ISSN 2415-3060 (print), ISSN 2522-4972 (online)
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JMBS 2021, 6(3): 96–101
https://doi.org/10.26693/jmbs06.03.096
Experimental Medicine and Morphology

Histological Changes in the Components of Aerogematic Barrier in 24 Hours after Modeling of Acute Renal Failure

Klishch I. P.
Abstract

Nowadays, acute renal failure remains one of the most complex problems in modern medicine. Multiple studies have proved that acute renal failure is frequently accompanied by the development of acute lung injury and its most severe form – acute respiratory distress syndrome. According to the literature, lethality in case of acute lung injury or acute respiratory distress syndrome is extremely high and is 30-65%. In case of combination of acute renal failure and acute lung injury or acute respiratory distress syndrome, the most frequently observed in critical patients, lethality reaches 80%. The purpose of the study was to study the possibility of ultrastructural changes of the respiratory tract in the lungs due to experimental modeling of acute renal failure. Materials and methods. The experiments were performed on 30 mature white male rats weighting 180-220 grams. Acute renal failure was induced by intramuscular administration of 50% glycerol water solution in dose of 10 ml per 1 kg of body mass. The sampling of lung tissue for electron microscopy study was carried out under the ketamine anaesthesia in 24 hours after beginning of the experiment. The pieces of lung tissue were fixed in 2.5% solution of gluteraldehyde with further postfixation in 1% solution of osmium tetroxide. After dehydration, the material was poured over epon araldite. The cuts, obtained on ultramicrotome “Tesla BS-490”, were studied using electron microscope “PEM-125K”. Results and discussion. In 24 hours after the beginning of the experiment, the changes in the alveolocytes of types I and II, endotheliocytes, alveolar macrophages are accompanied by the development of intracellular edema with ultrastructural disorder of organelles. Because of endotheliocytes edema and aggregation of forming blood elements, some blood capillaries lumens are closed or drastically narrowed. In some blood capillaries, we observe disorder of the luminal membrane integrity of endothelial cells accompanied by exit of the intracellular content into the micro blood vessel lumen. The expressed disorders of structural organization of the components of pulmonary aero-hematic barrier cause the exit of forming blood elements into the interstitial tissue and alveoli. Conclusion. Тhe detected changes in 24 hours of the experiment have a dystrophic-destructive character and are manifested by the development of edema in alveolocytes of types I and II, alveolar macrophages, endotheliocytes of hemocapillaries. Perspective for further research. Considering the severity of ultrastructural changes that develop in experimental acute renal failure, it would be reasonable to conduct a further study in order to find possible methods of prevention and timely correction

Keywords: lungs, respiratory part, experimental acute renal failure

Full text: PDF (Ukr) 558K

References
  1. Howrylak JM, Nakahira K. Inflammasomes: Key Mediators of Lung Immunity. Annu Rev Physiol. 2017; 79: 471-94. https://doi.org/10.1146/annurev-physiol-021115-105229
  2. Murtha LA, Schuilga MJ, Mabotuwana NS, Hardy SA, Waters DW, Burgess JK, et al. The processes and mechanisms of cardiac and pulmonary fibrosis. Front Physiol. 2017; 12(8): 777.
  3. Riviello ED, Buregeya E, Twagirumugabe T. Diagnosing acute respiratory distress syndrome in resource limited settings: the Kigali modification of the Berlin definition. Curr Opin Critt Care. 2017; 23: 18-23. https://doi.org/10.1097/MCC.0000000000000372
  4. Shankar-Hari M, Fan E, Ferguson ND. Acute respiratory distress syndrome (ARDS) phenotyping. Intensive Care Med. 2018; 45(4): 516-9. https://doi.org/10.1007/s00134-018-5480-6
  5. Domenech P, Perez T, Saldarini A, Uad P, Musso CG. Kidney-lung pathophysiological crosstalk: its charactteristics and importance. Int Urol Nephrol. 2017; 49: 1211-15. https://doi.org/10.1007/s11255-017-1585-z
  6. Ma T, Liu X, Liu Z. Role of asymmetric dimethylarginine in rat acute lung ingjury induced by acute ischemic kidney injury. Molecular medicine reports. 2015; 12: 1923-8. https://doi.org/10.3892/mmr.2015.3619
  7. Malek M, Hassanshahi J, Fartootzadeh R, Azizi F, Shahidani S. Nephrogenic acute respiratory distress syndrome: a nerrative review on pathophysiology and treatment. Chinese J Traumat. 2018; 21: 4-10.
  8. Oztay F, Kara-Kisla B, Orhan N, Yanardag R, Bolkent S. The protective effects of prostaglandin EI on lung injury following renal ischemia-reperfusion in rats. Toxicology and Industrial Health. 2016; 32(9): 1684-92. https://doi.org/10.1177/0748233715576615
  9. Rodrigo R, Trujillo S, Bosco C. Biochemical and ultrastructural lung damage indused by rhabdomyolysis in the rat. Exp Biol Med. 2006; 231: 1430-8. PMID: 16946412
  10. Im D, Shi W, Driscoll B. Pediatric Acute Respiratory Distress Syndrome: Fibrosis versus Repair. Front Pediatr. 2016; 4: 28. https://doi.org/10.3389/fped.2016.00028
  11. Slutsky AS, Ranieri VM. Ventilator-Induced Lung Injury. N Engl J Med. 2013; 369: 2126-36. https://doi.org/10.1056/NEJMral208707
  12. Whitsett JA, Alenghat T. Respiratory epithelial cells orchestrate pulmonary innate immunity. Nat Immonol. 2014; 16(1): 27-35. https://doi.org/10.1038/ni.3045
  13. Zaiats LM, Kuz UV, Zukov W. Correction of the ultrastructural changes of the respiratory department of the lungs by phosphatidylcholine liposomes due to multiple skeletal trauma with osteosynthesis in the experimental study. Journal of Education, Health and Sport. 2018; 8(8): 293-301.
  14. Perl M, Hohmann C, Denk S, Kellermann P, Lu D, Braumiiller S, et al. Role of activated neutrophils in chest trauma-induced septic acute lung injury. Shock. 2012; 38(1): 98-106. https://doi.org/10.1097/SHK.0b013e318254be6a