成都中医药大学
纸质出版:2017
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[1]马晖,谢春光.参芪复方对糖尿病大血管病变大鼠胸主动脉差异基因表达的影响[J].中医杂志,2017,58(10):863-867.
MA Hui, XIE Chunguang. Effect of Shenqi Compounds(参芪复方) on Differential Gene Expression in Thoracic Aorta of Rats with Diabetic Great Vascular Complications[J]. Journal of Traditional Chinese Medicine2017, 58(10): 863-867.
[1]马晖,谢春光.参芪复方对糖尿病大血管病变大鼠胸主动脉差异基因表达的影响[J].中医杂志,2017,58(10):863-867. DOI: 10.13288/j.11-2166/r.2017.10.014.
MA Hui, XIE Chunguang. Effect of Shenqi Compounds(参芪复方) on Differential Gene Expression in Thoracic Aorta of Rats with Diabetic Great Vascular Complications[J]. Journal of Traditional Chinese Medicine2017, 58(10): 863-867. DOI: 10.13288/j.11-2166/r.2017.10.014.
目的探讨参芪复方防治糖尿病大血管病变的可能分子机制。方法 160只自发性2型糖尿病GK大鼠给予高脂饲料喂养12周建立糖尿病大血管病变模型
随机分成模型组、西药组、参高组、参中组、参低组
每组32只。另设32只Wistar大鼠为空白组。造模后西药组给予二甲双胍片0.1 g/(kg·d)灌胃
参高、中、低组分别给予参芪复方2.88、1.44、0.72 g/(kg·d)灌胃
空白组和模型组给予生理盐水5 ml/(kg·d)灌胃
各组均灌胃16周。分别在给药前及给药第8、16周时检测空腹血糖;第8、16周时采用Masson染色观察胸主动脉病理形态
计算胶原纤维/血管壁面积(PVCA/LA);16周时进行差异基因筛选。结果与空白组同时间比较
模型组在给药前及给药8、16周时大鼠空腹血糖升高
第8、16周时PVCA/LA明显升高(P<0.05或P<0.01);第16周时西药组和参高、中、低组大鼠空腹血糖低于同时间模型组
PVCA/LA均显著下降(P<0.05或P<0.01)。参中组与模型组、模型组与空白组共同存在的显著性差异基因共15个
其中与糖尿病血管病变有关的基因为Elavl1、Lama4
且参中组Elavl1、Lama4基因较模型组下调。结论参芪复方防治糖尿病大血管病变作用机理可能与下调胸主动脉Elavl1、Lama4基因表达
从而抑制血管新生
减少胶原纤维产生有关。
Objective To explore the possible molecular mechanism of Shenqi Compounds(参芪复方) in preventing and treating diabetic great vascular complications. Methods Totally 160 Goto-Kakizaki(GK) rats with spontaneous type 2 diabetes were given high-fat diet for 12 weeks to establish diabetic great vascular complications model.The rats were then randomly divided into model group
western medicine group
Shenqi high
middle and low groups
with 32 rats in each group. Other 32 Wistar rats were set as blank group. After modeling
the western medicine group was given 0. 1 g/(kg·d) of diformin tablet for gavage
while the Shenqi high
middle and low groups were respectively given 2. 88
1. 44 or 0. 72 g/(kg·d) of Shenqi Compounds for gavage. The blank and model group were given5 ml/(kg·d) of saline for gavage. The medication were all for 16 weeks. Fasting blood-glucose was examined before giving medicine and in the 8th and 16 th week during treatment. In the 8th and 16 th week
Masson stain was adopted to observe pathomorphism of thoracic aorta and calculated perivascular circuferential area/lumen area(PVCA/LA).Differential genes screening was conducted in the 16 th week. Results Compared with the blank group at the same time point
fasting blood-glucose of rats increased before and in the 8th and 16 th week during giving medicine
and PVCA/LA remarkably increased in the 8th and 16 th week in the model group(P < 0. 05 or P < 0. 01); In the 16 th week
fasting blood-glucose of rats in the western medicine group and Shenqi high
middle and low groups were lower than that in the model group at the same time point and PVCA/LA all remarkably decreased(P < 0. 05 or P < 0. 01).There were in total 15 remarkable common differential genes between the Shenqi middle group and the model group
and the model and the blank group. Among them
Elavl1 and Lama4 were genes that had relationship with diabetic great vascular complications. Elavl1 and Lama4 genes in the Shenqi middle group decreased. Conclusion The possible functional mechanism of Shenqi Compounds in preventing and curing diabetic great vascular complications might be related with down-regulating Elavl1 and Lama4 gene expression in thoracic aorta and therefore inhibiting angiogenesis and reducing collagen fibers producing.
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