Brennan S S, Foster M E, Morgan A, Leaper D J
Dis Colon Rectum. 1984 Nov;27(11):723-5. doi: 10.1007/BF02554598.
In this study we report the effects of flurbiprofen and prostaglandin E2 on anastomotic tensile strength, collagen synthesis, and collagenolytic activity which are in a particularly fine balance in colonic healing. Colonic anastomoses were fashioned in 150 Sprague-Dawley rats which were allocated to receive either 20 mcg prostaglandin E2 in 1 ml saline, 1 ml saline alone (control) intraperitoneally for three days post-operatively, or oral 2.5 mg/kg flurbiprofen daily. Anastomotic bursting pressures, collagen content and collagenolytic activity were measured at three, six, and ten days. It was found that prostaglandin E2-treated animals had significantly weaker anastomoses at three days (102 +/- 6.1 mm Hg; m +/- SEM) compared with the control (126 +/- 7.3; P less than 0.02) or flurbiprofen group (128 +/- 4.6; P less than 0.01) with no differences at six and ten days. Collagen levels were higher in flurbiprofen-treated rats at three days (9.7 +/- 0.2 micrograms hydroxyproline/mg tissue) compared with the control (8.1 +/- 0.4 micrograms/mg; P 0.01) or prostaglandin E2 group (7.2 +/- 0.5 micrograms/mg; P 0.001). These differences were unchanged at six days but were not statistically different at ten days. Collagenolytic activity showed no differences in the three groups during the study. It is concluded that flurbiprofen enhances colonic healing with improved collagen synthesis without affecting collagenolytic activity.
在本研究中,我们报告了氟比洛芬和前列腺素E2对吻合口抗张强度、胶原蛋白合成及胶原酶活性的影响,这些因素在结肠愈合过程中保持着特别精细的平衡。在150只Sprague-Dawley大鼠身上制作结肠吻合口,将其分为三组,分别在术后三天腹腔内注射1毫升生理盐水加20微克前列腺素E2、单纯注射1毫升生理盐水(对照组),或每日口服2.5毫克/千克氟比洛芬。在术后三天、六天和十天测量吻合口破裂压力、胶原蛋白含量及胶原酶活性。结果发现,与对照组(126±7.3毫米汞柱;平均值±标准误)或氟比洛芬组(128±4.6毫米汞柱;P<0.01)相比,前列腺素E2处理组动物在术后三天时吻合口明显较弱(102±6.1毫米汞柱),而在术后六天和十天时无差异。与对照组(8.1±0.4微克/毫克;P<0.01)或前列腺素E2组(7.2±0.5微克/毫克;P<0.001)相比,氟比洛芬处理组大鼠在术后三天时胶原蛋白水平更高(9.7±0.2微克羟脯氨酸/毫克组织)。这些差异在术后六天时保持不变,但在术后十天时无统计学差异。在研究期间,三组的胶原酶活性无差异。结论是,氟比洛芬可通过改善胶原蛋白合成来促进结肠愈合,且不影响胶原酶活性。