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Acta Cirurgica Brasileira

versão impressa ISSN 0102-8650versão On-line ISSN 1678-2674

Acta Cir. Bras. v.24 n.1 São Paulo jan./fev. 2009

http://dx.doi.org/10.1590/S0102-86502009000100011 

11 - ORIGINAL ARTICLE
ISCHEMIA-REPERFUSION

 

Postconditioning ameliorates lipid peroxidation in liver ischemia-reperfusion injury in rats1

 

Pós-condicionamento melhora a peroxidação lipídica na lesão de isquemia-reperfusão hepática em ratos

 

 

Antonio Roberto Franchi TeixeiraI; Nilza T. MolanII; Márcia Saldanha KubruslyII; Marta Bellodi-PrivatoIII; Ana Maria CoelhoII; Kátia R. LeiteIV; Marcel Autran Cesar MachadoV; Telésforo BacchellaVI; Marcel Cerqueira César MachadoVII

IPh.D., Assistant Surgeon, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil
IIPharmacist, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil
IIIPharmacist, Post-Doctorate, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil
IVPh.D., Pathologist, Department of Urology, Faculty of Medicine, University of Sao Paulo, Brazil
VProfessor, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil
VIFull Professor and Surgeon-in Chief, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil
VIIFormer Chairman, Liver Transplantation and Surgery Unit, Department of Gastroenterology, Faculty of Medicine, University of Sao Paulo, Brazil

Correspondence

 

 


ABSTRACT

PURPOSE: Liver ischemia-reperfusion injury is a phenomenon presents in events like liver resections and transplantation. The restoration of blood flow may leads to local and systemic injury. Several techniques have been developed in order to avoid or ameliorate ischemia-reperfusion injury in clinical situations. The application of a sttuter reperfusion after the ischemic event (postconditioning) could alters the hydrodynamics and stimulates endogenous mechanisms that attenuate the reperfusion injury. The present study was designed to evaluate the potential protective effect of postconditioning in a model of ischemia-reperfusion in rats.
METHODS: Hepatic anterior pedicle of median and left anterolateral segments were exposed and clamped for 1 hour. Two hours later, clamp was released in two different ways: Control Group (n=7): clamp was release straightforward; Postconditioning Group (n=7): clamp was released intermittently. Lipid peroxidation (malondialdehyde) and expression of the glutathione-s-transferase-
α-3 gene were studied.
RESULTS: Lipid peroxidation was significantly decreased in ischemic and non-ischemic liver by postconditioning. GST-
α3 gene was overexpressed in postconditioned group, but not significantly.
CONCLUSION: Postconditioning induced hepatoprotection by reducing lipid peroxidation in the ischemic and non-ischemic liver.

Key words: Liver. Ischemia. Reperfusion. Lipid Peroxidation. Rats.


RESUMO

OBJETIVO: A lesão de isquemia-reperfusão hepática é um fenômeno presente em eventos tais como ressecções hepáticas e transplante de fígado. A restauração do fluxo sangüíneo após a isquemia gera lesões locais e sistêmicas. Várias técnicas foram desenvolvidas com o objetivo de evitar ou diminuir a lesão de isquemia-reperfusão hepática em situações clínicas. A utilização da reperfusão intermitente após o evento isquêmico (pós-condicionamento) pode alterar a hidrodinâmica e estimular mecanismos endógenos que atenuam o dano da reperfusão. O presente estudo foi realizado para avaliar o potencial efeito protetor do pós-condicionamento em um modelo de isquemia-reperfusão em ratos.
MÉTODOS: O pedículo dos lobos mediano e ântero-lateral foi isolado e clampeado por 1 hora. Após 2 horas, o pedículo foi liberado de duas maneiras diferentes: Grupo Controle (n=7): clampe liberado de uma só vez; Grupo Pós-condicionamento (n=7): clampe liberado de maneira intermitente. Malondialdeído (MDA) e expressão do gene GST-
α3 foram estudadas nos grupos.
RESULTADOS: A peroxidação lipídica foi significativamente diminuída no fígado isquêmico e no fígado não isquêmico pelo pós-condicionamento. A expressão do gene GST-
α3 aumentou, porém não significativamente, no grupo pós-condicionamento.
CONCLUSÃO: O pós-condicionamento induziu hepatoproteção pela redução da peroxidação lipídica nos fígados isquêmico e não isquêmico.

Descritores: Fígado. Isquemia. Reperfusão. Peroxidação de Lipídeos. Ratos.


 

 

Introduction

Ischemia-reperfusion injury is a known phenomenon presents in several events like liver resections and transplantation that results in metabolic, structural and functional changes which may lead to cell death1.

