Histological changes of adrenal gland under conditions of immobilization stress on the background of hypothyroidism

Authors

DOI:

https://doi.org/10.11603/bmbr.2706-6290.2022.4.13165

Keywords:

stress, adrenal gland, microscopic changes, hypothyroidism, endocrinocytes

Abstract

Summary. The action of the stress factor, regardless of its origin, causes a chain of protective reactions of the body. Adrenal gland is a stress-sensitive organ, the development of adaptation mechanisms under these conditions can be characterized by its morphological state.

The aim of the study – to investigate the features of histological changes in the adrenal glands of rats under the conditions of immobilization stress, which occurred on the background of experimental hypothyroidism.

Materials and Methods. The experiment was conducted on 20 sexually mature white male rats. Hypothyroidism was modeled by daily per os injection using a probe of the pharmacopoeial mercazole thyreostatics at a dose of 25 mg/kg during the 21st day. Immobilization stress was modeled by tying rats in a supine position by 4 limbs without restricting head mobility for 3 hours. The study was conducted 2 hours later (anxiety stage) after the end of the stressor. Histological studies were carried out according to generally accepted methods.

Results. Microscopic examination of the adrenal glands under conditions of immobilization stress revealed signs of destructive changes in the organ. Single blood-filled and dilated vessels were present. Cells with signs of destruction and swelling of the cytoplasm were determined. The presence of endocrinocytes with a small amount of lipid inclusions unevenly distributed in the cytoplasm of cells was characteristic. Microscopic studies of the adrenal glands 2 hours after the action of the stress factor on the background of hypothyroidism showed more significant changes in the structure of the organ. Perivascular edema was present. The connective tissue capsule was thickened. Single cells were necrotically altered and had pyknotic nuclei. Numerous endocrinocytes were poor in lipid inclusions, or completely devoid of them. In the medulla, there were destructively changed chromaffinocytes, with phenomena of edema and vacuolization of the cytoplasm. There were numerous blood vessels with blood-filled, dilated lumens.

Conclusions. Under conditions of stress, destructive changes in the structure of the organ were established, which were characterized by engorgement of blood vessels and swelling of their walls, destruction of endocrinocytes of all zones. Under the conditions of the combined effect of immobilization stress with hypothyroidism, more significant changes in the structure of the organ were observed – reorganization of the vessel walls, thickening of the organ capsule, disorganization of the structural components of the stroma of the organ, and the presence of destructively and necrotically altered endocrinocytes.

Author Biographies

I. M. Klishch, I. Horbachevsky Ternopil National Medical University

Doctor of Biological Sciences, Professor of the Department of Functional and Laboratory Diagnostics, I. Horbachevsky Ternopil National Medical University

P. H. Lykhatskyi, I. Horbachevsky Ternopil National Medical University

Doctor of Biological Sciences, Professor of the Department of Medical Biochemistry, I. Horbachevsky Ternopil National Medical University

H. O. Havryliuk-Skiba, О. Bohomolets National Medical University, Kyiv

PhD, Senior Teacher of the Department of Histology and Embryology, О. Boрomolets National Medical University

O. P. Andriyishyn, I. Horbachevsky Ternopil National Medical University

PhD, Associate Professor of the Department of Histology and Embryology, I. Horbachevsky Ternopil National Medical University

References

Walker C-D. Anand KJS, Plotsky PM. Development of the hypothalamic-pituitary-adrenal axis and the stress response. Comprehensive Physiology. 2011: 237-70.

Kanczkowski W, Sue M, Zacharowski K, Reincke M, Bornstein SR. The role of adrenal gland microenvironment in the HPA axis function and dysfunction during sepsis. Mol Cell Endocrinol. 2015;408: 241-8.

Di Lorenzo M, Barra T, Rosati L, Valiante S, Capaldo A, De Falco M, Laforgia V. Adrenal gland response to endocrine disrupting chemicals in fishes, amphibians and reptiles: a comparative overview. General and Comparative Endocrinology, 2020;297: 113-550. DOI:10.1016/j.ygcen. 2020.113550.

Berger I, Werdermann M, Bornstein SR, Steenblock C. The adrenal gland in stress – Adaptation on a cellular level. Journal of Steroid Biochemistry and Molecular Biology. 2019;1(190):198-206. DOI:10.1016/j.jsbmb.2019.04.006.

