Teke Zafer, Sacar Suzan, Yenisey Cigdem, Atalay A Ozgur, Kavak Tulay, Erdem Ergun
Department of Gastroenterological Surgery, Turkiye Yuksek Ihtisas Hospital, 06100, Sihhiye, Ankara, Turkey.
World J Surg. 2008 Nov;32(11):2434-43. doi: 10.1007/s00268-008-9696-4. Epub 2008 Aug 5.
Activated protein C (APC) is a serine protease with anticoagulant and anti-inflammatory activities. The delaying effects of intra-abdominal sepsis on wound healing process in colonic anastomoses have been previously demonstrated. This study was designed to investigate the role of APC on wound healing process in left colonic anastomoses in the presence of intra-abdominal sepsis.
The left colonic anastomosis was performed in 48 rats that were divided into four groups: (1) sham-operated group, laparatomy plus cecal mobilization (n = 12); (2) sham + APC group, identical to group I except for APC treatment (n = 12); (3) CLP group, cecal ligation and puncture (n = 12); 4) CLP + APC-treated group, 100 microg/kg, 15 min before the construction of colonic anastomosis (n = 12). Anastomotic bursting pressures were measured in vivo on day 7. Tissue samples were obtained for analyses of hydroxyproline (HP) contents, myeloperoxidase (MPO) acivity, malondialdehyde (MDA), and nitrate/nitrite (NO3(-) /NO2(-)) levels. The plasma levels of tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-6, and D-dimer also were measured.
Intra-abdominal sepsis led to significant decreases in colonic anastomotic bursting pressures and tissue HP contents, along with increases in MPO activity, MDA and NO3(-) /NO2(-) levels, and also plasma levels of TNF-alpha, IL-6, and D-dimer (P < 0.05). However, APC treatment led to significant increases in anastomotic bursting pressures and tissue HP ontents, along with decreases in MPO activity, MDA and NO3(-) /NO2(-) levels, and also plasma levels of TNF-alpha, IL-6, and D-dimer (P < 0.05).
This study clearly showed that APC treatment prevented the delaying effects of intra-abdominal sepsis on colonic anastomotic wound healing process. Further clinical studies are required to determine whether APC has a useful role in the enhancement of anastomotic healing during particular surgeries in which sepsis-induced injury occurs.
活化蛋白C(APC)是一种具有抗凝和抗炎活性的丝氨酸蛋白酶。此前已有研究表明,腹腔内脓毒症会延迟结肠吻合口的伤口愈合过程。本研究旨在探讨在腹腔内脓毒症存在的情况下,APC对左半结肠吻合口伤口愈合过程的作用。
对48只大鼠进行左半结肠吻合术,并将其分为四组:(1)假手术组,行剖腹术加盲肠游离(n = 12);(2)假手术+APC组,除接受APC治疗外,其余与第一组相同(n = 12);(3)CLP组,行盲肠结扎和穿刺术(n = 12);(4)CLP + APC治疗组,在结肠吻合术构建前15分钟给予100μg/kg(n = 12)。于第7天在体内测量吻合口破裂压力。获取组织样本以分析羟脯氨酸(HP)含量、髓过氧化物酶(MPO)活性、丙二醛(MDA)以及硝酸盐/亚硝酸盐(NO3(-)/NO2(-))水平。同时测量血浆中肿瘤坏死因子α(TNF-α)、白细胞介素(IL)-6和D-二聚体的水平。
腹腔内脓毒症导致结肠吻合口破裂压力和组织HP含量显著降低,同时MPO活性、MDA和NO3(-)/NO2(-)水平升高,以及血浆中TNF-α、IL-6和D-二聚体水平升高(P < 0.05)。然而,APC治疗导致吻合口破裂压力和组织HP含量显著增加,同时MPO活性、MDA和NO3(-)/NO2(-)水平降低,以及血浆中TNF-α、IL-6和D-二聚体水平降低(P < 0.05)。
本研究清楚地表明,APC治疗可预防腹腔内脓毒症对结肠吻合口伤口愈合过程的延迟作用。需要进一步的临床研究来确定在发生脓毒症诱导损伤的特定手术中,APC在促进吻合口愈合方面是否具有有益作用。