Morphological characteristics of the blood-brain barrier in 1 day of experimental blast-induced traumatic brain injury

Authors

  • Yu.V. Kozlova
  • N.S. Tryasak
  • G.A. Klopotskyi
  • K.S. Kozlova

Keywords:

blood-brain barrier, explosion, brain, trauma.

Abstract

Background. Blast-induced traumatic brain injury is becoming widespread in connection with the use of explosives in military conflicts all over the world and today in Ukraine, which needs the elaboration of modern pathogenetically based treatment methods of the acute period and prevention of remote complications. Scientists have established that one of the significant primary injuries, which is the basis for the realization of secondary ones, in the case of a mild blast-induced traumatic brain injury, is a violation not only of neurons themselves, but also of the blood-brain barrier. Aim. Morphological determination of changes in the blood-brain barrier in 1st day of experimental blast-induced traumatic brain injury using a proprietary device for simulating blast injury. Methods. Brain sections of 12 albino male Wistar rats (body mass 220-270 g, age 6-7 months) were examined using light microscopy. Rats were randomly divided into 2 groups: I – Experimental group (n=6), the animals of which were anesthetized with Halothane, fixed with their heads to the muzzle end of a self-made and patented device at a distance of 5 cm and subjected to the action of a blast wave of 26-36 kPa; II - Sham (n=6). After 1 day, the rats of both groups were euthanized and brains were removed, which were then fixed and sections were prepared and stained with hematoxylin and eosin according to standard methods. Results. Established credible signs of blood-brain barrier disruption using our own device to reproduce a blast-induced traumatic brain injury, which are primary damages as a result of the action of the blast wave and are the basis for triggering secondary damage mechanisms and lead to neurodegeneration processes. Conclusion. The mild blast-induced traumatic brain injury after using a proprietary device was confirmed by morphological changes in the blood-brain barrier in the 1st day of the post-traumatic period in the form of ruptured and paretically dilated capillaries and desquamation of the vascular endothelium, the presence of erythrocyte aggregates. Increased permeability of blood vessels led to swelling of brain tissue and neurocytes.

