ISCHEMIA REPERFUSION-INDUCED FELINE INTESTINAL DYSFUNCTION - IMPORTANCE OF GRANULOCYTE RECRUITMENT
ISCHEMIA REPERFUSION-INDUCED FELINE INTESTINAL DYSFUNCTION - IMPORTANCE OF GRANULOCYTE RECRUITMENT
复制标题
DOI:
10.1016/0016-5085(92)90010-v
复制
发表时间:
1992-09-01
期刊:
影响因子:
29.4
通讯作者:
GRANGER, DN
中科院分区:
文献类型:
--
作者:
KUBES, P;HUNTER, J;GRANGER, DN
Although previous studies have reported that neutrophils play an important role in mediating the microvascular injury observed after reperfusion of ischemic intestine, the contribution of these phagocytic cells to the mucosal dysfunction remains unclear. Three series of experiments consisting of an untreated group, a short-term monoclonal antibody (MAb) IB4treatment group (MAb IB4given on the day of the experiment), and a long-term MAb IB4treatment group (3-day pretreatment with MAb IB4) were performed using autoperfused segments of cat ileum exposed to 3 hours of ischemia followed by 1 hour of reperfusion. Mucosal myeloperoxidase activity, an index of mucosal granulocyte levels, increased from 12 to 25 U/g wet wt in the untreated group. In the short-term MAb IB4experiments, baseline values were very similar to those of the untreated group but no increase in myeloperoxidase activity was observed after ischemia/reperfusion. Long-term pretreatment with MAb IB4reduced baseline values of myeloperoxidase activity to approximately 1 U/g wet wt; the values remained at this level throughout the experiment. The permeability of the mucosal barrier was quantitated by measuring blood-to-lumen clearance to51Cr-ethylenediaminetetraacetic acid (EDTA). The water absorptive capacity of the intestine was also measured. In the untreated group, mucosal permeability to51Cr-EDTA increased sixfold and water absorption was abolished after reperfusion. Both short-term and long-term administration of MAb IB4prevented the net fluid loss into the lumen, but only long-term administration of MAb IB4blunted the increased mucosal permeability induced by ischemia/reperfusion. These data suggest that interstitial granulocytes contribute significantly to the mucosal dysfunction associated with reperfusion of the ischemic intestine.