Effects of Catechin, Quercetin and Taxifolin on Redox Parameters and Metabolites Linked with Renal Health in Rotenone-toxified Rats

Författare

  • A. C Akinmoladun

Nyckelord:

Flavonoids, nephrotoxicity, oxidative stress, structure-activity relationship

Abstract

Summary: Nephrotoxicity, with the attendant risk of progression to kidney failure, is a growing problem in many parts of the world. Current orthodox treatment options for nephrotoxicity and kidney failure are limited and there is need for alternative or complementary approaches. This study aimed at evaluating the effect of three structurally related flavonoids, catechin, quercetin and taxifolin on renal redox and metabolite biochemical disturbances in rotenone intoxicated animals. Male Wistar rats were administered 1.5 mg/kg rotenone (s.c.) for ten days followed by post-treatment with catechin (5, 10 or 20 mg/kg), quercetin (5, 10, or 20 mg/kg) and taxifolin (0.25, 0.5 or 1.0 mg/kg) (s.c.), for 3 days. Renal redox indices and levels of renal-related metabolites (creatinine, urea and uric acid) were assessed after sacrifice of animals. Catechin, quercetin and taxifolin significantly attenuated rotenone-induced effects on oxidative stress markers and metabolites linked to renal health. Quercetin was clearly more effective than catechin. The activity demonstrated by taxifolin, despite being administered at the lowest doses, was compelling. The results highlight the potential of these phytochemicals in the management of renal dysfunction. The findings additionally suggest a correlation between the structure of the flavonoids and their activity but also indicate that additional structural considerations beyond conventionally acknowledged ones may be involved.

Referenser

Abdel-Raheem, I. T., Abdel-Ghany, A. A., and Mohamed, G. A. (2009). Protective effect of quercetin against gentamicin-induced nephrotoxicity in rats. Biological & Pharmaceutical Bulletin, 32(1), 61–67.

Adil, M., Kandhare, A. D., Dalvi, G., Ghosh, P., Venkata, S., Raygude, K. S., and Bodhankar, S. L. (2016). Ameliorative effect of berberine against gentamicin-induced nephrotoxicity in rats via attenuation of oxidative stress, inflammation, apoptosis and mitochondrial dysfunction. Renal Failure, 38(6), 996–1006. https://doi.org/10.3109/0886022X.2016.1165120

Akinmoladun, A. C., Akinrinola, B. L., Olaleye, M. T., and Farombi, E. O. (2015). Kolaviron, a Garcinia kola biflavonoid complex, protects against ischemia/reperfusion injury: pertinent mechanistic insights from biochemical and physical evaluations in rat brain. Neurochemical Research, 40(4), 777–787. https://doi.org/10.1007/s11064-015-1527-z

Akimoladun, A. C., oladejo, C. O., Josiah, S. S., Famusiwa. C. D., Ojo, O. B. and Olaleye, M. T. (2018). Catechin, quercetin and taxifolin improve redox and biochemical imbalances in rotenone-induced hepatocellular dysfunction: Relevance for therapy in pesticide-induced liver toxicity? Pathophysiology, 25 (4): 365-371

Aldemir, O., Yildirim, H. K., & Sözmen, E. Y. (2018). Antioxidant and anti-inflammatory effects of biotechnologically transformed propolis. Journal of Food Processing and Preservation, 0(0), e13642. https://doi.org/10.1111/jfpp.13642

Amin, K. A., Ahmed, R. R., Hozayen, W. G., & Antar, A. (2017). Renoprotective and Antioxidant Effects of Silymarin and Propolis on Diclofenac Sodium - Induced Renal Toxicity in Rats. International Journal of Pure & Applied Bioscience, 5(2), 31–42. https://doi.org/10.18782/2320-7051.2421

Anetor, J. I., Anetor, G. O., Iyanda, A. A., & Adeniyi, F. (2008). Environmental chemicals and human neurotoxicity: magnitude, prognosis and markers. African Journal of Biomedical Research, 11(1). https://doi.org/10.4314/ajbr.v11i1.50675

Arnold, R., Issar, T., Krishnan, A. V., & Pussell, B. A. (2016). Neurological complications in chronic kidney disease. JRSM Cardiovascular Disease, 5, 204800401667768. https://doi.org/10.1177/2048004016677687

Arutyunyan, T. V., Korystova, A. F., Kublik, L. N., Levitman, M. K., Shaposhnikova, V. V., & Korystov, Y. N. (2013). Effects of taxifolin on the activity of angiotensin-converting enzyme and reactive oxygen and nitrogen species in the aorta of aging rats and rats treated with the nitric oxide synthase inhibitor and dexamethasone. AGE, 35(6), 2089–2097. https://doi.org/10.1007/s11357-012-9497-4

Benzie, I. F., & Strain, J. J. (1996). The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Analytical Biochemistry, 239(1), 70–76. https://doi.org/10.1006/abio.1996.0292

Beutler, E., Duron, O., & Kelly, B. M. (1963). Improved method for the determination of blood glutathione. The Journal of Laboratory and Clinical Medicine, 61, 882–888.

