIH3T3 细胞具有细胞增殖、抗氧化和迁移功能。研究还检测了两种 U. lactuca 提取物抑制脂多糖(LPS)刺激的 RAW 264.7 细胞中炎症细胞因子合成的能力。体内实验涉及四组白化小鼠(BALB/c;每组 10 只)。在所有小鼠背部全层皮肤上切除一个 1.0 平方厘米的伤口。第 I 组小鼠用乳酸乌头碱乙醇提取物(25 毫克/毫升)局部治疗 10 天;第 II 组小鼠用乳酸乌头碱水提取物(12.5 毫克/毫升)局部治疗 10 天;第 III 组小鼠局部使用磷酸盐缓冲生理盐水。第 IV 组伤口不做任何处理。两种提取物都能明显增加成纤维细胞的增殖。使用总抗氧化能力测定法测定了乳木果提取物的抗氧化活性。两种提取物都能抑制 RAW 264.7 细胞在 LPS 介导的炎症中释放肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-?这些提取物还能在促炎条件下上调 RAW 264.7 细胞中 Th2 细胞因子的表达,如转化生长因子 beta 1 (TGF-β1) 和白细胞介素 10 (IL-10)。两种提取物都能增强 NIH3T3 细胞的迁移能力。U. lactuca乙醇提取物可增强体内伤口愈合能力。这些结果表明,从U. lactuca提取物中提取的生物活性化合物有利于伤口愈合和抗炎治疗。
In vitro and in vivo evaluation of Ulva lactuca for wound healing
Ulva lactuca (U. lactuca) is an important seaweed species. Some ingredients in these seaweeds are thought to accelerate wound healing. However, limited data on the use of seaweed for wound healing exists. This study examined whether ethanol or aqueous extracts of U. lactuca promote antioxidant and anti-inflammatory properties in vitro and wound healing in vitro and in vivo. Cell proliferation, antioxidation, and migration were observed in NIH3T3 cells treated with U. lactuca extract in vitro. Both U. lactuca extracts were examined for their ability to inhibit inflammatory cytokine synthesis in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. In vivo experiments involved four groups of albino mice (BALB/c; 10 mice per group). One 1.0 cm2 wound was created via excision of full-thickness skin on the back of all mice. Mice in Group I mice were treated topically with the ethanol extract of U. lactuca (25 mg/mL) for 10 d. group II mice were treated topically with an aqueous extract of U. lactuca (12.5 mg/mL) for 10 d. Group III received topical application of phosphate-buffered saline solution. Group IV wounds were maintained without treatment. Both extracts significantly increased fibroblast proliferation. The antioxidant activity of the U. lactuca extract was determined using a total antioxidant capacity assay. Both extracts inhibited the release of tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-?? from LPS-mediated inflammation in RAW 264.7 cells. These extracts also upregulated the expression of Th2 cytokines such as transforming growth factor beta 1 (TGF-β1) and interleukin 10 (IL-10) in RAW 264.7 cells under pro-inflammatory conditions. Both extracts enhanced the migratory ability of NIH3T3 cells. U. lactuca ethanol extract enhances wound healing properties in vivo. These results suggest that bioactive compounds derived from U. lactuca extract are beneficial for wound healing and anti-inflammatory therapies.