Abstract
Objectives
Vanadium has been reported to possess relevant therapeutic properties such as anti-diabetic and anti-tumoral. This study aimed at determining the effects of vanadium on experimentally induced colitis in rats.
Methods
Forty-five male Wistar rats (103 ± 3.90 g, n=15) were used for this study and were divided into three groups. Group 1 (Untreated control) had nothing added to their drinking, while groups 2 and 3 received sodium metavanadate at a dose of 50 and 200 mg/L respectively in their drinking water for 10 weeks. Colitis was thereafter induced by intra colonic administration of 1.50 mL of 6% acetic acid. Animals were sacrificed on day 0 (pre-induction), three- and seven-days post induction. Blood samples were collected for haematological variables and the distal 8 cm of the colon was collected for macroscopic, histological and biochemical (malondialdehyde-MDA, superoxide dismutase-SOD, catalase-CAT, glutathione peroxidase- GPx and nitrite concentration- NO) assessment.
Results
Low dose vanadium proved beneficial in ameliorating acetic acid-induced colitis by improving both histopathological and haematological changes. Gross observation showed a faster healing rate in vanadium treated groups (50 and 200 mg/L) compared with untreated control at day 3 (40 and 26.20 vs. 2.50%) and day 7 (80 and 66.70 vs. 42%) respectively. Vanadium also appears to exert its beneficial effects on acetic acid-induced colitis via up regulation of antioxidant enzymes (SOD, CAT, GPx) and NO while decreasing the over production of MDA.
Conclusions
Vanadium at small concentration functions as an essential trace element and may be able to promote healing process during ulcerative colitis.
Acknowledgement
The authors are grateful to Dr John Ogunsola of the Department of Veterinary Medicine, University of Ibadan, Nigeria for the interpretation of the histological slides.
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Research funding: This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-public sectors.
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Author contributions: Author Olaleye SB and Omayone TP both conceive the idea and design the work. Data acquisition was done by author Omayone TP while, author Olaleye SB supervised the work. Both authors were involved in data analysis and interpretation. First draft of the manuscript was written by author Omayone TP and revised by Olaleye SB. Final approval of the version to be published was decided by both authors and both authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Not applicable.
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Ethical approval: The research has complied with the criteria outlined in the Guide for the Care and Use of Laboratory Animals prepared by the National Academy of Science, 2011.
References
1. Zeng, C, Xiao, J, Chang, M, Wang, J. Beneficial effects of THSG on acetic acid-induced experimental colitis: involvement of upregulation of PPAR-γ and inhibition of the Nf-Kb inflammatory pathway. Molecules 2011;16:8552–68. https://doi.org/10.3390/molecules16108552.Search in Google Scholar
2. Shrikant, VJ, Bhavin, AV, Payal, DS, Dinesh, RS, Shailesh, AS, Tejal, RG. Protective effect of aqueous extract of Oroxylum indicum Linn. (Root back) against DNBS-induced colitis in rats. Indian J Pharmacol 2011;43:656–61.10.4103/0253-7613.89821Search in Google Scholar
3. Kayal, M, Shah, S. Ulcerative colitis: current and emerging treatment strategies. J Clin Med 2020;9:1–12.10.3390/jcm9010094Search in Google Scholar
4. Kiernan, MG, Coffey, JC, Sahebally, SM, Tibbitts, P, Lyons, EM, O’leary, E, et al.. Systemic molecular mediators of inflammation differentiate between Crohn’s disease and ulcerative colitis, implicating threshold levels of IL-10 and reactive ratios of pro-inflammatory cytokines in therapy. J Crohns Colitis 2020;14:118–29. https://doi.org/10.1093/ecco-jcc/jjz117.Search in Google Scholar
5. Das, S, Kanodia, L. Effect of ethanolic extract of leaves of moringa olifera lam. on acetic acid induced colitis in albino rats. Asian J Pharmaceut Clin Res 2012;5:110–4.Search in Google Scholar
