ISSN 2415-3060 (print), ISSN 2522-4972 (online)
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JMBS 2022, 7(6): 45–50
https://doi.org/10.26693/jmbs07.06.045
Experimental Medicine and Morphology

The Effect of Polyphenols on Lipid Peroxidation and the Antioxidant System in the Submandular Salivary Glands during Combined Administration of Alcohol and S. typhi Lipopolysaccharide

Kozaeva R. S., Klymenko M. O.
Abstract

The purpose of the study was to study the effect of polyphenols (curcumin, epigallocatechin-3-gallate, and quercetin) on indicators of lipid peroxidation and antioxidant protection in the submandibular salivary glands of rats with alcohol damage against the background of lipopolysaccharide-induced systemic inflammatory response. Materials and methods. The studies were conducted on 35 rats of the Wistar line weighing 205–220 g, divided into 5 groups of seven animals in each: the 1st group (control) included animals receiving isotonic sodium chloride solution intragastrically twice a day; the 2nd group included rats exposed to alcohol (in a dose of 24 mg/kg intragastrically through gavage twice a day) for last 2 weeks during lipopolysaccharide-induced systemic inflammatory response; the rats of the 3rd, 4th and 5th groups were exposed to alcohol during lipopolysaccharide-induced systemic inflammatory response, which also received polyphenols, administered intragastrically: curcumin (diferuloylmethane, in a daily dose of 200 mg/kg), epigallocatechin-3-gallate (in a daily dose of 40 mg/kg), quercetin (in a daily dose of 200 mg/kg), respectively. The level of lipid peroxidation in the tissues of the submandibular salivary glands was assessed by the formation of compounds that react with thiobarbituric acid. The state of antioxidant protection was assessed by the increase in the concentration of thiobarbituric acid-active products during a 1.5-hour incubation in iron ascorbate buffer solution, as well as by the activity of superoxide dismutase. Results and discussion. When using curcumin under the experimental conditions, the concentration of thiobarbituric acid-reactants in the homogenate of submandibular salivary glands before and after incubation was 59.3 and 55.7% inferior to the corresponding results of the 2nd group, when prescribing epigallocatechin-3-gallate – by 55.7 and 51.2%, quercetin – by 67.0 and 61.0%, respectively. This was accompanied by a probable increase in the activity of superoxide dismutase in the tissues of the submandibular salivary glands. Conclusion. The use of curcumin and bioflavonoids (epigallocatechin-3-gallate and quercetin) under conditions of combined administration of 40% ethanol and S. typhi lipopolysaccharide significantly limits the development of lipid peroxidation in the tissues of the submandibular salivary glands, increases their antioxidant potential, superoxide dismutase activity

Keywords: lipopolysaccharide-induced systemic inflammatory response, salivary glands, lipid peroxidation, antioxidant protection, polyphenols, curcumin, epigallocatechin-3-gallate, quercetin