Several strategies have been described to avoid or ameliorate reperfusion injury in clinical situations. Ischemic preconditioning, intermittent vascular occlusion, anti TNF-α blockers and antioxidants have already been tested in liver reperfusion models2,3.

Recently a new strategy, named postconditioning, was described and showed promising results for cardiac reperfusion injury. It consists in application of a gradual, staged or stutter reperfusion after ischemic injury4,5.

Only one study in the English literature concerning postconditioning strategy in liver reperfusion injury was published so far. These authors studied the role of mitochondria in cell apoptosis and described a protective effect of ischemic postconditioning, using a gradual reperfusion6.

The aim of this study was to evaluate the protective effect of postconditioning using a different strategy, based on stutter reperfusion similar to those successfully used in cardiac postconditioning models.

 

Methods

This study was designed in accordance with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health and the Guidelines of Animal Experimentation of the University of São Paulo School of Medicine, Sao Paulo, SP, Brazil, for the care and use of laboratory animals. The experimental protocol was pre-approved by Ethics Commission of the University of Sao Paulo, Brazil.

Fourteen male Wistar rats weighing 250 ± 5 g were housed in cages with a controlled 12-h light/dark cycle, receiving water ad libitum. Before the day of experiment the animals fasted overnight but free access to water was allowed. Animals were anestethized with ketamin 5% (30 mg/kg) and xylazine 2% (30 mg/kg) intraperitonially. During the experiment animals were warmed by halogen light (45W, 127V) and corporeal temperature was controlled by digital thermometer (YSI Precision 4000A thermometer, USA) and kept around 37ºC. Animals were maintained in spontaneous ventilation with an oxygen-enriched mixture (40%) during all the procedure.

Experimental design

Median laparotomy was performed and the pedicle of median and left anterolateral segments was dissected, exposed and clamped with an atraumatic microvascular bulldog clamp (Figure 1).

 

 

After clamping abdominal wall was closed with ininterrupted 4-0 nylon suture. One hour later, the animals were reoperated and randomly divided in two groups: Control Group (CG): N=7, the clamp was released straightforward; Postconditioning Group (PG): N=7, the clamp was released in a stutter fashion, in 5 periods of 5 seconds of opening, followed of 5 seconds of clamping (Figure 2).

Abdominal wall was closed and animals were observed for two hours (reperfusion period). Animals were then anesthetized and liver was collected for analysis and identified as "ischemic liver" (lobes submitted to ischemia) and "normal liver" (paracaval non-ischemic lobes). Rats were sacrificed by aorta section.

Malondialdehyde analysis

Malondialdehyde levels in the samples were determined to obtain quantitative estimation of the membrane lipid oxidative damage. Malondialdehyde was assayed in terms of thiobarbituric acid reactive substrats. The thiobarbituric acid method was used to quantify lipid peroxidation in liver, measured as thiobarbituric acid-reactive substances. Liver tissues (100 mg/mL) were homogeneized in 1.15% KCl buffer, and centrifuged at 14,000 g for 20 min. The supernatant was then stores at -70ºC. an aliquot of the supernatant was added to a reaction mixture of 1.5 mL 0.8% thiobarbituric acid, 200 µL 8.1% (v/v) SDS, 1.5 mL 20% (v/v) acetic acid, pH 3.5, and 300 µL distilled H2O, and heated to 90ºC for 45 min. After cooling to room temperature, the samples were cleared by centrifugation at 10,000 g for 10 min, and their absorbance was measured at 532 nm using malondialdehyde bis (dimethyl acetal) as an external standard. The quantity of lipid peroxides is reported in nmol malondialdehyde equivalents/mg protein.

GST-α 3 quantitative RT-PCR Analysis: qRT-PCR analysis was performed in the Rotor-Gene RG-3000 (Corbett Research, Sidney, Australia) using SuperScriptTM III Platinum® SYBR® Green One-Step qRT-PCR kit (Invitrogen, Life Technologies) with 100 ng of total RNA and 0,2 µM sense/antisense primer per reaction, according to manufacturer's recommendations. The reaction was carried out under the following cycling conditions: 10 min at 50 ºC, 5 min at 95 ºC, followed by 35 cycles of 20 s at 95 ºC, 30 s at 57 ºC and 30s at 72 ºC. To verify amplification reaction specificity, melting curves were determined using the following parameters: 72 ºC ramping to 99 ºC at 0.2 ºC/s. Primer sets were designed to amplify two separate intron-spanning regions, enabling to assess the possible genomic DNA contamination: GST-α3 sense 5´-GGC GGATCT GGATGAAATAGT TCT-3´; GST-α3 antisense 5´-CAA CGA GAT AAT CTT GTC CAT GGC-3´; α-actin sense 5´-TGT CAC CAA CTG GGA CGA TA-3´ and α-actin antisense 5´-GGG GTG TTG AAG GTC TCAAA-3´. Specificity of product was ensured by melting point analysis and agarose gel electrophoresis to visualize the band for GST-α3 and α-actin with the correspondent size; 152 bp and 165 bp, respectively. RNA template concentrations (500 ng/µl, 100 ng/µl, 20 ng/µl, 4 ng/µl and 0.8 ng/µl) were used to generate a standard curve to evaluate the amplification efficiency of GST-α3 gene in comparison to α-actin. RNA content of GST-α3 was determined as the number of transcripts relative to those of α-actin and additionally normalized to the mean value of control pancreas and kidney.

