Morphometric indicators of changes in the kidneys of experimental rats under the conditions of administration of the venom of the viper Vipera berus berus
DOI:
https://doi.org/10.11603/2414-4533.2026.3.16692Keywords:
venom, vipers, kidneys, morphometry, inflammation, ratsAbstract
The aim of the study: to determine the morphometric changes in the kidneys of experimental rats under the conditions of administration of the venom of the viper Vipera berus berus.
Materials and Methods. The animals were divided into two groups: control and experimental (10 individuals each). Experimental rats received an intraperitoneal injection of a semi-lethal dose (LD50) of the venom of Vipera berus berus in saline at a concentration of 1.576 μg/g. The control group was administered only saline. After 24 h, the rats were euthanised by decapitation after anaesthesia. A morphometric study of the area of the epithelium of the proximal and distal tubules was performed.
Results. In the experimental group, oedema and dystrophy of the epithelial cells of the proximal convoluted tubules, along with reduction or even disappearance of their lumen, led to a statistically significant increase in their area compared with the control group. An increase in the standard deviation by 2.4 times indicates uneven manifestations of edematous and other pathological processes in the proximal tubules of the kidneys of rats. If some tubules remained unchanged or had moderate signs of pathology, others, on the contrary, had edematous epithelium and narrowed lumens. As a result of the cumulative effect of pathological changes in the epithelial cells of the distal tubules themselves, which caused their flattening, and in the surrounding tissues, in particular in the circulatory component, which led to obturation and deformation of the lumens of the tubules, the area of the epithelium in this experimental group decreased statistically significantly compared to the control group.
Conclusions. Morphometric analysis of changes in the kidneys of experimental rats under the conditions of administration of the venom of the viper Vipera berus berus revealed a statistically significant increase in the area of the epithelium of the proximal convoluted tubules against the background of a sharp decrease in the area of epithelial cells of the distal tubules.
References
1. Chaiyabutr N, Chanhome L, Vasaruchapong T, Laoungbua P, Khow O, Rungsipipat A, Sitprija V. The pathophysiological effects of Russell's viper (Daboia siamensis) venom and its fractions in the isolated perfused rabbit kidney model: A potential role for platelet activating factor. Toxicon X. 2020; 7:100046. DOI: 10.1016/j.toxcx.2020.100046. DOI: https://doi.org/10.1016/j.toxcx.2020.100046
2. Larréché S, Chippaux J.P, Chevillard L, Mathé S, Résière D, Siguret V, Mégarbane B. Bleeding and Thrombosis: Insights into Pathophysiology of Bothrops Venom-Related Hemostasis Disorders. Int J Mol Sci. 2021; 22 (17): 9643. DOI: 10.3390/ijms22179643. DOI: https://doi.org/10.3390/ijms22179643
3. Mora-Obando D, Salazar-Valenzuela D, Pla D, Lomonte B, Guerrero-Vargas JA, Ayerbe S, Calvete JJ. Venom variation in Bothrops asper lineages from North-Western South America. J Proteomics. 2020; 229:103945. DOI: 10.1016/j.jprot.2020.103945. DOI: https://doi.org/10.1016/j.jprot.2020.103945
4. Park EJ, Choi S, Kim HH, Jung YS. Novel Treatment Strategy for Patients with Venom-Induced Consumptive Coagulopathy from a Pit Viper Bite. Toxins (Basel). 2020; 12(5):295. DOI: 10.3390/toxins12050295. DOI: https://doi.org/10.3390/toxins12050295
5. Adisakwattana P, Chanhome L, Chaiyabutr N, Phuphisut O, Onrapak R, Thawornkuno C. Venom-gland transcriptomics of the Malayan pit viper (Calloselasma rhodostoma) for identification, classification, and characterization of venom proteins. Heliyon. 2023; 9(5): e15476. DOI: 10.1016/j.heliyon.2023.e15476. DOI: https://doi.org/10.1016/j.heliyon.2023.e15476
