Renal effects of the sulfur-containing aminoacid derivatives (ademetionine, taurin and glutathion) in conditionally healthy animals
DOI:
https://doi.org/10.24959/cphj.18.1472Keywords:
renal effects, ademetionine, taurine, glutathioneAbstract
Derivatives of sulfur-containing aminoacids (ademetionin, taurine and glutathione) selected for the experimental studies are used in various fields of practical medicine due to their multifaceted pleiotropic effects. The study of their renal effects in the conditions of the physiological norm makes it possible to expand and supplement their pharmacological characteristics, and forms the basis for further study of the nephroprotective potential in renal pathology.
Aim. To study the effect of sulfur-containing amino acid derivatives (ademetionine, taurine andglutathione) on the morphofunctional state of the rat kidneys in the daily administration for 7 days.
Materials and methods. The experiments were performed on mature non-linear white rats weighing 130-180 g. Animals were divided into 4 groups (n = 7): group I – intact control, group II – animals which were given ademetionine (“Geptral”, “Abbott SpA”, Italy) in the dose of 20 mg/kg, group III – animals received taurine (“Sigma-Aldrich”, USA) in the dose of 100 mg/kg, group IV – animals received glutathione (“TAD 600”, “Biomedica Foscama”, Italy) in the dose of 30 mg/kg. All drugs were injected intramuscularly for 7 days.
Results. The study of the renal effects of the sulfur-containing amino acid derivatives (SAD) under research in the daily administration for 7 days to conditionally healthy animals showed that these drugs had a weak diuretic effect, which was probably due to a decreased tubular reabsorption of water without significant changes in the glomerular filtration rate. Besides, the use of ademetionine resulted in a slight reduction of azotemia. There was not any significant change in the acid regulatory kidney function under the effect of SAD. Administration of ademetionine, taurine and glutathione resulted in a significant decrease in proteinuria, which was probably caused by the effect on the processes of protein reabsorption. The effect on the ion regulatory kidney function upon the course of SAD administration was characterized by an increase in urinary sodium excretion against the background of decreased relative sodium reabsorption, which was accompanied by intensification of distal transport of sodium ions due to the activation of the tubular-tubular balance. The morphological examination did not reveal any histopathological changes in the renal tissue, confirming the absence of nephrotoxicity of the SAD studied.
Conclusions. According to the data obtained the 7-day administration of ademetionine, taurine and glutathione to conditionally healthy animals moderately affects the processes of glomerular filtration and tubular transport in nephrons, which results in a slight increase in diuresis along with preservation of the renal mechanisms of autoregulation and the absence of histopathological changes in the kidneys.
References
Semidotckaia, Zh. D., Cherniakova, I. A., Pionova, E. N., Trifonova, N. S. (2017). East European Journal of Internal and Family Medicine, 1, 10–16.
Dennis, J. M., Witting, P. K. (2017). Protective Role for Antioxidants in Acute Kidney Disease. Nutrients, 9(7), 718. https://doi.org/10.3390/nu9070718
Ratliff, B. B., Abdulmahdi, W., Pawar, R., & Wolin, M. S. (2016). Oxidant Mechanisms in Renal Injury and Disease. Antioxidants & Redox Signaling, 25(3), 119–146. https://doi.org/10.1089/ars.2016.6665
Yurev, K. L. (2012). Ukrainskyi medychnyi chasopys, 1 (87), 10–16.
Zviahyntseva, T. D., Chernobai, A. Y., Hlushchenko, S. V. (2014). Ukrainskyi medychnyi chasopys, 3 (101), 56–59.
Anstee, Q. M., & Day, C. P. (2012). S-adenosylmethionine (SAMe) therapy in liver disease: A review of current evidence and clinical utility. Journal of Hepatology, 57(5), 1097–1109. https://doi.org/10.1016/j.jhep.2012.04.041
Geptral instrukciya, zastosuvannya preparatu. (n.d.). Available at: http://mozdocs.kiev.ua/likivi ew.php?id=31805
Traverso, N., Ricciarelli, R., Nitti, M., Marengo, B., Furfaro, A. L., Pronzato, M. A., … Domenicotti, C. (2013). Role of Glutathione in Cancer Progression and Chemoresistance. Oxidative Medicine and Cellular Longevity, 2013, 1–10. https://doi.org/10.1155/2013/972913
Saliga, N. O. (2013). Ukraïns’kij bìofarmacevtičnij žurnal, 85 (4), 40–47.
Forman, H. J., Zhang, H., & Rinna, A. (2009). Glutathione: Overview of its protective roles, measurement, and biosynthesis. Molecular Aspects of Medicine, 30(1-2), 1–12. https://doi.org/10.1016/j.mam.2008.08.006
Lushchak, V. I. (2012). Glutathione Homeostasis and Functions: Potential Targets for Medical Interventions. Journal of Amino Acids, 2012, 1–26. https://doi.org/10.1155/2012/736837
Hepaval. (n.d.). Available at: https://compendium.com.ua/info/220085/gepaval/
Ostapiv, R. D., Kystsiv, O. S., Manko, V. V. (2015). Visnyk Lvivskoho universytetu seriia Biolohiia, 69, 247–255.
Lambert, I. H., Kristensen, D. M., Holm, J. B., & Mortensen, O. H. (2014). Physiological role of taurine - from organism to organelle. Acta Physiologica, 213(1), 191–212. https://doi.org/10.1111/apha.12365
Yan-Jun, Xu., Amarjit, S. A., Paramjit, S. T., Naranjan, S. D. (2008). The potential health benefits of taurine in cardiovascular disease. Exp Clin Cardiol, 13(2), 57–65.
Kumari, N., Prentice, H., & Wu, J.-Y. (2013). Taurine and Its Neuroprotective Role. Taurine 8, 19–27. https://doi.org/10.1007/978-1-4614-6130-2_2
Shimada, K., Jong, C. J., Takahashi, K., & Schaffer, S. W. (2015). Role of ROS Production and Turnover in the Antioxidant Activity of Taurine. Advances in Experimental Medicine and Biology, 803, 581–596. https://doi.org/10.1007/978-3-319-15126-7_47
Taufon, instruktsiia, zastosuvannia preparatu. (n.d.). Available at: http://mozdocs.kiev.ua/likiview.php?id=31670
Council Directive 2010/63/EU of 22 September 2010 on the protection of animals used for scientific purposes. (2010). Official Journal of the European Communities, 276, 33–79.
Kamyshnikov, V. S. (2009). Spravochnik po kliniko-biokhimicheskim issledovaniiam i laboratornoi diagnostike, (3-edition). Moscow: «MEDpressinform», 896.
Downloads
Published
Issue
Section
License
Copyright (c) 2018 National University of Pharmacy
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).