Cellular Composition of Rat Thymus with Combined Effects of Carcinogen and Stress
https://doi.org/10.18499/2225-7357-2019-8-2-47-54
Abstract
The aim of the research was study the effects of experimental breast cancer and stress on the thymus of laboratory animals
Material and methods. Thymus 40 white nonlinear female rats of the same age were investigated using luminescent-histochemical, general histological and immunohistochemical methods . The animals were divided into 3 groups. In the 1st group were intact animals. Rats of the 2nd group were injected with N-methyl-N-nitrosourea, causing breast cancer. Animals of the 3rd group experienced a combined effect of carcinogen and water-immobilization stress.
Results. It was established that the administration of N-methyl-N-nitrosourea to female rats causes an increase in the size of the medullar and cortex of the thymus lobes. In cells of the premedullary and subcapsular zones, an increase in the level of serotonin and catecholamines is observed, and in cells of the premedullary zone, in the thymocytes of the cortex and medulla - a decrease in the level of histamine. The ratio (serotonin + histamine) / catecholamines decreases and the percentage of degranulated mast cells increases. Also, the number of mature T-lymphocytes and macrophages is increasing against the background of a decrease in the number of S-100+ cells. Combined effect of factors revealed a decrease in the size of the lobes of the organ, the replacement of the parenchyma with adipose and connective tissue, an increase in the content of serotonin and catecholamines, a significant decrease in histamine levels, with a decrease in the ratio (serotonin + histamine) / catecholamines in the same cells, an increase in mature forms of T-lymphocytes and macrophages, as well as a decrease in the percentage of dendritic cells.
Conclusion. The combined effect causes a more pronounced disorganization of the morphofunctional state of the thymus and leads to the 4th phase of the accidental involution of the thymus with the development of atrophy and sclerosis of the organ.
About the Authors
A. A. KotelkinaRussian Federation
Anastasiya Kotelkina
Moskovskii prospekt, 45, Cheboksary, Chuvash Republic , 428017
O. Yu. Kostrova
Russian Federation
Cheboksary
L. M. Merkulova
Russian Federation
Cheboksary
G. Yu. Struchko
Russian Federation
Cheboksary
M. N. Mikhailova
Russian Federation
Cheboksary
References
1. Keskinov АА, Shurin MR, Bukhman VM, Shprakh ZS. Impact of tumor-derived factors on dendritic cells in cancer. Russian Journal of Biotherapy. 2017; 16 (1): 12-23 (in Russian).
2. Kit OI, Zlatnik EYu, Nikipelova ЕА, Gevorkyan YuA, Averkin MA, Novikova IA, Dashkov AV. Peculiarities of general and local immunity at solitary and synchronous primary-multiple colon cancer. Modern problems of science and education. 2012; 5:38 (in Russian).
3. Kostrova OYu. Accidental thymic involution in rats in the background of a colon adenocarcinoma induced by administration of a carcinogen in different given dose. Fundamental research. 2013; 3-2:321-4 (in Russian).
4. Kostrova OYu, Stomenskaya IS, Merkulova LM, Struchko GYu, Mikhajlova MN, Lukiyanov MV, Filippov FN. Changes in adrenal glands of female rats with the combinet effect of carcinogen and stress. Stroenie organizma cheloveka i zhivotnykh v norme, patologii i ehksperimente. Minsk, 2017: 295-9 (in Russian).
5. Krokhina EM, Aleksandrov PN. Simpaticheskiy (adrenergicheskiy) komponent effektornoy innervatsii serdechnoy myshtsy. Kardiologiya. 1969; 3:97-102 (in Russian).
6. Lebedev KA, Ponyakina ID. Immunophysiological mechanisms of the origin and maintenance of tumor growth in humans. Human Physiology. 2010; 36(4):373-81 (in Russian).
7. Matkina O.V. Pathohistological changes in inbred white rats thymus and spleen during acute stress. Perm Medical Journal. 2014; 31(1):121-8 (in Russian).
