ULTRASTRUCTURAL CHANGES OF THE PINEAL GLAND IN EPILEPSY

Authors

DOI:

https://doi.org/10.21856/j-PEP.2023.3.12

Keywords:

epilepsy, experimental epileptic seizures, pineal gland, melatonin

Abstract

Circadian mechanisms modulate neuronal excitability at several levels, and their destruction can cause excessive uncontrolled excitability. Previous studies have shown that epilepsy is associated with melatonin levels. Melatonin is a powerful chronobiotic secreted from the pineal gland; helps to maintain normal circadian rhythms and is used to treat some neurological and psychiatric disorders. Circadian rhythms and sleep/wake mechanisms play role in the epilepsy. Melatonin deficiency can decrease seizure threshold, and hence could increase seizure activity. The aim of the study was to identify ultrastructural changes in the pineal gland in an experimental model of epilepsy.

Materials and methods. The experiment was carried out on Wistar rats, 5-6 months of age, weight of about 200 g, 36 experimental and 10 control animals. Electrically provoked experimental epileptic seizures model in rats was reproduced. The rats developed spontaneous generalized seizures after 9-14 stimulations. Material for histological examinations was taken after stable formation (for >1 month) of repeated seizures. Ultrathin sections, after contrast with Reynolds lead citrate, were studied under an electron microscope at an accelerating voltage of 75 kV. The increase was selected adequate to the study and ranged from 20,000 to 60,000 times.

Results. Experimental studies have confirmed the presence of stable dystrophic, up to apoptosis of some cells, morphological changes of the pineal gland in the experimental model of epilepsy in rats, which is the reason for the decrease in its functional activity.

Conclusions. Our experimental data on the morphological changes of the pineal gland confirm the conclusion about a stable, possibly irreversible, decrease in gland function in epilepsy due to damage and disruption of the structure of its cells. Given the polyfunctionality of melatonin, its deficiency can be one of the causes of changes in neural networks, impaired permeability of synaptic membranes, and as a consequence, increased epileptic activity of neurons.

References

Fiest KM, Sauro KM, Wiebe S, et al. Neurology 2017;88: 296-303. https://doi.org/10.1212/WNL.0000000000003509.

Griffiths G, Fox JT. Lancet 1938;232(5999): 409-416. https://doi.org/10.1016/S0140-6736(00)41614-4.

Nilsonne G, Tamm S, Schwarz J, et al. Sci Rep 2017;7: 9422. https://doi.org/10.1038/s41598-017-09744-7.

Razavi B, Fisher RS. Sleep and Epilepsy. In Sleep and Neurologic Disease: 129-140, available at: https://medicinainternaelsalvador.com/wp-content/uploads/ 2017/ 8/7.-leep-and-Epilepsy.pdf.

Wan L, Shi XY, Ge WR, Sun YL, et al. Front Neurol 2020;11: 497225. https://doi.org/10.3389/fneur.2020.497225.

Quigg M. Epilepsy Res 2020;42: 43–55. https://doi.org/10.1016/S0920-1211(00)00157-1.

Durazzo TS, Spencer SS, Duckrow RB, et al. Neurology 2008;70: 1265-1271. https://doi.org/10.1212/01.wnl.0000308938.84918.3f.

Tchopev ZN, Yeh PH, Morgan GW, et al. Front Neurol 2018;9: 6. https://doi.org/ 10.3389/fneur.2018.00006.

Lambert I, Roehri N, Giusiano B, et al. Epilepsia 2018;59: 235-243. https://doi.org/ 10.1111/epi.13958.

Kumar J, Solaiman A, Mahakkanukrauh P, et al. Front Pharmacol 2018;9: Article 1088. https://doi.org/10.3389/fphar.2018.01088.

Albrecht U. Neuron 2012;74(2): 246-260. https://doi.org/10.1016/j.neuron.2012.04.006.

Ko GY, Shi L, Ko ML. J Neurochemistry 2009;110(4): 1150-1169. https://doi.org/10.1111/j.1471-4159.2009.06223.x.

Itri JN. Vosko AM, Schroeder A, et al. J Neurophysiol 2010;103(2): 632-640. https://doi.org/10.1152/jn.00670.2009.

Gachon F, Fonjallaz P, Damiola F, et al. Genes Development 2004;18(12): 1397-1412. https://doi.org/10.1101/gad.301404.

Canales MT, Holzworth M, Bozorgmehri S, et al. Physiol Genomics 2019;51: 77-82. https://doi.org/10.1152/physiolgenomics.00091.2018.

