China Animal Husbandry & Veterinary Medicine ›› 2026, Vol. 53 ›› Issue (2): 870-878.doi: 10.16431/j.cnki.1671-7236.2026.02.032

• Genetics and Breeding • Previous Articles     Next Articles

Effect of L-alanine on Boar Semen Storage at Room Temperature

ZENG Guanghu1,2,3(), JIA Yuxuan1,2,3, HUANG Mengting1,2,3, SHEN Xiangyu1,2,3, LIU Jiawei1,2,3, DU Junhao1,2,3, GONG Ting1,2,3()   

  1. 1.Key Laboratory of Genetics,Breeding and Reproduction of Plateau and Mountain Animals,Ministry of Education,Guizhou University,Guiyang 550025,China
    2.Key Laboratory of Animal Genetics,Breeding and Reproduction of Guizhou Province,Guiyang 550025,China
    3.College of Animal Science,Guizhou University,Guiyang 550025,China
  • Received:2025-05-07 Online:2026-02-20 Published:2026-01-27
  • Contact: GONG Ting E-mail:guanghuzeng@163.com;tgong@gzu.edu.cn

Abstract:

Objective L-alanine (L-Ala) is a multifunctional additive that functions both as a sweetener and a pH buffer. This study aimed to investigate the effect of L-Ala on the effect of boar semen storage at room temperature and provide a theoretical basis for optimizing the formulation of semen diluents. Method Semen was collected from three healthy adult Duroc boars aged 1 to 2 years. Various concentrations (0, 20, 40, 80, 160, and 320 μg/mL) of L-Ala were added to Modena diluent. Sperm motility and motion parameters (straight-line (rectilinear) velocity (VSL), curvilinear velocity (VCL), average path velocity (VAP), and amplitude of lateral head (ALH)) were assessed at 17 ℃ on days 1, 3, 5, and 7 of storage. Samples showing significant changes were further analyzed for acrosome integrity, plasma membrane integrity, and oxidative stress indices. Result The effects of L-Ala on boar semen storage at room temperature were concentration- and time-dependent. During the first five days of storage, sperm motility parameters showed no significant differences in different concentration groups (0-320 μg/mL) (P>0.05). By days 7, 320 μg/mL L-Ala group exhibited the best performance, among which sperm motility increased by 9.73% (P<0.05), motility parameters (VSL, VAP, and ALH) increased by 11.33%, 13.08%, and 12.17% (P<0.05), and acrosome integrity rate and plasma membrane integrity rate increased by 43.71% and 26.54% (P<0.05), respectively, the total antioxidant capacity (T-AOC) increased by 1.14-fold (P<0.05), while malondialdehyde (MDA) content decreased by 54.91% (P<0.05). Conclusion Under the conditions of this experiment, L-Ala could effectively prolong the storage time of boar semen at room temperature, with 320 μg/mL being the optimal concentration. It significantly maintained sperm quality in the late storage period (7 days), the mechanism of action might be related to enhancing antioxidant capacity and reducing lipid peroxidation damage.

Key words: L-Ala; boar semen; storage at room temperature; sperm motility

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