Núcleo de Pesquisa em Biodiversidade e Biotecnologia-BIOTEC, Universidade Federal do Piauí-UFPI, Campus Ministro Reis Velloso-CMRV, Parnaíba, PI, Brazil.
Laboratório de Fisio-Farmacologia Experimental-LAFFEX, Universidade Federal do Piauí-UFPI, Campus Ministro Reis Velloso-CMRV, Parnaíba, PI, Brazil.
Food Res Int. 2017 Sep;99(Pt 2):959-968. doi: 10.1016/j.foodres.2017.01.017. Epub 2017 Jan 21.
This study investigated the anti-inflammatory activity of the extract (LEG) and purified (LPG) lycopene from guava (Psidium guajava L.), as well as some mechanisms possibly involved in this effect. The anti-inflammatory activity was initially assessed using paw edema induced by Carrageenan, Dextran, Compound 48/80, Histamine and Prostaglandin E2 in Swiss mice. A peritonitis model was used to evaluate neutrophil migration, the activity of myeloperoxidase (MPO) and reduced glutathione (GSH) concentration; while the effect on the expression of iNOS, COX-2 and NF-κB, was assessed by immunohistochemistry analysis. Results showed that oral and intraperitoneal administration of LEG and LPG inhibited inflammation caused by carrageenan. LPG (12.5mg/kg p.o.) significantly inhibited the edema formation induced by different phlogistic agents and immunostaining for iNOS, COX-2 and NF-κB. Leukocytes migration in paw tissue and peritoneal cavity was reduced, as well as MPO concentration, whereas GSH levels increased. Thus, lycopene-rich extract from red guava has beneficial effect on acute inflammation, offering protection against the consequences of oxidative stress by downregulating inflammatory mediators and inhibiting gene expression involved in inflammation.
本研究旨在探讨番石榴(Psidium guajava L.)提取物(LEG)和纯化(LPG)番茄红素的抗炎活性,以及可能涉及到的一些机制。首先使用角叉菜胶、葡聚糖、复合 48/80、组织胺和前列腺素 E2 诱导的爪水肿评估抗炎活性,然后使用腹膜炎模型评估中性粒细胞迁移、髓过氧化物酶(MPO)活性和还原型谷胱甘肽(GSH)浓度;通过免疫组化分析评估对 iNOS、COX-2 和 NF-κB 表达的影响。结果表明,LEG 和 LPG 的口服和腹腔内给药抑制了角叉菜胶引起的炎症。LPG(12.5mg/kg p.o.)显著抑制了不同致炎剂诱导的水肿形成,并抑制了 iNOS、COX-2 和 NF-κB 的免疫染色。爪组织和腹腔内白细胞迁移减少,MPO 浓度降低,而 GSH 水平升高。因此,富含番茄红素的红心番石榴提取物对急性炎症具有有益的作用,通过下调炎症介质和抑制炎症相关基因表达,提供了对抗氧化应激后果的保护。