Startseite Comparison of antithyroid effects and hepatic complications of methimazole with catechin and its nanoencapsulation form in adult male rats
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Comparison of antithyroid effects and hepatic complications of methimazole with catechin and its nanoencapsulation form in adult male rats

  • Esmaeil Mohamadizadeh , Mehdi Sheikh Arabi , Vida Hojati , Gholamhassan Vaezi ORCID logo EMAIL logo und Seyed Mehran Hosseini ORCID logo EMAIL logo
Veröffentlicht/Copyright: 2. August 2022

Abstract

Objectives

Methimazole is an antithyroid drug and is used clinically in hyperthyroidism. Liver dysfunction is one of the side effects of methimazole. Catechins are natural flavonoids and have antioxidant, antithyroid, and liver protection effects. Despite the wide range of biological properties of catechins, their effective use is limited due to poor water solubility, low stability, and low bioavailability. Catechin niosomal nanoencapsulation improves the properties of catechin and increases its antioxidant activities.

Methods

Niosomal vesicles were synthesized by the Thin Film Hydration method and their physicochemical characteristics, morphology, and percentage of trapped catechin in them were determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), and spectrophotometry, respectively. In this study, 32 adult male rats were divided into 4 groups: control, 50 mg/kg methimazole, 100 mg/kg catechin, and 100 mg/kg nanocapsule niosomal form of catechin. The drugs were administered orally and the duration of treatment was 8 weeks. Then, the serum concentration of thyroid hormones and thyroid stimulating hormone (TSH) by enzyme-linked immunosorbent assay (ELISA) method, and serum liver function tests were performed using an autoanalyzer. The activities of hepatic oxidative enzymes were measured spectrophotometrically.

Results

Our study showed that the percentage of catechin encapsulation in the niosome was calculated to be 51%. A significant difference was observed in the catechin and encapsulated catechin treatment groups compared to the methimazole group (p <0.0001). In all three treatment groups of methimazole, catechin, and niosomal nanocapsule catechin, serum levels of TT3, TT4, FT3, FT4, body weight and daily consumption of water and food were significantly reduced compared to the control group (p <0.0001).

Conclusions

The antithyroid effects of catechin and its encapsulated form were comparable to methimazole. Also, the encapsulation improved the hepatoprotective effects of catechin.


Corresponding authors: Gholamhassan Vaezi, Professor, Department of Biology, Faculty of Basic Sciences, Islamic Azad University, Cheshme Ali Blvd, Damghan, Iran, Phone: +98-367-163-9998, E-mail: ; and Seyed Mehran Hosseini, MD, PhD, Professor of Medical Physiology, Department of Physiology, School of Medicine, Golestan University of Medical Sciences, Gorgan, Golestan, Iran; Neuroscience Research Center, School of Medicine, Golestan University of Medical Sciences, Gorgan, Golestan, Iran, Phone: (98) 9113736634, Fax: (98) 1732452225, E-mail:

Acknowledgments

We would like to thank Dr. Esmaeil Samadian, Dr. Sahar Ardalan, Dr. Seyed Mostafa Mir, and Mr. Ahmad Abbasi for their kindly help in this study.

  1. Research funding: This research received no external funding.

  2. Author contributions: EM, MSA, GV, and SMH co-designed the research. EM and MSA performed the experiments and the measurements. EM and VH analyzed the data and the lab tests. EM, SMH, and GV wrote the manuscript and edited it. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors declare no conflict of interest.

  4. Ethical approval: This study has a research ethics certificate with approval ID: IR.GOUMS.REC.1397.227 from Golestan University of Medical Sciences.

References

1. Chandra, AK, De, N. Goitrogenic/antithyroidal potential of green tea extract in relation to catechin in rats. Food Chem Toxicol 2010;48:2304–11. https://doi.org/10.1016/j.fct.2010.05.064.Suche in Google Scholar

2. Cooper, DS. Antithyroid drugs: a review. N Engl J Med 2005;352:905–17. https://doi.org/10.1056/nejmra042972.Suche in Google Scholar

3. Sefi, M, Amara, IB, Troudi, A, Soudani, N, Hakim, A, Zeghal, KM, et al.. Effect of selenium on methimazole induced liver damage and oxidative stress in adult rats and their offspring. Toxicol Ind Health 2012;9:1–17.10.1177/0748233712462445Suche in Google Scholar

4. Woeber, KA. Methimazole-induced hepatotoxicity. Endocr Pract 2002;8:222–4. https://doi.org/10.4158/ep.8.3.222.Suche in Google Scholar