Full text: PDF (Ukr) 273K

References
  1. Kunavina KA, Opravin AS, Solov'yev AG. Characteristics of dental pathology in chronic alcohol intoxication. Narkolohiya. 2017;(12):72-80.
  2. Arya S, Pilania A, Kumar J, Talnia S. Diagnosis of bilateral parotid enlargement (Sialosis) by sonography: A case report and literature review. J Indian Acad Oral Med Radiol. 2019;31:79-83.
  3. Adhikari R, Soni A. Submandibular Sialadenitis and Sialadenosis [Updated 2021 Aug 14]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan. Available from: https://www.ncbi.nlm.nih.gov/books/ NBK562211/
  4. Kim SK, Hong SH, Chung JH, Cho KB. Association Between Alcohol Consumption and Metabolic Syndrome in a Community-Based Cohort of Korean Adults. Med Sci Monit. 2017;23:2104-10. PMID: 28465500. PMCID: PMC5424649. doi: 10.12659/MSM.901309
  5. Magis DC, Jandrain BJ, Scheen AJ. Alcohol, insulin sensitivity and diabetes. Rev Med Liege. 2003 Jul-Aug; 58(7-8):501-7.
  6. Stafeev IS, Menshikov MY, Tsokolaeva ZI, Shestakova MV, Parfyonova YV. Molecular Mechanisms of Latent Inflammation in Metabolic Syndrome. Possible Role of Sirtuins and Peroxisome Proliferator-Activated Receptor Type γ. Biochemistry. 2015;80(10):1217-26. PMID: 26567565. doi: 10.1134/S0006297915100028
  7. Yelins’ka AM, Shvaykovs’ka OO, Kostenko VO. Sources of production of reactive oxygen and nitrogen species in tissues of periodontium and salivary glands of rats under modeled systemic inflammation. Problemy ekolohiyi ta medytsyny. 2017;21(3-4):51-4.
  8. Kozaeva RS, Klymenko MO, Kostenko VО. Lipopolisakharyd-indukovana systemna zapalʹna vidpovidʹ obtyazhuye rozvytok okysno-nitrozatyvnoho stresu v slynnykh zalozakh shchuriv pry yikh alkoholʹnomu urazhenni [Lipopolysaccharide-induced systemic inflammatory response enhances the development of oxidative-nitrosative stress in salivary glands of rats under alcohol damage]. Fiziol Zh. 2021;67(6):60-7. [Ukrainian]. doi: 10.15407/fz67.06.060
  9. Yelins’ka AM, Shvaykovs’ka OO, Kostenko VO. Vplyv epihalokatekhinu-3-halatu na produktsiyu aktyvnykh form kysnyu i azotu v tkanynakh parodonta ta slynnykh zaloz shchuriv za umov systemnoyi zapalʹnoyi vidpovidi [Influence of epigallocatechin-3-gallate on production of reactive oxygen and nitrogen species in tissue of peridontium and salivary glands under systemic inflammatory response in rats]. Farmakolohiya ta likarsʹka toksykolohiya. 2018;(1):32-38. [Ukrainian]
  10. Yelins’ka AM, Shvaykovs’ka OO, Kostenko VO. Epigallocatechin-3-gallate prevents disruption of connective tissue in periodontium and salivary glands of rats during systemic inflammation. Wiad Lek. 2018;71(4):869-73.
  11. Shvaykovsʹka OO, Denysenko SV, Kostenko VO. Vplyv vodorozchynnoyi formy kvertsetynu na pokaznyky okysno-nitrozatyvnoho stresu v tkanynakh pidnyzhnʹoshchelepnykh slynnykh zaloz shchuriv za umov lipopolisakharyd-indukovanoyi systemnoyi zapalʹnoyi vidpovidi [Effect of water-soluble quercetin on indicators of oxidative-nitrosative stress in tissues of submandibular salivary glands of rats under lipopolysaccharide-induced systemic inflammatory response]. Aktualʹni problemy suchasnoyi medytsyny: Visn Ukrayinsʹkoyi med stomat akademiyi. 2021;21(2):175-81. [Ukrainian]. doi: 10.31718/2077-1096.21.2.175
  12. Kozaeva R, Klymenko MO, Katrushov OV, Kostenko VO. Bioflavonoids as agents for correcting nitro-oxidative stress and salivary gland functions in rats exposed to alcohol during modeled lipopolysaccharide-induced systemic inflammatory response. Wiad Lek. 2022;75(3):685-90.
