Effects of adrenomedullin and vascular endothelial growth factor on ischemia/reperfusion injury in skeletal muscle in rats

被引:24
作者
Kirisci, Mehmet [1 ]
Oktar, Gursel Levent [1 ]
Ozogul, Candan [2 ]
Oyar, Eser Oz [3 ]
Akyol, Seda Nur [2 ]
Demirtas, Canan Yilmaz [4 ]
Arslan, Mustafa [5 ]
机构
[1] Gazi Univ, Fac Med, Dept Cardiovasc Surg, TR-06510 Ankara, Turkey
[2] Gazi Univ, Fac Med, Dept Histol & Embryol, TR-06510 Ankara, Turkey
[3] Gazi Univ, Fac Med, Dept Physiol, TR-06510 Ankara, Turkey
[4] Gazi Univ, Fac Med, Dept Biochem, TR-06510 Ankara, Turkey
[5] Gazi Univ, Fac Med, Dept Anesthesiol & Reanimat, TR-06510 Ankara, Turkey
关键词
Ischemia/reperfusion; Adrenomedullin; VEGF; Skeletal muscle; Rat; Histopathology; ISCHEMIA-REPERFUSION INJURY; NITRIC-OXIDE; GRACILIS MUSCLE; VEGF; DAMAGE; MECHANISMS; PROTECTION; HYPOXIA; RELEASE; PEPTIDE;
D O I
10.1016/j.jss.2013.05.053
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: In this study we investigated the effects of adrenomedullin (AM) and vascular endothelial growth factor (VEGF) on skeletal muscle ischemia/reperfusion (I/R) injury in a rat model. Materials and methods: Thirty-six Wistar rats were randomized into six groups (n = 6). Laparotomy was performed in all groups under general anesthesia. Nothing else was done in Group S (Sham). The Group I/R underwent I/R performed by clamping and declamping of the infrarenal abdominal aorta for 120 min, respectively. Group VEGF and Group AM received intravenous infusion of VEGF (0.8 mu g/kg) or AM (12 mu g/kg) respectively, without I/R. Group I/R + VEGF and Group I/R + AM received intravenous infusion of VEGF (0.8 mu g/kg) or AM (12 mu g/kg) immediately after 2 h period of ischemia, respectively. At the end of reperfusion period, skeletal muscle samples of lower extremity were taken from all groups for biochemical and histopathologic examinations. Results: Tissue levels of malondialdehyde (MDA), superoxide dismutase (SOD), nitric oxide (NO), and hypoxia inducible factor 1 alpha (HIF 1 alpha) were found to be significantly higher in Group I/R than the levels in Group S (P < 0.05). Tissue levels of MDA, SOD, NO, and HIF 1 alpha were significantly lower in Group I/R + AM compared with the levels in Group I/R (P < 0.05). In Group I/R + VEGF, tissue levels of MDA and NO were significantly lower than the levels in Group I/R (P < 0.05). No statistically significant difference was found in the tissue levels of catalase among the groups. Histologic examination revealed a larger central muscular necrosis than the peripheral necrosis, red blood cells in the lumens of capillary vessels, and a stronger atrophy and elliptical or round shape in muscle fibers in Group I/R. Terminal deoxynucleotidyl transferase mediated dUPT nick end labeling (TUNEL)-positive cell count was significantly lower in groups I/R + AM and I/R + VEGF than Group I/R (P < 0.0001, P < 0.0001, respectively). Conclusions: These results indicate that AM and VEGF have protective effects on I/R injury in skeletal muscle in a rat model. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:56 / 63
页数:8
相关论文
共 46 条
[1]  
Antonio LGM, 2009, MINERVA CHIR, V64, P559
[2]   Curcumin Protects Against Ischemia/Reperfusion Injury in Rat Skeletal Muscle [J].
Avci, Gulden ;
Kadioglu, Huseyin ;
Sehirli, Ahmet O. ;
Bozkurt, Suleyman ;
Guclu, Oguz ;
Arslan, Emrah ;
Muratli, Sedit K. .
JOURNAL OF SURGICAL RESEARCH, 2012, 172 (01) :E39-E46
[3]  
BEYERSDORF F, 1991, J CARDIOVASC SURG, V32, P664
[4]   REACTIVE OXYGEN METABOLITES AND REPERFUSION INJURY - ABERRANT TRIGGERING OF RETICULOENDOTHELIAL FUNCTION [J].
BULKLEY, GB .
LANCET, 1994, 344 (8927) :934-936
[5]   Ischemia-reperfusion-induced muscle damage - Protective effect of corticosteroids and antioxidants in rabbits [J].
Bushell, A ;
Klenerman, L ;
Davies, H ;
Grierson, I ;
Jackson, MJ .
ACTA ORTHOPAEDICA SCANDINAVICA, 1996, 67 (04) :393-398
[6]   Ischaemic preconditioning of skeletal muscle 1. Protection against the structural changes induced by ischaemia/reperfusion injury [J].
Bushell, AJ ;
Klenerman, L ;
Taylor, S ;
Davies, H ;
Grierson, I ;
Helliwell, TR ;
Jackson, MJ .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2002, 84B (08) :1184-1188
[7]  
Da Silveira M, 2009, INT ANGIOL, V28, P412
[8]   Adrenomedullin and adrenomedullin binding protein-1 prevent acute lung injury after gut ischemia-reperfusion [J].
Dwivedi, Amit J. ;
Wu, Rongqian ;
Nguyen, Eric ;
Higuchi, Shinya ;
Wang, Haichao ;
Krishnasastry, Kambhampaty ;
Marini, Corrado P. ;
Ravikurnar, Thanjavur S. ;
Wang, Ping .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2007, 205 (02) :284-293
[9]  
Emrecan B, 2008, ULUS TRAVMA ACIL CER, V14, P182
[10]   VEGF: an update on biological and therapeutic aspects [J].
Farrara, N .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (06) :617-624