5. Angermuller, S, Islinger, M, Volkl, A. Peroxisomes and reactive oxygen species, a lasting challenge. Histochem Cell Biol 2009;131:459–63. https://doi.org/10.1007/s00418-009-0563-7.Suche in Google Scholar

6. Cano-Europa, E, Blas-Valdivia, V, Lopez-Galindo, GE, Franco-Colin, M, Pineda-Reynoso, M, Hernandez-Garcia, A, et al.. Methimazole-induced hypothyroidism causes alteration of the REDOX environment, oxidative stress, and hepatic damage; events not caused by hypothyroidism itself. Ann Hepatol 2010;9:80–8.10.1016/S1665-2681(19)31684-9Suche in Google Scholar

7. Kim, H, Lee, TH, Hwang, YS, Bang, MA, Kim, KH, Suh, JM, et al.. Methimazole as an antioxidant and immunomodulator in thyroid cells: mechanisms involving interferon-γ signaling and H2O2 scavenging. Mol Pharamacol 2001;60:972–80. https://doi.org/10.1124/mol.60.5.972.Suche in Google Scholar PubMed

8. Niknahad, H, Jamshidzadeh, A, Heidari, R, Hosseini, Z, Mobini, K, Khodaei, F, et al.. Paradoxical effect of methimazole on liver mitochondria: in vitro and in vivo. Toxicol Lett 2016;259:108–15. https://doi.org/10.1016/j.toxlet.2016.08.003.Suche in Google Scholar PubMed

9. Amara, IB, Hakim, A, Troudi, A, Soudani, N, Makni, FA, Zeghal, KM, et al.. Protective effects of selenium on methimazole-induced anemia and oxidative stress in adult rats and their offspring. Hum Exp Toxicol 2011;30:1549–60. https://doi.org/10.1177/0960327110392403.Suche in Google Scholar PubMed

10. De Souza Dos Santos, MC, Gonçalves, CF, Vaisman, M, Ferreira, AC, de Carvalho, DP. Impact of flavonoids on thyroid function: a review. Food Chem Toxicol 2011;49:2495–502.10.1016/j.fct.2011.06.074Suche in Google Scholar PubMed

11. Chandra, AK, De, N. Goitrogenic and antithyroid potential of green tea of indian origin: a review. J Bangladesh Soc Physiol 2014;9:105–16.10.3329/jbsp.v9i2.22807Suche in Google Scholar

12. Song, Q, Li, D, Zhou, Y, Yang, J, Yang, W, Zhou, G, et al.. Enhanced uptake and transport of (+)-catechin and (–)-epigallocatechin gallate in niosomal formulation by human intestinal Caco-2 cells. Int J Nanomed 2014;9:2157–65. https://doi.org/10.2147/ijn.s59331.Suche in Google Scholar

13. Huang, Y-B, Tsai, M-J, Wu, P-C, Tsai, Y-H, Wu, Y-H, Fang, J-Y. Elastic liposomes as carriers for oral delivery and the brain distribution of (+)-catechin. J Drug Target 2011;19:709–18. https://doi.org/10.3109/1061186x.2010.551402.Suche in Google Scholar PubMed

14. Chandra, AK, De, N, Choudhury, SR. Effect of different doses of un-fractionated green and black tea extracts on thyroid physiology. Hum Exp Toxicol 2010;30:884–96. https://doi.org/10.1177/0960327110382563.Suche in Google Scholar PubMed

15. Chengelis, CP, Kirkpatrick, JB, Regan, KS, Radovsky, AE, Beck, MJ, Morita, O, et al.. 28-Day oral (gavage) toxicity studies of green tea catechins prepared for beverages in rats. Food Chem Toxicol 2008;46:978–89. https://doi.org/10.1016/j.fct.2007.10.027.Suche in Google Scholar PubMed

16. Lin, AM, Chyi, BY, Wu, LY, Hwang, LS, Ho, LT. The antioxidative property of green tea against iron-induced oxidative stress in rat brain. Chin J Physiol 1998;41:189–94.Suche in Google Scholar

17. Tabassum, H, Parvez, S, Rehman, H, Banerjee, BD, Raisuddin, S. Catechin as an antioxidant in liver mitochondrial toxicity: inhibition of tamoxifen-induced protein oxidation and lipid peroxidation. J Biochem Mol Toxicol 2007;21:110–7. https://doi.org/10.1002/jbt.20167.Suche in Google Scholar PubMed

18. Mehra, P, Garg, M, Koul, A, Bansal, DD. Effect of (+)-catechin hydrate on oxidative stress induced by high sucrose and high fat diet in male Wistar rats. Indian J Exp Biol 2013;51:823–7.Suche in Google Scholar

