Does propofol or caffeic acid phenethyl ester prevent lung injury after hindlimb ischaemia-reperfusion in ventilated rats?

被引:37
作者
Akyol, A [1 ]
Ulusoy, H
Imamoglu, M
Çay, A
Yulug, E
Alver, A
Ertürk, E
Kosucu, M
Besir, A
Akyol, A [1 ]
Özen, I
机构
[1] Karadeniz Tech Univ, Dept Anesthesiol & Crit Care, Fac Med, TR-61080 Trabzon, Turkey
[2] Macka Vocat Sch, Trabzon, Turkey
来源
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED | 2006年 / 37卷 / 05期
关键词
propofol; caffeic acid phenethyl ester; ischaemia-reperfusion; lung injury; rat;
D O I
10.1016/j.injury.2006.01.004
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: To investigate the effects of propofol and caffeic acid phenethyl ester (CAPE) on prevention of lung injury as a remote organ after performing hindlimb ischaemia-reperfusion (IR) in a rat model. Methods: The animals were divided randomly into one of four groups: sham, no IR (n = 8), control, IR, (n = 8), CAPE group, IR with CAPE, (n = 8), propofol group, IR with P, (n = 8). After the rats were anaesthetised, the animals in the CAPE group received CAPE of 10 mu mol, in the propofol group received propofol 50 mg/kg, in the control group received a similar volume of saline solution by means of intraperitoneal injection 1 h before reperfusion. After 4 h of ischaemia the tourniquet was removed and the animals were released for reperfusion for 4 h thereafter. At the end of the reperfusion period, a median sternotomy was performed. A blood sample was obtained for plasma malondialdehyde (MDA). The lung tissues were also removed for MDA assays, myeloperoxidase (MPO) activity, and histopathological examination. Results: Plasma and lung MDA levels, and lung MPO activity were significantly higher in the control group compared to the other groups (p < 0.0005). In the CAPE group, these were significantly lower compared to the control group (p < 0.0005). Also, propofol caused a marked reduction in the MDA levels and MPO activity compared with control group (p < 0.0005), with no significant difference compared to that of the sham group. Histopathologically, the scores resulted in a grade zero (8/8) in the sham group, 3 (3/8) or 4 (5/8) in the control group, 1 (2/8) or 2 (6/8) in the CAPE group, and 1 (3/8) or 2 (5/8) in the propofol group. Conclusion: Propofol and CAPE seem to be effective in protecting against lung injury caused by increased oxidative stress and neutrophil accumulation after hindlimb IR in a rat model. (C) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:380 / 387
页数:8
相关论文
共 22 条
[1]   THE WIDELY USED ANESTHETIC AGENT PROPOFOL CAN REPLACE ALPHA-TOCOPHEROL AS AN ANTIOXIDANT [J].
AARTS, L ;
VANDERHEE, R ;
DEKKER, I ;
DEJONG, J ;
LANGEMEIJER, H ;
BAST, A .
FEBS LETTERS, 1995, 357 (01) :83-85
[2]   FK506 to prevent lung injury after hindlimb ischemia and reperfusion in a rat model: An electron microscopic study [J].
Akgun, S ;
Tekeli, A ;
Isbir, SC ;
Civelek, A ;
Ak, K ;
Sirvanci, S ;
Arbak, S ;
Yaylim, I ;
Arsan, S .
SURGERY TODAY, 2004, 34 (08) :678-684
[3]  
[Anonymous], METHODS ENZYMOLOGY
[4]   Ischemia and reperfusion injury: Prevention of pulmonary hypertension and leukosequestration following lower limb ischemia [J].
Bengisun, U ;
Koksoy, C ;
Bengisun, JS ;
Bayraktaroglu, G ;
Camur, A ;
Aras, N .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1997, 56 (02) :117-120
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]  
Bulkley G B, 1987, Br J Cancer Suppl, V8, P66
[7]   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
[8]   SPECIFICITY AND PROPERTIES OF PROPOFOL AS AN ANTIOXIDANT FREE-RADICAL SCAVENGER [J].
GREEN, TR ;
BENNETT, SR ;
NELSON, VM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 129 (01) :163-169
[9]   Serum myeloperoxidase concentration in a healthy population:: biological variations, familial resemblance and new genetic polymorphisms [J].
Hoy, A ;
Trégouët, D ;
Leininger-Muller, B ;
Poirier, O ;
Maurice, M ;
Sass, C ;
Siest, G ;
Tiret, L ;
Visvikis, S .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (10) :780-786
[10]  
KAHRAMAN S, 1997, BRIT J ANAESTH, V4, P265