Del Vecchio R P, Matsas D J, Fortin S, Sponenberg D P, Lewis G S
Department of Animal Science, College of Agriculture and Life Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061 USA.
Theriogenology. 1994 Feb;41(2):413-21. doi: 10.1016/0093-691x(94)90077-v.
Postpartum Holstein (n=21) and Jersey (n=4) cows were used to determine if uterine infections are associated with elevated plasma concentrations of 13,14-dihydro-15-keto-prostaglandin F(2)alpha (PGFM). Based upon clinical examinations and bacterial content of intrauterine fluid samples, cows detected with uterine infections between 21 and 28 d post partum were used (infected; n=14). These cows were matched with herdmates that were free of infection (control; n=11). Beginning on the day the cows were assigned to the experiment (Day 1), blood samples were collected on alternate days for the next 14 to 15 d. Plasma samples were stored at -20 degrees C until assayed. From Day 1 until the end of the experiment, uterine fluid samples were collected transcervically twice weekly for aerobic bacterial culture. Endometrial biopsies were collected between Days 6 and 8 and Days 13 and 15. Control cows did not show signs of uterine infection throughout the trial, and bacterial cultures indicated that there were no significant bacterial populations in the uteri of the control cows. The uteri of infected cows harbored numerous microbes. Actinomyces pyogenes was most prominent. Various species of Streptococcus and Pasteurella were also prevalent in the infected cows. Escherichia coli was present in the uterus of both infected and control cows. Biopsies showed that infected cows had more (P<0.05) neutrophils, plasma cells and lymphocytes in the endometrium than did the control cows. As determined by plasma progesterone concentrations, 83% of the control and 50% of the infected cows had functional luteal tissue during the 2-wk sampling period. Plasma PGFM profiles were linear (P<0.03) and did not differ between treatment groups (P>0.01). However, average plasma PGFM concentrations were greater (P<0.0001) in infected than in control cows. These data indicate that plasma PGFM concentrations are greater in postpartum cows with spontaneous uterine infections then in herdmates free of infection.
选用产后荷斯坦奶牛(n = 21)和泽西奶牛(n = 4)来确定子宫感染是否与血浆中13,14 - 二氢 - 15 - 酮 - 前列腺素F₂α(PGFM)浓度升高有关。根据临床检查和子宫内液体样本的细菌含量,选取产后21至28天检测出子宫感染的奶牛(感染组;n = 14)。这些奶牛与未感染的同群奶牛(对照组;n = 11)进行匹配。从奶牛被分配到实验的当天(第1天)开始,在接下来的14至15天内隔天采集血样。血浆样本储存在-20℃直至检测。从第1天到实验结束,每周经宫颈采集两次子宫内液体样本进行需氧细菌培养。在第6至8天以及第13至15天采集子宫内膜活检样本。在整个试验过程中,对照奶牛未表现出子宫感染的迹象,细菌培养表明对照奶牛子宫内没有显著的细菌菌群。感染奶牛的子宫内有大量微生物。化脓放线菌最为突出。各种链球菌和巴斯德氏菌在感染奶牛中也很常见。大肠杆菌在感染奶牛和对照奶牛的子宫内均有存在。活检显示,感染奶牛子宫内膜中的中性粒细胞、浆细胞和淋巴细胞比对照奶牛更多(P < 0.05)。根据血浆孕酮浓度测定,在为期2周的采样期内,83%的对照奶牛和50%的感染奶牛有功能性黄体组织。血浆PGFM曲线呈线性(P < 0.03),且处理组之间无差异(P > 0.01)。然而,感染奶牛的血浆PGFM平均浓度高于对照奶牛(P < 0.0001)。这些数据表明,自然发生子宫感染的产后奶牛血浆PGFM浓度高于未感染的同群奶牛。