天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2013年
12期
1180-1183
,共4页
白彝华%王家平%王剑松%连希艳%蒋红樱%李龙
白彝華%王傢平%王劍鬆%連希豔%蔣紅櫻%李龍
백이화%왕가평%왕검송%련희염%장홍앵%리룡
肾病%间质干细胞%骨髓移植%间质干细胞移植%疾病模型,动物%大鼠, Sprague-Dawley%阿霉素
腎病%間質榦細胞%骨髓移植%間質榦細胞移植%疾病模型,動物%大鼠, Sprague-Dawley%阿黴素
신병%간질간세포%골수이식%간질간세포이식%질병모형,동물%대서, Sprague-Dawley%아매소
nephrosis%mesenchymal stem cells%bone marrow transplantation%mesenchymal stem cell transplantation%dis-ease models,animal%rats,Sprague-Dawley%adriamycin-induced nephropathy
目的:探索骨髓间充质干细胞(BMSCs)经不同输注方式移植入阿霉素慢性肾病大鼠体内对肾损伤的影响。方法 SD大鼠左侧肾切除后以2.5 mg/kg剂量给大鼠尾静脉注射阿霉素,1次/周,连续2次,慢性肾病模型成功后,将成模大鼠36只随机均分为3组:阿霉素慢性肾病对照(ADR)组、干细胞经肾动脉移植(M-A)组、干细胞经外周静脉移植(M-V)组,另选12只正常大鼠设正常对照(N)组。BMSCs经体外培养后,以2×106个/mL经肾动脉注射到M-A组大鼠体内,2×106个/mL经尾静脉注射到M-V组大鼠体内,2周后再次同样方法注射等量BMSCs。检测移植当周、移植后1周、2周大鼠血尿素氮、血肌酐、24 h尿蛋白、24 h尿微量蛋白,末次注射干细胞后第1周于激光聚焦显微镜下观察大鼠肾脏病理和干细胞在肾脏内分布情况。结果 M-A组、M-V组和ADR组在各观察时点血尿素氮、血肌酐、24 h尿蛋白总量、24 h尿微量蛋白均明显高于N组(P<0.01)。移植后1、2周M-A组的24 h尿微量蛋白低于ADR组(P<0.01),且M-A组的血肌酐较ADR组和M-V组均降低(P<0.01)。移植后1周,M-A组24 h尿蛋白、24 h尿微量蛋白明显低于M-V组(P<0.01);但2周时尿蛋白和微量蛋白与M-V组的差异无统计学意义。结论 BMSCs移植可以改善阿霉素慢性肾病的肾损伤情况,在BMSCs移植后一段时间,BMSCs经肾动脉移植的效果优于经外周静脉移植。
目的:探索骨髓間充質榦細胞(BMSCs)經不同輸註方式移植入阿黴素慢性腎病大鼠體內對腎損傷的影響。方法 SD大鼠左側腎切除後以2.5 mg/kg劑量給大鼠尾靜脈註射阿黴素,1次/週,連續2次,慢性腎病模型成功後,將成模大鼠36隻隨機均分為3組:阿黴素慢性腎病對照(ADR)組、榦細胞經腎動脈移植(M-A)組、榦細胞經外週靜脈移植(M-V)組,另選12隻正常大鼠設正常對照(N)組。BMSCs經體外培養後,以2×106箇/mL經腎動脈註射到M-A組大鼠體內,2×106箇/mL經尾靜脈註射到M-V組大鼠體內,2週後再次同樣方法註射等量BMSCs。檢測移植噹週、移植後1週、2週大鼠血尿素氮、血肌酐、24 h尿蛋白、24 h尿微量蛋白,末次註射榦細胞後第1週于激光聚焦顯微鏡下觀察大鼠腎髒病理和榦細胞在腎髒內分佈情況。結果 M-A組、M-V組和ADR組在各觀察時點血尿素氮、血肌酐、24 h尿蛋白總量、24 h尿微量蛋白均明顯高于N組(P<0.01)。移植後1、2週M-A組的24 h尿微量蛋白低于ADR組(P<0.01),且M-A組的血肌酐較ADR組和M-V組均降低(P<0.01)。移植後1週,M-A組24 h尿蛋白、24 h尿微量蛋白明顯低于M-V組(P<0.01);但2週時尿蛋白和微量蛋白與M-V組的差異無統計學意義。結論 BMSCs移植可以改善阿黴素慢性腎病的腎損傷情況,在BMSCs移植後一段時間,BMSCs經腎動脈移植的效果優于經外週靜脈移植。
목적:탐색골수간충질간세포(BMSCs)경불동수주방식이식입아매소만성신병대서체내대신손상적영향。방법 SD대서좌측신절제후이2.5 mg/kg제량급대서미정맥주사아매소,1차/주,련속2차,만성신병모형성공후,장성모대서36지수궤균분위3조:아매소만성신병대조(ADR)조、간세포경신동맥이식(M-A)조、간세포경외주정맥이식(M-V)조,령선12지정상대서설정상대조(N)조。BMSCs경체외배양후,이2×106개/mL경신동맥주사도M-A조대서체내,2×106개/mL경미정맥주사도M-V조대서체내,2주후재차동양방법주사등량BMSCs。검측이식당주、이식후1주、2주대서혈뇨소담、혈기항、24 h뇨단백、24 h뇨미량단백,말차주사간세포후제1주우격광취초현미경하관찰대서신장병리화간세포재신장내분포정황。결과 M-A조、M-V조화ADR조재각관찰시점혈뇨소담、혈기항、24 h뇨단백총량、24 h뇨미량단백균명현고우N조(P<0.01)。이식후1、2주M-A조적24 h뇨미량단백저우ADR조(P<0.01),차M-A조적혈기항교ADR조화M-V조균강저(P<0.01)。이식후1주,M-A조24 h뇨단백、24 h뇨미량단백명현저우M-V조(P<0.01);단2주시뇨단백화미량단백여M-V조적차이무통계학의의。결론 BMSCs이식가이개선아매소만성신병적신손상정황,재BMSCs이식후일단시간,BMSCs경신동맥이식적효과우우경외주정맥이식。