8. Moskvichev EV, Merkulova LM, Struchko GYu, Mikhajlova MN, Kostrova OYu. Age-related involution and acute thymic atrophy in experimental carcinogenesis. Journal of Volgograd State Medical University. 2014; 3 (51):127-9 (in Russian).
9. Parakhonskij AP. Mekhanizmy povysheniya ehffektivnosti protivoopukholevogo immuniteta. V mire nauchnykh otkrytij: materialy XVI mezhdunarodnoj nauchno-prakticheskoj konferentsii: sbornik nauchnykh trudov. Moscow; 2015: 21-6 (in Russian).
10. Pirs E. Histochemistry theoretical and applied. Moscow: 1962. 962 (in Russian).
11. Rodzaevskaya EB. Peculiarities of the thymus accidental involution under plumbum acetate-containing ration at experiment. Natural sciences. 2017; 4:166-71 (in Russian).
12. Skotarenko LV, Vorotnikov IK, Kadagidze ZG, Shamilov FA. The specific features of T cell immunity in breast cancer. Tumors of female reproductive system. 2011; 4:24-8 (in Russian).
13. Solopova A, Idrisova L, Chukanova E, Alipov V. Neuroimmunology in oncology: impact of stress on disease. Vrach. 2017; 9:14-16 (in Russian).
14. Tillyashajkhov MN, Kamyshov SV. Osobennosti kletochnogo statusa immuniteta u bol'nykh rakom shejki matki. European Science. 2018; 5 (37): 75-80 (in Russian).
15. Frantsiyants EM, Kaplieva IV, Trepitaki LK, Cheryarina ND. Correlation between some growth factors and hormones in blood of rats during liver metastasis. Modern problems of science and education. 2015; 3:205 (in Russian).
16. Shalyapina VG, Vershinina EA, Rakitskaya VV, Ryzhova LYu, Semenova MG, Semenova OG. Alteration of active and passive Wistar rats adaptive behavior in water-immersion model of depression. Zh Vyssh Nerv Deiat Im I P Pavlova. 2006 Jul-Aug;56(4):543-7] (in Russian).
17. Bojkova B, Kajo K, Kubatka P, Solar P, Pec M, Adamkov M. Metformin and melatonin improve histopathological outcome of NMU-induced mammary tumors in rats. Pathol Res Pract. 2019; 215(4):722-9. doi:i0.i0i6/j.prp.20i9.0i.007
18. Cross SAM, Ewen SWB., Rost EWD. A study of the methods owailable for the cytochemical Fnflam-matory of histamine by fluorescence induced with o-phthalaldehyde or acetaldehyde. J. Histochem. 1971; 6:471-6.
19. Csaba G. The immunoendocrine thymus as a pacemaker of lifespan. Acta Microbiologica et Immunologica. 2016; 63(2):139-58.
20. Faustino-Rocha А, Gama А, Neuparth М, et al. Mast Cells in Mammary Carcinogenesis: Host or Tumor Supporters. Anticancer Res. 2017; 37(3):1013-21.
21. Kazakov OV, Kabakov AV, Ishchenko IY, Pove-shchenko AF, Raiter TV, Strunkin DN, Konenkov VI. The Thymus in Experimental Mammary Carcinogenesis and Polychemotherapy. Bulletin of Experimental Biology and Medicine. 2017; 162(4): 479-82. doi:10.1007/s10517-017-3644-y
22. Wang W, Xu ZZ, Costanzo M, Boone C, Lange CA, Myers CL. Pathway-based discovery of genetic interactions in breast cancer PLoS Genet. 2017; 13(9). doi:i0.i37i/journal.pgen.i006973
Review
For citations:
Kotelkina A.A., Kostrova O.Yu., Merkulova L.M., Struchko G.Yu., Mikhailova M.N. Cellular Composition of Rat Thymus with Combined Effects of Carcinogen and Stress. Journal of Anatomy and Histopathology. 2019;8(2):47-54. (In Russ.) https://doi.org/10.18499/2225-7357-2019-8-2-47-54