Proteolisis status in the oral mucosa of rats after “mild” stress
DOI:
https://doi.org/10.12775/JEHS.2025.85.67653Keywords
stress, proteolysis, oral cavityAbstract
Background. Stress is one of the main causes of the development of most diseases. The role of proteolysis in the pathogenesis of post-stress reactions is not sufficiently elucidated.
Aim. To investigate the effect of “mild” stress on the state of proteolysis in the oral mucosa (OM).
Methods. Rats were subjected to “mild” stress by holding them at −20 °C for 5 minutes. In the OM, in blood serum, liver, kidneys and pancreas, proteolysis activity was determined by the rate of hydrolysis of two substrates: casein and BAEE (benzoyl-arginine ethyl ether).
Results. It has been established that OM has a high proteolytic activity, which begins to decrease already 5 hours after stress. In blood serum, on the contrary, the activity of proteolysis (substrate casein) increases after stress. The activity of BAEE-esterase does not change significantly after stress.
Conclusion. The level of proteolysis in OM is several times higher than the corresponding indicator for blood serum and rat liver. "Mild" stress causes an increase in the level of proteolysis in the blood serum as early as 5 hours after stress, while the level of proteolysis in the OM after stress tends to decrease. Activation of proteolysis in the blood after stress requires antiprotease actions using protease inhibitors.
References
1. Selye H. Stress and the General Adaptation Syndrome. Br. Med. J. 1950;1(4667):1383. doi:https://doi.org/10.1136/bmj.1.4667.1383
2. Goldstein DS, 1, Kopin IJ. Evolution of concepts of stress. Stress. 2007;10(2):109-120. doi: 10.1080/10253890701288935
3. Ray PD, Huang BW, Tsuji Y. Reactive Oxygen Species (ROS) Homeostasis and Redox Regulation in Cellular Signaling. Cellular Signalling. 2012;24:981-990. https://doi.org/10.1016/j.cellsig.2012.01.008
4. Reddy VP. Oxidative Stress in Health and Disease. Biomedicines. 2023;11(11): 2925. doi: 10.3390/biomedicines11112925
5. Rodney G, Swanson AL, Wheeler LM, Smith GN. The effect of a series of flavonoids on hyaluronidase and some other related enzymes. Journal of Biological Chemistry. 1950;183(2):739-747. DOI:10.1016/S0021-9258(19)51199-1
6. Lambert GP. Stress-induced gastrointestinal barrier dysfunction and its inflammatory effects. J Anim Sci. 2009;87(14):E101-108. doi: 10.2527/jas.2008-1339.
7. Levitsky AP. Digestive enzymes of the salivary glands / Abstract of a doctoral dissertation. Odessa, 1974:58. (in Russian).
8. Levitsky AP, Barabash RD, Vovchuk SV. Detection, isolation and properties of kallikrein from rat and golden hamster Grisatus suratus saliva. Journal of Evolutionary Biochemistry and Physiology. 1974;5:510-512. (in Russian)
9. Levitsky AP. Disbiotic syndrome: etiology, pathogenesis, clinic, prevention and treatment. Dentistry Bulletin. 2019;10(special issue):14-20. (in Russian)
10. Levitsky AP, Makarenko OA, Demyanenko SA. Methods of experimental dentistry. Simferopol, Tarpan, 2018:78. (in Russian)
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