6. Ungaro, R, Mehandru, S, Allen, PB, Peyrin-Biroulet, L, Colombel, JF. Ulcerative colitis. Lancet 2017;389:1756–70. https://doi.org/10.1016/s0140-6736(16)32126-2.Search in Google Scholar
7. Gitter, AH, Wullstein, F, Fromm, M, Schulzke, JD. Epithelial barrier defects in ulcerative colitis: characterization and quantification by electrophysiological imaging. Gastroenterology 2001;121:1320–8. https://doi.org/10.1053/gast.2001.29694.Search in Google Scholar
8. Gummow, B. Vanadium-environmental pollution and health effects. Townsville; QUB, Australia: School of Veterinary and Biomedical Sciences, James Cook University Elsevier P.V.; 2011:628–36 pp.10.1016/B978-0-444-52272-6.00661-9Search in Google Scholar
9. Goldfine, AB, Simondson, DC, Folli, F, Patti, ME, Kahn, F. Metabolic effects of sodium metavanadate in humans with insulin dependent and non-insulin dependent diabetes mellitus in vivo and in vitro studies. J Clin Endocrinol Metab 1995;80:3311–20. https://doi.org/10.1210/jcem.80.11.7593444.Search in Google Scholar
10. Boden, G, Chen, X, Riuz, J, van Rossum, JD, Turco, S. Effects of vanadyl sulphate on carbohydrate and lipid metabolism in patients with non-insulin dependent diabetes mellitus. Metabolism 1996;45:1130–5. https://doi.org/10.1016/s0026-0495(96)90013-x.Search in Google Scholar
11. Halberstam, M, Cohen, N, Shlimovich, P, Rossetti, L, Shamoon, H. Oral vanadyl sulphate improves insulin sensitivity in NIDDM but not in obese nondiabetic subjects. Diabetes 1996;45:659–66. https://doi.org/10.2337/diabetes.45.5.659.Search in Google Scholar
12. Adam, AMA, Naglah, AM, Al-Omar, MA, Refat, MS. Synthesis of a new insulin-mimetic anti-diabetic drug containing vitamin A and vanadium (IV) salt: chemico-biological characterizations. Int J Immunopathol Pharmacol 2017;30:272–81. https://doi.org/10.1177/0394632017719601.Search in Google Scholar PubMed PubMed Central
13. Huang, Y, Liu, F, Zhang, F, Liu, P, Xu, T, Ding, W. Vanadium (IV)-chlorodipicolinate alleviates hepatic lipid accumulation by inducing autophagy via the LKB1/AMPK signaling pathway in vitro and in vivo. J Inorg Biochem 2018;183:66–76. https://doi.org/10.1016/j.jinorgbio.2018.03.006.Search in Google Scholar
14. Kanna, PS, Mahendrakumar, CB, Chakraborty, T, Hemalatha, P, Banerjee, P, Chatterjee, M. Effect of vanadium on colonic aberrant crypt foci induced in rats by 1,2-dimethyl hydrazine. World J Gastroenterol 2003;9:1020–7. https://doi.org/10.3748/wjg.v9.i5.1020.Search in Google Scholar
15. Li, X, Lu, Y, Yang, JH, Jin, Y, Hwang, S, Chang, HW. Natural vanadium-containing Jeju groundwater inhibits immunoglobulin E-mediated anaphylactic reaction and suppresses eicosanoid generation and degranulation in bone marrow derived mast cells. Biol Pharm Bull 2012;35:216–22. https://doi.org/10.1248/bpb.35.216.Search in Google Scholar
16. Enns, R, Sutherland, L. Adverse events of medical therapy for the treatment for inflammatory bowel disease. In: Campieri, M, Bianchiporro, G, Fiocchi, C, Scholmerich, J, editors. Clinical challenges in inflammatory bowel disease diagnosis, prognosis and treatment. London: Kluwer Academic Publishers; 1998:113–23 pp.10.1097/00054725-199805000-00013Search in Google Scholar
17. Kozuch, PL, Hanauer, SB. Treatment of inflammatory bowel disease: a review of medical therapy. World J Gastroenterol 2008;14:354–77. https://doi.org/10.3748/wjg.14.354.Search in Google Scholar
18. Coskun, ZK, Kerem, M, Gurbuz, N, Omeroglu, S, Pasaogly, H, Demirtas, C, et al.. The study of biochemical and histopathological effects of spirulina in rats with TNBS-induced colitis. Bratisl Lek Listy 2011;112:235–43.Search in Google Scholar
19. Dai, S, Vera, E, McNeill, JH. Lack of haematological effect of oral vanadium treatment in rats. Pharmacol Toxicol 1995;76:263–8. https://doi.org/10.1111/j.1600-0773.1995.tb00141.x.Search in Google Scholar
20. Omayone, TP, Salami, AT, Oluwole, FS, Olaleye, SB. Gastroprotective effect of vanadium in rats- roles of gastric acid and nitric oxide. J Afr Ass Physiol Sci 2016;4:32–40.Search in Google Scholar
