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. 2022 Nov 17;50(2):1059–1068. doi: 10.1007/s11033-022-08061-1

Table 3.

Frequency of chromosomal aberrations induced in mouse spermatocytes after treatment with vinblastine

Treatment and doses Total abnormal metaphases No and (%) of metaphases with different types of chromosome aberration
No Mean(%) ± SE X–Y univalent Autosomal univalent X–y u + A-u Fragment and/or Break Chain IV Polyp
I. Control (Non-treated) 19 3.80 ± 0.37a 17(3.40) 2(0.40)
II. Vinblastine a-Single dose
 3 mg/kg 40 8.0 ± 0.77b 25(5.0) 12(2.40) 1(0.20) 2(0.40)
 4.5 mg/kg 44 8.80 ± 0.37b,c 28(5.60) 12(2.40) 1(0.20) 3(0.60)
 6 mg/kg 52 10.40 ± 0.93c,d 23(4.60) 20(4.0) 1(0.20) 3(0.60) 1(0.20) 4(0.80)
 10 mg/kg 66 13.20 ± 1.16e 45(9.0) 17(3.40) 2(0.40) 2(0.20)
b-3 successive dose treatment
 3 mg/kg 51 10.20 ± 0.86b,c,d 27(5.40) 18(3.60) 4(0.40) 1(0.20) 1(1.0)
 4.5 mg/kg 55 11.0 ± 0.83c,d,e 41(8.20) 8(1.60) 5(1.0) 1(1.0)
 6 mg/kg 61 12.20 ± 0.37d,e 30(6.0) 18(3.60) 6(1.20) 7(1.40)

A total of 500 cells were analyzed (five mice per group; 100 cells/mouse). X–Y u X–Y univalent, A-u Autosomal univalent, Polyp Polyploidy. One way ANOVA–Tukey’s multiple comparisons test was used. The values having different superscript letters in each column are significantly different from one another