Changes of Prooxidant-Antioxidant Systems in Experimental Acute Pancreatitis
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Keywords

acute pancreatitis
lipid peroxidation
products of thiobarbituric acid
diene conjugates
catalase

How to Cite

Cherkasova, V., & Zaiats, L. (2017). Changes of Prooxidant-Antioxidant Systems in Experimental Acute Pancreatitis. Galician Medical Journal, 24(3). https://doi.org/10.21802/gmj.2017.3.13

Abstract

Mortality in acute destructive pancreatitis, despite the development and introduction of new methods of treatment, remains stable high and in severe forms reaches 25-85%. Activation of neutrophils and macrophages in acute pancreatitis leads to an "oxygen burst", which is closely linked with the activation of lipid peroxidation.

Goals. The purpose is to establish dynamic changes in the indexes of prooxidant-antioxidant systems in acute L-arginine-induced pancreatitis.

Materials and methods. The study was performed on 62 white male rats of Wistar line weighing 180-220g, with modeled acute pancreatitis. Blood for analysis have been taken: the blood serum on 12, 24, 48 and 72 hours of experiment to determine the activity level of thiobarbituric acid products, diene conjugates, catalase and lactate for assessment of the intensity of oxidative stress and antioxidant systems.

Results. The obtained results of the study showed that acute L-arginine-induced pancreatitis is accompanied by an intensification of lipid peroxidation processes (LPO). Revealed that the most pronounced increase in all blood parameters is observed 24 hours after the beginning of the study. A significant increase in the active products of tiobarbituric acid (TBA-AP) and diene conjugates (DC) was detected - 1.98 and 2.7 times, respectively, and 2.2 times the growth of catalase (CT). At the next stage of the experiment there is a slowdown in the rate of LPO, as evidenced by the following values. Thus, for 48 years in the 3rd group: TBA-AP - they increased by 5.1% (p> 0.05), DC - by 3.3% (p> 0.05), and the level of CT - by 43.4% (P <0.05), compared with data for 24 hours. It is important to note that at 72 hours, the CT level decreased by 23.3% (p> 0.05), which may indicate an exhaustion of antioxidant systems. Indicators of LPO on 72 hours compared with 48 hours in group III: TBA-AP - increased by 1.7% (p> 0.05), DC - by 5.7% (p> 0.05).

Conclusions. Acute L-arginine-induced pancreatitis is accompanied by an intensification of lipid peroxidation-oxidation processes that can potentiate the development of multiple organ failure in pancreatic inflammation. The most pronounced changes in lipid peroxidation-oxidation rates are observed for 24 hours of study.

https://doi.org/10.21802/gmj.2017.3.13
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References

Kryvoruchko I. Differencionny podhod k vyboru metoda lechenia psevdokist podzheludochnoi zhelezy. Clin Hirurgia. 2013. 7:16-19.

Daciuk О, Shaprynskiy V, Shlapak I. Osoblyvosti infuzijnoi terapii u hvoryh za tyazhkoho hostroho destruktyvnoho pankreatytu. Clin Hirurhiya. 2013. 9:22-25.

Singh VK, Bollen TL, Wu BU, Repas K, Maurer R, Yu S, et al. An assessment of the severity of interstitial pancreatitis. Clin. Gastroenterol. Hepatol. 2011. Dec;9(12):1098-103.

Lytvynenko O, Homolyako I, Kalyuzhka A. Alternative methods of prognosis for acute pancreatitis. Clin Surgery. 2013. 4:28-31.

Bernyk O, Savchu O, Dvorshchenko K, Berehova T, Ostapchenko L. Peroksydne okysnennia bilkiv pechinky za umov hypoacydnoho stanu. Fizyka zhyvoho. 2010. 18(3):89-92.

Besjkiy V, Hryshchuk L, Marushchak M. Pokaznyky vilnoradykalnoho okysnennia krovi ta bronhoalveolyarnoho lavazhu pry syndromi hostroho ushkodzhennia lehenj. Suchasni Med Tech. 2014. 2:48-54.

Gavrilov V, Gavrilova A, Hmara N. Izmenenie dienovyh koniuhatov v plazme po ultrafioletovomu pohloshcheniju heptanovyh I izopropilnyh ekstraktov. Lab Delo. 1988. 2:60-64.

Korobeynikova E. Modyfikacija izmereniya produktov perekisnoho okislenija lipidov v reakciji s tiobarbiturovoj kislotoj. Lab Delo. 1989. 1:8-10.

Babenko G. Vyznachennia mikroelementiv i metalofermentiv v klinichnyh laboratoriyah. Кiev: Zdorovia; 1968.

Chooklin S, Bihalskyy I, Pereyaslov A. Markery oksydacijnogo stresu jak pokaznyki tyazhkosti gostroho pankreatytu. Ukr J Hirurgii. 2011. 6(15):159-163.

Maksymiuk V. Suchasni pidhody do diagnostyki, prohnozuvannya perebigu ta likuvannya hostroho nekrotychnoho pankreatytu. Med Extr Staniv. 2014. 7(62):84-87.

Cruz-Santamaria DM, Taxonera C, Іner M. Update on pathogenesis and clinical management of acute pancreatitis. World J Gastrointest. Pathophisiol. 2012. 3(3):60-70.

Esrefoglu M. Experimental and clinical evidence of antioxidant therapy in acute pancreatitis. World J Gastrointest. 2012. 18(39):5533-5541.

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