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出 处:《中国药房》2016年第13期1788-1790,共3页China Pharmacy
基 金:吉林省科技发展计划项目(No.20130302025YY)
摘 要:目的:研究壮骨伸筋胶囊对骨质疏松模型大鼠的改善作用及其机制。方法:将72只SD大鼠随机分为6组,即空白对照组(生理盐水)、模型组(生理盐水)、骨疏康颗粒组[阳性药物,3 g(生药)/kg]和壮骨伸筋胶囊低、中、高剂量组[1.4、2.7、5.4 g(生药)/kg]。除空白对照组ig生理盐水外,其余各组大鼠于每周一、四ig醋酸泼尼松片(4.5 mg/kg)复制骨质疏松模型,并同时于每周一至六ig相应药物,连续13周。测定大鼠股骨骨密度、骨形态计量指标[骨小梁体积百分比、骨小梁矿化率(MAR)和骨皮质矿化率(mAR)]、肾组织中肌节同源盒基因Msx-2 mRNA及其蛋白的表达。结果:与空白对照组比较,模型组大鼠骨密度、骨小梁体积百分比降低,mAR升高,肾组织中Msx-2 mRNA及其蛋白表达减弱(P<0.05或P<0.01)。与模型组比较,骨疏康颗粒组和壮骨伸筋胶囊高剂量组大鼠骨小梁体积百分比升高、m AR降低,肾组织中Msx-2 mRNA表达增强;各给药组大鼠骨密度增加、Msx-2蛋白表达增强;中剂量组骨小梁体积百分比升高,以上差异均有统计学意义(P<0.05或P<0.01);MAR差异无统计学意义(P>0.05)。结论:壮骨伸筋胶囊对泼尼松致大鼠骨质疏松有一定的改善作用,其机制可能与上调肾组织中Msx-2基因的表达有关。OBJECTIVE:To study the improvement effects of Zhuanggu shenjin capsules(ZGSJC)on prednisone-induced osteoporosis model rats and its mechanism. METHODS:72 SD rats were randomly divided into 6 groups as blank control group(normal saline),model group(normal saline),Gushukang granule group [positive drug,3 g(crude drug)/kg] and ZGSJC low-dose,medium-dose and high-dose groups [1.4,2.7,5.4 g(crude drug)/kg]. Except for intragastric administration of normal saline in blank control group,other groups were given Prednisone acetate tablet 4.5 mg/kg intragastricallly every Monday and Thursday to induce osteoporosis model,and given relevant medicine intragastrically from Monday to Saturday for consecutive 13 weeks. Bone density(BMD),bone histomorphometry indicators [volume percentage of bone trabecula,mineralization rate of bone trabecular(MAR)and mineralization rate of bone cortical(mAR)] and the expression of muscle segment homeebox gene Msx-2 mRNA and protein were all determined. RESULTS:Compared with blank control group,BMD,volume percentage of bone trabecula and the expression of Msx-2 mRNA and protein in renal tissue decreased,while m AR increased in model group(P〈0.05 or P〈0.01).Compared with model group,volume percentage of bone trabecula and the expression of Msx-2 mRNA in renal tissue increased in Gushukang granule group and ZGSJC high-dose group,while mAR decreased;BMD and the expression of Msx-2 protein increased in treatment groups,as well as the volume percentage of bone trabecula increased in ZGSJC medium-dose group,with statistical significance(P〈0.05 or P〈0.01),while the difference of MAR without statistic significance(P〉0.05). CONCLUSIONS:ZGSJC can protect rats against prednisone-induced osteoporosis,and its mechanism may be associated with the up-regulation of Msx-2 expression in renal tissue.
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