Morphological features of heart remodeling in the postcompression period of crush syndrome

Summary. In the postcompression period of crush syndrome regenerative processes develop restorative processes in target organs, in particular in the heart. However, the dynamics of myocardial regenerative changes in the postcompression period in crush syndrome is insufficiently covered in professional literature and requires comprehension study and clarified. The aim of the study – to find out features of regenerative changes in heart of laboratory rats in the dynamics in the postcompression period of crush syndrome. Materials and Methods. Light-optical and polarization were performed examination of the myocardium of 48 laboratory rats after 1, 3, 7 and 14 days (12 animals in each period) after cessation of 6 hour compression of the thigh right pelvic limb. Crush syndrome was modeled under anesthesia by intraperitoneal input of ketamine hydrochloride (100 mg/kg body weight) in a specially designed device, the compression force was 7 kg/cm2, the compressive surface area – 5 cm2. The control group consisted of 12 animals. Results. The stages of myocardial remodeling in the postcompression period are noted, reflecting its structural recovery. In the early postcompression period light-optical disorders predominated microcirculation and alternate changes in acquired cardiomyocytes maximum development after 3 days. After 7 days in myocardial stroma registered cellular infiltrates in which predominate lymphocytes and fybroblasts. Cardiomyocytes lose a compact, gait cells became fortuous, microfoci of contractures were detected and fragmentation, there was a weak proliferation of collagen fibers. After 14 days in the late postcompression period the manifestation do not fade microcirculation disorders. Processes were registered in some areas collagen formation. Conclusions. In the first three days after the cessation of compression of compression of the lower extremity dystrophic–necrotic changes of the myocardium persist in combination with microcirculatory disorders. After 7 days the development of interstitial lympho–histiocytic infiltration is observed against the background of a gradual decrease alternative and hemodynamic processes. After 14 days registration a restoration of myocardial histostructure with residual processes of microfocal contracture of cardiomyocyte degeneration and increased collagen formation are registere

crush syndrome, myocardium, rats

https://doi.org/10.11603/bmbr.2706-6290.2022.1.12979

[1] Niccoli G, Kharbanda RK, Crea F, Banning AP. No-reflow: again prevention is better than treatment. Eur Heart J. 2010;31(20): 2449-55. DOI: 10.1093/eurheartj/ehq299.

[2] Goldenthal MJ. Mitochondrial involvement in myocyte death and heart failure. Heart Fail Rev. 2016;21(2): 137-55. DOI:10.1007/s10741-016-9531-1.

[3] Shemarova  IV,  Nesterov  VP,  Korotkov  SM,  Sobol KV. [Participation of Ca2+ in the development of ischemic disorders  of  myocardial  contractile  function].  Zhurnal evolyucionnoj  biohimii  i  fiziologii.  2017;53(5):  328-37. Russian.

[4] Khubulava  GG,  Shishkevich  AN,  Mikhailov  SS, Bessonov   EYu. [Myocardial   reperfusion   syndrome. Pathogenesis,  clinic,  diagnosis].  Bulletin  of  the  Russian military medical academy. 2020;22(1): 196-200. Russian.

[5] Kloner  RA.  Stunned  and  Hibernating  myocardium: Where are we nearly 4 decades later? J Am Heart Assoc. 2020;9(3): e015502. DOI:10.1161/JAHA.119.015502.

[6] Tang X, Liu B, Wang X, Yu Q, Fang R. Epidermal growth factor, through alleviating oxidative stress, protect IPEC-J2 cells from lipopolysaccharides-induced apoptosis. Int J Mol Sci. 2018;19(3): 848. DOI:10.3390/ijms19030848.

[7] Galushko  OA,  Nedashkivsky`j  SM,  Dzyuba  DO, Babak SI, Yurkiv VV. [Infectious and toxic shock: traditions and  modern  approaches].  Hostri  ta  nevidkladni  stany  u praktytsi likaria. 2014;6(42): 26-34. Ukrainian.

[8] Virzì  GM,  Clementi  A,  Brocca  A,  Ronco  C. Endotoxin  effects  on  cardiac  and  renal  functions  and cardiorenal  syndromes.  Blood  Purif.  2017;44(4):  314-6. DOI:10.1159/000480424.

[9] Nechaev  EA,  Revskoj AK,  Savickij  GG.  Prolonged compression syndrome: Guide for doctors. [Синдром дли-тельного сдавления : руководство для врачей] Moscow: Meditsina; 1993. Russian

[10] Yuryk  YaI,  Kryvyi  PD,  Bodnar  YaYa,  Yuryk II,  Petrechko  IR,  Sharyk  MV.  inventors;  [Adjustable compression  device  for  experimental  modeling  of  the syndrome  of  tightness  and  traumatic  shock]:  Ukrainian patent UA 146513, No u 202006295. 2020 September 29. Int. Cl. A61B 17/00. Ukrainian.

[11] Directive  2010/63/EU  of  the  European  Parliament and of the Council of 22 September 2010 on the protection of  animals  used  for  scientific  purposes.  Official  Journal of  the  European  Union  [Internet].  2010;L276:33-79. Aviable  from:  https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=celex%3A32010L0063

[12] National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals. Guide for the Care and Use of Laboratory Animals. 8th ed. Washington (DC): National Academies Press (US); 2011. DOI:10.17226/12910.