Silva A R, Pinheiro A M, Souza C S, Freitas S R V-B, Vasconcellos V, Freire S M, Velozo E S, Tardy M, El-Bachá R S, Costa M F D, Costa S L
Departamento de Biofunção, Laboratório de Neuroquímica e Biologia Celular, Instituto de Ciências da Saúde, Universidade Federal da Bahia, Salvador, Brazil.
Cell Biol Toxicol. 2008 Jan;24(1):75-86. doi: 10.1007/s10565-007-9017-y. Epub 2007 Jun 5.
Astrocyte and microglia cells play an important role in the central nervous system (CNS). They react to various external aggressions by becoming reactive and releasing neurotrophic and/or neurotoxic factors. Rutin is a flavonoid found in many plants and has been shown to have some biological activities, but its direct effects on cells of the CNS have not been well studied. To investigate its potential effects on CNS glial cells, we used both astrocyte primary cultures and astrocyte/microglia mixed primary cell cultures derived from newborn rat cortical brain. The cultures were treated for 24 h with rutin (50 or 100 micromol/L) or vehicle (0.5% dimethyl sulfoxide). Mitochondrial function on glial cells was not evidenced by the MTT test. However, an increased lactate dehydrogenase activity was detected in the culture medium of both culture systems when treated with 100 micromol/L rutin, suggesting loss of cell membrane integrity. Astrocytes exposed to 50 micromol/L rutin became reactive as revealed by glial fibrillary acidic protein (GFAP) overexpression and showed a star-like phenotype revealed by Rosenfeld's staining. The number of activated microglia expressing OX-42 increased in the presence of rutin. A significant increase of nitric oxide (NO) was observed only in mixed cultures exposed to 100 micromol/L rutin. Enhanced TNFalpha release was observed in astrocyte primary cultures treated with 100 micromol/L rutin and in mixed primary cultures treated with 50 and 100 micromol/L, suggesting different sensitivity of both activated cell types. These results demonstrated that rutin affects astrocytes and microglial cells in culture and has the capacity to induce NO and TNFalpha production in these cells. Hence, the impact of these effects on neurons in vitro and in vivo needs to be studied.
星形胶质细胞和小胶质细胞在中枢神经系统(CNS)中发挥着重要作用。它们通过变得具有反应性并释放神经营养和/或神经毒性因子来应对各种外部侵害。芦丁是一种存在于许多植物中的类黄酮,已被证明具有一些生物学活性,但其对中枢神经系统细胞的直接影响尚未得到充分研究。为了研究其对中枢神经系统胶质细胞的潜在影响,我们使用了源自新生大鼠皮质脑的星形胶质细胞原代培养物和星形胶质细胞/小胶质细胞混合原代细胞培养物。将培养物用芦丁(50或100微摩尔/升)或溶剂(0.5%二甲亚砜)处理24小时。MTT试验未证明芦丁对胶质细胞线粒体功能有影响。然而,当用100微摩尔/升芦丁处理时,在两种培养系统的培养基中均检测到乳酸脱氢酶活性增加,这表明细胞膜完整性丧失。暴露于50微摩尔/升芦丁的星形胶质细胞通过胶质纤维酸性蛋白(GFAP)过表达而变得具有反应性,并通过罗森菲尔德染色显示出星形表型。在芦丁存在的情况下,表达OX-42的活化小胶质细胞数量增加。仅在暴露于100微摩尔/升芦丁的混合培养物中观察到一氧化氮(NO)显著增加。在用100微摩尔/升芦丁处理的星形胶质细胞原代培养物以及用50和100微摩尔/升处理的混合原代培养物中观察到肿瘤坏死因子α(TNFα)释放增强,这表明两种活化细胞类型的敏感性不同。这些结果表明芦丁会影响培养中的星形胶质细胞和小胶质细胞,并具有诱导这些细胞产生NO和TNFα的能力。因此,需要研究这些作用在体外和体内对神经元的影响。