19. Catterall, F, King, LJ, Clifford, MN, Ioannides, C. Bio-availability of dietary doses of 3H-labelled tea anti-oxidants (+)-catechin and (–)-epicatechin in rat. Xenobiotica 2003;33:743–53. https://doi.org/10.1080/0049825031000108315.Suche in Google Scholar PubMed

20. Zhang, L, Kosaraju, SL. Biopolymeric delivery system for controlled release of polyphenolic antioxidants. Eur Polym J 2007;43:2956–66. https://doi.org/10.1016/j.eurpolymj.2007.04.033.Suche in Google Scholar

21. Dang, S, Gupta, S, Bansal, R, Ali, J, Gabrani, R. Nano-encapsulation of a natural polyphenol, green tea catechins: way to preserve its antioxidative potential. In: Book: free radicals in human health and disease. India: Springer; 2015:397–415 pp.10.1007/978-81-322-2035-0_25Suche in Google Scholar

22. Niu, G, Yousefi, B, Qujeq, D, Marjani, A, Asadi, J, Wang, Z, et al.. Melatonin and doxorubicin co-delivered via a functionalized graphene-dendrimeric system enhances apoptosis of osteosarcoma cells. Mater Sci Eng C 2021;119:111554. https://doi.org/10.1016/j.msec.2020.111554.Suche in Google Scholar PubMed

23. Anand, P, Sundaram, C, Jhurani, S, Kunnumakkara, AB, Aggarwal, BB. Curcumin and cancer: an “old-age” disease with an “age-old” solution. Cancer Lett 2008;267:133–64. https://doi.org/10.1016/j.canlet.2008.03.025.Suche in Google Scholar

24. Samanta, A, Bandyopadhyay, B, Das, N. Formulation of catechin hydrate nanocapsule and study of its bioavailability. Med Chem 2016;6:399–404. https://doi.org/10.4172/2161-0444.1000376.Suche in Google Scholar

25. Mir, SM, Tehrani, SS, Goodarzi, G, Jamalpoor, Z, Asadi, J, Khelghati, N, et al.. Shelterin complex at telomeres: implications in ageing. Clin Interv Aging 2020;15:827. https://doi.org/10.2147/cia.s256425.Suche in Google Scholar

26. Safayee, S, Karbalaei, N, Noorafshan, A, Nadimi, E. Induction of oxidative stress, suppression of glucose-induced insulin release, ATP production, glucokinase activity, and histomorphometric changes in pancreatic islets of hypothyroid rat. Eur J Pharmacol 2016;79:1147–156. https://doi.org/10.1016/j.ejphar.2016.08.024.Suche in Google Scholar

27. Mondal, C, Sinha, S, Chakraborty, A, Chandra, AK. Studies on goitrogenic/antithyroidal potentiality of thiocyanate, catechin and after concomitant exposure of thiocyanate-catechin. IJPCR 2016;8:108–16.Suche in Google Scholar

28. Ajala, MO, Ogunro, PS, Fasanmade, OA. Relationship between liver function tests and thyroid hormones in thyroid disorders. Niger Postgrad Med J 2013;20:188–92.10.4103/1117-1936.164708Suche in Google Scholar

29. Bun, SS, Bun, H, Gue´don, C, Rosier, E, Ollivier, A. Effect of green tea extracts on liver functions in Wistar rats. Food Chem Toxicol 2006;44:1108–13. https://doi.org/10.1016/j.fct.2006.01.006.Suche in Google Scholar

30. Goth, L. A simple method for determination of serum catalase activity and revision of reference range. Clin Chim Acta 1991;196:143–51. https://doi.org/10.1016/0009-8981(91)90067-m.Suche in Google Scholar

31. Marklund, S, Marklund, G. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem 1974;47:469–74. https://doi.org/10.1111/j.1432-1033.1974.tb03714.x.Suche in Google Scholar

32. Hagar, HH, Etter, EE, Arafa, M. Taurine attenuates hypertension and renal dysfunction induced by cyclosporine A in rats. Clin Exp Pharmacol Physiol 2006;33:189–96. https://doi.org/10.1111/j.1440-1681.2006.04345.x.Suche in Google Scholar

33. Bradford, MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–54. https://doi.org/10.1016/0003-2697(76)90527-3.Suche in Google Scholar

34. Sung, H, Nah, J, Chun, S, Park, H, Yang, SE, Min, WK. In vivo antioxidant effect of green tea. Eur J Clin Nutr 2000;54:527–9. https://doi.org/10.1038/sj.ejcn.1600994.Suche in Google Scholar PubMed

35. Ye, JH, Augustin, MA. Nano- and micro-particles for delivery of catechins: physical and biological performance. Crit Rev Food Sci Nutr 2018;59:1–17. https://doi.org/10.1080/10408398.2017.1422110.Suche in Google Scholar PubMed

