Table 2.
Dose (%) | S9‐Mixure | G | B | D | R | g | b | Int | Itr | Other | AFa |
---|---|---|---|---|---|---|---|---|---|---|---|
Short‐term treatment (3 hr) | |||||||||||
Negative controlb | + | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
Positive controlc | + | 0 | 3 | 13 | 0 | 0 | 5 | 4 | 1 | 0 | 26/200* |
S. sanghuang mycelia 1.25 | + | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1/200 |
S. sanghuang mycelia 0.625 | + | 0 | 0 | 0 | 1 | 0 | 1 | 0 | 0 | 0 | 2/200 |
S. sanghuang mycelia 0.3125 | + | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
Negative controlb | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
Positive controld | − | 0 | 3 | 2 | 1 | 0 | 6 | 23 | 4 | 0 | 39/200* |
S. sanghuang mycelia 5 | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
S. sanghuang mycelia 2.5 | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
S. sanghuang mycelia 1.25 | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
Long‐term treatment (20 hr) | |||||||||||
Negative controlb | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
Positive controld | − | 0 | 1 | 3 | 0 | 0 | 11 | 10 | 3 | 0 | 28/200* |
S. sanghuang mycelia 5 | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
S. sanghuang mycelia 2.5 | − | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0/200 |
S. sanghuang mycelia 1.25 | − | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 1/200 |
Chromosome gaps were recorded separately but not included in aberrant cells. b, chromatid break; B, chromosome break; D, dicentric; g, chromatid gap; G, chromosome gap; Int, interchange; Itr, intrachange; R, ring.
Aberration frequency: Number of cells with chromosome aberration in 200 metaphase cells (n/200).
Ham's F‐12 Culture medium with 10% fetal bovine serum.
25 μg/ml cyclophosphamide.
2 μg/ml mitomycin C.
Statistically significant (p < .05) when compared to the control group.