机构地区:[1]中山大学附属第一医院儿科,广东广州510080 [2]中山大学附属第二医院儿科,广东广州510120
出 处:《中山大学学报(医学科学版)》2006年第1期67-71,共5页Journal of Sun Yat-Sen University:Medical Sciences
基 金:广东省卫生厅科研基金资助项目(A2003168);广东省自然科学基金博士启动基金资助项目(04300346)
摘 要:目的探讨肾病综合征(NS)鼠骨代谢的变化特点及芪归合剂对其的作用。方法制备大鼠阿霉素NS模型,设模型组、激素治疗组、芪归治疗组、激素芪归治疗组及正常对照组,每组8只,用药时间为3周。测量各组尿蛋白、血生化指标和右股骨长度;用HologicQDR-2000+DEXA行股骨全段骨密度(BMD)测定;以放射免疫法测定血清骨钙素(OC)、I型前胶原氨基端伸展肽(PINP)、I型胶原羧基端关联肽原(ICTP)水平。结果模型组股骨长度(3.35±0.09)cm,低于正常组(3.53±0.11)cm(P<0.05);芪归治疗组(3.46±0.09)cm,高于模型组(P<0.05);激素芪归组(3.28±0.07)cm,高于激素治疗组(3.16±0.11)cm(P<0.01);激素治疗组低于模型组(P<0.05)。模型组股骨全段BMD(0.1357±0.0137)g/㎝2,低于正常组(0.1599±0.0101)g/㎝2(P<0.01);激素治疗组(0.1208±0.0123)g/㎝2,低于模型组(P<0.05)。模型组血OC(16.31±3.87)μg/L和PINP(2.02±0.51)μg/L水平,低于正常组,分别(31.49±4.16)μg/L、(3.58±0.46)μg/L(P<0.01);芪归治疗组血OC(25.90±8.26)μg/L和PINP(3.42±1.07)μg/L水平,高于模型组(分别P<0.05和P<0.01);激素芪归组血OC(12.01±1.97)μg/L和PINP(2.47±0.88)μg/L水平,高于激素治疗组,分别(6.12±3.26)μg/L、(1.63±0.74)μg/L(P<0.05);激素治疗组低于模型组(P<0.05)。激素治疗组的ICTP(10.15±3.77)μg/L高于模型组(8.71±3.29)μg/L(P<0.05)。结论NS鼠存在骨代谢的异常,激素治疗使骨代谢异常进一步加剧,而芪归合剂治疗对其有改善作用。[Objective] To investigate the change of bone metabolism in rats with nephrotic syndrome (NS) and the role of Astragalus and Angelica mixture (A&A). [ Methods] Forty male SD rats (six weeks old) were randomly divided into five groups: control group, NS model group, NS group treated with A&A, NS group treated with dexamethasone (Dex), NS group treated with A&A and Dex. Urine protein, serum biochemical levels and the femur length were measured. The bone mineral density (BMD) of whole part of femur was measured by Hologic ODR-2000+DEXA. Serum osteocalcin (OC), aminoterminal propeptide of type Ⅰ procollagen (PINP) and carboxytenninal telopeptide of type Ⅰ collagen (ICTP) levels were assayed by radioimmunoassay technique. [Results] The length of femur of NS group treated with A&A and NS group treated with A&A and Dex were higher than those in NS model group and NS group treated with Dex, respectively (P 〈 0.05 and P 〈 0.05). The length of femur of NS group treated with Dex was lower than that of NS model group (P 〈 0.05). The length of femur of NS model group was lower than that of control group (P 〈 0.05). The BMD of femur in NS model group was lower than that of control group (P 〈 0.01). The serum levels of OC and PINP in NS model group were lower than those in control group (P 〈 0.01). The serum levels of OC and PINT in NS group treated with A&A and NS group treated with A&A and Dex were higher than those in NS model group and NS group treated with Dex, respectively (P 〈 0.05 and P 〈 0.01,respectively). The serum levels of OC and PINP in NS group treated with Dex were lower than those in NS model group (P 〈 0.05). The serum levels of ICTP in NS group treated with Dex were higher than that of NS model group (P 〈 0.05).[Conclusion] The abnormality of bone metabolism exists in nephrotic rats. Dexamethasone treatment can aggravate this abnormality, which can be improved by Astragalus and Angelica mixture.
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