Mineral water Vincentka and its influence on mucosal ulcers
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
36647913
PubMed Central
PMC9906663
DOI
10.33549/physiolres.935013
PII: 935013
Knihovny.cz E-zdroje
- MeSH
- gastritida * chemicky indukované patologie MeSH
- krysa rodu Rattus MeSH
- lidé MeSH
- minerální vody * MeSH
- pilotní projekty MeSH
- potkani Wistar MeSH
- vřed MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- minerální vody * MeSH
Gastropathy is one of the most common diseases of the human gastrointestinal tract. Apart from its consequences in the stomach, it is also manifested in other parts of the digestive tract, particularly in the duodenum. The aim of this pilot study was to verify on animal model the empirically observed alleviation of gastropathy symptoms in patients who underwent a drinking treatment of Vincentka natural mineral water during their spa treatment. Sixteen male Wistar rats were included in the study. The animals were randomly divided into two groups: experimental group (E; n=8) and control group (C; n=8). The experimental protocol consisted of three phases: (1) handling phase (7 days); (2) mineral water (E)/tap water (C) administration (7 days); (3) acute gastritis induction (1 day). Twenty-four hours after the induction of acute gastritis, the animals were sacrificed. The collected tissues (stomach and duodenum) and blood were examined by standard histological microscopy, and by immunohistochemical and biochemical methods. Histopathological analysis revealed significantly reduced damage to the gastric mucosa in the experimental group. Significantly different values of blood plasma antioxidant capacity, oxidative stress parameters and blood plasma biochemical parameters were also found. Based on these results, we conclude that the mineral water Vincentka has a positive impact on development and symptoms of acute gastric ulcers.
Zobrazit více v PubMed
Mihály E, Micsik T, Juhász M, Herszényi L, Tulassay Z. Gastritis and gastropathy. (Article in Hungarian) Orv Hetil. 2014;155:43–61. doi: 10.1556/OH.2014.29807. PubMed DOI
Nel WA. Gastritis and gastropathy: More than meets the eye. Cont Med Educ. 2012;30:61–66.
Kayaçetin S, Güreşçi S. What is gastritis? What is gastropathy? How is it classified? Turk J Gastroenterol. 2014;25:233–247. doi: 10.5152/tjg.2014.7906. PubMed DOI
Yoshikawa T, Naito Y. The role of neutrophils and inflammation in gastric mucosal injury. Free Radic Res. 2000;33:785–794. doi: 10.1080/10715760000301301. PubMed DOI
Narayanan M, Reddy KM, Marsicano E. Peptic ulcer disease and Helicobacter pylori infection. Mo Med. 2018;115:219–224. PubMed PMC
Lewis JH. Treatment of gastric ulcer. What is old and what is new. Arch Intern Med. 1983;143:264–274. doi: 10.1001/archinte.143.2.264. PubMed DOI
Bi W-P, Man H-B, Man M-Q. Efficacy and safety of herbal medicines in treating gastric ulcer: a review. World J Gastroenterol. 2014;20:17020–17028. doi: 10.3748/wjg.v20.i45.17020. PubMed DOI PMC
Jandová D. Balneologie. 1. vydání. Grada Publishing; Praha: 2009.
Třískala Z, Jandová D. Medicína přírodních léčivých zdrojů. 1. vydání. Grada Publishing; Praha: 2019. p. 208.
