Biochemical state of brain-liver axis of rats under restraint-induced stress and 2-oxoglutarate impact

  • O. Dyomshyna Oles Honchar Dnipro National University
  • O. Dovban Oles Honchar Dnipro National University
  • G. Ushakova Oles Honchar Dnipro National University
Keywords: restraint-induced stress; antioxidant system; catalase; superoxide dismutase; cytochrome C; liver; brain; 2-oxoglutarate.

Abstract

Environmental factors play a significant role in affecting the overall health of organisms, with stress being a notable contributor. The process of urbanization and globalization in modern society introduces additional stressors, exacerbating population health issues. Consequently, there is a need for thorough examination, analysis, and exploration of strategies to mitigate the adverse effects of stress. 2-Oxoglutarate, an essential intracellular metabolite and mediator with metabolite trophic properties, emerges as a promising candidate for intervention. In this study, we aimed to evaluate the combined impact of restraint-induced stress and 2-oxoglutarate on the oxidative-reducing balance, antioxidant system effectiveness, and the functional status of the liver and brain in rats. Restraint-induced stress was found to elevate oxidative stress levels, as evidenced by increased concentrations of malonic dialdehyde and oxidative-modified proteins, particularly in the brain. Additionally, signs of lactic acidosis were observed in the liver, indicating physiological changes in response to stress. Furthermore, restraint-induced stress significantly altered bioenergy components, with decreased superoxide dismutase activity and increased cytochrome C concentration, potentially indicating mitochondrial dysfunction and increased membrane permeability. The incorporation of a 2% solution of 2-oxoglutarate into the diet demonstrated a reduction in malonic dialdehyde and carbonylated protein formation, leading to more effective restoration of oxidative-reducing balance in the brain compared to the liver. Additionally, normalization of the lactate/pyruvate concentration ratio and decreased lactate dehydrogenase activity, alongside elevated alanine aminotransferase levels, suggested a decrease in oxidative stress in the liver. Moreover, exogenous 2-oxoglutarate exhibited a positive effect on superoxide dismutase activity and cytochrome C concentration, indicating a reduction in oxidative tension in the liver and progressive mitochondrial function recovery. Based on these findings, exogenous 2-oxoglutarate emerges as a promising metabolitotrope and adaptogen for managing oxidative stress and improving mitochondrial function.

References

Andreeva, L. Y., Kozhemjakyn, L. A., & Kyshkun, A. A. (1988). Modification of the method for the determination of lipid peroxides in the test with thiobarbituric acid. Laboratornoe Delo, 2, 41–43 (in Russian).

Arulselvan, P., Fard, M. T., Tan, W. S., Gothai, S., Fakurazi, S., Norhaizan, M. E., & Kumar, S. S. (2016). Role of antioxidants and natural products in inflammation. Oxidative Medicine and Cellular Longevity, 2016, 5276130.

Baulies, A., Montero, J., Matías, N., Insausti, N., Terrones, O., Basañez, G., Vallejo, C., Conde de La Rosa, L., Martinez, L., Robles, D., Morales, A., Abian, J., Car-rascal, M., Machida, K., Kumar, D. B. U., Tsukamoto, H., Kaplowitz, N., Gar-cia-Ruiz, C., & Fernández-Checa, J. C. (2018). The 2-oxoglutarate carrier pro-motes liver cancer by sustaining mitochondrial GSH despite cholesterol loading. Redox Biology, 14, 164–177.

Bayliak, M. M., & Lushchak, V. I. (2021). Pleiotropic effects of alpha-ketoglutarate as a potential anti-ageing agent. Ageing Research Reviews, 66, 101237.

Bhattacharya, R., Gujar, N. L., Kumar, D., & John, J. J. (2017). Protective efficacy of various carbonyl compounds and their metabolites, and nutrients against acute toxicity of some cyanogens in rats: Biochemical and physiological studies. In-terdisciplinary Toxicology, 10(1), 1–10.

Burtis, C. A., Ashwood, E. R., & Bruns, D. E. (Eds.). (2007). Tietz fundamentals of clinical chemistry. 6th ed. Saunders Elsevier, St. Louis.