Relative quantification was calculated using the mathematical model based on GST-α 3 and α-actin genes amplification efficiency. All samples were analyzed in duplicate. The results were expressed in arithmetic mean and standard deviation (sd). Collected data were stored in a computer and plot in spread sheets of the Excel program (Microsoft, Seattle, WA, USA).

Statistical analysis

Comparisons between groups were statistically analyzed using GraphPad Prism 4 software (San Diego, CA, USA). Nonparametric test (Mann-Whitney) was performed since the data distribution was considered as non-Gaussian. Mean values and SEM were displayed in graphics only as additional information. Differences were considered statistically significant when p < 0.05.

 

Results

The concentration of malondialdehyde was elevated after reperfusion in Control Group (CG) both in ischemic (3.6 ±0.53); and non-ischemic (3.22 ±0.52) lobes. In the postconditioned group (PG), malondialdehyde was significantly lower in ischemic (1.56 ±0.33) and non-ischemic (0.67 ±0.26) portions of the liver (Figure 3).

 

 

Analysis of gene expression of glutathione s-transferase in Control Group (CG) was slightly lower than in the postconditioned group (PG), in ischemic and non-ischemic liver samples, but differences was not significant (Figure 4).

 

 

Discussion

Lipid peroxidation generates a complex variety of products, many of which react with protein and DNA and as a result are toxic and mutagenic7. Amajor target site of lipid peroxidation damage is the cellular membrane because it contains polyunsaturated fatty acids. Toxicity of partially reduced oxygen species arises from the peroxidation of polyunsaturated fatty acid of membrane phospholipids, which may cause membrane disintegration. In liver ischemia-reperfusion injury, this mechanism is exacerbated. The consequent damage to liver cells by reperfusion results in mitochondrial dysfunction and it can also induce microcirculatory disturbances8.

Our experiment showed that lipid peroxidation was decreased in the ischemic portion of the liver by postconditioning. This beneficial effect of postconditioning was also identified by Sun et al.6. Using a similar model of liver ischemiareperfusion in rats, but with a different protocol of postconditioning, they related that gradual reperfusion minimizes lipid peroxidation and also depress synthesis of free oxygen radicals, preserving mitochondrial ultrastructure and function6. Using a rapid stutter reperfusion, we found an important lipid peroxidation reduction in non-ischemic liver that has not been previously described.

In cardiac reperfusion models, postconditioning beneficial effects are related to adenosine. Philipp et al.9 described that the protective effect of postconditioning in the rabbit heart is dependent on the occupancy of adenosine receptors9 and requires PI3-K and guanylyl cyclase activation10. Two reports indicate that endogenous adenosine elicits the infarct-sparing effect of postconditioning by the activation of A2B receptor9,11. Adenosine is a very important substrate to rebalance the energetic metabolism after reperfusion and it is a potent vasodilator of the microvasculature.

In the liver, we hypothesized that the decrease of lipid peroxidation may also be related to the protective effects of adenosine that remains inside the parenchyma, like in the heart12. In our model, we believe that when the clamp is released straightway, reperfusion flow washes out the endogenous protective substances (adenosine amongst them) that have been produced inside the tissue. When a stutter postconditioning is applied, the slow and soft reperfusion flow keeps adenosine and other protective substances inside the liver parenchyma. This also benefits the non-ischemic liver (figure 5).

 

 

The glutathione-s-transferases (GSTs) family comprises cytosolic, mitochondrial and microsomal enzymes involved in the detoxification of endogenous compounds such as peroxidised lipids. They are also important in the metabolism of xenobiotics13.

In order to investigate if GST alpha-3 pathway was involved in the protective effect of postconditioning, we performed a real-time RNA analysis. GST-α3 gene was overexpressed in the posconditioned group, both in ischemic and non-ischemic liver. This data, although not significant, reveals a proper tendency.

The application of liver postconditioning strategies in the clinical setting may be useful. In liver transplantation and liver resection, ischemia is very usual and sometimes mandatory. The release of vascular clamps after ischemia is normally done straightaway. The intermittent clamp release is a very simple maneuver that may preserve endogenous protective substances inside the liver. Further studies will be addressed in this way.