6. Al Shammari AK, Abd El-Aziz TM, Al-Sabi A. Snake Venom: A Promising Source of Neurotoxins Targeting Voltage-Gated Potassium Channels. Toxins (Basel). 2023; 16(1):12. DOI: 10.3390/toxins16010012. DOI: https://doi.org/10.3390/toxins16010012
7. Frangieh J, Rima M, Fajloun Z, Henrion D, Sabatier JM, Legros C, Mattei C. Snake Venom Components: Tools and Cures to Target Cardiovascular Diseases. Molecules. 2021; 26(8):2223. DOI: 10.3390/molecules26082223. DOI: https://doi.org/10.3390/molecules26082223
8. Siigur J, Siigur E. Biochemistry and toxicology of proteins and peptides purified from the venom of Vipera berus berus. Toxicon X. 2022; 15:100131. DOI: 10.1016/j.toxcx.2022.100131. DOI: https://doi.org/10.1016/j.toxcx.2022.100131
9. Albert V, Hall MN. mTOR signaling in cellular and organismal energetics. Curr Opin Cell Biol. 2015; 33:55-66. DOI: 10.1016/j.ceb.2014.12.001. DOI: https://doi.org/10.1016/j.ceb.2014.12.001
10. Chun Y, Kim J. AMPK-mTOR Signaling and Cellular Adaptations in Hypoxia. Int J Mol Sci. 2021; 22(18):9765. DOI: 10.3390/ijms22189765. DOI: https://doi.org/10.3390/ijms22189765
11. Fantus D, Rogers NM, Grahammer F, Huber TB, Thomson AW. Roles of mTOR complexes in the kidney: implications for renal disease and transplantation. Nat Rev Nephrol. 2016; 12(10):587-609. DOI: 10.1038/nrneph.2016.108. DOI: https://doi.org/10.1038/nrneph.2016.108
12. Toyama EQ, Herzig S, Courchet J, Lewis TLJr, Losón OC, Hellberg K, Shaw RJ. Metabolism. AMP-activated protein kinase mediates mitochondrial fission in response to energy stress. Science. 2016; 351(6270):275-281. DOI: 10.1126/science.aab4138. DOI: https://doi.org/10.1126/science.aab4138
13. Zhang H, Xu R, Wang Z. Contribution of Oxidative Stress to HIF-1-Mediated Profibrotic Changes during the Kidney Damage. Oxid Med Cell Longev. 2021; 6114132. DOI: 10.1155/2021/ 6114132. DOI: https://doi.org/10.1155/2021/6114132
14. Palikaras K, Tavernarakis N. Mitochondrial homeostasis: the interplay between mitophagy and mitochondrial biogenesis. Exp Gerontol. 2016; 56:182-88. DOI: 10.1016/j.exger.2014.01.021. DOI: https://doi.org/10.1016/j.exger.2014.01.021
15. Singh JP, Singh AP, Bhatti R. Explicit role of peroxisome proliferator-activated receptor gamma in gallic acid-mediated protection against ischemia-reperfusion-induced acute kidney injury in rats. J Surg Res. 2016; 187(2):631-39. DOI: 10.1016/j.jss.2013.11.1088. DOI: https://doi.org/10.1016/j.jss.2013.11.1088
16. Whitaker RM, Corum D, Beeson CC, Schnellmann RG. Mitochondrial Biogenesis as a Pharmacological Target: A New Approach to Acute and Chronic Diseases. Annu Rev Pharmacol Toxicol. 2016; 56:229-49. DOI: 10.1146/annurev-pharmtox- 010715-103155. DOI: https://doi.org/10.1146/annurev-pharmtox-010715-103155
17. Zhang J, Pan W, Zhang Y, Tan M, Yin Y, Li Y, Li H. Comprehensive overview of Nrf2-related epigenetic regulations involved in ischemia-reperfusion injury. Theranostics. 2022; 12(15):6626-45. DOI: 10.7150/thno.77243. DOI: https://doi.org/10.7150/thno.77243
18. Sitprija V. Snakebite nephropathy (Review Article). Nephrology. 2006; 11:442-8. DOI: 10.1111/j.1440-1797.2006. 00599.x. DOI: https://doi.org/10.1111/j.1440-1797.2006.00599.x
19. Alvitigala BY, Gooneratne LV, Gnanathasan CA, Wijewickrama ES. Snakebite-associated acute kidney injury in South Asia: narrative review on epidemiology, pathogenesis and management. Transactions of The Royal Society of Tropical Medicine and Hygiene. 2025; 119(6):648-4. DOI: 10.1093/trstmh/trae077. DOI: https://doi.org/10.1093/trstmh/trae077
20. Meena P, Bhargava V, Gupta P, Panda S, Bhaumik S. The kidney histopathological spectrum of patients with kidney injury following snakebite envenomation in India: scoping review of five decades. BMC nephrology. 2024; 25(1): 112. DOI: 10.1186/s12882-024-03508-y DOI: https://doi.org/10.1186/s12882-024-03508-y
21. Vikrant S, Jaryal A, Parashar A. Clinicopathological spectrum of snake bite-induced acute kidney injury from India. World journal of nephrology. 2017; 6(3):150-61. DOI: 10.5527/wjn.v6.i3.150. DOI: https://doi.org/10.5527/wjn.v6.i3.150
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