Chen, Z., Tian, R., She, Z., Cai, J., & Li, H. (2020). Role of oxidative stress in the pathogenesis of nonalcoholic fatty liver disease. Free Radical Biology and Medicine, 152, 116–141.

Choi, S., & Swanson, J. M. (1995). Interaction of cytochrome с with cardiolipin: An infrared spectroscopic study. Biophysical Chemistry, 54, 271–278.

Ding, J. H., Jin, Z., Yang, X. X., Lou, J., Shan, W. X., Hu, Y. X., Du, Q., Liao, Q. S., Xie, R., & Xu, J. Y. (2020). Role of gut microbiota via the gut-liver-brain axis in digestive diseases. World Journal Gastroenterology, 26, 6141–6162.

Diniz, L. R. L., Bezerra Filho, C. D. S. M., Fielding, B. C., & de Sousa, D. P. (2020). Natural antioxidants: A review of studies on human and animal coronavirus. Oxidative Medicine and Cellular Longevity, 2020, 3173281.

D'Mello, C., & Swain, M. G. (2011). Liver-brain inflammation axis. American Journal of Physiology-Gastrointestinal and Liver Physiology, 301(5), 749–761.

Dyomshyna, O. O., Ushakova, G. A., & Stepchenko, L. M. (2017). The effect of biologically active feed additives of humilid substances on the antioxidant sys-tem in liver mitochondria of gerbils. Regulatory Mechanisms in Biosystems, 8(2), 185–190.

Ehtramolsadat, S., Maghsoud Peeri, M., Hosseini, M.-J., & Azarbyjani, M. A. (2018). Cardiac oxidative stress following maternal separation stress was miti-gated following adolescent voluntary exercise in adult male rats. Physiology and Behavior, 183, 39–45.

Giuffrè, M., & Moretti, R. (2023). The gut-liver-brain axis: From the head to the feet. International Journal of Molecular Sciences, 24(21), 15662.

Gong, S., Miao, Y. L., Jiao, G. Z., Sun, M. J., Li, H., Lin, J., Luo, M. J., & Tan, J. H. (2015). Dynamics and correlation of serum cortisol and corticosterone under different physiological or stressful conditions in mice. PLoS One, 10(2), e0117503.

Hendricks, B., Quinn, T. D., Price, B. S., Dotson, T., Claydon, E. A., & Miller, R. (2023). Impact of stress and stress mindset on the prevalence of cardiovascular disease risk factors among first responders. BMC Public Health, 23(1), 1929.

Koroliuk, M. A., Ivanova, L. I., Mayorova, I. G., & Tokarev, V. E. (1988). A method of determining catalase activity. Laboratornoe Delo, 1, 16–19 (in Russian).

Kostjuk, V. A., Potapovych, A. Y., & Kovaleva, Z. V. (1990). Prostoy i chuvstvi-tel'nyy metod opredeleniya aktivnosti superoksiddismutazy, osnovannyy na reaktsii okisleniya kvertsetina [A simple and sensitive method for determining the activity of superoxide dismutase, based on the oxidation reaction of quercetin]. Questions of Medical Chemistry, 36(2), 88–91 (in Russian).

Kovalenko, T. N., Ushakova, G. A., Osadchenko, I., Skibo, G. G., & Pierzynowski, S. G. (2011). The neuroprotective effect of 2-oxoglutarate in the experimental ischemia of hippocampus. Journal Physiology Pharmacology, 62(2), 239–246.

Li, S., Li, H., Xu, X., Saw, P. E., & Zhang, L. (2020). Nanocarrier-mediated antioxi-dant delivery for liver diseases. Theranostics, 10(3), 1262–1280.

Lushchak, V. I. (2014). Free radicals, reactive oxygen species, oxidative stress and its classification. Chemico-Biological Interactions, 224, 164–175.

Lushchak, V. I. (2015). Free radicals, reactive oxygen species, oxidative stresses and their classifications. Ukrainian Biochemical Journal, 87(6), 11–18.

Lushchak, V. I., Semchyshyn, H. M., & Lushchak, O. V. (2011). The classic methods to measure oxidative damage: Lipid peroxides, thiobarbituric acid reactive substances, and protein carbonyls. In: Abele, D., Vázquez-Medina, J.P., & Zenteno-Savín, T. (Eds.). Oxidative stress in aquatic ecosystems. John Wiley & Sons, Inc., New Jersey. Pp. 420–431.

