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. 2022 Jan;10(2):38. doi: 10.21037/atm-21-4800

Table 1. PDS-C increased the colony formation of granulocytic, erythroid, and megakaryocytic progenitor cells in normal mice (x¯±s, n=8).

PDS-C (mg/L) CFU-GM number (increasing %) CFU-E number (increasing %) CFU-MK number (increasing %)
0 97.0±11.5 117.0±11.2 56.0±6.5
5 108.2±12.8 (11.5±2.2) 132.0±12.9 (12.8±2.3) 63.1±7.7 (13.1±2.1)
10 125.7±14.8** (28.5±3.4) 148.4±15.7** (26.5±3.2) 70.0±8.7** (25.7±3.1)
25 137.5±16.4** (41.6±4.3) 168.0±16.7** (42.4±4.5) 78.2±8.5** (39.3±4.4)
50 138.5±16.3** (42.2±4.6) 167.2±16.9** (41.2±4.4) 79.3±8.6** (40.9±4.3)
100 128.5±15.7** (31.6±3.5) 153.4±15.9** (30.4±3.3) 71.8±7.8** (28.6±3.2)
Testosterone 10−7 M 110.0±11.6 (13.5±2.3) 169.8±18.4** (45.1±4.6) 69.9±7.8** (24.3±2.6)

**, P<0.01, vs. untreated control cells. PDS-C, panaxadiol saponins component; CFU-GM, colony formation unit granulocyte and macrophage; CFU-E, colony formation unit-erythroid; CFU-MK, colony formation unit megakaryocytic progenitor.