Blood aminothiol levels in patients with typical alcoholic delirium tremens: results of an original study

 

Authors

 

A.V. Sakharov

National Scientific Center for Addictology ‒ Branch of the Federal State Budgetary Institution “National Medical Research Center for Psychiatry and Addictology named after V.P. Serbsky" of the Ministry of Health of the Russian Federation, Moscow, Russian Federation

S.E. Golygina

Federal State Budgetary Educational Institution of Higher Education “Chita State Medical Academy” of the Ministry of Health of the Russian Federation, Chita, Russian Federation

 

https://doi.org/10.26617/1810-3111-2026-1(130)-18-28

 

Journal: Siberian Herald of Psychiatry and Addiction Psychiatry. 2026; 1 (130):  18-28.

 

Abstract

Introduction. The thiol-disulfide oxidation-reduction system is a key functional element of the mechanism of non-specific resistance and adaptation of the organism to environmental factors. The state of the thiol-disulfide system of key aminothiols in individuals with alcohol dependence has been insufficiently studied. Objective: to study aminothiol levels in the blood serum of patients with typical alcoholic delirium before therapy. Material and Methods. The study included 30 patients with typical alcoholic delirium before therapy with an ICD-10 diagnosis of withdrawal state with delirium (classical delirium) (F10.40) – the main group. The control group consisted of 35 conditionally healthy male volunteers, comparable with patients in the main group by age. Aminothiol levels in the blood serum were determined by liquid chromatography. Results. In typical alcoholic delirium tremens, an increase in cysteine (Cys) levels is observed relative to the values in the control group: total – by 1.5 times, reduced – by 1.4 times, oxidized – by 1.3 times. A 1.5-fold increase in the content of reduced glutathione (GSH) was recorded, while its oxidized form decreased by 1.6 times. The level of homocysteine (Hcy) was elevated: total – by 1.3 times, reduced – by 1.6 times. Conclusion. The findings indicate a significant disturbance of the redox balance in alcoholic delirium. The observed imbalance may act as an important pathogenetic link in this condition, in particular, mediating the development of concomitant endothelial dysfunction. Further in-depth research is needed to determine the exact pathogenetic significance of the identified changes.

 

Keywords: alcohol dependence syndrome, delirium tremens, aminothiols.

 

Article (pdf)

 

Contacts

This email address is being protected from spambots. You need JavaScript enabled to view it.

 

Materials  

For citation: Sakharov A.V., Golygina S.E. Blood aminothiol levels in patients with typical alcoholic delirium tremens: results of an original study. Siberian Herald of Psychiatry and Addiction Psychiatry.2026; 1 (130): 18-28. https://doi.org/10.26617/1810-3111-2026-1(130)-18-28

 