Majmundar, A. J., Wong, W. J., & Simon, M. C. (2010). Hypoxia-inducible factors and the response to hypoxic stress. Molecular Cell, 40(2), 294–309.

Mariño, G., Pietrocola, F., Eisenberg, T., Kong, Y., Malik, S. A., Andryushkova, A., Schroeder, S., Pendl, T., Harger, A., Niso-Santano, M., Zamzami, N., Scoazec, M., Durand, S., Enot, D. P., Fernández, Á. F., Martins, I., Kepp, O., Senovilla, L., Bauvy, C., Morselli, E., & Kroemer, G. (2014). Regulation of autophagy by cytosolic acetyl-coenzyme A. Molecular Cell, 53(5), 710–725.

Mifsud, K. R., & Reul, J. M. H. M. (2018). Mineralocorticoid and glucocorticoid receptor-mediated control of genomic responses to stress in the brain. Stress, 21(5), 389–402.

Munujos, P., Coll-Cantí, J., González-Sastre, F., & Gella, F. J. (1993). Assay of succinate dehydrogenase activity by a colorimetric-continuous method using iodonitrotetrazolium chloride as electron acceptor. Analytical Biochemistry, 212(2), 506–509.

Nguyen, H. H., & Swain, M. G. (2023). Avenues within the gut-liver-brain axis linking chronic liver disease and symptoms. Frontiers in Neuroscience, 17, 1171253.

Okuyama, J., Seto, S., Fukuda, Y., Funakoshi, S., Amae, S., Onobe, J., Izumi, S., Ito, K., & Imamura, F. (2021). Mental health and physical activity among children and adolescents during the covid-19 pandemic. The Tohoku Journal of Experimental Medicine, 253(3), 203–215.

Osborne, M. T., Shin, L. M., Mehta, N. N., Pitman, R. K., Fayad, Z. A., & Tawakol, A. (2020). Disentangling the links between psychosocial stress and cardiovascular disease. Circulation: Cardiovascular Imaging, 13(8), e010931.

Pandurangan, M., & Kim, D. H. (2015). ZnO nanoparticles augment ALT, AST, ALP and LDH expressions in C2C12 cells. Saudi Journal Biological Science, 22(6), 679–684.

Panov, A., & Orynbayeva, Z. (2018). Determination of mitochondrial metabolic phenotype through investigation of the intrinsic inhibition of succinate dehydrogenase. Analytical Biochemistry, 552, 30–37.

Rostami, R., Eslamifar, Z., Nazemi, S., Hosseini, S. Z., Behvandi, M. M., & Jafari-pour, L. (2022). The effect of thyme essential oil on liver injuries caused by renal ischemia-reperfusion in rats. BioMed Research International, 2022, 2988334.

Samad, N., Ali, A., Yasmin, F., Ullah, R., & Bari, A. (2020). Behavioral and bio-chemical effects of Makia madrespatana following single immobilization stress on rats. Medicina (Kaunas), 56(7), 350.

Satpute, R., Lomash, V., Hariharakrishnan, J., Rao, P., Singh, P., Gujar, N., & Bhat-tacharya, R. (2014). Oxidative stress and tissue pathology caused by subacute exposure to ammonium acetate in rats and their response to treatments with al-pha-ketoglutarate and N-acetyl cysteine. Toxicology and Industrial Health, 30(1), 12–24.

Sawa, K., Uematsu, T., Korenaga, Y., Hirasawa, R., Kikuchi, M., Murata, K., Zhang, J., Gai, X., Sakamoto, K., Koyama, T., & Satoh, T. (2017). Krebs cycle inter-mediates protective against oxidative stress by modulating the level of reactive oxygen species in neuronal ht22 cells. Antioxidants, 6(1), 21.

Selen, E. S., Rodriguez, S., Cavagnini, K. S., Kim, H. B., Na, C. H., & Wolfgang, M. J. (2022). Requirement of hepatic pyruvate carboxylase during fasting, high fat, and ketogenic diet. The Journal of Biological Chemistry, 298(12), 102648.