Birsoy, K., Wang, T., Chen, W. W., Freinkman, E., Abu-Remaileh, M., & Sabatini, D. M. (2015). An Essential Role of the Mitochondrial Electron Transport Chain in Cell Proliferation Is to Enable Aspartate Synthesis. Cell, 162(3), 540–551.

https://doi.org/10.1016/j.cell.2015.07.016

Bonet-Ponce, L., Saez-Atienzar, S., Da, C. C., Sancho-Pelluz, J., Barcia, J. M., Martinez-Gil, N., … Galindo, M. F. (2016). Rotenone Induces the Formation of 4-Hydroxynonenal Aggresomes. Role of ROS-Mediated Tubulin Hyperacetylation and Autophagic Flux Disruption. Molecular Neurobiology, 53(9), 6194–6208. https://doi.org/10.1007/s12035-015-9509-3

Bowers, L. D., & Wong, E. T. (1980). Kinetic serum creatinine assays. II. A critical evaluation and review. Clinical Chemistry, 26(5), 555–561.

Cao, X., Nie, X., Xiong, S., Cao, L., Wu, Z., Moore, P. K., & Bian, J.-S. (2018). Renal protective effect of polysulfide in cisplatin-induced nephrotoxicity. Redox Biology, 15, 513–521.

https://doi.org/10.1016/j.redox.2018.01.012

Chen, L., Teng, H., Xie, Z., Cao, H., Cheang, W. S., Skalicka-Woniak, K., … Xiao, J. (2018). Modifications of dietary flavonoids towards improved bioactivity: An update on structure–activity relationship. Critical Reviews in Food Science and Nutrition, 58(4), 513–527.

https://doi.org/10.1080/10408398.2016.1196334

Csepregi, K., Neugart, S., Schreiner, M., & Hideg, É. (2016). Comparative Evaluation of Total Antioxidant Capacities of Plant Polyphenols. Molecules (Basel, Switzerland), 21(2). https://doi.org/10.3390/molecules21020208

Dai, Y., Cheng, S., Wang, Z., Zhang, R., Yang, Z., Wang, J., … Chen, X. (2018). Hypochlorous Acid Promoted Platinum Drug Chemotherapy by Myeloperoxidase-Encapsulated Therapeutic Metal Phenolic Nanoparticles. ACS Nano, 12(1), 455–463. https://doi.org/10.1021/acsnano.7b06852

Degrossoli, A., Müller, A., Xie, K., Schneider, J. F., Bader, V., Winklhofer, K. F., … Leichert, L. I. (2018). Neutrophil-generated HOCl leads to non-specific thiol oxidation in phagocytized bacteria. ELife, 7, e32288. https://doi.org/10.7554/eLife.32288

Dorman, D. (2015). Chapter 13 - Extrapyramidal system neurotoxicity: animal models. In M. Lotti & M. L. Bleecker (Eds.), Handbook of Clinical Neurology (Vol. 131, pp. 207–223). Elsevier.

https://doi.org/10.1016/B978-0-444-62627-1.00012-3

Eiserich, J. P., Hristova, M., Cross, C. E., Jones, A. D., Freeman, B. A., Halliwell, B., & van der Vliet, A. (1998). Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils. Nature, 391(6665), 393–397. https://doi.org/10.1038/34923

Feriani, A., Contreras, M. del M., Talhaoui, N., Gómez-Caravaca, A. M., Taamalli, A., Segura-Carretero, A., … Allagui, M. S. (2017). Protective effect of Globularia alypum leaves against deltamethrin-induced nephrotoxicity in rats and determination of its bioactive compounds using high-performance liquid chromatography coupled with electrospray ionization tandem quadrupole–time-of-flight mass spectrometry. Journal of Functional Foods, Complete(32), 139–148. https://doi.org/10.1016/j.jff.2017.02.015

Gupta, R. C. (2012). Chapter 52 - Rotenone. In Veterinary Toxicology (Second Edition) (pp. 620–623). Boston: Academic Press. https://doi.org/10.1016/B978-0-12-385926-6.00052-1

Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1974). Glutathione S-Transferases THE FIRST ENZYMATIC STEP IN MERCAPTURIC ACID FORMATION. Journal of Biological Chemistry, 249(22), 7130–7139.

