Steamed Panax notoginseng attenuates renal anemia in an adenine-induced mouse model of chronic kidney disease

被引:14
作者
Gao, Min [1 ,2 ]
Zhang, Zejun [1 ,2 ]
Zhang, Yiming [1 ,2 ]
Li, Minghui [1 ,2 ]
Che, Xiaoyan [1 ,2 ]
Cui, Xiuming [1 ,2 ]
Wang, Mei [3 ,4 ,5 ]
Xiong, Yin [1 ,2 ,3 ]
机构
[1] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Peoples R China
[2] Kunming Univ Sci & Technol, Yunnan Key Lab Panax Notoginseng, Kunming 650500, Peoples R China
[3] Leiden Univ, European Ctr Chinese Med & Nat Cpds, Inst Biol Leiden, NL-2333 BE Leiden, Netherlands
[4] Bomed B V, NL-2333 BE Leiden, Netherlands
[5] Ctr Drug Discovery & Technol Dev Yunnan Tradit Med, Kunming 650217, Peoples R China
基金
中国国家自然科学基金;
关键词
Steamed Panax notogensing; Renal anemia; Chronic kidney disease; Hematopoiesis; HEPATOCYTE GROWTH-FACTOR; FIBROSIS; APOPTOSIS; MECHANISMS; FAILURE; ERYTHROPOIETIN; GINSENG; SYSTEM; DEATH;
D O I
10.1016/j.jep.2021.114941
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Panax notoginseng (PN) (Burk.) F. H. Chen is a medicinal herb used to treat blood disorders since ancient times, of which the steamed form exhibits the anti-anemia effect and acts with a "blood-tonifying " function according to the traditional use. However, its pharmacological effect and mechanism on alleviating renal anemia (RA) are still unclear.& nbsp;Aims of the study: The study aims to investigate the effect of steamed Panax notoginseng (SPN) to attenuate RA and its underlying mechanism based on the model of adenine-induced RA mice.& nbsp;Materials and methods: Seventy mice were randomly divided into seven groups of ten: the control group, model group, the erythropoietin (EPO) group, the Fufang E'jiao Jiang (FEJ) group, the high-dose steamed PN (H-SPN) group, the middle-dose steamed PN (M-SPN) group, and the low-dose steamed PN (L-SPN) group. The adenine induction RA model was applied to assess the "blood enriching " function of SPN. The blood routine indexes, erythrocyte fragility, pathologic morphology of kidney tissue and the expression levels of related cytokines and proteins in the mice were detected after 3-week administration with SPN and positive drugs.& nbsp;Results: Our study provided evidences that SPN could ameliorate RA. Compared with the control group, SPN could attenuate RA by significantly increasing the numbers of peripheral blood cells (p < 0.01), improving the erythrocyte fragility (p < 0.01), and restoring the expression of EPO mRNA in the kidneys and EPO receptor mRNA in bone marrow nucleated cells. The expression of TGF-beta(1) mRNA was declined and the expression of HGF mRNA was significantly increased in a dose-dependent way after the treatment of SPN. Additionally, the expression of Bcl-2 and Bcl-2/Bax ratio in the kidneys were significantly increased. In contrast, there was a highly significant decrease in the expression of Bax (p < 0.01), following SPN treatment.& nbsp;Conclusion: SPN could alleviate RA by promoting the overall hematopoiesis and inhibiting the progress of renal injury in mice.
引用
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页数:9
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