REFERENCES

  1. Klimenko TV, Kozlov AA. Current state, achievements, problem aspects and prospects for developing a system providing the medical care in the field of addiction psychiatry. Journal of Addiction Problems. 2018;9(169): 5-17 (in Russian).
  2. Nemtsov AV. Cardiovascular and other deaths in Russia, 2004-2016. Social Aspects of Population Health. 2018;2:6 (in Russian).
  3. GBD 2016 Alcohol Collaborators. Alcohol use and burden for 195 countries and territories, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2018 Sep 22;392(10152):1015-1035. https://doi.org/10.1016/S0140-6736(18)31310-2. Epub 2018 Aug 23. Erratum in: Lancet. 2018 Sep 29;392(10153):1116. https://doi.org/10.1016/S0140-6736(18)32338-9. Erratum in: Lancet. 2019 Jun 22;393(10190):e44. https://doi.org/10.1016/S0140-6736(19)31050-5. PMID: 30146330; PMCID: PMC6148333.
  4. Yang M, Zhou X, Tan X, Huang X, Yuan L, Zhang Z, Yang Y, Xu M, Wan Y, Li Z. The status of oxidative stress in patients with alcohol dependence: A meta-analysis. Antioxidants (Basel). 2022 Sep 28;11(10):1919. https://doi.org/10.3390/antiox11101919. PMID: 36290642; PMCID: PMC9598131.
  5. UzbekovMG. Lipid peroxidation and antioxidant systems in mental disorders. Part II. Social and Clinical Psychiatry. 2015;25(4):92-101 (in Russian).
  6. Razvodovsky YuE. Amino acids in the pathogenesis and treatment of alcoholism. Narcology. 2010; 6:88-97 (inRussian).
  7. Semenchuk AK, Lelevich VV. The content of sulfur-containing amino acids and related compounds in the blood plasma of rats with various types of alcohol intoxication. Journal of Grodno State Medical University. 2021;19(2):170-175. https://doi.org/10.25298/2221-8785-2021-19-2-170-175 (in Russian).
  8. Dontsov VV, Zybin DI, Ivanov AV, Popov MA., Agafonov EG, Shumakov DV. The effect of coronary bypass surgery on blood aminothiols in patients with coronary heart disease. Bulletin of the N.I. Pirogov National Medical and Surgical Center. 2024;19(4):86-92.https://doi.org/10.25881/20728255_2024_19_4_86 (in Russian).
  9. Koriakin AM, Epifantseva NN, Eshcheva LA, Dementjeva LA, Yakimovskikh AV. Damage, inflammation of the vascular endothelium, hypercoagulable as risk factors for heart diseases in patients with chronic alcoholism. Siberian Medical Journal. 2014;29(4):52-55 (in Russian).
  10. Vorontsova AS, Vorobyova NA, Malyshkina NA, Belova NI. Mechanisms of regulation of homocysteine and folate metabolism in norm and pathology: a tutorial. Arkhangelsk: Publishing house of the Northern State Medical University, 2023:135 (in Russian).
  11. Mashkovsky MD. Medicines. 16th edition, revised, corrected and supplemented. Moscow: Novaya Volna, 2012:1216 (in Russian).
  12. Studentsov EP, Ramsh SM, Kazurova NG., Neporozhneva OV, Garabadzhiu AV, Kochina TA, Voronkov MG, Kuznetsov VA, Krivorotov DV. Adaptogens and related groups of drugs – 50 years of searching. Reviews of clinical pharmacology and drug therapy. 2013;11(4):3-43 (in Russian).
  13. Borisenok OA, Bushma MI, Basalai ON, Radkovec AYu. Glutathione deficiency: consequence and correction.Medical News. 2019;11(302):10-15 (in Russian).
  14. Basalaj ON, Radkovets AYu, Bushma MI. Taurine: the metabolic regulator and the drug. Medical News. 2017;5:3-7 (in Russian).
  15. Giles NM, Watts AB, Giles GI, Fry FH, Littlechild JA, Jacob C. Metal and redox modulation of cysteine protein function. Chem Biol. 2003 Aug;10(8):677-93. https://doi.org/10.1016/s1074-5521(03)00174-1. PMID: 12954327.
  16. Razak MA, Begum PS, Viswanath B, Rajagopal S. Multifarious beneficial effect of nonessential amino acid, glycine: A review. Oxid Med Cell Longev. 2017; 2017:1716701. https://doi.org/10.1155/2017/1716701. Epub 2017 Mar 1. Erratum in: Oxid Med Cell Longev. 2022 Feb 23;2022:9857645.https://doi.org/10.1155/2022/9857645. PMID: 28337245; PMCID: PMC5350494.
  17. Gundersen Y, Vaagenes P, Dreiem A, Fonnum F. Glysin [Glycine]. Tidsskr Nor Laegeforen. 2004 Mar 18;124(6):773-5. Norwegian. PMID: 15039805.
  18. Zhong Z, Wheeler MD, Li X, Froh M, Schemmer P, Yin M, Bunzendaul H, Bradford B, Lemasters JJ. L-Glycine: a novel anti-inflammatory, immunomodulatory, and cytoprotective agent. Curr Opin Clin Nutr Metab Care. 2003 Mar;6(2):229-40. https://doi.org/10.1097/00075197-200303000-00013. PMID: 12589194.
