Cao Bin, Li Ning, Wang Yong, Li Jie-Shou
The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
World J Gastroenterol. 2005 May 21;11(19):2994-7. doi: 10.3748/wjg.v11.i19.2994.
To investigate the protective effect and possible mechanism of L-arginine preconditioning on ischemia and reperfusion injury associated with small bowel transplantation (SBT).
Male inbred Wistar rats weighting between 180 and 250 g were used as donors and recipients in the study. Heterotopic rat SBT was performed according to the techniques of Li and Wu. During the experiment, intestinal grafts were preserved in 4 degrees Ringer's solution for 8 h before being transplanted. Animals were divided into three groups. In group 1, donors received intravenous L-arginine (50 mg/kg, 1 mL) injection 90 min before graft harvesting. However, donors in control group were given normal saline (NS) instead. In group 3, six rats were used as sham-operated control. Specimens were taken from intestinal grafts 15 min after reperfusion. Histological grading, tissue malondialdehyde (MDA) and myeloperoxidase (MPO) levels were assessed. The graft survival of each group was monitored daily until 14 d after transplantation.
Levels of MDA and MPO in intestine of sham-operated rats were 2.0+/-0.22 mmol/g and 0.66+/-0.105 U/g. Eight hours of cold preservation followed by 15 min of reperfusion resulted in significant increases in tissue MDA and MPO levels. Pretreatment with L-arginine before graft harvesting resulted in lower enhancement of tissue levels of MDA and MPO and the differences were significant (4.71+/-1.02 mmol/g vs 8.02+/-3.49 mmol/g, 1.03+/-0.095 U/g vs 1.53+/-0.068 U/g, P<0.05). Besides, animals in L-arginine pretreated group had better histological structures and higher 2-wk graft survival rates comparing with that in NS treated group (3.3+/-0.52 vs 6+/-0.1, 0/6 vs 6/6, P<0.05 or 0.01).
L-arginine preconditioning attenuates ischemia and reperfusion injury in the rat SBT model, which was due to antioxidant activities partially.
探讨L-精氨酸预处理对小肠移植(SBT)缺血再灌注损伤的保护作用及可能机制。
选取体重180~250 g的雄性近交系Wistar大鼠作为供体和受体。参照Li和Wu的技术进行大鼠异位SBT。实验过程中,肠移植物在4℃林格液中保存8 h后再进行移植。动物分为三组。第1组,供体在获取移植物前90 min静脉注射L-精氨酸(50 mg/kg,1 mL)。而对照组供体给予生理盐水(NS)。第3组,6只大鼠作为假手术对照。再灌注15 min后从肠移植物取材。评估组织学分级、组织丙二醛(MDA)和髓过氧化物酶(MPO)水平。每天监测每组移植物存活情况直至移植后14 d。
假手术大鼠肠组织中MDA和MPO水平分别为2.0±0.22 mmol/g和0.66±0.105 U/g。8 h冷保存后再灌注15 min导致组织MDA和MPO水平显著升高。移植物获取前用L-精氨酸预处理可使组织MDA和MPO水平升高幅度降低,差异有统计学意义(4.71±1.02 mmol/g对8.02±3.49 mmol/g,1.03±0.095 U/g对1.53±0.068 U/g,P<0.05)。此外,与NS处理组相比,L-精氨酸预处理组动物具有更好的组织结构和更高的2周移植物存活率(3.3±0.52对6±0.1,0/6对6/6,P<0.05或0.01)。
L-精氨酸预处理减轻大鼠SBT模型中的缺血再灌注损伤,部分原因是其抗氧化活性。