Hassan, S. S., Thomann, C., Ettarh, R., & Ahmad, Z. (2017). Possible protective role of silybin against polymyxin E-induced toxic effect in rat kidneys: A biochemical approach. Neurourology and Urodynamics, 36(8), 2003–2010. https://doi.org/10.1002/nau.23249

Hayek, T., Fuhrman, B., Vaya, J., Rosenblat, M., Belinky, P., Coleman, R., … Aviram, M. (1997). Reduced Progression of Atherosclerosis in Apolipoprotein E–Deficient Mice Following Consumption of Red Wine, or Its Polyphenols Quercetin or Catechin, Is Associated With Reduced Susceptibility of LDL to Oxidation and Aggregation. Arteriosclerosis, Thrombosis, and Vascular Biology, 17(11), 2744–2752.

https://doi.org/10.1161/01.ATV.17.11.2744

Hsiao, Y.-P., Huang, H.-L., Lai, W.-W., Chung, J.-G., & Yang, J.-H. (2009). Antiproliferative effects of lactic acid via the induction of apoptosis and cell cycle arrest in a human keratinocyte cell line (HaCaT). Journal of Dermatological Science, 54(3), 175–184.

https://doi.org/10.1016/j.jdermsci.2009.02.012

Jaiswal, N., & Rizvi, S. I. (2014). Onion extract (Allium cepa L.), quercetin and catechin up‐regulate paraoxonase 1 activity with concomitant protection against low‐density lipoprotein oxidation in male Wistar rats subjected to oxidative stress. Journal of the Science of Food and Agriculture, 94(13), 2752–2757. https://doi.org/10.1002/jsfa.6620

Jiang, X.-W., Qiao, L., Feng, X., Liu, L., Wei, Q.-W., Wang, X.-W., & Yu, W.-H. (2017). Rotenone induces nephrotoxicity in rats: oxidative damage and apoptosis. Toxicology Mechanisms and Methods, 27(7), 528–536. https://doi.org/10.1080/15376516.2017.1333553

Jung, D., Biggs, H., Erikson, J., & Ledyard, P. U. (1975). New Colorimetric reaction for end-point, continuous-flow, and kinetic measurement of urea. Clinical Chemistry, 21(8), 1136–1140.

Kakkar, P., Das, B., & Viswanathan, P. N. (1984). A modified spectrophotometric assay of superoxide dismutase. Indian Journal of Biochemistry & Biophysics, 21(2), 130–132.

Kalai Selvi, I., & Nagarajan, S. (2018). Separation of catechins from green tea ( Camellia sinensis L.) by microwave assisted acetylation, evaluation of antioxidant potential of individual components and spectroscopic analysis. LWT, 91, 391–397. https://doi.org/10.1016/j.lwt.2018.01.042

Kataria, A., Trasande, L., & Trachtman, H. (2015). The effects of environmental chemicals on renal function. Nature Reviews. Nephrology, 11(10), 610–625. https://doi.org/10.1038/nrneph.2015.94

Kay, C., de Gesso, J., Warner, E., Amin, H., de Ferrars, R., Edwards, M., … O’Connell, M. (2015). The bioactivity of flavonoids is likely the result of cumulative low exposure to a variety of structurally similar phenolic metabolites. The FASEB Journal, 29(1_supplement), 118.4. https://doi.org/10.1096/fasebj.29.1_supplement.118.4

Kim, S. Y., & Moon, A. (2012). Drug-Induced Nephrotoxicity and Its Biomarkers. Biomolecules & Therapeutics, 20(3), 268–272. https://doi.org/10.4062/biomolther.2012.20.3.268

Krieg, M., Gunsser, K. J., Steinhagen-Thiessen, E., & Becker, H. (1986). [Comparative quantitative clinico-chemical analysis of the characteristics of 24-hour urine and morning urine]. Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 24(11), 863–869.

