1. 福建中医药大学附属人民医院
2. 福建中医药大学
纸质出版:2016
移动端阅览
[1]艾斯,郑健,邱彩霞,卢小露,王思佳,刘运军.肾康灵对阿霉素肾病大鼠尿蛋白质组学的影响[J].中医杂志,2016,57(07):610-614.
AI Si, ZHENG Jian, QIU Caixia, et al. Impact of Shenkangling( 肾康灵) on the Urinary Proteomics of Adriamycin Nephropathy Model Rats[J]. Journal of Traditional Chinese Medicine2016, 57(7): 610-614.
[1]艾斯,郑健,邱彩霞,卢小露,王思佳,刘运军.肾康灵对阿霉素肾病大鼠尿蛋白质组学的影响[J].中医杂志,2016,57(07):610-614. DOI: 10.13288/j.11-2166/r.2016.07.018.
AI Si, ZHENG Jian, QIU Caixia, et al. Impact of Shenkangling( 肾康灵) on the Urinary Proteomics of Adriamycin Nephropathy Model Rats[J]. Journal of Traditional Chinese Medicine2016, 57(7): 610-614. DOI: 10.13288/j.11-2166/r.2016.07.018.
目的探讨原发性肾病综合征的诊断标志物和中药肾康灵药物治疗靶点。方法将50只SD大鼠随机分为正常组、模型组、泼尼松组、中西药组、肾康灵组各10只。除正常组外其余各组大鼠于实验第1天按5.5 mg/kg剂量一次性尾静脉注射阿霉素建立阿霉素肾病大鼠模型。造模后1周
正常组和模型组上、下午各灌服蒸馏水3 ml;泼尼松组上午灌服泼尼松悬液5.5 mg/kg
下午经灌服蒸馏水3 ml;肾康灵组上午灌服肾康灵煎剂1.5 g/100 g
下午经胃灌服蒸馏水3 ml;中西药组上午灌服泼尼松悬液5.5 mg/kg
下午经胃灌服肾康灵煎剂1.5 g/100 g。各组均连续灌胃22天后收集大鼠尿液
利用i TRAQ定量分析技术联合质谱分析法鉴定各组差异蛋白。结果模型组与正常组大鼠的显著差异蛋白3个
其中高表达的蛋白是afamin
isoform CRA
a
低表达的蛋白是gro和Cystatin related protein 2。中西药组与模型组比较
显著差异表达的蛋白有6个
其中高表达的蛋白是apolipoprotein A-Ⅱ
Apolipoprotein A-Ⅳ
Vitronectin
osteopontin
Coagulation factorⅫ
低表达的蛋白是afamin
isoform CRA
a
。肾康灵组与模型组比较
显著差异表达的蛋白有6个
其中高表达的蛋白是apolipoprotein A-Ⅱ
Complement factor B
Vitronectin
osteopontin
Coagulation factorⅫ
低表达的蛋白是afamin
isoform CRA
a
。结论 gro、Cystatin related protein 2、afamin
isoform CRA
a
可作为原发性肾病综合征的诊断标志物
afamin
isoform CRA
a
、apolipoprotein A-Ⅱ、Complement factor B、Vitronectin
osteopontin、Coagulation factorⅫ可作为肾康灵的药物治疗靶点。
Objective To explore the diagnostic marker of primary nephrotic syndrome( PNS) and the therapeutic target of Shenkangling( 肾康灵) decoction. Methods Fifty SD rats were randomized into normal group
model group
prednisone group
the herb-western medicine group and the Shenkangling group
10 in each group. Except for the normal group rats in other groups were injected adriamycin 5. 5 mg / kg by tail vein on the first day of the test to establish adriamycin nephropathy rats models. One week after modeling
the normal group and the model group were given 3 ml distilled water in the morning and in the afternoon respectively by gavage. The prednisone group was given prednisone suspension 5. 5 mg / kg in the morning by gavage
3ml distilled water in the afternoon. The Shenkangling group was given Shenkangling decoction 1. 5 g /100 g in the morning by gavage
3ml distilled water in the afternoon. The herb-western medicine group was given prednisone suspension 5. 5 mg / kg in the morning by gavage
Shenkangling decoction 1. 5 g /100 g in the afternoon. After 22 days
urine was collected and differential proteins in all groups were examined by isobaric tags for relative and absolute quantitation( i TRAQ) quantitative analysis technology combined with mass spectrometric method. Results There were three significantly differential proteins in the model group and the normal group
including highly expressed protein afamin
isoform CRA
a
as well as lowly expressed proteins gro and Cystatin related protein 2. Compared the herb-western medicine group with the model group
there were six significantly differential proteins
including highly expressed proteins apolipoprotein A-Ⅱ
Apolipoprotein A-Ⅳ
Vitronectin
osteopontin and Coagulation factor Ⅻ
as well as lowly expressed protein afamin
isoform CRA
a. Compared the Shenkangling group with the model group
there were six significantly differential proteins
including highly expressed proteins apolipoprotein A-Ⅱ
Complement factor B
Vitronectin
osteopontin and Coagulation factor Ⅻ
as well as lowly expressed protein afamin
isoform CRA
a. Conclusion Gro
Cystatin related protein 2
afamin and isoform CRA
a might be used as the diagnostic markers of PNS. Afamin
isoform CRA
a
apolipoprotein A-Ⅱ
Complement factor B
Vitronectin
osteopontin and Coagulation factor Ⅻ might be used as the therapeutic target of Shenkangling.
0
浏览量
224
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010102007558号