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作 者:赖满香[1] 陈侠[1] 冯娟[1] 何丽霞[2] 杨丽[2]
机构地区:[1]广东食品药品职业学院,广州510520 [2]暨南大学药学院,广州510560
出 处:《中国药房》2016年第10期1318-1321,共4页China Pharmacy
基 金:广东省医学科学技术研究基金项目(No.B2015063);广东食品药品职业学院自然科学基金项目(No.2014YZ003)
摘 要:目的:研究中药单体梓醇在成骨细胞(OB)-破骨细胞(OC)共育体系中对OC活性、凋亡的影响及其作用机制。方法:分别选用1~3 d龄和5~7 d龄SD乳鼠分离培养OB和OC,建立OB-OC共育体系。通过倒置显微镜观察0(空白对照)、0.05、0.5、5、50、100 mg/L梓醇培养48、72、96 h后OC的骨吸收陷窝数目,以反映OC活性;以0(空白对照)、0.05 mg/L梓醇培养细胞48、72、96h,检测OC中抗酒石酸酸性磷酸酶(TRACP)活性,计算OC的凋亡率;以0(空白对照)、0.05 mg/L梓醇培养细胞并检测OB中骨保护素(OPG)m RNA的表达。结果:在OB-OC共育体系中,0.05~50 mg/L梓醇作用下所形成骨吸收陷窝数目显著低于空白对照(P〈0.01),表明梓醇可抑制OC活性,其中质量浓度为0.05 mg/L时作用最明显。与空白对照比较,0.05 mg/L梓醇作用后OC中TRACP的活性降低、OC的凋亡率升高(P〈0.05);OB的OPG m RNA表达上调(P〈0.01)。结论:在OB-OC共育体系中,梓醇可抑制OC活性、诱导OC凋亡,其机制可能与上调OB的OPG m RNA表达有关。OBJECTIVE:To study the effect of catalpol on the activity and apoptosis of osteoclasts(OC) in the osteoblasts(OB)-OC co-culture system and its mechanism. METHODS:OB and OC were isolated respectively from the SD rats of 1-3 days and 5-7 days old to establish OB-OC co-culture system. After treated with 0(blank control),0.05,0.5,5,50 and 100 mg/L catalpol for 48,72 and 96 h,the number of bone absorption lacuna for OC was observed by inverted microscope to reflect OC activity.After treated with 0(blank control)and 0.05 mg/L catalpol for 48,72 and 96 h,the activity of tartrate resistant acid phosphatase(TRACP)in OC was detected,and the apoptosis rate of OC was calculated. After treated with 0(blank control)and 0.05 mg/L catalpol,m RNA expression of osteoprotegerin(OPG)in OB was detected. RESULTS:In OB-OC co-culture system,the number of bone absorption lacuna in 0.05-50 mg/L catalpol groups was significantly lower than blank control group(P0.01),indicating catalpol could inhibit OC activity,especially 0.05 mg/L catapol. Compared with blank control,0.05 mg/L catapol lowered the activity of TRACP but increased the apoptosis rate of OC(P0.05);m RNA expression of OPG was up-regulated in OB(P0.01). CONCLUSIONS:In OB-OC co-culture system,catalpol can inhibit the activity of OC and induce the apoptosis of OC,and its mechanism may be associated with the m RNA expression up-regulation of OPG in OB.
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