21. National Research Council. Guide for the care and use of laboratory animals, 8th ed. The National Academies Press; 2011. Available from: https://www.nap.edu/catalog/12910/guide-for-the-care-and-use-of-laboratory-animals-eighth; https://doi.org/10.17226/12910.10.17226/12910Search in Google Scholar
22. Jagtap, AG, Shirke, SS, Phadkef, AS. Effect of polyherbal formulation on experimental models of inflammatory bowel disease. J Ethnopharmacol 2004;90:195–204. https://doi.org/10.1016/j.jep.2003.09.042.Search in Google Scholar
23. Morris, GP, Beck, PL, Herrigge, MS, Depew, WT, Szewcdzuk, MR, Wallace, JL. Hapten induced model of chronic inflammation and ulceration in the rat colon. Gastroenterology 1989;96:795–803. https://doi.org/10.1016/s0016-5085(89)80079-4.Search in Google Scholar
24. Harputluoglu, MM, Demirel, U, Yuxwk, N, Karadag, N, Temel, I, Firat, S, et al.. The effects of Gingko biloba extract on acetic acid-induced colitis in rats. Turk J Gastroenterol 2006;17:177–82.Search in Google Scholar
25. Misra, HP, Fridovich, I. The role of superoxide anion in the autooxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170–5. https://doi.org/10.1016/s0021-9258(19)45228-9.Search in Google Scholar
26. Claiborne, A. Catalase activity. In: Greenwald, RA, editor. Handbook of methods for oxygene radical research. Boca Raton, FL: CRC Press; 1985.Search in Google Scholar
27. Rotruck, JT, Pope, AL, Ganther, HE, Swanson, AB, Hafeman, DG, Hoekstra, WG. Selenium: biochemical role as a component of glutathione peroxidase. Science 1973;179:588–90. https://doi.org/10.1126/science.179.4073.588.Search in Google Scholar
28. Varshney, R, Kale, RK. Effect of calmodulin antagonists on radiation induced lipid peroxidation in microsomes. Int J Biol 1990;158:733–41. https://doi.org/10.1080/09553009014552121.Search in Google Scholar
29. Gornal, AG, Bardawill, CJ, David, MM. Determination of serum protein by means of Biuret reaction. J Biol Chem 1949;177:571–6.10.1016/S0021-9258(18)57021-6Search in Google Scholar
30. Matkowskyj, KA, Chen, ZE, Rao, MS, Yang, GY. Dysplastic lesions in inflammatory bowel disease. Arch Pathol Lab Med 2013;137:338–50. https://doi.org/10.5858/arpa.2012-0086-ra.Search in Google Scholar
31. Bitar, VA, Laham, S. Methylsulfonylmethane and green tea extract reduced oxidative stress and inflammation in an ulcerative colitis. Asian J Pharmaceut Clin Res 2013;6:974–2441.Search in Google Scholar
32. Zeng, C, Xiao, JH, Chang, MJ, Wang, JL. Beneficial effects of THSG on acetic acid-induced experimental colitis: involvement of upregulation of PPAR-γ and inhibition of the Nf-Κb inflammatory pathway. Molecules 2011;16:8552–68. https://doi.org/10.3390/molecules16108552.Search in Google Scholar PubMed PubMed Central
33. Kockerling, A, Sorgenfrei, D, Fromm, M. Electrogenic Na+ absorption of rat distal colon confined to surface epithelium: a voltage-scanning study. Am J Physiol 1993;264:C1285–93. https://doi.org/10.1152/ajpcell.1993.264.5.c1285.Search in Google Scholar PubMed
34. Krośniak, M, Szklarzewicz, J, Gryboś, R, Tatar, B, Yildirim, M, Sahin, B, et al.. The influence of chronic supply of vanadium compounds on organ weights and body mass in animal diabetes model (NZO). Sci Technol Innov 2019;4:63–73.10.5604/01.3001.0013.1563Search in Google Scholar
35. Kirsner, JB, Shorter, RG. Recent developments in “nonspecific” inflammatory bowel disease (first of two parts). N Engl J Med 1982;306:775–85. https://doi.org/10.1056/nejm198204013061304.Search in Google Scholar
36. Jewell, DP, Patel, C. Immunology of inflammatory bowel disease. Scand J Gastroenterol 1985;114:119–26. https://doi.org/10.3109/00365528509093772.Search in Google Scholar PubMed
37. Xing, J, Sun, J, Sun, J, Hu, S, Guo, C, Wang, M, et al.. Protective effect of shikimic acid on acetic acid induced colitis in rats. J Med Plants Res 2012;6:2011–8.10.5897/JMPR11.1748Search in Google Scholar
