Dong Guo-Hua, Wang Chang-Tian, Li Yun, Xu Biao, Qian Jian-Jun, Wu Hai-Wei, Jing Hua
Department of Cardiothoracic Surgery, Jinling Hospital, Clinical Medicine School of Nanjing University, Nanjing, Jiangsu Province, China.
World J Gastroenterol. 2009 Jul 7;15(25):3166-72. doi: 10.3748/wjg.15.3166.
To investigate microvascular injury quantitatively in the small bowel with respect to cardiopulmonary bypass (CPB) and related mechanisms.
In 10 male SD rats, normothermic CPB was established and continued with a flow rate of 100-150 mL/kg per minute for 60 min, while another 10 sham-operated animals served as controls. An approximate 10-cm loop of the terminal ileum was exteriorized for observation by means of intravital fluorescence microscopy. The small bowel microcirculatory network including arterioles, capillaries, and collecting venules was observed prior to CPB, CPB 30 min, CPB 60 min, post-CPB 60 min and post-CPB 120 min. The intestinal capillary perfusion, microvascular permeability and leukocyte adherence were also measured.
The systemic hemodynamics remained stable throughout the experiment in both groups. In CPB animals, significant arteriolar vasoconstriction, blood velocity reduction and functional capillary density diminution were found. As concomitances, exaggerated albumin extravasation and increased leukocyte accumulation were also noted. These changes were more pronounced and there were no signs of restitution at the end of the observation period.
CPB induces significant microcirculatory injury of the small bowel in rats. The major underlying mechanisms are blood flow redistribution and generalized inflammatory response associated with CPB.
定量研究体外循环(CPB)对小肠微血管损伤及其相关机制。
选取10只雄性SD大鼠,建立常温CPB并以每分钟100 - 150 mL/kg的流量持续60分钟,另10只假手术动物作为对照。将近端回肠约10厘米的肠袢外置,通过活体荧光显微镜进行观察。在CPB前、CPB 30分钟、CPB 60分钟、CPB后60分钟和CPB后120分钟观察小肠微循环网络,包括小动脉、毛细血管和集合小静脉。同时测量肠毛细血管灌注、微血管通透性和白细胞黏附情况。
两组动物在整个实验过程中全身血流动力学均保持稳定。在CPB动物中,发现小动脉显著收缩、血流速度降低和功能性毛细血管密度减小。同时,还观察到白蛋白外渗增加和白细胞聚集增多。这些变化更为明显,且在观察期末未见恢复迹象。
CPB可导致大鼠小肠显著的微循环损伤。主要潜在机制是与CPB相关的血流重新分布和全身性炎症反应。