Histomorphometric study of rat liver during the treatment of the acute toxic injury
- Autores: Baygildin S.S.1, Repina E.F.1, Gimadieva A.R.2, Kudoyarov E.R.1, Smolyankin D.A.1, Mustafin A.G.2, Valova Y.V.1
-
Afiliações:
- Ufa Research Institute of Occupational Health and Human Ecology
- Ufa Institute of Chemistry UFRC RAS
- Edição: Volume 100, Nº 11 (2021)
- Páginas: 1283-1286
- Seção: PREVENTIVE TOXICOLOGY AND HYGIENIC STANDARTIZATION
- ##submission.datePublished##: 06.12.2021
- URL: https://bulletin.ssaa.ru/0016-9900/article/view/638780
- DOI: https://doi.org/10.47470/0016-9900-2021-100-11-1283-1286
- ID: 638780
Citar
Texto integral
Resumo
Introduction. There are a few effective therapies are available for acute liver injury at present.
The aim of the study was to investigate histological and morphometric changes in the liver using models of toxic damage caused by carbon tetrachloride (ССl4 ) and acetaminophen during correction with Oxymethyluracil (OMU).
Material and methods. A total of ninety rats were divided into 18 groups. The treatment of acute liver damage models caused by a single injection of ССl4 or acetaminophen was carried out using “Heptor”, “Mexidol”, and OMU. The correction was carried out twice (sacrificed 24 hours after intoxication) and four times (sacrificed 72 hours after intoxication). Liver tissues were processed using standard histological techniques (H&E). A semi-quantitative assessment was performed using a scale based on the severity of liver cell deaths.
Results. Twenty-four hours after administration of ССl4 or 72 hours after administration of acetaminophen, the treatment with OMU led to a decrease in liver cell death compared to the group with administration of only ССl4 or acetaminophen. Seventy-two hours after ССl4 and 24 hours after acetaminophen intoxication, these groups with the OMU treatment did not differ from those of the carbon tetrachloride- or acetaminophen-induced liver injury groups, respectively.
Conclusion. Thus, on the model of ССl4 liver injury, the treatment with OMU is more effective for 24 hours. In the case of acetaminophen intoxication, the effectiveness of treatment with OMU is better for 72 hours. The results obtained are possibly associated with a different mechanism of the damaging effect of the studied toxicants.
Contribution:
Baygildin S.S. — collection and processing of material, statistical processing, writing a text;
Repina E.F. — the concept and design of the study, editing;
Gimadieva A.R., Mustafin A.G. — oxymethyl uracil synthesis;
Kudoyarov E.R. — collection and processing of material, statistical processing;
Smolyankin D.A., Valova Y.V. — collection and processing of material.
All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version.
Conflict of interest. The authors declare no conflict of interest.
Acknowledgement. The work was carried out at the expense of subsidies for the implementation of a state task within the framework of the sectoral research program of the Federal Service for Supervision in Protection of the Rights of Consumer and Man Wellbeing (Rospotrebnadzor): “Hygienic scientific substantiation of minimizing risks to the health of the population of Russia” for 2016-2020 on topic 3.5, the state no. registration AAAA-A16-116022610045-4. The 5-hydroxy-6-methyl uracil composition was synthesized under the Ufa Institute of Chemistry of the Ufa Federal Research Center of the Russian Academy of Sciences (State Registration No. AAAA-A19-119011790021-4).
Conclusion of the bioethical commission: the study was approved by the bioethical commission of the Ufa Research Institute of Occupational Medicine and Human Ecology, carried out under the European Convention for the Protection of Vertebrate Animals Used for Experiments or Other Scientific Purposes (ETS No. 123), the directive of the European Parliament and the Council of the European Union 2010/63 / EC of September 22, 10 on the protection of animals used for scientific purposes.
Received: July 19, 2021 / Accepted: September 28, 2021 / Published: November 30, 2021
Sobre autores
Samat Baygildin
Ufa Research Institute of Occupational Health and Human Ecology
Autor responsável pela correspondência
Email: baigildin.samat@yandex.ru
ORCID ID: 0000-0002-1856-3173
MD, junior researcher of the department of toxicology and genetics with an experimental clinic of laboratory animals Ufa Research Institute of Occupational Health and Human Ecology, Ufa, 450106, Russian Federation.