Levine, R. L., Garland, D., Oliver, C. N., Amici, A., Climent, I., Lenz, A. G., … Stadtman, E. R. (1990). Determination of carbonyl content in oxidatively Ocular Toxicology, 0(0), 1–6. https://doi.org/10.1080/15569527.2018.1442842

Thiffault, C., Langston, J. W., & Di Monte, D. A. (2000). Increased striatal dopamine turnover following acute administration of rotenone to mice. Brain Research, 885(2), 283–288.

Tian, R., Ding, Y., Peng, Y.-Y., & Lu, N. (2017). Inhibition of Myeloperoxidase- and Neutrophil-Mediated Hypochlorous Acid Formation in Vitro and Endothelial Cell Injury by (-)-Epigallocatechin Gallate. Journal of Agricultural and Food Chemistry, 65(15), 3198–3203. https://doi.org/10.1021/acs.jafc.7b00631

Topal, F., Nar, M., Gocer, H., Kalin, P., Kocyigit, U. M., Gülçin, İ., & Alwasel, S. H. (2016). Antioxidant activity of taxifolin: an activity–structure relationship. Journal of Enzyme Inhibition and Medicinal Chemistry, 31(4), 674–683. https://doi.org/10.3109/14756366.2015.1057723

Trouillas, P., Marsal, P., Siri, D., Lazzaroni, R., & Duroux, J.-L. (2006). A DFT study of the reactivity of OH groups in quercetin and taxifolin antioxidants: The specificity of the 3-OH site. Food Chemistry, 97(4), 679–688. https://doi.org/10.1016/j.foodchem.2005.05.042

Tu, S., Xiao, F., Min, X., Chen, H., Fan, X., & Cao, K. (2018). Catechin Attenuates Coronary Heart Disease in a Rat Model by Inhibiting Inflammation. Cardiovascular Toxicology, 1–7. https://doi.org/10.1007/s12012-018-9449-z

Varshney, R., & Kale, R. K. (1990). Effects of calmodulin antagonists on radiation-induced lipid peroxidation in microsomes. International Journal of Radiation Biology, 58(5), 733–743.

Vazquez Prieto, M. A., Bettaieb, A., Lanzi, C. R., Soto, V. C., Perdicaro, D. J., Galmarini, C. R., Fawaz G. H.,

Roberto M. M. & Oteiza, P. I. (2015). Catechin and quercetin attenuate adipose inflammation in fructose-fed rats and 3T3-L1 adipocytes. Molecular Nutrition & Food Research, 59(4), 622–633. https://doi.org/10.1002/mnfr.201400631

Wang, Y.-H., Wang, W.-Y., Chang, C.-C., Liou, K.-T., Sung, Y.-J., Liao, J.-F., … Shen, Y.-C. (2006). Taxifolin ameliorates cerebral ischemia-reperfusion injury in rats through its anti-oxidative effect and modulation of NF-kappa B activation. Journal of Biomedical Science, 13(1), 127–141. https://doi.org/10.1007/s11373-005-9031-0

Weber, E. J., Himmelfarb, J., & Kelly, E. J. (2017). Concise review: Current and emerging biomarkers of nephrotoxicity. Current Opinion in Toxicology, 4, 16–21. https://doi.org/10.1016/j.cotox.2017.03.002

Weidmann, A. E. (2012). Dihydroquercetin: More than just an impurity? European Journal of Pharmacology, 684(1–3), 19–26. https://doi.org/10.1016/j.ejphar.2012.03.035

Wootton-Beard, P. C., Moran, A., & Ryan, L. (2011). Stability of the total antioxidant capacity and total polyphenol content of 23 commercially available vegetable juices before and after in vitro digestion measured by FRAP, DPPH, ABTS and Folin–Ciocalteu methods. Food Research International, 1(44), 217–224. https://doi.org/10.1016/j.foodres.2010.10.033

Zhao, P., Chen, K., Zhang, G., Deng, G., & Li, J. (2017). Pharmacological Basis for Use of Selaginella moellendorffii in Gouty Arthritis: Antihyperuricemic, Anti-Inflammatory, and Xanthine Oxidase Inhibition. Evidence-Based Complementary and Alternative Medicine : ECAM, 2017. https://doi.org/10.1155/2017/2103254

Publicerad

2019-06-30

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Full Length Research Articles

Referera så här

Effects of Catechin, Quercetin and Taxifolin on Redox Parameters and Metabolites Linked with Renal Health in Rotenone-toxified Rats. (2019). Nigerian Journal of Physiological Sciences, 34(1), 001-010. https://ojshostng.com/index.php/njphysiologicalsciences/article/view/1918

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