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Vasconcellea cundinamarcensis 蛋白水解部分(P1G10)在皮肤创伤切除模型中的愈合活性。

Healing activity of proteolytic fraction (P1G10) from Vasconcellea cundinamarcensis in a cutaneous wound excision model.

机构信息

Departamentos de Farmacologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

Departamentos de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Biomed Pharmacother. 2017 Dec;96:269-278. doi: 10.1016/j.biopha.2017.09.109. Epub 2017 Oct 6.

Abstract

The proteolytic enzymes from Vasconcellea cundinamarcensis have demonstrated efficacy to accelerate healing of skin lesions. We report here the efficacy of the proteolytic fraction - P1G10 during repair of excisional wounds in rodent model and analyze possible mediators involved. Using 0.05% P1G10 we observed on day 3rd increased wound contraction accompanied by an increase in activated neutrophils and VEGF relative to the control. On day 7th neutrophils returned to normal levels, and at 0.01% P1G10, an increase in NAG activity used to monitor monocyte/macrophage, was observed. On the other hand, on day 7th, we observed a decrease in TGF-β at 0.05% P1G10, accompanied by an increased transformation of the latent TGF-β to its active form. Also, on day 7th a reduction in MMP-9 activity and the number of apoptotic cells was observed along with an increase in fibroblast levels. Morphometrically, it appears that treatment with P1G10 accelerates the decline of initial inflammatory phase and reduces some unwanted effects likely caused by remaining TGF-β or MMPs, thus enhancing the quality of scar. Overall, these data suggest that the active proteolytic fraction P1G10 enhances the efficacy of repair in excisional cutaneous wounds.

摘要

来自 Vasconcellea cundinamarcensis 的蛋白水解酶已被证明能有效加速皮肤损伤的愈合。我们在此报告蛋白水解部分 - P1G10 在啮齿动物模型中修复切除性伤口的功效,并分析可能涉及的介质。使用 0.05%的 P1G10,我们观察到第 3 天伤口收缩增加,与对照组相比,激活的中性粒细胞和 VEGF 增加。第 7 天,中性粒细胞恢复正常水平,而在 0.01%的 P1G10 下,监测单核细胞/巨噬细胞的 NAG 活性增加。另一方面,第 7 天,我们观察到在 0.05%的 P1G10 下 TGF-β 的减少,伴随着潜伏 TGF-β向其活性形式的转化增加。此外,第 7 天还观察到 MMP-9 活性降低和凋亡细胞数量减少,同时成纤维细胞水平增加。从形态学上看,用 P1G10 治疗似乎加速了初始炎症阶段的下降,并减少了可能由残留的 TGF-β 或 MMPs 引起的一些不良影响,从而提高了疤痕的质量。总的来说,这些数据表明,活性蛋白水解部分 P1G10 增强了切除性皮肤伤口修复的功效。

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