EVALUATION OF CYTOTOXIC EFFECTS OF DIFFERENT DOSES OF VINBLASTINE ON MOUSE SPERMATOGENESIS BY FLOW-CYTOMETRY

Citation
Gc. Jagetia et al., EVALUATION OF CYTOTOXIC EFFECTS OF DIFFERENT DOSES OF VINBLASTINE ON MOUSE SPERMATOGENESIS BY FLOW-CYTOMETRY, Toxicology, 112(3), 1996, pp. 227-236
Citations number
27
Categorie Soggetti
Toxicology,"Pharmacology & Pharmacy
Journal title
ISSN journal
0300483X
Volume
112
Issue
3
Year of publication
1996
Pages
227 - 236
Database
ISI
SICI code
0300-483X(1996)112:3<227:EOCEOD>2.0.ZU;2-W
Abstract
The cytotoxic effects of different doses (0 to 8 mg/kg body weight) of vinblastine on mouse spermatogenesis were studied at 7 to 70 days pos t-treatment. First the gross changes in testicular weight were studied : the doses from 0.05 to 0.5 mg/kg body weight of vinblastine did not show any significant change in testicular weight. However, a dose of 1 mg/kg at day 21 and 28, and 2 mg/kg at all the intervals studied show ed a significant decline in testicular weight (P < 0.003 and < 0.03 fo r 1 and 2 mg/kg, respectively). A further increase in vinblastine dose resulted in a significant decline in testis weight from 7 to 35 days post-treatment. Flow cytometric DNA content measurements were carried out in monocellular suspensions of mouse testis that revealed five qua ntifiable populations: elongated spermatids (HC), round spermatids (1C ), spermatogonia (2C), genial cells and primary spermatocytes synthesi zing DNA (S-phase), and primary spermatocytes (4C) in the control anim als. Administration of vinblastine resulted in significant changes in the relative percentages of different germ cell populations as a conse quence of which the complete germ cell transformation ratio (HC:2C) de clined significantly (P < 0.04) at 21 and 35 days post-treatment (1 an d 2 mg/kg). The HC:2C ratio is further divided into 4C:2C, 1C:4C and 1 C:2C ratios. The 4C:2C ratio (transformation of spermatogonia to prima ry spermatocyte) significantly declined at all the post-treatment inte rvals for 1 and 2 mg/kg vinblastine (P < 0.01). A significant decline in 1C:4C ratio (meiotic transformation) was observed at all the interv als for 0.5 mg/kg (P < 0.004, 0.05, 0.001 and 0.0002 at 7, 14, 21, 28 and 35 days, respectively). This decline in 1C:4C ratio continued at h igher doses, i.e. 1 mg/kg (P < 0.0001) and 2 mg/kg (P < 0.0001, 0.005 and 0.0001, respectively) at 14, 21 and 28 days post-treatment. The 1C :2C ratio (spermatocytogenesis) decreased significantly for all the do ses by day 14 and 35, except for 0.01 mg/kg (P < 0.04 to 0.0001). Our data suggest that doses of 0.5 mg/kg vinblastine were already cytotoxi c to various germ cell populations.