e-mail: baigildin.samat@yandex.ru
RússiaElvira Repina
Ufa Research Institute of Occupational Health and Human Ecology
Email: noemail@neicon.ru
ORCID ID: 0000-0001-8798-0846
Rússia
Alfiya Gimadieva
Ufa Institute of Chemistry UFRC RAS
Email: noemail@neicon.ru
ORCID ID: 0000-0002-2995-310X
Rússia
Eldar Kudoyarov
Ufa Research Institute of Occupational Health and Human Ecology
Email: noemail@neicon.ru
ORCID ID: 0000-0002-2092-1021
Rússia
Denis Smolyankin
Ufa Research Institute of Occupational Health and Human Ecology
Email: noemail@neicon.ru
ORCID ID: 0000-0002-7957-2399
Rússia
Akhat Mustafin
Ufa Institute of Chemistry UFRC RAS
Email: noemail@neicon.ru
ORCID ID: 0000-0002-8342-8787
Rússia
Yana Valova
Ufa Research Institute of Occupational Health and Human Ecology
Email: noemail@neicon.ru
ORCID ID: 0000-0001-6605-9994
Rússia
Bibliografia
- Munakarmi S., Chand L., Shin H.B., Jang K.Y., Jeong Y.J. Indole-3-carbinol derivative DIM mitigates carbon tetrachloride-induced acute liver injury in mice by inhibiting inflammatory response, apoptosis and regulating oxidative stress. Int. J. Mol. Sci. 2020; 21(6): 2048. https://doi.org/10.3390/ijms21062048
- Ye X., He L., Ma J., Li Y., Zhang M., Yang J., et al. Downregulation of Glt25d1 aggravates carbon tetrachloride induced acute hepatic injury through activation of the TGF β1/Smad2 signaling pathway. Mol. Med. Rep. 2018; 18(4): 3611–8. https://doi.org/10.3892/mmr.2018.9392
- Lee Y.S., Cho I.J., Kim J.W., Lee M.K., Ku S.K., Choi J.S., et al. Hepatoprotective effects of blue honeysuckle on CCl4‐induced acute liver damaged mice. Food Sci. Nutr. 2019; 7(1): 322–38. https://doi.org/10.1002/fsn3.893
- Ramachandran A., Jaeschke H. Acetaminophen hepatotoxicity. Semin. Liver Dis. 2019; 39(2): 221–34. https://doi.org/10.1055/s-0039-1679919
- Kuvandik G., Duru M., Nacar A., Yonden Z., Helvaci R., Koc A., et al. Effects of erdosteine on acetaminophen-induced hepatotoxicity in rats. Toxicol. Pathol. 2008; 36(5): 714–9. https://doi.org/10.1177/0192623308320800
- Ramachandran R., Kakar S. Histological patterns in drug-induced liver disease. J. Clin. Pathol. 2009; 62(6): 481–92. https://doi.org/10.1136/jcp.2008.058248
- Repina E.F., Myshkin V.A., Karimov D.O., Khusnutdinova N.Yu., Kutlina T.G., Baygil’din S.S., et al. Comparative hepatoprotective efficiency of oximethyluracyl and bemythyl in hepatotoxicity. Meditsina truda i ekologiya cheloveka. 2019; (1): 78–81. https://doi.org/10.24411/2411-3794-2019-10013 (in Russian)
- Lazareva D.N., Alekhin E.K., Plechev V.V. Oxymethyluracil (immureg) – is an immunostimulant. Meditsinskiy vestnik Bashkortostana. 2007; 2(6): 70–5. (in Russian)
- Zhu R.Z., Di Xiang C.X., Li J.J., Hu J.J., He H.L., Yuan Y.S., et al. Protective effect of recombinant human IL-1Ra on CCl4-induced acute liver injury in mice. World J. Gastroenterol. 2010; 16(22): 2771–9. https://doi.org/10.3748/wjg.v16.i22.2771
- Grzhibovskiy A.M., Ivanov S.V., Gorbatova M.A. Analysis of nominal and ordinal data using Statistica and SPSS software. Nauka i zdravookhranenie. 2016; (6): 5–39. (in Russian)
- Naiki-Ito A., Asamoto M., Naiki T., Ogawa K., Takahashi S., Sato S., et al. Gap junction dysfunction reduces acetaminophen hepatotoxicity with impact on apoptotic signaling and connexin 43 protein induction in rat. Toxicol. Pathol. 2010; 38(2): 280–6. https://doi.org/10.1177/0192623309357951
- Blondet N.M., Messner D.J., Kowdley K.V., Murray K.F. Mechanisms of hepatocyte detoxification. In: Physiology of the Gastrointestinal Tract. Elsevier; 2018: 981–1001. https://doi.org/10.1016/B978-0-12-809954-4.00043-8
- Myshkin V.A., Enikeev D.A. Oxymethyluracil and experimental pathology of the liver. Meditsinskiy vestnik Bashkortostana. 2009; 4(2): 147–51. (in Russian)
- Aleksunes L.M., Slitt A.M., Cherrington N.J., Thibodeau M.S., Klaassen C.D., Manautou J.E. Differential expression of mouse hepatic transporter genes in response to acetaminophen and carbon tetrachloride. Toxicol. Sci. 2005; 83(1): 44–52. https://doi.org/10.1093/toxsci/kfi013
- Li M., Wang S., Li X., Kou R., Wang Q., Wang X., et al. Diallyl sulfide treatment protects against acetaminophen-/carbon tetrachloride-induced acute liver injury by inhibiting oxidative stress, inflammation and apoptosis in mice. Toxicol. Res. (Camb.) 2019; 8(1): 67–76. https://doi.org/10.1039/c8tx00185e
Arquivos suplementares