Tseilikman V, Komelkova M, Kondashevskaya MV, Manukhina E, Downey HF, Chereshnev V, et al. A rat model of post-traumatic stress syndrome causes phenotype-associated morphological changes and hypofunction of the adrenal gland. International Journal of Molecular Sciences. 2021;22(24): 13235. DOI:10.3390/ijms222413235.

Bali A, Jaggi AS. Preclinical experimental stress studies: protocols, assessment and comparison. Eur J Pharmacol 2015;746: 282-92. https://doi.org/https://doi.org/10.1016/j.ejphar.2014.10.017.

Brook ChGD, Clayton PE, R.S. Brown The adrenal cortex and its disorders. Brook's clinical pediatric endocrinology. 2010: 283-326.

Wang M, Milic M, Gericke A, Mercieca K, Liu H, Ruan Y, Jiang S, van Beers T, von Pein HD, Müller MB, Prokosch V. Chronic social defeat stress causes retinal vascular dysfunction. Exp Eye Res. 2021;213: 108853. DOI: 10.1016/j.exer.2021.108853. Epub 2021 Nov 18. PMID: 34800481.

Zaki SM, Abdelgawad FA, El-Shaarawy EAA, Radwan RAK, Aboul-Hoda BE. Stress-induced changes in the aged-rat adrenal cortex. Histological and histomorphometric study. Folia Morphol (Warsz). 2018;77(4): 629-641.

DOI: 10.5603/FM.a2018.0035. Epub 2018 Apr 3. PMID: 29611160.

Kozhemyakin YuM, Hromov OS, Filonenko MA, Sajfetdinova GA. Scientific and practical recommendations for keeping laboratory animals and working with them. [Науково-практичні рекомендації з утримання лабораторних тварин та роботи з ними] Kyiv: Interservis; 2017. Ukrainian.

Isman CA. Methimazole-induced hypothyroidism in rats ameliorates oxidative injury in experimental colitis. J Endocrinol. 2003;177(3): 471-6.

Argumedo GS, Sanz CR, Olguín HJ. Experimental models of developmental hypothyroidism. Horm Metab Res. 2012;44(2): 79-85. DOI: 10.1055/s-0031-1297941. Epub 2011 Dec 27. PMID: 22203441.

Lyubovich ОYe, Klishch IM. Features of the cytokine profile of rats blood in thedynamics of immobilization stress on the background of hypothyroidism. [Особливості цитокінового профілю крові щурів в динаміці іммобілізаційного стресу на тлі гіпотиреозу] Bulletin of Problems in Biology and Medicine-Вісник проблем біології та медицини. 2019;1(1): 140-4. Ukrainian.

Horalskyi LP, Khomych VT, & Kononskyi OI. Fundamentals of histological technique and morphofunctionalmethods of research in normal and pathology. [Основи гістологічної техніки і морфофункціональні методи досліджень у нормі та при патології]. Zhytomyr: Polissia; 2015. Ukrainian.

Zhurakivska OIa, Zhurakivskyi VM, Dutchak UM, Kulynych HB, Tkachuk YuL. [Morphofunctional changes in the adrenal glands in the early deadline of the development of streptosotocin diabetes mellitus]. Klin anatom i operat khirurhiia. 2019;2: 82-8. Ukrainian.

Kniazevych-Chorna TV, Mykhailiuk IO, Rudiak OM, Tarasevych NR. [The functional state of the adrenal glands in combination with their morphological restructuring at different stages of the post-hypothermic period]. Visn Vinnyts nats med univer. 2019;1(23): 41-5. DOI: 10.31393/reports-vnmedical-2019-23(1)-06.

Gannouni N, Mhamdi A, El May M, Tebourbi O, Rhouma KB. Morphological changes of adrenal gland and heart tissue after varying duration of noise exposure in adult rat. Noise Health 2014;16: 416-21. DOI: 10.4103/1463-1741.144424.

Published

2022-12-14

How to Cite

Klishch, I. M., Lykhatskyi, P. H., Havryliuk-Skiba, H. O., & Andriyishyn, O. P. (2022). Histological changes of adrenal gland under conditions of immobilization stress on the background of hypothyroidism . Bulletin of Medical and Biological Research, (4), 14–19. https://doi.org/10.11603/bmbr.2706-6290.2022.4.13165