Saeki Isamu, Matsuura Toshiharu, Hayashida Makoto, Taguchi Tomoaki
Kyushu University, Fukuoka, Japan.
Pediatr Surg Int. 2011 Aug;27(8):857-62. doi: 10.1007/s00383-010-2810-3. Epub 2010 Nov 28.
To investigate the protective effect of ischemic preconditioning (IPC) and remote ischemic preconditioning (RIPC) against cold ischemia-reperfusion injury (IRI) associated with small bowel transplantation (SBT).
Male Lewis rats weighing 200-300 g were used for this study. The rats were assigned to three groups: control, ischemic preconditioning (IPC), or remote ischemic preconditioning (RIPC). Heterotopic SBT was thereafter performed. The recipient rats were killed 3, 6, 12 and 24 h after transplantation. Specimens from the intestine were histologically scored according to a grading system (Park et al.). Serum lactate dehydrogenase (LDH), aspirate aminotransferase (AST), alanine aminotransferase (ALT) were examined and heme oxygenase-1 (HO-1) were analyzed by ELISA where HO-1 served as an indicator of protection against IRI.
The values of tissue injury were significantly lower in the IPC and RIPC groups than in control group at 3 h after SBT. The serum LDH, AST and ALT levels also significantly decreased in the IPC and RIPC groups at 3 h after SBT, but these protective effects against cold IRI diminished by 12 and 24 h after SBT. The serum HO-1 level significantly increased in the IPC and RIPC groups 3 h after SBT.
Both IPC and RIPC were found to ameliorate ischemia-reperfusion injury after rat SBT in the early phase. HO-1 may therefore play a protective role against cold IRI.
探讨缺血预处理(IPC)和远程缺血预处理(RIPC)对小肠移植(SBT)相关的冷缺血再灌注损伤(IRI)的保护作用。
本研究使用体重200 - 300 g的雄性Lewis大鼠。将大鼠分为三组:对照组、缺血预处理(IPC)组或远程缺血预处理(RIPC)组。随后进行异位SBT。移植后3、6、12和24小时处死受体大鼠。根据分级系统(Park等人)对肠组织标本进行组织学评分。检测血清乳酸脱氢酶(LDH)、天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT),并通过酶联免疫吸附测定法(ELISA)分析血红素加氧酶-1(HO-1),其中HO-1作为抗IRI保护作用的指标。
SBT后3小时,IPC组和RIPC组的组织损伤值显著低于对照组。SBT后3小时,IPC组和RIPC组的血清LDH、AST和ALT水平也显著降低,但这些对冷IRI的保护作用在SBT后12和24小时减弱。SBT后3小时,IPC组和RIPC组的血清HO-1水平显著升高。
发现IPC和RIPC均可在大鼠SBT后的早期改善缺血再灌注损伤。因此,HO-1可能对冷IRI起保护作用。