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Chinese Journal of Critical Care Medicine(Electronic Edition) ›› 2018, Vol. 11 ›› Issue (02): 78-82. doi: 10.3877/cma.j.issn.1674-6880.2018.02.002

Special Issue:

• Original Article • Previous Articles     Next Articles

Intervention effect of invigorating kidney and activating blood in mice with chronic aplastic anemia

Ju Sun1, Mei Liu1, Dijiong Wu2, Wenbin Liu2, Huijin Hu2, Baodong Ye2,()   

  1. 1. The First Clinical Medical Institute, Zhejiang Chinese Medical University, Hangzhou 310053, China
    2. Department of Hematology, the First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou 310006, China
  • Received:2018-02-17 Online:2018-04-01 Published:2018-04-01
  • Contact: Baodong Ye
  • About author:
    Corresponding author: Ye Baodong, Email:

Abstract:

Objective

To explore the intervention effect of invigorating kidney and activating blood in mice with chronic aplastic anemia (CAA) and its mechanism.

Methods

The mice model of kidney deficiency complicated with CAA was established. Totally 30 mice were divided into the medicine group, model group and control group, 10 mice in each group. Mice in the medicine group were given orally herbal soup (0.2 mL each time, 2 times a day for 60 days), and mice in the model group and control group only received the same dose of normal saline. The general condition was observed. The levels of white blood cells, hemoglobin and platelets were detected after injection of benzene for 16 and 25 times. The levels of serum vascular endothelial growth factor (VEGF) and stromal cell-derived factor-1a (SDF-1a) were determined by enzyme linked immunosorbant assay. Meanwhile, the bone marrow nucleated cells were counted under electron microscope, and the bone marrow pathological features were observed through hatmatoxylin-eosin (HE) staining.

Results

The mice in the medicine group and model group gradually showed weight loss, fatigue, dry and sparse hair, pale limbs and so on, and as the Chinese medicine intervention prolonged, the mice in the medicine group recovered to varying degrees. The levels of white blood cells, hemoglobin and platelets all showed significant differences among three groups (F=16.536, 9.273, 5.667; all P<0.05). Above indicators at the same time in the model group and medicine group were much lower than those in the control group (all P<0.05), and above indicators after benzene injection for 25 times in the medicine group were much higher than those in the model group (all P<0.05). The levels of VEGF, SDF-1a and bone marrow nucleated cells also showed significant differences among three groups (F=11.231, 7.924, 8.455; all P<0.05). The levels of VEGF [(342 ± 11), (235 ± 13), (278 ± 13) ng/L], SDF-1a [(110 ± 13), (85 ± 11), (93 ± 12) ng/L] and bone marrow nucleated cells [(94 ± 15), (72 ± 11), (83 ± 13)/HP] in the model group and medicine group decreased more obviously compared with the control group, and they decreased most in the model group (all P<0.05). HE staining revealed that granulocyte, erythrocyte and megakaryocyte series decreased in the model group and medicine group, and the model group was less severe.

Conclusion

Invigorating kidney and activating blood may improve mice with CAA through enhancing the levels of serum VEGF and SDF-1a.

Key words: Anemia, aplastic, Mice, Intervention studies, Invigorating kidney and activating blood

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