Skip to main content
. 2025 Jan 2;15:447. doi: 10.1038/s41598-024-84184-8

Fig. 7.

Fig. 7

Brca2wt/mut male rats reveal deteriorated sperm quality. (a) Design of experiments regarding the characterization of spermatozoa. (b) Representative images of Eosin Y-Nigrosin staining (bar = 20 μm; arrowhead, viable spermatozoa; arrow, dead spermatozoa). (c) Number of spermatozoa and (d) vitality of spermatozoa are decreased in Brca2wt/mut group both at 11 weeks and 8 months (n = 5). (e) Motility of sperms from Brca2wt/mut rats is not deteriorated at 11 weeks but decreased at 8 months (n = 5). (f) Representative morphology of abnormal sperms. AH, abnormal head sperm; TL, tailless sperm; ST, short tail sperm; SH, small head sperm; LH, large head sperm. (g) Abnormal sperm was more abundant in Brca2wt/mut than Brca2wt/wt both at 11 weeks and 8 months. (h) Representative images of the sperms stained with acridine orange (arrowhead, damaged sperm DNA as D; arrow, undamaged sperm DNA as UD). (i) Comparison of the proportion of spermatozoa with DNA fragmentation within a sperm sample detected from SCSA (n = 5). This proportion of spermatozoa with DNA fragmentation is commonly referred to as DNA fragmentation index, DFI. Both at 11 weeks and 8 months, the spermatozoa of the Brca2wt/mut rats show more DNA fragmentation than those of Brca2wt/wt. SCSA, sperm chromatin structure assay. (j) Summary of the findings.