Moyanova S, De Fusco A, Santolini I, et al. Int J Mol Sci 2018;19: 1973. https://doi.org/10.3390/ijms19071973.

Mosi´nska P, Socała K, Nieoczym D, et al. Behav Brain Res 2016;307: 199-207. https://doi.org/10.1016/j.bbr.2016.03.036.

Gerstner JR, Smith GG, Lenz O, et al. Front Syst Neurosci 2014;8: 121. https://doi.org/10.3389/fnsys.2014.001.

Li P, Fu X, Smith NA, et al. Neuron 2017;96: 387-401. https://doi.org/10.1016/j.neuron.2017.09.044.

Ramanathan C, Kathale ND, Liu D, et al. PLoS Genet 2018;14: e1007369. https://doi.org/10.1371/journal.pgen.1007369.

Koene L, van Grondelle SE, Proietti OM, et al. Ann Clin Transl Neurol 2019;6: 1273-1291. https://doi.org/10.1002/acn3.50829.

Ricos MG, Hodgson BL, Pippucci T, et al. Ann Neurol 2016;79: 120-131. https://doi.org/10.1002/ana.245.

International guiding principles for biomedical research involving animals. Counsil for International Organizations of Medical Sciences (CIOMS), Geneva, 1985, available at: https://cioms.ch/publications/product/international-guiding-principles-for-biomedical-research-involving-animals-2/.

Guide for the care and use of laboratory animals. National Academy press, Washington, 1996, available at: http://www.nap.edu/openbook.php?record_id=5140&page=8.

Reiter RJ, Sharma R, Rosales-Corral SA, et al. Advances in Characterizing Recently-Identified Molecular Actions of Melatonin: Clinical Implications. In: Bizzarri M (ed.), Approaching Complex Diseases, Human Perspectives in Health Sciences and Technology 2, Springer Nature Switzerland AG, 2020. https://doi.org/10.1007/978-3-030-32857-3_14.

Guo JF, Yao BZ. Chinese J Contemporary Pediatrics 2009;11(4): 288-290.

Bazil CW, Short D, Crispin D, Zheng W. Neurology 2000;55(11): 1746-1748. https://doi.org/10.1212/wnl.55.11.1746.

Molina-Carballo A, Muñoz-Hoyos A, Sánchez-Forte M, et al. Neuropediatrics 2007;38(3): 122-125. https://doi.org/10.1055/s-2007-985138.

Schapel GJ, Beran RG, Kennaway DL, et al. Epilepsia 1995;36(1): 75-78. https://doi.org/10.1111/j.1528-1157.1995.tb01669.x.

Ardura J, Andres J, Garmendia JR, Ardura F. J Child Neurol 2010;25(7): 888-891. https://doi.org/10.1177/0883073809351315.

Fauteck J, Schmidt H, Lerchl A, et al. Biol Sign Recept 1999;8(1-2): 105-110. https://doi.org/10.1159/000014577.

Peled N, Shorer Z, Peled E, Pillar G. Epilepsia 2001;42(9): 1208-1210. https://doi.org/10.1046/j.1528-1157.2001.28100.x.

Jou MJ, Peng TI, Reiter RJ, et al. J Pineal Res 2004;37: 55-70. https://doi.org/10.1111/j.1600-079X.2004.00140.x.

Karbowski M, Youle RJ. Curr Opin Cell Biol 2011;23(4): 476-482. https://doi.org/10.1016/j.ceb.2011.05.007.

Lacoste B, Angeloni D, Dominguez-Lopez S, et al. J Pineal Res 2015;58(4): 397-417. https://doi.org/10.1111/jpi.12224.

Bhattacharya P, Pandey AK, Paul S, Patnaik R. Life Sci 2014;100(2): 97-109. https://doi.org/10.1016/j.lfs.2014.01.085.

Hardeland R. Int J Molec Sci 2019;20(5): 1223. https://doi.org/10.3390/ijms20051223.

Domínguez-Alonso A, Valdés-Tovar M, Solís-Chagoyán H, Benítez-King G. Int J Molec Sci 2015;16(1): 1907-1927. https://doi.org/10.3390/ijms16011907.

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Published

2023-09-15

How to Cite

Litovchenko, T., Dubenko, A., Sazonov, S., Florikian, V., Zavalna, O., & Sukhonosova, O. (2023). ULTRASTRUCTURAL CHANGES OF THE PINEAL GLAND IN EPILEPSY. Problems of Endocrine Pathology, 80(3), 94–104. https://doi.org/10.21856/j-PEP.2023.3.12

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