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Extracts of Portulaca oleracea promote wound healing by enhancing angiology regeneration and inhibiting iron accumulation in mice
马齿苋提取物通过促进小鼠血管再生和抑制铁积累促进伤口愈合
Portulaca oleraceaの抽出物は、脈管学の再生を促進し、マウスの鉄の蓄積を阻害することにより、創傷治癒を促進します
Portulaca oleracea 추출물은 생쥐에서 혈관 재생을 강화하고 철분 축적을 억제하여 상처 치유를 촉진합니다.
Los extractos de Portulaca oleracea promueven la cicatrización de heridas al mejorar la regeneración angiológica e inhibir la acumulación de hierro en ratones
Les extraits de Portulaca oleracea favorisent la cicatrisation des plaies en améliorant la régénération de l'angiologie et en inhibant l'accumulation de fer chez la souris
Экстракты Portulaca oleracea способствуют заживлению ран, усиливая регенерацию сосудов и подавляя накопление железа у мышей
Jinglin Guo 郭景琳 ¹, Juan Peng 彭娟 ², Jing Han 韩晶 ¹, Ke Wang 王珂 ³, Ruijuan Si 司瑞娟 ¹, Hui Shan 山慧 ¹, Xiaoying Wang 王晓莹 ¹, Ju Zhang 张菊 ¹
¹ School of Nursing, Qingdao University, Qingdao 266071, China
中国 青岛 青岛大学护理学院
² Surgery of Traditional Chinese Medicine, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300150, China
中国 天津 天津中医药大学第二附属医院中医外科
³ School of Pharmacy, Qingdao University, Qingdao 266071, China
中国 青岛 青岛大学药学院
Chinese Herbal Medicines, 26 February 2022
Abstract

Objective

To investigate the role of Portulaca oleracea (POL) in promoting revascularization and re-epithelization as well as inhibiting iron aggregation and inflammation of deep tissue pressure injury (DTPI).

Methods

The hydroalcoholic extract of POL (P) and aqueous phase fraction of POL (PD) were prepared based on maceration and liquid–liquid extraction. The number of new blood vessels and VEGF-A expression level were assessed using H&E stain and Western blot on injured muscle to examine the role of POL different extracts in vascularization. The iron distribution and total elemental iron of injured muscle were detected using laser ablation inductively coupled plasma mass spectrometry (ICP-MS) and Perls’ staining to determine whether POL extracts can inhibit the iron accumulation. Besides, the ability of POL extracts to promote wound healing by combining re-epithelization time, inflammation degree and collagen deposition area were comprehensively evaluated.

Results

In vitro, we observed a significant increase in HUVEC cell viability, migration rate and the number of the tube after P and PD treatment (P < 0.05). In vivo, administration of P and PD impacted vascularization and iron accumulation on injured tissue, evident from more new blood vessels, higher expression of VEGF-A and decreased muscle iron concentration of treatment groups compared with no-treatment groups (P < 0.05). Besides, shorter re-epithelization time, reduced inflammatory infiltration and distinct collagen deposition were associated with administration of P and PD (P < 0.05).

Conclusion

POL extract administration groups have high-quality wound healing, which is associated with increased new blood vessels, collagen deposition and re-epithelization, along with decreased iron accumulation and inflammatory infiltration. Our results suggest that that POL extract is beneficial to repair injured muscle after ischemia–reperfusion, highlighting the potential of POL in the DTPI treatment.
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