You are here

HEMORAJİK ŞOKU İZLEYEN İSKEMİ- REPERFÜZYON HASARININ KARACİĞER OKSİDAN-ANTİOKSİDAN DURUMUNA ETKİSİ

THE EFFECT OF ISCHEMIA REPERFUSION INJURY AFTER HAEMORRHAGE ON LIVER OXIDANT-ANTIOXIDANT STATUS

Journal Name:

Publication Year:

Abstract (2. Language): 
Aim: Various types of haemorrhage can cause hypovolemic shock. Volume replacement for prevention of hypovolemic shock results with reperfusion. The aim of this study was to determine the hepatic tissue MDA, XO, SOD and AOA levels after reperfusion following ischemia with duration of 30 minutes. Method: Twenty four female Spraque-Dawley rats were divided into four groups of six rats in each. Group A was the control group and B, C, and D groups were ischemia-reperfusion groups which were reperfused for 1 hour, 3 hours and 24 hours after 30 minutes hemorrhagic ischemia, respectively. In the ischemia-reperfusion groups at the end of the reperfusion periods, rats were sacrified and the liver tissue samples were collected. In group A rats were only anesthetized for one hour and then they were sacrified and the liver tissue samples were collected. MDA, XO, SOD and AOA analyses were performed in liver tissues. Results: MDA and XO levels were significantly increased in the ischemia- reperfusion groups when compared with the control group (p<0,05). SOD and AOA levels were significantly decreased in ischemia- reperfusion groups when compared with the control group (p<0,05). These changes were most obvious in the first hour. Conclusion: Our findings showed that volume replacement therapy after hypovolemic shock was lead to reperfusion injury. Because MDA, XO, SOD ve AOA changes were more significant in the first hour of the reperfusion than the 3th and 24th hours; we suggest maintenance of antioxidant suplements with replacement theraphy to decrease the reperfusion injury. For the supplemental management antioxidants such as alpha tocopherol, ascorbic acid and melathonin can be prefered in the first hour of reperfusion especially.
Abstract (Original Language): 
Amaç: Çeşitli şekillerde oluşan hemoraji hipovolemik şoka neden olabilir. Hemorajik şoku önlemek için uygulanan volüm replasmanı ise reperfüzyona neden olmaktadır. Çalışmamızda 30 dakikalık iskemi sonrası yapılan reperfüzyonun karaciğer dokusu malondialdehit (MDA), ksantin oksidaz (XO), süperoksit dismutaz (SOD) ve antioksidan aktivite (AOA) düzeylerine olası etkisini değerlendirmeyi amaçladık. Yöntem: Çalışmamızda Spraque-Dawley cinsi 24 adet rat kullanıldı. Ratlar 4 gruba ayrıldı: A grubu kontrol, B, C, ve D grupları iskemi-reperfüzyon grupları olarak planlandı. İskemi-reperfüzyon gruplarında femoral venden kan alınarak 30 dakikalık iskemi oluşturuldu. İskemi süresinin sonunda alınan kan tekrar verilip reperfüzyon oluşturulmasını takiben, B, C ve D gruplarında sırası ile 1, 3 ve 24. saatin sonunda ratlar sakrifiye edilerek karaciğer doku örnekleri çıkarıldı. Kontrol grubunda ise sadece 60 dakika süreli anesteziyi takiben ratlar sakrifiye edilerek karaciğer doku örnekleri çıkarıldı. Karaciğer dokusunda MDA, XO, SOD ve AOA analizleri yapıldı. Bulgular: İskemi-reperfüzyon gruplarında karaciğer doku MDA düzeyleri ve XO aktivitelerinin kontrol grubuna oranla önemli oranda (p<0,05) arttığı, SOD ve AOA değerlerinin ise önemli oranda (p<0,05) azaldığı görülmüştür. Bu artış ve azalmalar özellikle reperfüzyon sonrası birinci saatte en belirgin olmuştur. Sonuç: Bulgularımız göstermektedir ki; hipovolemik iskemi sonrası uygulanan volüm replasmanı reperfüzyon hasarına neden olmuştur. Reperfüzyonun birinci saatindeki MDA, XO, SOD ve AOA değişimlerinin üçüncü ve yirmidördüncü saatlerden daha belirgin olması nedeniyle volüm replasmanı uygulamasına ilaveten reperfüzyon hasarını azaltıcı antioksidan destek uygulanmasını öneriyoruz. Bunun için α-tokoferol, askorbik asit ve melatonin gibi antioksidanlar reperfüzyonun özellikle ilk saatinde tercih edilmelidir.
203-210

