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. 2022 May 31;49(2):110–116. doi: 10.5653/cerm.2021.04861

Table 2.

Sperm membrane function, DNA damage, intracellular ROS, and MMP of raw, control, and post-thaw human sperm samples supplemented with different concentrations of aqueous NSE

Group Raw semen control Vitrified semen control NSE
1% 2% 3% 4% 5% 6%
Sperm membrane function 65.2±2.4 33.6±2.8a) 67.1±2.5b) 68.3±2.2b) 70.3±2.9b) 70.9±2.8b) 69.2±2.1b) 69.1±2.1b)
MMP 59.5±5.4 29.2±5.7a) 37.7±5.4b) 38.6±5.9b) 42.2±5.1b) 43.4±5.7b) 41.3±5.1b) 41.4±5.3b)
DNA damage 7.4±4.3 10.5±4.1a) 3.6±1.3b) 3.5±1.8b) 2.2±1.5b) 2.2±1.5b) 2.2±1.1b) 2.2±1.1b)
Intracellular ROS 32.3±7.2 53.1±7.5a) 43.9±7.5b) 43.2±7.8b) 39.7±7.4b) 38.1±7.6b) 39.3±7.1b) 39.1±7.0b)

Values are presented as mean±standard error.

ROS, reactive oxygen species; MMP, mitochondrial membrane potential; NSE, Nigella sativa extract.

a)

p<0.05, significant differences compared to the raw semen control group;

b)

p<0.05, significant differences compared to the vitrified semen control group.