Nilakantan Vani, Zhou Xianghua, Hilton Gail, Roza Allan M, Adams Mark B, Johnson Christopher P, Pieper Galen M
Department of Surgery, Division of Transplant Surgery, Milwaukee, WI 53226, USA.
Mol Cell Biochem. 2005 Feb;270(1-2):39-47. doi: 10.1007/s11010-005-3639-2.
Reactive oxygen and nitrogen may mediate inflammation injury, but the status of the antioxidant defense system that might influence this process is unknown. In the present study, we examined the expression profile of the antioxidant enzymes, manganese superoxide dismutase (MnSOD), catalase and glutathione peroxidase (GPX) in acutely rejecting cardiac allografts and the potential role of inducible nitric oxide synthase (iNOS) in modulating antioxidant gene expression and activity. Donor hearts from Lewis (isograft) or Wistar-Furth (allograft) rats were transplanted into Lewis recipient rats. A subset of the allografts received L-N6-(1-imino-ethyl) lysine (L-NIL), a specific iNOS inhibitor, beginning the day of surgery until the day of harvesting. Catalase and glutathione peroxidase (GPX) protein levels were significantly decreased by postoperative day 4 (POD4) and postoperative day 5 (POD5), respectively, in allografts compared to isografts. While CuZn superoxide dismutase (CuZn SOD) levels were unchanged, there was a 50% decrease in MnSOD protein in allografts at postoperative day 6 (POD6). The sequential loss in antioxidant protein levels was not due to transcriptional regulation since there was no change in RNA levels for any of the genes tested. L-NIL did not alter catalase protein; however, the loss of MnSOD protein at POD6 was prevented by L-NIL. Consistent with a decrease in antioxidant protein levels, there was a sequential loss in enzyme activity for MnSOD, catalase and GPX. L-NIL however, restored MnSOD and GPX activities but not catalase activity. Treatment with CsA restored both protein and enzyme activities of GPX and MnSOD but not catalase. These results indicate that the loss in MnSOD and GPX protein and activity in allografts occurs via an iNOS-dependent mechanism whereas the decrease in catalase appears to be iNOS-independent. This suggests a differential role for iNOS in regulating post-translational modification of individual antioxidant enzymes in acute cardiac transplantation.
活性氧和氮可能介导炎症损伤,但可能影响这一过程的抗氧化防御系统的状态尚不清楚。在本研究中,我们检测了急性排斥反应心脏同种异体移植中抗氧化酶、锰超氧化物歧化酶(MnSOD)、过氧化氢酶和谷胱甘肽过氧化物酶(GPX)的表达谱,以及诱导型一氧化氮合酶(iNOS)在调节抗氧化基因表达和活性中的潜在作用。将来自Lewis(同基因移植)或Wistar-Furth(同种异体移植)大鼠的供体心脏移植到Lewis受体大鼠体内。一部分同种异体移植从手术当天开始直至收获当天接受L-N6-(1-亚氨基乙基)赖氨酸(L-NIL),一种特异性iNOS抑制剂。与同基因移植相比,同种异体移植中过氧化氢酶和谷胱甘肽过氧化物酶(GPX)蛋白水平在术后第4天(POD4)和术后第5天(POD5)分别显著降低。虽然铜锌超氧化物歧化酶(CuZn SOD)水平未变,但同种异体移植中MnSOD蛋白在术后第6天(POD6)降低了50%。抗氧化蛋白水平的顺序性降低并非由于转录调控,因为所检测的任何基因的RNA水平均无变化。L-NIL未改变过氧化氢酶蛋白;然而,L-NIL可防止POD6时MnSOD蛋白的丢失。与抗氧化蛋白水平降低一致,MnSOD、过氧化氢酶和GPX的酶活性也顺序性降低。然而,L-NIL可恢复MnSOD和GPX活性,但不能恢复过氧化氢酶活性。环孢素A(CsA)治疗可恢复GPX和MnSOD的蛋白及酶活性,但不能恢复过氧化氢酶活性。这些结果表明,同种异体移植中MnSOD和GPX蛋白及活性的丧失通过iNOS依赖性机制发生,而过氧化氢酶的降低似乎与iNOS无关。这表明iNOS在急性心脏移植中调节单个抗氧化酶的翻译后修饰方面具有不同作用。