Table 1.

Thalidomide-induced vascular defect during the development of zebrafish embryos


Concentration

Dorsal artery presence, % (no.)

Dorsal artery absence, % (no.)

No. embryos
Thalidomide    
    Control   100 (250)   0 (0)   250  
    100 μM   100 (240)   0 (0)   240  
    200 μM   89 (212)   11 (27)   239  
    400 μM   41 (147)   59 (210)   357  
    800 μM   7 (49)   93 (641)   690  
C2-ceramide    
    Control   100 (250)   0 (0)   250  
    2.5 μM   80 (187)   20 (47)   234  
    5.0 μM   48 (118)   52 (127)   245  
    10 μM   27 (95)   73 (256)   351  
    20 μM   12 (54)   88 (397)   451  
    40 μM
 
0 (0)
 
100 (535)
 
535
 

Concentration

Dorsal artery presence, % (no.)

Dorsal artery absence, % (no.)

No. embryos
Thalidomide    
    Control   100 (250)   0 (0)   250  
    100 μM   100 (240)   0 (0)   240  
    200 μM   89 (212)   11 (27)   239  
    400 μM   41 (147)   59 (210)   357  
    800 μM   7 (49)   93 (641)   690  
C2-ceramide    
    Control   100 (250)   0 (0)   250  
    2.5 μM   80 (187)   20 (47)   234  
    5.0 μM   48 (118)   52 (127)   245  
    10 μM   27 (95)   73 (256)   351  
    20 μM   12 (54)   88 (397)   451  
    40 μM
 
0 (0)
 
100 (535)
 
535
 

Zebrafish embryos were treated at 75% epiboly stage (8 hpf) with various concentrations of thalidomide or C2-ceramide, and then the defect of dorsal artery was determined by assessing the loss of blood flow under microscopy at the 48-hpf stage.

Close Modal

or Create an Account

Close Modal
Close Modal