  19. Ruiz-Ramírez A, Ortiz-Balderas E, Cardozo-Saldaña G, Diaz-Diaz E, El-Hafidi M. Glycine restores glutathione and protects against oxidative stress in vascular tissue from sucrose-fed rats. Clin Sci (Lond). 2014 Jan 1;126(1):19-29. https://doi.org/10.1042/CS20130164. PMID: 23742196.
  20. Borisenok OA, Bushma MI, Basalai ON, Radkovec AYu. Glutathione biological role. Medical News. 2019;7(398):3-8 (in Russian).
  21. Abduganieva EA. The role of homocysteine as a pathogenetic factor in the development of thrombophilic conditions. Siberian Medical Review. 2023;2(140):8-16. https://doi.org/10.20333/25000136-2023-2-8-16 (in Russian).
  22. Nikitin IA, Mutallibzoda Sh, Balashova MS, Orlova OYu, Klokonos MV, Velina DA. High homocysteine levels as a risk factor for folate cycle disorders. Effective Healthcare Management: Innovation Strategies. III International Scientific and Practical Conference: collection of materials. Saratov, 2022:234-237(in Russian).
  23. Mattson MP, Shea TB. Folate and homocysteine metabolism in neural plasticity and neurodegenerative disorders. Trends Neurosci. 2003 Mar;26(3):137-46.https://doi.org/10.1016/S0166-2236(03)00032-8. PMID: 12591216.
  24. Golimbet VE, Lebedeva IS, Alfimova MV, Barkhatova AN, Lezheiko TV, Kolesina NYu, Borozdina SA, Abramova LI. Homocysteine-related genes and attention in patients with schizophrenia and schizoaffective psychosis. S.S. Korsakov Journal of Neurology and Psychiatry. 2010;110(6):86-89 (in Russian).
  25. Kaplan ED. Association between homocyst(e)ine levels and risk of vascular events. Drugs Today (Barc). 2003 Mar;39(3):175-92. https://doi.org/10.1358/dot.2003.39.3.799452. PMID: 12730702.
  26. Miroshnichenko II, Kalmykov YuM, Yаkovleva OB, Ptitsina SN. Homocysteine and mental health. Psychiatry. 2010;2(44):67-71 (in Russian).
  27. Cybikov NN, Cybikova EA, Nikitin DA. Dynamics of homocysteine levels in the blood serum and cerebrospinal fluid of patients with delirium tremens. Narcology. 2008;7(7;79):77-79 (in Russian).
  28. Kopylova VS, Boronovskiy SE, Nartsissov YaR. Simulation modeling of glutamate-cysteine ligase activity. Biophysics. 2023;68(2):218-229. https://doi.org/10.31857/S0006302923020023(in Russian).
  29. Maksimova MYu, Ivanov AV, Nikiforova KA, Virus ED, Suanova ET, Ochtova FR, Piradov MA, Kubatiev AA. Aminothiols in blood plasma at different subtypes of ischemic stroke. S.S. Korsakov Journal of Neurology and Psychiatry. 2020;120(8-2):17-23. https://doi.org/10.17116/jnevro202012008217 (in Russian).
  30. Uzbekov MG. Lipid peroxidation and antioxidant systems in mental illnesses. Communication IV. Social and Clinical Psychiatry. 2016;26(3):65-71 (in Russian).
  31. Tsermpini EE, Plemenitaš Ilješ A, Dolžan V. Alcohol-induced oxidative stress and the role of antioxidants in alcohol use disorder: A systematic review. Antioxidants (Basel). 2022 Jul 15;11(7):1374.https://doi.org/10.3390/antiox11071374. PMID: 35883865; PMCID: PMC9311529.
  32. Prokopieva VD, Vetlugina TP. Features of oxidative stress in alcoholism. Biomedical Chemistry. 2023;69(2):83-96. https://doi.org/10.18097/PBMC20236902083 (in Russian).
  33. Vasiliev AG, Morozova KV, Brus TV, Zabezhinskij MM, Kravcova AA, Balashov LD, Vasilieva AV, Pyurveev SS, Kosova AN. The role of homocysteine metabolism disorders in pathological processes. Russian Biomedical Research. 2022;7(1):44-59 (in Russian).
  34. Sibireva OF, Zhavoronok TV, Kalyuzhina EV, Kalyuzhin VV. Hereditary risk factors for intravascular coagulation and homocysteine levels in patients with chronic alcoholism. Narcology. 2019;18(3):52-58. https://doi.org/10.25557/1682-8313.2019.03.52-58 (in Russian).
  35. Dubchenko EA, Ivanov AV, Boiko AN, Spirina NN, Gusev EI, Kubatiev AA. Hyperhomocysteinemia and endothelial dysfunction in patients with cerebral vascular and autoimmune diseases. S.S. Korsakov Journal of Neurology and Psychiatry. 2019;119(11):133-138. https://doi.org/10.17116/jnevro2019119111133 (in Russian).
  36. Lutz UC. Alterations in homocysteine metabolism among alcohol dependent patients – clinical, pathobiochemical and genetic aspects. Curr Drug Abuse Rev. 2008 Jan;1(1):47-55.https://doi.org/10.2174/1874473710801010047. PMID: 19630705.
  37. Gauthier TW, Kable JA, Burwell L, Coles CD, Brown LA. Maternal alcohol use during pregnancy causes systemic oxidation of the glutathione redox system. Alcohol Clin Exp Res. 2010 Jan;34(1):123-30.https://doi.org/10.1111/j.1530-0277.2009.01072.x. Epub 2009 Oct 23. PMID: 19860801; PMCID: PMC2851176.