Cheleschi S, Tenti S, Seccafico I, Gálvez I, Fioravanti A, Ortega E. Balneotherapy year in review 2021: focus on the mechanisms of action of balneotherapy in rheumatic diseases. Environ Sci Pollut Res Int. 2022;29:8054–8073. doi: 10.1007/s11356-021-17780-0. PubMed DOI
Cheleschi S, Gallo I, Tenti S. A comprehensive analysis to understand the mechanism of action of balneotherapy: why, how, and where they can be used? Evidence from in vitro studies performed on human and animal samples. Int J Biometeorol. 2020;64:1247–1261. doi: 10.1007/s00484-020-01890-4. PubMed DOI PMC
Gálvez I, Torres-Piles S, Ortega-Rincón E. Balneotherapy, immune system, and stress response: a hormetic strategy? Int J Mol Sci. 2018;19:1687. doi: 10.3390/ijms19061687. PubMed DOI PMC
O VINCENTCE [Internet] Vincentka; [cited 2022 Oct 23]. Available from: https://www.vincentka.cz/o-vincentce/
Yamasaki K, Ishiyama H, Imaizumi T, Kanbe T, Yabuuchi Y. Effect of OPC-12759, a novel antiulcer agent, on chronic and acute experimental gastric ulcer, and gastric secretion in rats. Jpn J Pharmacol. 1989;49:441–448. doi: 10.1016/S0021-5198(19)43019-9. PubMed DOI
Kim YS, Jeong M, Han YM, Park JM, Kwon SO, Hong SP, Hahm KB. Combined extracts of artemisia and green tea, mitigated alcoholic gastritis via enhanced heat-shock protein 27. Korean J Gastroenterol. 2018;71:132–142. doi: 10.4166/kjg.2018.71.3.132. PubMed DOI
Keller A, Mohamed A, Dröse S, Brandt U, Fleming I, Brandes RP. Analysis of dichlorodihydrofluorescein and dihydrocalcein as probes for the detection of intracellular reactive oxygen species. Free Radic Res. 2004;38:1257–1267. doi: 10.1080/10715760400022145. PubMed DOI
Pederson TC, Buege JA, Aust SD. Microsomal electron transport. The role of reduced nicotinamide adenine dinucleotide phosphate-cytochrome c reductase in liver microsomal lipid peroxidation. J Biol Chem. 1973;248:7134–7141. doi: 10.1016/S0021-9258(19)43371-1. PubMed DOI
Reznick AZ, Packer L. Oxidative damage to proteins: spectrophotometric method for carbonyl assay. Methods Enzymol. 1994;233:357–363. doi: 10.1016/S0076-6879(94)33041-7. PubMed DOI
Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 1968;25:192–205. doi: 10.1016/0003-2697(68)90092-4. PubMed DOI
Chaturvedi S, Gupta P. Chapter 8 - Plant secondary metabolites for preferential targeting among various stressors of metabolic syndrome. In: ATTA-UR-RAHMAN, editor. Studies in Natural Products Chemistry. Elsevier; 2021. pp. 221–261. DOI
Wallace JL. Prostaglandins, NSAIDs, and gastric mucosal protection: why doesn’t the stomach digest itself? Physiol Rev. 2008;88:1547–1565. doi: 10.1152/physrev.00004.2008. PubMed DOI
Naito Y, Yoshikawa T. Oxidative stress involvement and gene expression in indomethacin-induced gastropathy. Redox Rep. 2006;11:243–253. doi: 10.1179/135100006X155021. PubMed DOI
Zhang J, Wang X, Vikash V, Ye Q, Wu D, Liu Y, Dong W. ROS and ROS-mediated cellular signaling. Oxid Med Cell Longev. 2016;2016:e4350965. doi: 10.1155/2016/4350965. PubMed DOI PMC
Sies H, Jones DP. Reactive oxygen species (ROS) as pleiotropic physiological signalling agents. Nat Rev Mol Cell Biol. 2020;21:363–383. doi: 10.1038/s41580-020-0230-3. PubMed DOI
Hagfors L, Leanderson P, Sköldstam L, Andersson J, Johansson G. Antioxidant intake, plasma antioxidants and oxidative stress in a randomized, controlled, parallel, Mediterranean dietary intervention study on patients with rheumatoid arthritis. Nutr J. 2003;2:5. doi: 10.1186/1475-2891-2-5. PubMed DOI PMC
Tan BL, Norhaizan ME, Liew W-P-P, Sulaiman Rahman HS. Antioxidant and oxidative stress: a mutual interplay in age-related diseases. Front Pharmacol. 2018;9:1162. doi: 10.3389/fphar.2018.01162. PubMed DOI PMC
Wang Y, Yang M, Lee S-G, Davis CG, Kenny A, Koo SI, Chun OK. Plasma total antioxidant capacity is associated with dietary intake and plasma level of antioxidants in postmenopausal women. J Nutr Biochem. 2012;23:1725–1731. doi: 10.1016/j.jnutbio.2011.12.004. PubMed DOI
Herken EN, Kocamaz E, Erel O, Celik H, Kucukatay V. Effect of sulfite treatment on total antioxidant capacity, total oxidant status, lipid hydroperoxide, and total free sulfydryl groups contents in normal and sulfite oxidase-deficient rat plasma. Cell Biol Toxicol. 2009;25:355–362. doi: 10.1007/s10565-008-9089-3. PubMed DOI
Gunnison AF, Palmes ED. Persistence of plasma S-sulfonates following exposure of rabbits to sulfite and sulfur dioxide. Toxicol Appl Pharmacol. 1973;24:266–278. doi: 10.1016/0041-008X(73)90147-6. PubMed DOI
Carbajo JM, Maraver F. Sulphurous mineral waters: new applications for health. Evid Based Complement Alternat Med. 2017;2017:e8034084. doi: 10.1155/2017/8034084. PubMed DOI PMC