38. Diegelmann, RF, Evans, MC. Wound healing: an overview of acute, fibrotic and delayed healing. Front Biosci 2004;9:283–9. https://doi.org/10.2741/1184.Search in Google Scholar PubMed
39. Kunwar, A, Priyadarsini, KI. Free radicals, oxidative stress and importance of antioxidants in human health. J Med Allied Sci 2011;1:53–60.Search in Google Scholar
40. Mateos, R, Lecumberri, E, Ramos, S, Goya, L, Bravo, L. Determination of Malondialdehyde (MDA) by high-performance liquid chromatography in serum and liver as a biomarker for oxidative stress. Application to a rat model for hypercholesterolemia and evaluation of the effect of diets rich in phenolic antioxidants from fruits. J Chromatogr B 2005;827:76–82. https://doi.org/10.1016/j.jchromb.2005.06.035.Search in Google Scholar PubMed
41. Kemeir, MEA. The protective effect of vanadium sulphate on ethanol-induced gastric ulcer. Bahrain Med Bull 2013;35:9. https://doi.org/10.12816/0004441.Search in Google Scholar
42. Valko, M, Morris, H, Cronnin, MTD. Metals, toxicity and oxidative stress. Curr Med Chem 2005;12:1161–208. https://doi.org/10.2174/0929867053764635.Search in Google Scholar PubMed
43. Leonard, SS, Harris, GK, Shi, XL. Metal-induced oxidative stress and signal transduction. Free Radic Biol Med 2004;37:1921–42. https://doi.org/10.1016/j.freeradbiomed.2004.09.010.Search in Google Scholar PubMed
44. Senturk, H, Bayramoglu, G, Dokumacioglu, A, Aral, E, Kanbak, G, İnal, M, et al.. Protective effects of Echinacea purpurea in an acetic acid induced rat model of colitis. Biol Divers Conserv 2012;5:59–65.Search in Google Scholar
45. Farombi, EO, Adedara, IA, Ajayi, BO, Ayepola, OR, Egbeme, EE. Kolaviron, a natural antioxidant and anti-inflammatory phytochemical prevents dextran sulphate sodium-induced colitis in rats. Basic Clin Pharmacol Toxicol 2013;113:49–55. https://doi.org/10.1111/bcpt.12050.Search in Google Scholar PubMed
46. Das, S, Kanodia, L, Mukherjee, A, Hakim, A. Effect of ethanolic extract of leaves of Paederia foetida Linn. on acetic acid induced colitis in albino rats. Indian J Pharmacol 2013;45:453–7. https://doi.org/10.4103/0253-7613.117728.Search in Google Scholar PubMed PubMed Central
47. Sobhani, I, Hochlaf, S, Denizot, Y, Vissuzaine, C, Rene, E, Benveniste, J, et al.. Raised concentrations of platelet activating factor incolonic mucosa of Crohn’s disease patients. Gut 1992;33:1220–5. https://doi.org/10.1136/gut.33.9.1220.Search in Google Scholar PubMed PubMed Central
48. Hirayama, K, Yokoi, Y, Sakaguchi, T, Nakamura, T, Kashiwabara, H, Sunayama, K, et al.. Platelet-activating factor, a critical mediator in the pathogenesis of dextransulfate sodium-induced colitis in rats. Dis Colon Rectum 2003;46:100–10. https://doi.org/10.1007/s10350-004-6503-7.Search in Google Scholar PubMed
49. Kanwar, S, Kubes, P. Nitric oxide is an antiadhesive molecule for leukocytes. New Horiz 1995;3:93–104.Search in Google Scholar
50. Gaboury, J, Woodman, RC, Granger, DN, Reinhardt, P, Kubes, P. Nitric oxide prevents leukocyte adherence: role of superoxide. Am J Physiol 1993;265:H862–7. https://doi.org/10.1152/ajpheart.1993.265.3.h862.Search in Google Scholar PubMed
51. Kim-Shapiro, DB, Schechter, AN, Gladwin, MT. Unraveling the reactions of nitric oxide, nitrite, and hemoglobin in physiology and therapeutics. Arterioscler Thromb Vasc Biol 2006;26:697–705. https://doi.org/10.1161/01.atv.0000204350.44226.9a.Search in Google Scholar PubMed
52. Kiss, J, Lamarque, D, Delchier, JC, Whittle, BJ. Time-dependent actions of nitric oxide synthase inhibition on colonic inflammation induced by trinitrobenzene sulphonic acid in rats. Eur J Pharmacol 1997;336:219–24. https://doi.org/10.1016/s0014-2999(97)01246-6.Search in Google Scholar
53. Miller, MJS, Sadowska-Krowicka, H, Chotinaruemol, S. Amelioration of chronic ileitis by nitric oxide synthase inhibition. J Pharmacol Exp Therapeut 1993;264:11–6.Search in Google Scholar
54. Rachmilewitz, D, Stamler, JS, Bachwich, D, Karmeli, F, Ackerman, Z, Podolsky, DK. Enhanced colonic nitric oxide generation and nitric oxide synthase activity in ulcerative colitis and Crohn’s disease. Gut 1995;36:718–23. https://doi.org/10.1136/gut.36.5.718.Search in Google Scholar