REFERENCES

References: 

1. Scafer M, Krahenbuhl L. Effect of
laparoscopy on intraabdominal blood flow.
Surgery. 2001;129(4):385-9.
2. Eleftheriadis E, Kotzampassi K, Heliadis N,
Sarris K. Gut ischemia, oxidative stress,
and bacterial translocation in elevated
abdominal pressure in rats. World J Surg.
1996;20(1):11-6.
3. Yilmaz S, Koken T, Tokyol C, Kahraman
A, Akbulut G, Serteser M, et al. Can
preconditioning reduce laparoscopy–
induced tissue injury? Surg Endosc.
2003;17(5):819-24.
4. Liu Z, Xu Z, Shen W, Li Y, Zhang J, Ye X.
Effect of pharmacologic preconditioning
with tetrandrine on subsequent ischemia/
reperfusion injury in rat liver. World
Journal Of Surgery 2004;28(6):620-4.
5. Cheng F, Li YP, Cheng JQ, Feng L, Li SF.
The protective mechanism of Yisheng
Injection against hepatic ischemia
reperfusion injury in mice. World journal
of gastroenterology 2004;10(8):1198-203.
6. Garrison RN, Conn AA, Haris PD, Zakaria
ER. Direct peritoneal resuscitation as
adjunct to conventional resuscitation from
hemorrhagic shock: a beter outcome.
Surgery 2004;136(4):900-8.
7. Aydemir EO, Var A, Uyanik BS, Ilkgul
O, Aydede H, Sakarya A. The protective
mechanisms of defibrotide on liver
ischaemia–reperfusion injury. Cell
Biochem Funct. 2003;21(4):307–10.
8. Giakoustidis D, Papageorgiou G,
Kostopoulou E, Iliadis S, Giakoustidis A,
Kontos N, et al. High dose intravenous
immunoglobulin g pretreatment: effect on
lipid peroxidation and reperfusion injury
to the liver. World J Surg. 2003;27(12):
1300–5.
9. Sener G, Tosun O, Sehirli AO, Kacmaz
A, Arbak S, Ersoy Y, et al. Melatonin
and N-acetylcysteine have beneficial
effects during hepatic ischemia and
reperfusion.Life Sci 2003;72(24):2707-18.
10. Peralta C, Bulbena O, Xaus C, Prats
N, Cutrin JC, Poli G, et al. Ischemýc
preconditioning: a defense mechanism
against the reactive oxygen species
generated after hepatic ischemia
reperfusion. Transplantation. 2002;73(8):
1203-11.
11. Erdogan O, Yildiz S, Basaran A, Demirbas
A, Yesilkaya A. Effect of intraportal
verapamil infusion on hepatic ischemiareperfusion injury. Pol J Pharmacol.
2001;53(2):137-41.
12. Yuan GJ, Ma JC, Gong ZJ, Sun XM,
Zheng SH, Li X. Modulation of liver
oxidant-antioxidant system by ischemic
preconditioning during ischemia/
reperfusion injury in rats. World J
Gastroenterol. 2005;11(12):1825-8.
13. Bertuglia S, Giusti A. Influence of ACTH-
(1-24) and plasma hyperviscosity on free
radical production and capillary perfusion
after hemorrhagic shock Microcirculation.
2004;11(3):227–38.
14. Lowry OH, Rosebrough NJ, Farr AL,
Randall RJ. Protein measurement with
the Folin phenol reagent. J Biol Chem.
1951;193(1):265–75.
15. Hammouda A el-R, Khalil MM, Salem A.
Lipid peroxidation products in pleural
fluid for seperation of transudates and
exudates. Clin Chem 1995;41(9):1314-5.
