Université de Tunis El Manar, Faculté des Sciences de Tunis, 2092 Tunis, Tunisia; Centre de Biotechnologie de Borj-Cédria, LR15CBBC06 Laboratoire des Plantes Aromatiques et Médicinales, BP 901, 2050 Hammam-Lif, Tunisia; Université de Bretagne Occidentale, Faculté de Médecine et des Sciences de la Santé, EA 4324 Laboratoire de Physiologie ORPHY, 29200 Brest, France.
Université de Bretagne Occidentale, Faculté de Médecine et des Sciences de la Santé, EA 4324 Laboratoire de Physiologie ORPHY, 29200 Brest, France.
Biomed Pharmacother. 2017 Nov;95:1404-1411. doi: 10.1016/j.biopha.2017.09.068. Epub 2017 Sep 21.
Limoniastrum guyonianum is used in several regions of North Africa as a folk medicine. The objective of this study was to determine the in vitro antioxidant activities of L. guyonianum roots and their cytoprotective action on HO-challenged rat small intestine epithelial cells (IEC-6 cells). To assess the cytoprotective effect of L. guyonianum extract (LGE), IEC-6 cells were pre-incubated with different LGE concentrations. Then, IEC-6 cultures were exposed to 40μM HO during 4h. Modulation of endogenous antioxidant system including SOD, CAT, MDA, GSH and the expression of possibly involved MAPKs was evaluated. Main results reported that L. guyonianum was rich in polyphenols and exhibited an important antioxidant activity as revealed by different tests (DPPH Assay, IC=1.6μg/mL; ABTS test, IC=27μg/mL; Fe-reducing power, EC=44μg/mL). HPLC analysis showed that quercetin, catechin, and isorhamnetin-3-O-rutinoside were major phenolics. The exposure of IEC-6 cells to 40μM HO during 4h resulted in oxidative stress manifested by (i) over 70% cell mortality, (ii) over-activity of CAT (246%), (iii) decrease in GSH level (10.4nmol/mg), (iv) excess in MDA content (18.4nmol/mg), and (v) a trigger of JNK phosphorylation. Pretreatment with LGE, especially at 0.25μg/mL, restored cell viability to 100%, and normal cell morphology in HO-chalenged cells. In addition, this extract maintained a high CAT activity, enhanced SOD capacity (120%) and increased GSH level (45.5nmol/mg). Furthermore, reducing cell death seems to be due to dephosphorylated JNK MAPK exerted by L. guyonianum bioactive compounds. In all, L. guyonianum components provided a cross-talk between regulatory pathways, implying their role as cytoprotector against oxidative stress.
利蒙尼亚斯图姆·盖约尼亚努姆在北非的几个地区被用作民间药物。本研究的目的是确定 L. guyonianum 根的体外抗氧化活性及其对 HO 挑战的大鼠小肠上皮细胞 (IEC-6 细胞) 的细胞保护作用。为了评估 L. guyonianum 提取物 (LGE) 的细胞保护作用,将 IEC-6 细胞用不同浓度的 LGE 预孵育。然后,IEC-6 培养物在 4 小时内暴露于 40μM HO。评估内源性抗氧化系统的调节,包括 SOD、CAT、MDA、GSH 和可能涉及的 MAPKs 的表达。主要结果表明,L. guyonianum 富含多酚,具有不同测试(DPPH 测定法,IC=1.6μg/mL;ABTS 测试法,IC=27μg/mL;还原铁能力,EC=44μg/mL)显示出重要的抗氧化活性。HPLC 分析表明,槲皮素、儿茶素和异鼠李素-3-O-芸香糖苷是主要的酚类化合物。IEC-6 细胞暴露于 40μM HO 4 小时会导致氧化应激,表现为(i)超过 70%的细胞死亡率,(ii)CAT 过度活跃(246%),(iii)GSH 水平下降(10.4nmol/mg),(iv)MDA 含量增加(18.4nmol/mg),以及(v)JNK 磷酸化的触发。用 LGE 预处理,尤其是在 0.25μg/mL 时,可将细胞活力恢复到 100%,并恢复 HO 挑战细胞的正常细胞形态。此外,该提取物保持高 CAT 活性,增强 SOD 能力(120%)并增加 GSH 水平(45.5nmol/mg)。此外,减少细胞死亡似乎是由于 L. guyonianum 生物活性化合物使 JNK MAPK 去磷酸化所致。总之,L. guyonianum 成分在调节途径之间提供了一种交流,表明它们在对抗氧化应激方面具有细胞保护作用。