Smith J R, Gabler W L
Department of Biological Structure and Function, School of Dentistry, Oregon Health Sciences University, Portland 97201, USA.
Res Commun Mol Pathol Pharmacol. 1995 Jun;88(3):303-15.
In rats splanchnic artery occlusion (SAO) of the celiac and superior mesenteric arteries for 1 hr., followed by a period of reperfusion initiates a severe form of circulatory shock, which typically leads to death within 2 hrs, characterized by multiorgan failure in which neutrophils play a central role. Doxycycline (Dc) pretreatment (10mg/kg; 2 hrs. prior to occlusion) significantly increased the survival time and leukocytes retention in circulation and decreased the hemoglobin levels in the contents of the small intestine. Dc did not influence serum alanine aminotransferase or amylase levels (marker enzymes for liver and pancreas damages respectively) at the time of death. Creatinine phosphate kinase, a marker of cardiotoxicity, was significantly increased in serum from Dc-treated rats. We conclude that pretreatment with Dc has a protective effect in the SAO rat model and this protection cannot be ascribed directly to a specific sparing influence on the liver, pancreas, or heart.
在大鼠中,闭塞腹腔干和肠系膜上动脉1小时,随后进行一段时间的再灌注,会引发一种严重的循环性休克,通常会在2小时内导致死亡,其特征为多器官功能衰竭,中性粒细胞在其中起核心作用。强力霉素(Dc)预处理(10mg/kg;闭塞前2小时)显著延长了存活时间,增加了循环中的白细胞滞留,并降低了小肠内容物中的血红蛋白水平。死亡时,Dc对血清丙氨酸转氨酶或淀粉酶水平(分别为肝脏和胰腺损伤的标志物酶)没有影响。磷酸肌酸激酶是心脏毒性的标志物,在接受Dc治疗的大鼠血清中显著升高。我们得出结论,Dc预处理在SAO大鼠模型中具有保护作用,且这种保护不能直接归因于对肝脏、胰腺或心脏的特定保护作用。