RESUMO
The objective of this study was to evaluate the impact of cows' calving ages and newborn calf body weight on the pre-weaning growth rates of calves under the farming conditions of a northeastern European country. The females were purebred Charolais cows that calved between 2019 and 2022. A total of 130 calves (bulls = 76; heifers = 54) were observed during the evaluation. The investigation showed that, based on gender, bulls had a 4.28% higher birth weight than heifers (p < 0.05). The gender of the calves affected their weight, indicating that newborns bulls were significantly heavier. Calf gender affected calf growing performance. Male calves' weight gain was higher than that of females in the time before weaning (210 days). The highest gain of bulls was observed from 211 days to 365 days after birth. The average daily weight of male calves during this period was 6.16% (p < 0.001) higher compared to the period up to 210 days after birth. Heifers had a higher daily weight in the period up to 210 days after birth, and the daily weight gain was 12.9% (p < 0.001) higher in this period compared to the period from 211 to 365 days after birth. We observed a higher weight gain in calves from mothers with a higher number of calvings. Being born from cows with four or more calvings had a significant effect on the weight gain of calves in the period up to 210 days (p < 0.05). In the period up to 210 days, the weight gain of calves born from cows with two calvings was the lowest and was 9.79% lower compared to calves born from cows with four and more calvings (p < 0.05). The best weights were obtained from calves born in the spring and autumn seasons. Calves born in spring, summer, and autumn differed in weight by 0.37 kg. The calves of cows that were inseminated in the autumn season had the highest gain in the period up to 210 days and also from 210 to 365 days (p < 0.05). In our study, significantly higher average birth weight of calves was detected in autumn compared to summer and winter (p < 0.05). Also, the highest gain was found from 211 to 365 days after birth in the summer season, but the difference was only 1.47% (p < 0.05).
RESUMO
Objective: The purpose of this study was to investigate the possible cytotoxic and genotoxic impact of new-generation 206 nm femtosecond solid-state laser irradiation on murine skin cells in vitro, and to compare the cell and DNA damage caused by different wavelength (206 vs. 257 nm) femtosecond laser pulses. Background data: The first attempts to evaluate the possible genotoxic impact of ultrashort laser pulses on the murine bone marrow cells in vitro revealed the unlooked-for DNA-damaging effect. However, the impact of far-ultraviolet (UV) radiation on genetic material of internal and external organs' cells may differ due to differences in size, structure, and biochemical composition of the cells. Methods: Mouse skin cells were exposed to different doses of 206 and 257 nm wavelength femtosecond laser, and 254 nm UV lamp irradiation. Comet assay in two versions-the standard alkaline and the enzyme-linked-was used for the evaluation of DNA damage. Results: The irradiation determined by different parameters demonstrated intensity-dependent genotoxic impact. The pyrimidine dimers made up the greater part of DNA photodamage, but with rising exposure dose the increase of relative amount of more energy-consuming primary damage-DNA strand breaks-was detected. Conclusions: The 206 nm femtosecond laser irradiation was much more cytotoxic but caused less primary DNA damage than the same pulse duration longer wavelength (257 nm) laser irradiation. DNA-damaging effect of 206 nm femtosecond laser pulses with extremely low penetration force may highly depend on the size, structure, and biochemical composition of the cells of organ or tissue targets.
