Cell Culture Laboratory, Post-Graduation Program in Biotechnology, Taquari Valley University-Univates, Lajeado, RS, Brazil.
MARE-Marine and Environmental Sciences Centre, ESTM, Polytechnic University of Leiria, 2520-641, Peniche, Portugal.
Inflammopharmacology. 2024 Oct;32(5):3327-3345. doi: 10.1007/s10787-024-01547-3. Epub 2024 Aug 12.
Wounds or chronic injuries are associated with high medical costs so, develop healing-oriented drugs is a challenge for modern medicine. The identification of new therapeutic alternatives focuses on the use of natural products. Therefore, the main goal of this study was to evaluate the healing potential and anti-inflammatory mechanism of action of extracts and the main compounds derived from Myrciaria plinioides D. Legrand leaves. The antimicrobial activity of leaf extracts was analyzed. Cell viability, cytotoxicity and genotoxicity of plant extracts and compounds were also assessed. Release of pro- and anti-inflammatory cytokines and TGF-β by ELISA, and protein expression was determined by Western Blot. The cell migration and cell proliferation of ethanol and aqueous leaf extracts and p-coumaric acid, quercetin and caffeic acid compounds were also evaluated. The aqueous extract exhibited antibacterial activity and, after determining the safety concentrations in three assays, we showed that this extract induced p38-α MAPK phosphorylation and the same extract and the p-coumaric acid decreased COX-2 and caspase-3, -8 expression, as well as reduced the TNF-α release and stimulated the IL-10 in RAW 264.7 cells. In L929 cells, the extract and p-coumaric acid induced TGF-β release, besides increasing the process of cell migration and proliferation. These results suggested that the healing properties of Myrciaria plinioides aqueous extract can be associated to the presence of phenolic compounds, especially p-coumaric acid, and/or glycosylated metabolites.
伤口或慢性损伤与高昂的医疗费用有关,因此,开发以愈合为导向的药物是现代医学的一项挑战。新治疗方法的选择重点在于天然产物的使用。因此,本研究的主要目标是评估源自 Myrciaria plinioides D. Legrand 叶的提取物及其主要化合物的愈合潜力和抗炎作用机制。分析了叶提取物的抗菌活性。还评估了植物提取物和化合物的细胞活力、细胞毒性和遗传毒性。通过 ELISA 测定促炎和抗炎细胞因子和 TGF-β的释放,并通过 Western Blot 测定蛋白表达。还评估了乙醇和水提叶提取物以及对羟基肉桂酸、槲皮素和咖啡酸化合物的细胞迁移和细胞增殖。水提物表现出抗菌活性,在三项测定中确定了安全浓度后,我们表明该提取物诱导了 p38-α MAPK 磷酸化,相同的提取物和对羟基肉桂酸降低了 COX-2 和 caspase-3、-8 的表达,减少了 TNF-α的释放并刺激了 RAW 264.7 细胞中的 IL-10。在 L929 细胞中,提取物和对羟基肉桂酸诱导 TGF-β释放,同时增加细胞迁移和增殖过程。这些结果表明,Myrciaria plinioides 水提物的愈合特性可能与存在酚类化合物有关,尤其是对羟基肉桂酸和/或糖基化代谢物。