Abstract. Supplementation of semen extender with caffeine and CaCl2 for artificial insemination (AI) of fresh spermatozoa has been demonstrated to reduce recruitment of uterine polymorphonuclear leukocytes (PMNs) and the activity of phagocytosis. Here, we determined if addition of caffeine and CaCl2 to semen extender improves the fertility of frozen-thawed boar semen. In experiment 1, gilts were cervically inseminated twice with froxzen-thawed boar spermatozoa (25 × 10 8 cells per dose) suspended in Modena solution (n=7) or modified Beltsville Thawing Solution supplemented with caffeine and CaCl2 (BCC, n=7). The gilts were slaughtered 4 h later, and their oviducts and uterine horns plus the body of the uterus were flushed to recover PMNs and non-phagocytosed spermatozoa. There was no difference in the total number of uterine PMNs between gilts inseminated with Modena solution and those inseminated with BCC (3.8 × 10 8 vs. 1.5 × 10 8 cells, respectively); however, the total number of uterine spermatozoa was higher when gilts were inseminated with BCC (40.6 × 10 6 cells) compared with those inseminated with Modena solution (1.4 × 10 6 cells, P<0.05). In experiment 2, gilts and sows were subjected to intrauterine insemination twice with frozen-thawed spermatozoa suspended (25 × 10 8 sperm per dose) in Modena (n=21) or BCC (n=21). The overall pregnancy and farrowing rates were higher in females inseminated with BCC (71.4 and 61.9%, respectively) compared with those inseminated with Modena solution (38.1 and 28.6%, respectively, P<0.05). However, no significant difference in litter size of piglets was observed between treatments (7.2 ± 1.6 piglets for Modena solution vs. 8.2 ± 0.9 piglets for BCC solution). In conclusion, we demonstrated that use of BCC solution for frozen-thawed boar semen produced better pregnancy and farrowing rates following AI than Modena solution, probably by reducing the phagocytosis of spermatozoa. Key words: Artificial insemination, Caffeine and CaCl2, Frozen-thawed boar semen, Polymorphonuclear leukocytes (J. Reprod. Dev. 55: [645][646][647][648][649] 2009) uring artificial insemination (AI) in sows, a large quantity of semen is deposited into the uterus. However, at the same time, a considerable amount of spermatozoa is rapidly lost from the uterus; only less than 2% of the inseminated spermatozoa are reported to be recovered from the uterus at 4 h after AI [1]. The backflow of semen and phagocytosis of spermatozoa by polymorphonuclear leukocytes (PMNs) appear to be the two main mechanisms responsible for the reduction in the amount of spermatozoa [2]. In gilts, although the influx of PMNs into the uterus can persist for as long as 36 h after insemination, the number of uterine spermatozoa and the clearance time from the uterus are highly dependent on the presence or absence of seminal plasma [3]. It has been shown that seminal plasma inhibits neutrophil chemotaxis in vitro [4] and protects spermatozoa from an inflamed uterine environment, resulting in improved fertility [5,6]. In the c...