The influence of iloprost on acute lung injury induced by hind limb ischemia-reperfusion in rats

被引:26
作者
Koksel, O
Ozdulger, A
Aytacoglu, B
Tamer, L
Polat, A
Sucu, N
Yildirim, C
Degirmenci, U
Kanik, A
机构
[1] Mersin Univ, Sch Med, Dept Thorac Surg, Mersin, Turkey
[2] Mersin Univ, Sch Med, Dept Cardiovasc Surg, Mersin, Turkey
[3] Mersin Univ, Sch Med, Dept Biochem, Mersin, Turkey
[4] Mersin Univ, Sch Med, Dept Pathol, Mersin, Turkey
[5] Mersin Univ, Sch Med, Dept Biostat, Mersin, Turkey
关键词
lung injury; iloprost; myeloperoxidase; Na+-K+ ATPase; antioxidant capacity;
D O I
10.1016/j.pupt.2004.12.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The local ischemia-reperfusion (I/R) process gains a systemic nature and affects distal organs. The remote effects of I/R are most frequently observed in the lungs and pulmonary damage may vary from acute lung injury with mild dysfunction to severe respiratory failure or the acute respiratory distress syndrome. In this hind limb I/R induced experimental lung injury model two groups of rats as IR and ILO were determined. Both groups underwent 60 min of ischemia and 120 min of reperfusion. While ILO group received iloprost in saline, IR group received only saline before reperfusion period intravenously. Serum myeloperoxidase (MPO) activity, malondialdehyde (MDA) levels and total antioxidant capacity (TAC) and lung tissue MPO activity, MDA levels and Na+-K+ ATPase activity were measured and light microscopic analyses of lung specimens were performed. The MPO activities in serum and lung homogenates were found to be significantly decreased in ILO group (P <= 0.01). The MDA levels in lung homogenates were found to be significantly decreased in ILO group (P <= 0.01), but the decreases were not significant in serum MDA levels (P = 0.052). Serum TAC and lung tissue Na+-K+\ ATPase activity levels were found to be increased in ILO group compared to IR group (P <= 0.01). Lung histology showed marked improvement by iloprost compared to the IR group in this study. Iloprost has been found to be effective in attenuating ischemia reperfusion-induced remote organ damage, in this case, lung injury, in rats. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:235 / 241
页数:7
相关论文
共 43 条
[1]   PULMONARY LEUKOSEQUESTRATION INDUCED BY HINDLIMB ISCHEMIA [J].
ANNER, H ;
KAUFMAN, RP ;
KOBZIK, L ;
VALERI, CR ;
SHEPRO, D ;
HECHTMAN, HB .
ANNALS OF SURGERY, 1987, 206 (02) :162-167
[2]  
[Anonymous], METHODS ENZYMOLOGY
[3]   CYTOPROTECTIVE ACTIONS OF PROSTACYCLIN DURING HYPOXIA IN THE ISOLATED PERFUSED CAT LIVER [J].
ARAKI, H ;
LEFER, AM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1980, 238 (02) :H176-H181
[4]  
BISHOP ML, 1996, FREE RADICALS CLIN C, P765
[5]   The effects of caffeic acid phenethyl ester on tissue damage in lung after hindlimb ischemia-reperfusion [J].
Çalikoglu, M ;
Tamer, L ;
Sucu, N ;
Coskun, B ;
Ercan, B ;
Gul, A ;
Calikoglu, I ;
Kanik, A .
PHARMACOLOGICAL RESEARCH, 2003, 48 (04) :397-403
[6]  
Carden DL, 2000, J PATHOL, V190, P255, DOI 10.1002/(SICI)1096-9896(200002)190:3<255::AID-PATH526>3.0.CO
[7]  
2-6
[8]  
Crinnion J N, 1993, Cardiovasc Surg, V1, P317
[9]   Exogenous human recombinant interleukin-10 attenuates hindlimb ischemia-reperfusion injury [J].
Engles, RE ;
Huber, TS ;
Zander, DS ;
Hess, PJ ;
Welborn, MB ;
Moldawer, LL ;
Seeger, JM .
JOURNAL OF SURGICAL RESEARCH, 1997, 69 (02) :425-428
[10]   BIOCHEMISTRY OF REOXYGENATION INJURY [J].
ERNSTER, L .
CRITICAL CARE MEDICINE, 1988, 16 (10) :947-953