55. Conner, EM, Chen, Y, Grisham, MB. Effect of nitric oxide synthase (NOS) inhibition on dextran sulfate sodium (DSS)-induced colitis in rats and mice. Gastroenterology 1995;108:A801.10.1016/0016-5085(95)27512-6Search in Google Scholar
© 2021 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Reviews
- An insight on safety, efficacy, and molecular docking study reports of N-acetylcysteine and its compound formulations
- Public health approach of Unani medicine to cope and stay safe in hot environmental conditions
- Original Articles
- Kinetic characterization of rat brain acetylcholinesterase modulated by lead and cartap: the ameliorative effect of Citrus limon fruit juice
- Attenuation of potassium dichromate and sodium arsenite toxicities by methanol extract of Rauvolfia vomitoria in mice
- Chronic exposure of industrial grade calcium carbide and ethylene glycol alter histological architecture of systemic organs by disrupting redox balance in rat
- Biochemical and histopathological effects of low dose vanadium in the healing of acetic acid-induced colitis in male wistar rats
- Glycine and L-Arginine supplementation ameliorates gastro-duodenal toxicity in a rat model of NSAID (Diclofenac)-gastroenteropathy via inhibition of oxidative stress
- Cocos nucifera L. oil alleviates lead acetate-induced reproductive toxicity in sexually-matured male Wistar rats
- Intracellular signaling molecules of nerve tissue progenitors as pharmacological targets for treatment of ethanol-induced neurodegeneration
- Glatiramer acetate treatment inhibits inflammatory responses and improves survival in a mice model of cecal ligation and puncture-induced sepsis
- Ciprofloxacin-induced cutaneous adverse drug events: a systematic review of descriptive studies
- Aqueous extract of Adansonia digitata prevents Cadmium Chloride-induced testicular damage in Wistar Rats
- Exposure to prolonged unpredictable light impairs spatial memory via induction of oxidative stress and tumor necrosis factor-alpha in rats
- Tamarindus indica. Linn leaves ameliorates experimental induced heart failure in Wistar rats
Articles in the same Issue
- Frontmatter
- Reviews
- An insight on safety, efficacy, and molecular docking study reports of N-acetylcysteine and its compound formulations
- Public health approach of Unani medicine to cope and stay safe in hot environmental conditions
- Original Articles
- Kinetic characterization of rat brain acetylcholinesterase modulated by lead and cartap: the ameliorative effect of Citrus limon fruit juice
- Attenuation of potassium dichromate and sodium arsenite toxicities by methanol extract of Rauvolfia vomitoria in mice
- Chronic exposure of industrial grade calcium carbide and ethylene glycol alter histological architecture of systemic organs by disrupting redox balance in rat
- Biochemical and histopathological effects of low dose vanadium in the healing of acetic acid-induced colitis in male wistar rats
- Glycine and L-Arginine supplementation ameliorates gastro-duodenal toxicity in a rat model of NSAID (Diclofenac)-gastroenteropathy via inhibition of oxidative stress
- Cocos nucifera L. oil alleviates lead acetate-induced reproductive toxicity in sexually-matured male Wistar rats
- Intracellular signaling molecules of nerve tissue progenitors as pharmacological targets for treatment of ethanol-induced neurodegeneration
- Glatiramer acetate treatment inhibits inflammatory responses and improves survival in a mice model of cecal ligation and puncture-induced sepsis
- Ciprofloxacin-induced cutaneous adverse drug events: a systematic review of descriptive studies
- Aqueous extract of Adansonia digitata prevents Cadmium Chloride-induced testicular damage in Wistar Rats
- Exposure to prolonged unpredictable light impairs spatial memory via induction of oxidative stress and tumor necrosis factor-alpha in rats
- Tamarindus indica. Linn leaves ameliorates experimental induced heart failure in Wistar rats