Aitken S L, Karcher E L, Rezamand P, Gandy J C, VandeHaar M J, Capuco A V, Sordillo L M
Department of Large Animal Clinical Sciences, Michigan State University, East Lansing 48824, USA.
J Dairy Sci. 2009 Feb;92(2):589-98. doi: 10.3168/jds.2008-1551.
The incidence and severity of mastitis can be high during the period of transition from pregnancy to lactation when dairy cattle are susceptible to oxidative stress. Oxidative stress may contribute to the pathogenesis of mastitis by modifying the expression of proinflammatory genes. The overall goal of this study was to determine the relationship between critical antioxidant defense mechanisms and proinflammatory markers in normal bovine mammary tissue during the periparturient period. Mammary tissue samples were obtained from 12 cows at 35, 20, and 7 d before expected calving and during early lactation (EL, 15 to 28 d in milk). Enzyme activities for cytosolic glutathione peroxidase and phospholipid hydroperoxide glutathione peroxidase were relatively low during the dry period, but increased during EL, whereas activity of thioredoxin reductase 1 did not change significantly as a function of time. In contrast, gene expression for these antioxidant selenoproteins and for heme oxygenase-1 gradually decreased as parturition approached and then increased during EL. The expression of intercellular vascular adhesion molecule-1 and vascular cell adhesion molecule-1 followed a similar trend where mRNA abundance gradually declined as parturition approached with a slight rebound in EL. Gene expression of the pro-oxidant, 15-lipoxygenase 1, which is known to increase during times of oxidative stress, also increased dramatically in mammary tissue from EL cows. Expression of the proinflammatory cytokines, IL-1beta, IL-6, and IL-8 did not change significantly during the periparturient period. Strong positive correlations were found between several antioxidant enzymes (cytosolic glutathione peroxidase, thioredoxin reductase 1, and heme oxygenase-1) and vascular adhesion molecules (intercellular vascular adhesion molecule-1, vascular cell adhesion molecule-1) suggesting a protective response of these antioxidants to an enhanced proinflammatory state. Ability to control oxidative stress through manipulation of key antioxidant enzymes in the future may modify the proinflammatory state of periparturient cows and reduce incidence and severity of some diseases such as mastitis.
在奶牛从怀孕过渡到泌乳的时期,乳腺炎的发病率和严重程度可能很高,此时奶牛易受氧化应激影响。氧化应激可能通过改变促炎基因的表达而促进乳腺炎的发病机制。本研究的总体目标是确定围产期正常牛乳腺组织中关键抗氧化防御机制与促炎标志物之间的关系。在预期产犊前35天、20天和7天以及泌乳早期(EL,产奶15至28天)从12头奶牛获取乳腺组织样本。胞质谷胱甘肽过氧化物酶和磷脂氢过氧化物谷胱甘肽过氧化物酶的酶活性在干奶期相对较低,但在泌乳早期增加,而硫氧还蛋白还原酶1的活性并未随时间显著变化。相比之下,这些抗氧化硒蛋白和血红素加氧酶-1的基因表达随着分娩临近逐渐降低,然后在泌乳早期增加。细胞间血管黏附分子-1和血管细胞黏附分子-1的表达遵循类似趋势,即随着分娩临近mRNA丰度逐渐下降,在泌乳早期略有反弹。促氧化剂15-脂氧合酶1的基因表达在氧化应激时会增加,在泌乳早期奶牛的乳腺组织中也显著增加。促炎细胞因子IL-1β、IL-6和IL-8的表达在围产期没有显著变化。在几种抗氧化酶(胞质谷胱甘肽过氧化物酶、硫氧还蛋白还原酶1和血红素加氧酶-1)与血管黏附分子(细胞间血管黏附分子-1、血管细胞黏附分子-1)之间发现了强正相关,表明这些抗氧化剂对增强的促炎状态有保护反应。未来通过操纵关键抗氧化酶来控制氧化应激的能力可能会改变围产期奶牛的促炎状态,并降低乳腺炎等一些疾病的发病率和严重程度。