Semchyshyn, H. M., & Lushchak, V. I. (2012). Interplay between oxidative and carbonyl stresses: Molecular mechanisms, biological effects and therapeutic strategies of protection. In: Lushchak, V. I., & Semchyshyn, H. M. (Eds.). Oxidative stress – molecular mechanisms and biological effects. IntechOpen Limited, London. Pp. 15–46.

Shobatake, R., Ota, H., Takahashi, N., Ueno, S., Sugie, K., & Takasawa, S. (2022). The impact of intermittent hypoxia on metabolism and cognition. International Journal of Molecular Science, 23(21), 12957.

Song, T., Song, X., Zhu, C., Patrick, R., Skurla, M., Santangelo, I., Green, M., Harper, D., Ren, B., Forester, B. P., Öngür, D., & Du, F. (2021). Mitochondrial dys-function, oxidative stress, neuroinflammation, and metabolic alterations in the progression of Alzheimer's disease: A meta-analysis of in vivo magnetic reson-ance spectroscopy studies. Ageing Research Reviews, 72, 101503.

Stepchenko, L., Dyomshyna, O., & Ushakova, G. (2021). The impact of the humate nature feed additives on the antioxidative status of erythrocytes, liver, and muscle in chickens, hens, and gerbils. Biointerface Research in Applied Chemistry, 11(5), 13202–13213.

Su, Y., Wang, T., Wu, N., Li, D., Fan, X., Xu, Z., Mishra, S. K., & Yang, M. (2019). Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and acti-vating AMPK. Aging, 11(12), 4183–4197.

Tkachenko, V., Kovalchuk, Y., Bondarenko, N., Bondarenko, О., Ushakova, G., & Shevtsova, A. (2018). The cardio- and neuroprotective effects of corvitin and 2-oxoglutarate in rats with pituitrin-isoproterenol-induced myocardial damage. Biochemistry Research International, 2018, 9302414.

Waller-Evans, H., Hue, C., Fearnside, J., Rothwell, A. R., Lockstone, H. E., Caldéra-ri, S., Wilder, S. P., Cazier, J. B., Scott, J., & Gauguier, D. (2013). Nutrigenomics of high-fat diet-induced obesity in mice suggests relationships between sus-ceptibility to fatty liver disease and the proteasome. PLoS One, 8, e82825.

Wang, X., & Michaelis, E. K. (2010). Selective neuronal vulnerability to oxidative stress in the brain. Frontiers in Aging Neuroscience, 2, 12.

Warillea, A. A., Altunc, G., Elamina, A. A., Kaplanc, A. A., Mohameda, H., Yurtc, K. K., & Elhaj, A. E. (2017). Skeptical approaches concerning the effect of ex-posure to electromagnetic fields on brain hormones and enzyme activities. Journal of Microscopy and Ultrastructure, 5, 177–184.

Weiner, H. (1996). Use of animal models in peptic ulcer disease. Psychosomatic Medicine, 58(6), 524–545.

Yaribeygi, H., Panahi, Y., Sahraei, H., Johnston, T. P., & Sahebkar, A. (2017). The impact of stress on body function: A review. EXCLI Journal, 16, 1057–1072.

Zdzisińska, B., Żurek, A., & Kandefer-Szerszeń, M. (2017). Alpha-ketoglutarate as a molecule with pleiotropic activity: Well-known and novel possibilities of therapeutic use. Archivum Immunologiae et Therapiae Experimentalis, 65(1), 21–36.

Zeng, X., Wu, J., Wu, Q., & Zhang, J. (2015). L-malate enhances the gene expres-sion of carried proteins and antioxidant enzymes in the liver of aged rats. Phy-siological Research, 64(1), 71–78.

Zhao, J., Jiang, Y., Sun, X., Liu, X., Liu, F., Song, M., & Zhang, L. (2020). The mechanism and role of intracellular α-ketoglutarate reduction in hepatic stellate cell activation. Bioscience Reports, 40(3), BSR20193385.

Published
2024-04-29
How to Cite
Dyomshyna, O., Dovban, O., & Ushakova, G. (2024). Biochemical state of brain-liver axis of rats under restraint-induced stress and 2-oxoglutarate impact . Regulatory Mechanisms in Biosystems, 15(2), 306-314. https://doi.org/10.15421/022444