Objective To investigate the effectiveness of bone marrow mesenchymal stem cell (MSC) and different transplantation methods of MSC on adriamycin (ADR) model of nephropathy in rats. Methods The ADR model of nephrop-athy was induced by left nephrectomy plus injection of ADR (2.5 mg/kg) in Sprague-Dawley (SD) rats, once a week for two weeks. The model rats with nephropathy were randomly divided into three groups: adriamycin nephropathic model control group (ADR, n=12), MSCs transplantation through right renal artery group (M-A, n=12) and MSCs transplantation through peripheral veins group (M-V, n=12). Another 12 SD rats were served as normal controls (N, n=12). MSCs were cultured, transplanted via right renal artery (2×106/mL) to rats in M-A group, and were transplanted via peripheral veins 2×106/mL) to rats in M-V group. The same procedure was repeated in two weeks. The blood urea nitrogen, serum creatinine, 24 h urine protein and 24 h uromicroprotein were detected before transplantation and in one and two weeks after the second transplanta-tion. The renal morphology and labeled cells were examined in the kidney one week after the second transplantation. Results The values of blood urea nitrogen, serum creatinine, 24 h urine protein and 24 h uromicroprotein were significant-ly higher in M-A group, M-V group and ADR group than those of N group (P<0.01). The level of 24 h uromicroprotein was significantly lower before the second transplantation in M-A group than that of ADR group (P<0.01). The serum level of cre-atinine was significantly decreased in M-A group than that of ADR group and M-V group (P<0.01). The levels of 24 h urine protein and 24 h uromicroprotein were significantly lower after one week transplantation in M-A group than those of M-V group (P<0.01). The serum level of creatinine was significantly lower two weeks after the second transplantation in M-A group than that of ADR group and M-V group (P<0.01), but no significant differences in the levels of urine protein and uro-microprotein between M-A group and M-V group. Conclusion Transplantation of MSCs can alleviate renal damage of chronic ADR-induced nephropathy, which is more effective in rats with MSCs transplantation via renal artery than that in rats with MSCs transplantation via peripheral vein.