References

  1. Zhang JK, Botterbush KS, Bagdady K, Lei CH, Mercier P, Mattei TA. Blast-related traumatic brain injuries secondary to thermobaric explosives: implications for the War in Ukraine. World Neurosurg. 2022;22:1878-8750. DOI: 10.1016/j.wneu.2022.08.073.
  2. Rusiecki J, Levin LI, Wang L, Byrne C, Krishnamurthy J, Chen L, Galdzicki Z, French LM. Blast traumatic brain injury and serum inflammatory cytokines: a repeated measures case-control study among U.S. military service members. J Neuro inflammation. 2020;17(1):20. DOI: 10.1186/s12974-019-1624-z.
  3. Yamamoto S, DeWitt DS, Prough DS. Impact & blast traumatic brain injury: implications for therapy. Molecules. 2018;23(2):245. DOI: 10.3390/molecules23020245.
  4. Ratliff WA, Mervis RF, Citron BA, Schwartz B, Rubovitch V, Schreiber S, Pick CG. Mild blast-related TBI in a mouse model alters amygdalar neurostructure and circuitry. Exp Neurol. 2019;315:9-14. DOI: 10.1016/j.expneurol.2019.01.020.
  5. Kozlova YuV, Abdul-Ogly LV, Kosharnyj AV, Kytova IV, Korzachenko MA, inventors; Kozlova YuV, asignee. Device for studying the effect of the shock wave of an explosion on the body. Ukrainian patent UA 146858. 2021 Mar. Int. CI. G09B 23/28, B01J 3/00. Ukrainian. Available from: https://base.uipv.org/searchINV/search.php?action=viewdetails&IdClaim=275099
  6. Sundar S, Ponnalagu A. Biomechanical analysis of head subjected to blast waves and the role of combat protective headgear under blast loading: a review. J Biomech Eng. 2021;143(10):100801. DOI: 10.1115/1.4051047. PMID: 33954580.
  7. Marsh JL, Bentil SA. Cerebrospinal fluid cavitation as a mechanism of blast-induced traumatic brain injury: a review of current debates, methods, and findings. Front Neurol. 2021;12:626393. DOI: 10.3389/fneur.2021.626393.
  8. Vogel EW, Panzer MB, Morales FN, Varghese N, Bass CR, Meaney DF, Morrison B. Direct observation of low strain, high rate deformation of cultured brain tissue during primary blast. Ann Biomed Eng. 2020;48(4):1196-1206. DOI: 10.1007/s10439-019-02437-4.
  9. Fan K, Ma J, Xiao W, Chen J, Wu J, Ren J, Hou J, Hu Y, Gu J, Yu B. Mangiferin attenuates blast-induced traumatic brain injury via inhibiting NLRP3 inflammasome. Chem Biol Interact. 2017;271:15-23. DOI: 10.1016/j.cbi.2017.04.021.
  10. Kawoos U, Abutarboush R, Gu M, Chen Y, Statz JK, Goodrich SY, Ahlers ST. [Blast-induced temporal alterations in blood-brain barrier properties in a rodent model]. Sci Rep. 2021;11(1):5906.
  11. Kozhemyakin YuM, Khromov OS, Boldyreva NE, Dobrelya V, Saifetdinova GA. [Scientific and practical recommendations for keeping and working with laboratory animals]. Interservice. 2017;1:150-182. Ukrainian.
  12. Bagriy MM, Dibrova VA, Popadynets OG, Grischuk MI, authors; Bagriy MM, Dibrova VA, editors. Metodu morfologichnogo doslidzennya [Methods of morphological research]. Vinnitsa: New book; 2016. 328 p. Ukrainian.
  13. Kuriakose M, Rama Rao KV, Younger D, Chandra N. Temporal and spatial effects of blast overpressure on blood-brain barrier permeability in traumatic brain injury. Sci Rep. 2018;8(1):8681. DOI: 10.1038/s41598-018-26813-7.
  14. Benz F, Liebner S. Structure and function of the blood-brain barrier (BBB). Handb Exp Pharmacol. 2022;273:3-31. DOI: 10.1007/164_2020.
  15. Kadry H, Noorani B, Cucullo L. A blood-brain barrier overview on structure, function, impairment, and biomarkers of integrity. Fluids Barriers CNS. 2020;17(1):69. DOI: 10.1186/s12987-020.
  16. Murugan M, Ravula A, Gandhi A, Vegunta G, Mukkamalla S, Mujib W, Chandra N. Chemokine signaling mediated monocyte infiltration affects anxiety-like behavior following blast injury. Brain Behav Immun. 2020;88:340-352. DOI: 10.1016/j.bbi.2020.03.029.
  17. Kuriakose M, Younger D, Ravula AR, Alay E, Rama Rao KV, Chandra N. Synergistic role of oxidative stress and blood-brain barrier permeability as injury mechanisms in the acute pathophysiology of blast-induced neurotrauma. Sci Rep. 2019; 9(1):7717. DOI: 10.1038/s41598-019-44147-w.
  18. Ritzel RM, He J, Li Y, Cao T, Khan N, Shim B, Sabirzhanov B, Aubrecht T, Stoica BA, Faden AI, Wu LJ, Wu J. Proton extrusion during oxidative burst in microglia exacerbates pathological acidosis following traumatic brain injury. Glia. 2021;69(3):746-764. DOI: 10.1002/glia.23926.
  19. Rand D, Ravid O, Atrakchi D, Israelov H, Bresler Y, Shemesh C, Omesi L, Liraz-Zaltsman S, Gosselet F, Maskrey TS, Beeri MS, Wipf P, Cooper I. Endothelial Iron homeostasis regulates blood-brain barrier integrity via the HIF2α-Ve-Cadherin pathway. Pharmaceutics. 2021;13(3):311. DOI: 10.3390/pharmaceutics13030311.
  20. Xie BS, Wang YQ, Lin Y, Mao Q, Feng JF, Gao GY, Jiang JY. Inhibition of ferroptosis attenuates tissue damage and improves long-term outcomes after traumatic brain injury in mice. CNS Neurosci Ther. 2019;25(4):465-475. DOI: 10.1111/cns.13069.
  21. Needham EJ, Helmy A, Zanier ER, Jones JL, Coles AJ, Menon DK. The immunological response to traumatic brain injury. J Neuroimmunol. 2019;332:112-125. DOI: 10.1016/j.jneuroim.2019.04.005.

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Published

2022-10-15

How to Cite

Kozlova, Y. ., Tryasak, N. ., Klopotskyi, G. ., & Kozlova, K. . (2022). Morphological characteristics of the blood-brain barrier in 1 day of experimental blast-induced traumatic brain injury. Морфологія / Morphologia / Morfologìâ, 16(3), 148–152. Retrieved from https://morphology.dma.edu.ua/article/view/282008

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