 

Conclusion

Postconditioning induced hepatoprotection by reducing lipid peroxidation in the ischemic and non-ischemic liver in this model of liver ischemia-reperfusion injury in rats.

 

References

1. Crisostomo PR, Wairiuko GM, Wang M, Tsai BM, Morrell ED, Meldrum DR. Preconditioning versus postconditioning: mechanisms and therapeutic potentials. J Am Coll Surg. 2006;202:797-812.         [ Links ]

2. Minor T, Isselhard W, Yamaguchi T. Involvement of platelet activating factor in microcirculatory disturbances after global hepatic ischemia. J Surg Res. 1995;58:536-40.         [ Links ]

3. Glantzounis GK, Salacinski HJ, Yang W, Davidson BR, Seifalian AM. The contemporary role of antioxidant therapy in attenuating liver ischemia-reperfusion injury: a review. Liver Transplant. 2005;11:1031-47.         [ Links ]

4. Okamoto F, Allen BS, Buckberg GD, Bugyi H, Leaf J. Reperfusion conditions: importance of ensuring gentle versus sudden reperfusion during relief of coronary occlusion. J Thorac Cardiovasc Surg. 1986;92:613-20.         [ Links ]

5. Zhao ZQ, Corvera JS, Halkos ME, Kerendi F, Wang NP, Guyton RA, Vinten-Johansen J. Inhibition of myocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol. 2003;285:H579-88.         [ Links ]

6. Sun K, Liu ZS, Sun Q. Role of mitochondria in cell apoptosis during hepatic ischemia-reperfusion injury and protective effect of ischemic postconditioning. World J Gastroenterol. 2004;10:1934-8.         [ Links ]

7. Marnett LJ. Lipid peroxidation-DNA damage by malondialdehyde. Mutat Res. 1999;424:83-95.         [ Links ]

8. Giakoustidis D, Papageorgiou G, Iliadis S, Giakoustidis A, Kostopoulou E, Kontos N, Botsoglou E, Tsantilas D, Papanikolaou V, Takoudas D. The protective effect of alpha-tocopherol and GdCl3 against hepatic ischemia/reperfusion injury. Surg Today. 2006;36:450-6.         [ Links ]

9. Philipp S, Yang XM, Cui L, Davis AM, Downey JM, Cohen MV. Postconditioning protects rabbit hearts through a protein kinase C-adenosine A2b receptor cascade. Cardiovasc Res. 2006;70:308-14.         [ Links ]

10. Yang XM, Philipp S, Downey JM, Cohen MV. Postconditioning's protection is not dependent on circulating blood factors or cells but involves adenosine receptors and requires PI3-kinase and guanylyl cyclase activation. Basic Res Cardiol. 2005;100:57-63.         [ Links ]

11. Kin H, Zatta AJ, Lofye MT, Amerson BS, Halkos ME, Kerendi F, Zhao ZQ, Guyton RA, Headrick JP, Vinten-Johansen J. Postconditioning reduces infarct size via adenosine receptor activation by endogenous adenosine. Cardiovasc Res. 2005;67:124-33.         [ Links ]

12. Ajamieh HH, Candelario-Jalil E, Fernández OS, Gerbes AL. Ischaemic and pharmacological preconditionings protect liver via adenosine and redox status following hepatic ischaemia-reperfusion in rats. Clin Sci. 2008;115(2):69-77.         [ Links ]

13. Boyer TD. The glutathione S-transferases: an update. Hepatology. 1989;9:486-96.         [ Links ]

 

 

Correspondence:
Dr. Antonio Roberto Franchi Teixeira
Laboratory of Medical Investigation #LIM37
School of Medicine, University of Sao Paulo
Av. Dr. Arnaldo, 455/3206
01246-903 Sao Paulo - SP Brazil
Phone: (55 11)3061-8319 / 8558-8426
drrteixeira@uol.com.br

Received: August 27, 2008
Review: October 23, 2008
Accepted: November 25, 2008
Conflict of interest: none
Financial source: none

 

 

How to cite this article
Teixeira ARF, Molan NT, Kubrusly MS, Bellodi-Privato M, Coelho AM, Leite KR, Machado MAC, Bacchella T, Machado MCC. Postconditioning ameliorates lipid peroxidation in liver ischemia-reperfusion injury in rats. Acta Cir Bras. [serial on the Internet] 2009 Jan-Feb;24(1). Available from URL: http://www.scielo.br/acb
1 Research performed at Transplantation Division, Laboratory of Medical Investigation #LIM37, Department of Gastroenterology, Medicine School, University of Sao Paulo (USP), Sao Paulo, Brazil.

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