16. Prajda N, Weber G. Malignant
transformation–linked imbalance:
decreased xhantine oxidase activity in
hepatomas. FEBS Lett 1975;59(2):245–9.
17. Sun Y, Oberley LW, Li Y. A simple method
for clinical assay of superoxide dismutase.
Clin Chem. 1988;34(3),497-500.
18. Durak I, Yurtaslanı Z, Canbolat O, Akyol O.
A methodological approach to superoxide
dismutase (SOD) activity assay based on
inhibition of nitrobluetetrazolium (NBT)
reduction. Clin Chim Acta 1993;214:103-4.
19. Koracevic D, Koracevic G, Djordjevic V,
Andrejevic S, Cosic V. Method for the
measurement of antioxidant activity in
human fluids. J Clin Pathol. 2001;54(5):
356-61.
20. Gedik E, Girgin S, Obay BD, Ozturk H,
Ozturk H, Buyukbayram H. Iloprost, a
prostacyclin (PGI2) analogue, reduces
liver injury in hepatic ischemia-reperfusion
in rats. Acta Cir Bras. 2009;24(3):226-
32.
21. Baltalarli A, Ozcan V, Bir F, Aybek H, Sacar
M, Onem G, et al. Ascorbic acid (vitamin
C) and iloprost attenuate the lung injury
caused by ischemia/reperfusion of the
lower extremities of rats. Ann Vasc Surg.
2006;20:49-55.
22. Zulfikaroglu B, Koc M, Soran A, Isman
F, Cinel I. Evaluation of oxidative stress
in laparoscopic cholecystectomy. Surg
Today. 2002;32(10):869-74.
23. Sare M, Yilmaz I, Hamamci D, Birincioglu
M, Özmen M, Yesilada O. The effect of
carbon dioxide pneumoperitoneum on
free radicals. Surg Endosc. 2000;14(7):
649-52.
24. Kanko M, Maral H, Akbas MH, Ozden M,
Bulbul S, Omay O, et al. Protective effects
of clopidogrel on oxidant damage in a rat
model of acute ischemia. Tohoku J Exp
Med. 2005;205(2):133-9.
25. Issekutz TB. Effects of six different
cytokines on lymphocyte adherence
to microvascular endothelium and in
vivo lymphocyte migration in the rat. J
Immunol. 1990;144(6):2140-6.
26. Tsujimoto M, Yokota S, Vilcek J,
Weissmann G. Tumor necrosis factor
provokes superoxide anion generation
from neutrophils. Biochem Biophys Res
Commun. 1986;137(3):1094-100.
27. Meyer JD, Yurt RW, Duhaney R, Hesse DG,
Tracey KJ, Fong YM, et al. Tumor necrosis
factor-enhanced leukotriene B4 generation
and chemotaxis in human neutrophils.
Arch Surg. 1988 Dec;123(12):1454-58.
28. Guneli E, Cavdar Z, Islekel H, Sarioglu
S, Erbayraktar S, Kiray M, Sokmen S, et
al. Erythropoietin protects the intestine
against ischemia/ reperfusion injury in
rats. Mol Med. 2007;13(9-10):509-17.
29. Kart A, Cigremis Y, Ozen H, Dogan O.
Caffeic acid phenethyl ester prevents
ovary ischemia/reperfusion injury in
rabbits. Food Chem Toxicol. 2009;47(8):
1980-4.
30. Xu GX, Xiao ZY, Xie MS, Feng YL, Guo J,
Fu LX. Protective effects of melatonin on
cultural human retinal pigment epithelial
cells against oxidative damage in vitro.
Zhonghua Yan Ke Za Zhi. 2009;45(6):
528-32.

Thank you for copying data from http://www.arastirmax.com