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作 者:齐洪娜[1,2] 崔洁[1] 刘磊[1] 卢飞飞[3] 宋成洁[1] 石玥[1] 闫长栋[1,3]
机构地区:[1]徐州医学院生理学教研室,徐州221002 [2]徐州医学院心血管研究所,徐州221002 [3]徐州医学院江苏省麻醉学重点实验室,徐州221002
出 处:《生理学报》2012年第4期425-432,共8页Acta Physiologica Sinica
基 金:supported by the Natural Science Foundation of Jiangsu Province;China (No. BK2009088);Graduate Innovation Program of Jiangsu Province;China (No. CX095-0272)
摘 要:本文旨在观察硫化氢(hydrogen sulfide,H2S)供体硫氢化钠(NaHS)预处理对人脐静脉内皮细胞老化的影响及机制。原代人脐静脉内皮细胞株(HUVECs)传代培养到第12代为老年组;自第4代细胞(年轻组)起,给予NaHS孵育到第12代即为NaHS组。细胞衰老β-半乳糖苷酶(SAβ-gal)染色法检测细胞老化程度,DAPI荧光染色法检测细胞凋亡,免疫印迹法测定细胞黄嘌呤氧化酶(XOD)、锰-超氧化物歧化酶(Mn-SOD)和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶亚单位蛋白表达,化学比色法检测HUVECs内SOD活性和过氧化氢(H2O2)含量。结果显示,与年轻组相比,老年组内皮细胞SAβ-gal阳性率和凋亡率显著增加(P<0.01),而NaHS预处理能明显减少细胞SAβ-gal阳性率和凋亡率(P<0.01)。与年轻组相比,老年组内皮细胞XOD和NADPH氧化酶亚单位p67phox蛋白表达增加,Mn-SOD蛋白表达减少;NaHS组与老年组相比,XOD和p67phox蛋白表达减少,Mn-SOD蛋白表达增加(P<0.05)。与年轻组相比,老年组SOD活性降低,H2O2含量增加;NaHS组与老年组相比,SOD活性提高,H2O2含量减少(P<0.01)。以上结果提示,NaHS预处理能减轻老化HUVECs氧化应激水平,起到延缓HUVECs老化的作用。The present study was aimed to investigate the effect of pretreatment with hydrogen sulfide (H2S) on human umbilical vein endothelial cells (HUVECs) senescence and the underlying mechanism. Cultured HUVECs at twelfth and fourth passages were taken as old and young groups, respectively. Sodium hydrosulfide (NariS, donor of H2S) group was treated with NariS from fourth to twelfth passage. The cell senescence was determined by senescence-associated I)-galactosidase (SA I)-gal) staining. DAPI fluorescent dye was used to detect cellular apoptosis. Western blot was used to analyze the expression levels of xanthine oxidase (XOD), Manga- nese-superoxide dismutase (Mn-SOD) and the subunits p67phox of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase in the HUVECs. Colorimetric method was used to detect SOD activity and cellular hydrogen peroxide (H2O2) level. The results showed that, compared with young group, the old group exhibited higher SA β-gal positive rate and cellular apoptosis, while NariS pretreatment decreased SA β-gal positive rate and cellular apoptosis. Compared with the young group, the old group showed increased expression levels of XOD and p67^phox, as well as lower Mn-SOD expression level. With the pretreatment of NariS, the up-regulations of XOD and p67^phox levels and down-regulation of Mn-SOD level were inhibited. Compared with the young group, the old group showed lower SOD activity and higher H2O2 level, whereas NariS pretreatment reversed the changes of SOD activity and H2O2 level. These results suggest that H2S delays senescence of HUVECs through lessening oxidative stress.
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