Davoodi Farshid, Mohammadi Rahim, Asri-Rezaei Siamak, Behfar Mehdi, Dezfoulian Omid, Raisi Abbas
Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Surgery. 2025 Aug;184:109453. doi: 10.1016/j.surg.2025.109453. Epub 2025 Jun 10.
Wound healing is a dynamic process that begins following the destruction of the skin's normal anatomy. This study evaluated effects of pyrroloquinoline quinone on skin wounds in mice.
Thirty-six male mice were randomly divided in to 3 groups: (1) Sham group, where wounds were created but no treatment was administered; (2) Soybean oil, where soybean oil was applied topically to wounds for 9 days; and (3) pyrroloquinoline quinone group, where pyrroloquinoline quinone dissolved in soybean oil was applied topically. Four mice per group were used in an incisional wound model for biomechanical testing. Hematoxylin and eosin, Masson trichrome, immunohistochemical staining of caspase 3, vascular endothelial growth factor and tumor growth factor beta, oxidative stress biomarkers, and Western blot assay for tumor necrosis factor alpha and nuclear factor kappa B were performed on days 7 and 14. Biomechanical parameters were evaluated on day 10 post wounding.
Pyrroloquinoline quinone significantly reduced the wound area. In the treatment group, malondialdehyde and total oxidant status significantly reduced and total antioxidant capacity was increased compared with other groups. Levels of hydroxyproline was significantly higher in the pyrroloquinoline quinone group in comparison to 2 other groups. In Western blot assay, tumor necrosis factor alpha significantly reduced in the treatment group. Histopathologic evaluation confirmed improved wound healing in the pyrroloquinoline quinone group, with reduced expression of caspase 3 and tumor growth factor beta. Vascular endothelial growth factor expression increased on day 7 but decreased on day 14 in the pyrroloquinoline quinone group. Biomechanical parameters including, strain, ultimate strength, and maximum energy stored, showed significant improvements.
These findings suggested that pyrroloquinoline quinone may accelerate wound healing in mice.
伤口愈合是一个动态过程,始于皮肤正常解剖结构遭到破坏之后。本研究评估了吡咯喹啉醌对小鼠皮肤伤口的影响。
将36只雄性小鼠随机分为3组:(1)假手术组,造伤口但不给予治疗;(2)大豆油组,将大豆油局部涂抹于伤口,持续9天;(3)吡咯喹啉醌组,将溶于大豆油的吡咯喹啉醌局部涂抹。每组4只小鼠用于切开伤口模型的生物力学测试。在第7天和第14天进行苏木精-伊红染色、Masson三色染色、半胱天冬酶3、血管内皮生长因子和肿瘤生长因子β的免疫组化染色、氧化应激生物标志物检测,以及肿瘤坏死因子α和核因子κB的蛋白质印迹分析。在伤口形成后第10天评估生物力学参数。
吡咯喹啉醌显著减小了伤口面积。与其他组相比,治疗组丙二醛和总氧化剂状态显著降低,总抗氧化能力增加。吡咯喹啉醌组羟脯氨酸水平显著高于其他两组。在蛋白质印迹分析中,治疗组肿瘤坏死因子α显著降低。组织病理学评估证实吡咯喹啉醌组伤口愈合改善,半胱天冬酶3和肿瘤生长因子β的表达降低。吡咯喹啉醌组血管内皮生长因子表达在第7天增加,但在第14天下降。包括应变、极限强度和最大储能在内的生物力学参数显示出显著改善。
这些发现表明吡咯喹啉醌可能加速小鼠伤口愈合。