Lüttgenau J, Wellnitz O, Kradolfer D, Kalaitzakis E, Ulbrich S E, Bruckmaier R M, Bollwein H
Clinic of Reproductive Medicine, Vetsuisse Faculty, University of Zurich, CH-8057 Zurich, Switzerland.
Clinic of Reproductive Medicine, Vetsuisse Faculty, University of Zurich, CH-8057 Zurich, Switzerland; Veterinary Physiology, Vetsuisse Faculty, University of Bern, CH-3001 Bern, Switzerland.
J Dairy Sci. 2016 May;99(5):4018-4031. doi: 10.3168/jds.2015-10641. Epub 2016 Feb 28.
Data from various studies indicate that the ovarian function in dairy cows can be compromised during intramammary infections. Therefore, in this study, we investigated if an experimentally induced mastitis has an effect on corpus luteum (CL) function in 14 lactating cows. On d 9 of the estrous cycle (d 1=ovulation), cows received a single dose of 200 μg of Escherichia coli lipopolysaccharide (LPS; dissolved in 10 mL of NaCL; n=8) or 10 mL of saline (control; n=6) into one quarter of the mammary gland. Measurements included plasma cortisol, haptoglobin, and progesterone (P4) concentrations, as well as luteal size (LTA) and relative luteal blood flow (rLBF). Sampling was performed on d 1, 4, and 8. On d 9, the main examination day, sampling was performed immediately before (0 h), every 1h (or at 3-h intervals for LTA and rLBF) until 9 h, as well as 12 and 24 h after treatment. Thereafter, measurements were taken on d 12, 15, 18, and then every 2 d until ovulation. Luteal tissue was collected for biopsy 24 h before and 6 h after treatment. Quantitative real-time PCR was applied to assess mRNA expression of steroidogenic factors (STAR, HSD3B), caspase 3, toll-like receptors (TLR2, -4), tumor necrosis factor α (TNFA), and prostaglandin-related factors (PGES, PGFS, PTGFR). Intramammary LPS infusion caused considerable inflammatory responses in the treated udder quarters. No decrease in plasma P4 concentrations was noted after LPS-challenge, and P4 levels did not differ between LPS-treated and control cows. Furthermore, LTA and rLBF values were not decreased after LPS challenge compared with the values obtained immediately before treatment. However, LPS infusion increased plasma levels of cortisol and haptoglobin compared with the control group. In the CL, mRNA abundance of TLR2 and TNFA was increased in cows after LPS-challenge (but not in control cows), whereas TLR4, steroidogenic, and prostaglandin-related factors remained similar to the mRNA abundance before treatment. In conclusion, intramammary LPS challenge induces systemic inflammatory reactions which alter the luteal mRNA abundance of TLR2 and TNFA but does not induce lysis of the CL.
来自各项研究的数据表明,奶牛的卵巢功能在乳房内感染期间可能会受到损害。因此,在本研究中,我们调查了实验性诱导的乳腺炎对14头泌乳奶牛的黄体(CL)功能是否有影响。在发情周期的第9天(第1天=排卵),奶牛在一个乳腺象限接受单剂量200μg的大肠杆菌脂多糖(LPS;溶解于10mL氯化钠中;n=8)或10mL生理盐水(对照组;n=6)。测量指标包括血浆皮质醇、触珠蛋白和孕酮(P4)浓度,以及黄体大小(LTA)和相对黄体血流量(rLBF)。在第1、4和8天进行采样。在主要检查日第9天,在治疗前(0小时)、每1小时(或对于LTA和rLBF每3小时)直至9小时以及治疗后12和24小时进行采样。此后,在第12、15、18天进行测量,然后每2天测量一次直至排卵。在治疗前24小时和治疗后6小时收集黄体组织进行活检。应用定量实时PCR评估类固醇生成因子(STAR、HSD3B)、半胱天冬酶3、 Toll样受体(TLR2、-4)、肿瘤坏死因子α(TNFA)和前列腺素相关因子(PGES、PGFS、PTGFR)的mRNA表达。乳房内注入LPS在治疗的乳房象限引起了相当大的炎症反应。LPS激发后未观察到血浆P4浓度降低,LPS处理的奶牛和对照奶牛之间的P4水平没有差异。此外,与治疗前立即获得的值相比,LPS激发后LTA和rLBF值没有降低。然而,与对照组相比,注入LPS增加了血浆皮质醇和触珠蛋白水平。在CL中,LPS激发后奶牛的TLR2和TNFA的mRNA丰度增加(但对照奶牛中未增加),而TLR4、类固醇生成和前列腺素相关因子与治疗前的mRNA丰度保持相似。总之,乳房内LPS激发诱导全身炎症反应,这改变了黄体中TLR2和TNFA的mRNA丰度,但不诱导CL的溶解。