Hebra A, Hong J, McGowan K L, Smith C, McKernan M L, Ross A J
David Paley Lichtenstein Laboratory of Surgical Metabolism and Nutrition, Children's Hospital of Philadelphia, PA 19104.
J Pediatr Surg. 1994 Feb;29(2):280-5; discussion 285-7. doi: 10.1016/0022-3468(94)90333-6.
The authors previously reported that mesenteric ischemia and reperfusion (I/R) in a chronic newborn piglet model creates dysfunctional intestinal motility. Whether this leads to inadequate bacterial clearance and translocation (BT) through the gastrointestinal tract remains unclear. To test this hypothesis the authors used their chronic piglet model (weight, 3.5 +/- 0.3 kg; age, 18 +/- 4 days; on formula feeding); nonocclusive mesenteric ischemia was induced via reversible pericardial tamponade. Mesenteric flow (SMA Doppler measurement via the retroperitoneal approach) was decreased to 25% +/- 5% of baseline for 300 minutes in the ischemia group (n = 7) and followed by 14 hours of reperfusion in the I/R group (n = 6). Control subjects had a sham operation (n = 7). Mesenteric lymph nodes (MLN), liver (L), spleen (S), ileum, peritoneum, and blood were harvested for blind quantitative microbial analysis. Subjects in the control group had no cultures positive for growth. Eighty-five percent of animals in the ischemia group had positive MLN cultures only (P < .05 v control). All piglets in the I/R group had positive MLN cultures (P < .05 v control), and one third of them manifested bacteremia. Histological examination did not show mucosal disruption in any group. The validity of this model is confirmed by the negative cultures in the control group and by the presence of normal ileal flora in all animals. In the ischemia and I/R groups, MLN cultures were consistently positive with gram-negative bacilli (Escherichia coli and/or Klebsiella pneumoniae). When subjects of the I/R group had more than 1,000 colonies in the MLN, bacteremia with the translocating organisms was also identified.(ABSTRACT TRUNCATED AT 250 WORDS)
作者之前报道,慢性新生仔猪模型中的肠系膜缺血再灌注(I/R)会导致肠道运动功能障碍。目前尚不清楚这是否会导致胃肠道细菌清除不足和细菌移位(BT)。为了验证这一假设,作者使用了他们的慢性仔猪模型(体重3.5±0.3千克;年龄18±4天;人工喂养);通过可逆性心包填塞诱导非闭塞性肠系膜缺血。缺血组(n = 7)通过经腹膜后途径的SMA多普勒测量使肠系膜血流降至基线的25%±5%,持续300分钟,然后I/R组(n = 6)再灌注14小时。对照组进行假手术(n = 7)。采集肠系膜淋巴结(MLN)、肝脏(L)、脾脏(S)、回肠、腹膜和血液进行盲法定量微生物分析。对照组受试者培养物均无生长阳性。缺血组85%的动物仅MLN培养阳性(与对照组相比,P <.05)。I/R组所有仔猪MLN培养均阳性(与对照组相比,P <.05),其中三分之一表现为菌血症。组织学检查在任何组中均未显示黏膜破坏。对照组培养阴性以及所有动物回肠菌群正常证实了该模型的有效性。在缺血组和I/R组中,MLN培养物革兰氏阴性杆菌(大肠杆菌和/或肺炎克雷伯菌)始终呈阳性。当I/R组受试者的MLN中有超过1000个菌落时,也可识别出移位菌引起的菌血症。(摘要截断于250字)