Department of Pathobiology and Population Sciences, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Herts AL9 7TA, UK.
Agri-Food and Biosciences Institute, Newforge Lane, Upper Malone Road, Belfast BT9 5PX, UK.
Int J Mol Sci. 2023 Jun 8;24(12):9906. doi: 10.3390/ijms24129906.
Cows can live for over 20 years, but their productive lifespan averages only around 3 years after first calving. Liver dysfunction can reduce lifespan by increasing the risk of metabolic and infectious disease. This study investigated the changes in hepatic global transcriptomic profiles in early lactation Holstein cows in different lactations. Cows from five herds were grouped as primiparous (lactation number 1, PP, 534.7 ± 6.9 kg, = 41), or multiparous with lactation numbers 2-3 (MP2-3, 634.5 ± 7.5 kg, = 87) or 4-7 (MP4-7, 686.6 ± 11.4 kg, = 40). Liver biopsies were collected at around 14 days after calving for RNA sequencing. Blood metabolites and milk yields were measured, and energy balance was calculated. There were extensive differences in hepatic gene expression between MP and PP cows, with 568 differentially expressed genes (DEGs) between MP2-3 and PP cows, and 719 DEGs between MP4-7 and PP cows, with downregulated DEGs predominating in MP cows. The differences between the two age groups of MP cows were moderate (82 DEGs). The gene expression differences suggested that MP cows had reduced immune functions compared with the PP cows. MP cows had increased gluconeogenesis but also evidence of impaired liver functionality. The MP cows had dysregulated protein synthesis and glycerophospholipid metabolism, and impaired genome and RNA stability and nutrient transport (22 differentially expressed solute carrier transporters). The genes associated with cell cycle arrest, apoptosis, and the production of antimicrobial peptides were upregulated. More surprisingly, evidence of hepatic inflammation leading to fibrosis was present in the primiparous cows as they started their first lactation. This study has therefore shown that the ageing process in the livers of dairy cows is accelerated by successive lactations and increasing milk yields. This was associated with evidence of metabolic and immune disorders together with hepatic dysfunction. These problems are likely to increase involuntary culling, thus reducing the average longevity in dairy herds.
奶牛的寿命可以超过 20 年,但它们的生产寿命平均只有首次产犊后约 3 年。肝功能障碍会增加代谢和传染病的风险,从而缩短寿命。本研究调查了不同泌乳期荷斯坦奶牛在泌乳早期肝脏整体转录组谱的变化。来自五个牛群的奶牛被分为初产(泌乳次数 1,PP,534.7 ± 6.9kg,n = 41)或经产 2-3 次(MP2-3,634.5 ± 7.5kg,n = 87)或 4-7 次(MP4-7,686.6 ± 11.4kg,n = 40)。奶牛在产后约 14 天进行肝脏活检以进行 RNA 测序。测量血液代谢物和产奶量,并计算能量平衡。MP 和 PP 奶牛之间的肝脏基因表达存在广泛差异,MP2-3 和 PP 奶牛之间有 568 个差异表达基因(DEGs),MP4-7 和 PP 奶牛之间有 719 个 DEGs,MP 奶牛中下调的 DEGs 占主导地位。两个年龄组的 MP 奶牛之间的差异中等(82 个 DEGs)。基因表达差异表明,与 PP 奶牛相比,MP 奶牛的免疫功能降低。MP 奶牛的糖异生增加,但也有肝功能受损的证据。MP 奶牛的蛋白质合成和甘油磷脂代谢失调,基因组和 RNA 稳定性以及营养物质转运受损(22 个差异表达溶质载体转运蛋白)。与细胞周期停滞、细胞凋亡和抗菌肽产生相关的基因上调。更令人惊讶的是,初产奶牛在开始第一次泌乳时就出现了肝纤维化的炎症迹象。因此,本研究表明,奶牛肝脏的衰老过程因连续泌乳和产奶量的增加而加速。这与代谢和免疫紊乱以及肝功能障碍的证据有关。这些问题可能会增加非自愿淘汰,从而降低奶牛群的平均寿命。