Key result
Ginsenoside Rk3 and Rh4 restored red blood cell count, hemoglobin, and hematocrit to normal values in mice with ribavirin-induced anemia, with effects superior to erythropoietin.
Why the study?
Do ginsenoside Rk3 and Rh4 improve ribavirin-induced anemia in mice?
RCT (n=100)
randomly divided
Do ginsenoside Rk3 and Rh4 improve ribavirin-induced anemia in mice?
Ginsenoside Rk3 and Rh4 effectively treat ribavirin-induced anemia in mice by promoting hematopoiesis, suggesting potential as new therapeutic drugs for anemia.
Ginsenosides show no immediate clinical role in anemia; leaves open translation from murine hematopoiesis data to human trials.
Ginsenoside Rk3 (Rk3) and ginsenoside Rh4 (Rh4) have been reported to have therapeutic effects on a variety of diseases including some hematological diseases. The aim of the present study was to treat ribavirin-induced anemia in mice with Rk3 and Rh4 and explore the therapeutic mechanisms. All the experimental mice were randomly divided into 10 groups (the normal group, the control group, the model group, the erythropoietin (EPO) group, and 6 groups of different doses of Rk3 and Rh4, n = 10 per group). The changes in the hemograms, the content of cytokines, the number of hematopoietic cells and viscera damage were observed in the experiment. The results showed that the red blood cell count, the hemoglobin amount and the hematocrit of mice in the ginsenoside groups could be restored to normal values in a short time, and the effects of both Rk3 and Rh4 are obviously better than those of EPO. Moreover, some positive regulators (EPO, erythroid transcription factor-1, and interleukin-3) related to hematopoiesis increased and some negative regulators (interferon-γ and tumour necrosis factor-α) decreased in vivo after the injection of Rk3 or Rh4. These two ginsenosides did little damage to viscera and produced different degrees of increase in the hematopoietic cells in the bone marrow and spleen, which indicated that Rk3 promoted bone marrow and extramedullary haematopoiesis while Rh4 promoted extramedullary hematopoiesis. Therefore, both Rk3 and Rh4 could be considered new therapeutic drugs for treating anemia.
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Wei et al. (2018) conducted an RCT in ribavirin-induced anemia (n=100). Ginsenoside Rk3 and ginsenoside Rh4 vs. erythropoietin (EPO), normal, control, and model groups was evaluated on changes in hemograms (red blood cell count, hemoglobin amount, and hematocrit). Ginsenoside Rk3 and Rh4 restored red blood cell count, hemoglobin, and hematocrit to normal values in mice with ribavirin-induced anemia, with effects superior to erythropoietin.
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