Cryopreservation of boar semen is a technique used to extend the shelf life over that of cooled semen, which is useful to preserve genetic material for long periods (Qian, Yu, & Zhou, 2016). Artificial insemination (AI) was the first studied in 1957 (Hess, Teague, Ludwick, & Martig, 1957) and swine industry has been applying this biotechnology for several decades (Rath et al., 2009). On the other hand, this procedure does not exceed 1% of all the swine industry farm worldwide (Yeste, 2015). Frozen semen is commonly used in cattle due to the quality of semen after freezing and the satisfactory conception rate. However, the quality of boar semen after freezing has not been satisfactory. It results in a low conception rate and litter size that is not high enough to meet the requirements of the manufacturer. The issue occurs because of the low semen quality and low survival rate of spermatozoa after the freezing process (Eriksson, Petersson, & Rodriguez-Martinez, 2002). It was found that boar semen are sensitive to exposure to temperatures below 12°C, which induces destabilizing sperm membrane changes called "cold shock" as expressed by decreased sperm motility that appears to be the critical temperature to spermatozoa.