  13. Kozaeva R, Klymenko MO, Kostenko VO. Resveratrol inhibits reactive oxygen and nitrogen species formation in rats’ salivary glands and their functions under alcohol exposure and lipopolysaccharide-induced systemic inflammatory response. Pharmacol OnLine. 2021;3:106-115. PMID: 35522879. doi: 10.36740/WLek202203121
  14. Yeroshenko GA, Shevchenko KV, Yakushko OS. Morphometric characteristics of rat salivary glands hemomicrovasculature capacity component under normal conditions and in ethanol chronic intoxication. Svit Med ta Biol. 2018;(3):149-52. doi: 10.26724/2079-8334-2018-3-65-149-152
  15. Yelins’ka AM, Shvaykovs’ka OO, Kostenko VO. Epigallocatechin-3-gallate prevents disruption of connective tissue in periodontium and salivary glands of rats during systemic inflammation. Wiad Lek. 2018;71(4):869-73.
  16. Akimov OYe, Kostenko VO. Oksydatyvno-nitrozatyvnyy stres ta metody yoho doslidzhennya [Oxidative-nitrosative stress and methods of its research]. Lviv: Magnolia; 2021. [Ukrainian]
  17. Yelins’ka AM, Shvaykovs’ka OO, Kostenko VO. Vplyv pirolidyndytiokarbamatu amoniyu na produktsiyu aktyvnykh form kysnyu i azotu v tkanynakh parodonta ta slynnykh zaloz shchuriv za umov systemnoho vvedennya lipopolisakharydu [Influence of ammonium pyrrolidine dithiocarbamate on the production of reactive oxygen and nitrogen species in tissues of periodontium and salivary glands in rats exposed to Salmonella typhi lipopolisaccharide]. Fiziol Zh. 2018;64(5):63-69. [Ukrainian]. doi: 10.15407/fz64.05.063
  18. Yavtushenko IV, Kostenko VO. Pryhnichennya transkryptsiynykh chynnykiv NF kappa B ta AP-1 obmezhuye rozvytok okysno-nitrozatyvnoho stresu v tkanyni velykykh pivkulʹ holovnoho mozku shchuriv pislya vidtvorennya eksperymentalʹnoyi cherepno-mozkovoyi travmy [Inhibition of transcription factors NF kappa B and AP-1 limits the progression of oxidative-nitrosative stress in the tissue of cerebral hemispheres in rats after modelled traumatic brain injury]. Aktualʹni problemy suchasnoyi medytsyny: Visn Ukr med stomatol akad. 2020;20(1):80-5. [Ukrainian]. doi: 10.31718/2077-1096.20.1.80
  19. Frenkel YuD, Cherno VS, Kostenko VO. Nrf2 induction alleviates metabolic disorder and systemic inflammatory response in rats under a round-the-clock lighting and high-carbohydrate-lipid diet. Romanian J Diabetes Nutrit Metabolic Dis. 2022;29(2):194-201.
  20. Mendonca P, Soliman KFA. Flavonoids Activation of the Transcription Factor Nrf2 as a Hypothesis Approach for the Prevention and Modulation of SARS-CoV-2 Infection Severity. Antioxidants (Basel). 2020 Jul 24;9(8):659. PMID: 32722164. PMCID: PMC7463602. doi: 10.3390/antiox9080659
  21. Zhang DD, Chapman E. The role of natural products in revealing NRF2 function. Nat Prod Rep. 2020 Jun 1;37(6):797-826. PMID: 32400766. PMCID: PMC7316599. doi: 10.1039/C9NP00061E
  22. Wang Y, Tang Q, Duan P, Yang L. Curcumin as a therapeutic agent for blocking NF-κB activation in ulcerative colitis. Immunopharmacol Immunotoxicol. 2018 Dec;40(6):476-82. PMID: 30111198. doi: 10.1080/08923973.2018.1469145
  23. Kang CH, Choi YH, Moon SK, Kim WJ, Kim GY. Quercetin inhibits lipopolysaccharide-induced nitric oxide production in BV2 microglial cells by suppressing the NF-κB pathway and activating the Nrf2-dependent HO-1 pathway. Int Immunopharmacol. 2013 Nov;17(3):808-13. PMID: 24076371. doi: 10.1016/j.intimp.2013.09.009
  24. Shanmugam MK, Rane G, Kanchi MM, Arfuso F, Chinnathambi A, Zayed ME, et al. The multifaceted role of curcumin in cancer prevention and treatment. Molecules. 2015;20(2):2728-69. PMID: 25665066. PMCID: PMC6272781. doi: 10.3390/molecules20022728