Figure 3.

Effect of DBP, MBP, and ATBC exposure on the viability of antral follicle follicles in vitro. Early antral follicles (n = 6–12 follicles per treatment) were obtained from the ovaries of untreated CD-1 mice and cultured as described in Materials and Methods section. At the end of each culture, the ATP concentration within each follicle was determined using a luminescence assay. Data were normalized to the DMSO vehicle control and are presented as mean normalized luminescence ± SEM with asterisks (*) indicating significantly different from control.