36. Moghassemi, S, Hadjizadeh, A. Nano-niosomes as nanoscale drug delivery systems: an illustrated review. J Contr Release 2014;185:22–36. https://doi.org/10.1016/j.jconrel.2014.04.015.Suche in Google Scholar PubMed

37. Cakic-Milosevic, M, Korac, A, Davidovic, V. Methimazole-induced hypothyroidism in rats: effects on body weight and histological characteristics of thyroid gland. Jugosl Med Biohemija 2004;23:143–7. https://doi.org/10.2298/jmh0402143c.Suche in Google Scholar

38. Messarah, M, Boumendjel, A, Chouabia, A, Klibet, F, Abdennour, C, Boulakoud, MS, et al.. Influence of thyroid dysfunction on liver lipid peroxidation and antioxidant status in experimental rats. Exp Toxicol Pathol 2010;62:301–10. https://doi.org/10.1016/j.etp.2009.04.009.Suche in Google Scholar PubMed

39. Nadkarni, GD, Deshpande, UR, Pahuja, DN. Effects of propylthiouracil, methimazole and thyroidectomy on liver and plasma proteins: differential response to thyroxine. Exp Clin Endocrinol 1983;81:291–6. https://doi.org/10.1055/s-0029-1210239.Suche in Google Scholar PubMed

40. Jin, X, Zheng, RH, Li, YM. Green tea consumption and liver disease: a systematic review. Liver Int 2008;28:990–6. https://doi.org/10.1111/j.1478-3231.2008.01776.x.Suche in Google Scholar PubMed

41. Kao, YH, Hiipakka, RA, Liao, S. Modulation of endocrine systems and food intake by green tea epigallocatechin gallate. Endocrinology 2000;141:980–7. https://doi.org/10.1210/endo.141.3.7368.Suche in Google Scholar PubMed

42. Venditti, P, Balestrieri, M, Meo, S, Leo, T. Effect of thyroid state on lipid peroxidation, antioxidant defences and susceptibility to oxidative stress in rat tissues. J Endocrinol 1997;155:151–7. https://doi.org/10.1677/joe.0.1550151.Suche in Google Scholar PubMed

43. Goel, A, Kunnumakkara, AB, Aggarwal, BB. Curcumin as “Curecumin”: from kitchen to clinic. Biochem Pharmacol 2008;75:787–809. https://doi.org/10.1016/j.bcp.2007.08.016.Suche in Google Scholar PubMed

44. Rocha, S, Generalov, R, Pereira, MC, Peres, I, Juzenas, P, Coelho, MA. Epigallocatechin gallate-loaded polysaccharide nanoparticles for prostate cancer chemoprevention. Nanomedicine 2011;6:79–87.10.2217/nnm.10.101Suche in Google Scholar PubMed

Received: 2022-03-14
Accepted: 2022-07-04
Published Online: 2022-08-02

© 2022 Walter de Gruyter GmbH, Berlin/Boston

Artikel in diesem Heft

  1. Frontmatter
  2. Reviews
  3. Evidence implementation among complementary medicine practitioners: a meta-summary
  4. Phytochemical: a treatment option for heavy metal induced neurotoxicity
  5. The effects of curcumin-containing supplementations on inflammatory markers and lipid profiles in patients with chronic kidney diseases: a systematic review and meta-analysis of randomized controlled trials
  6. A systematic review on traditional medicinal Animal’s parts and products used for the treatment of respiratory tract disorders in Ethiopia
  7. Review on nutraceuticals: phase transition from preventive to protective care
  8. A study of effect of Centella asiatica on oxidative markers in the hippocampus of offsprings born to alcohol-fed pregnant rats and the correlation with their cognitive functions
  9. Anxiogenic and anxiolytic effects of memantine injected into the ventral hippocampus in male stressed mice
  10. Research Articles
  11. Comparison of antithyroid effects and hepatic complications of methimazole with catechin and its nanoencapsulation form in adult male rats
  12. Almond oil restores blood parameters, liver function, blood and liver antioxidants and DNA, and liver histology more efficiently than olive oil in favism
  13. Highly efficient microencapsulation of phytonutrients by fractioned cellulose using biopolymer complexation technology
  14. Ocimum basilicum alleviates blood glucose, lipid profile and iNOS in diabetes gestational rat model
  15. Blood pressure and blood sugar-lowering effects of purified gambir on diabetic hypertensive Wistar Kyoto rats
  16. Assessment of anti-inflammatory and antioxidant activity of quercetin–rutin blend (SophorOx™) – an invitro cell based assay
  17. Subchronic toxicological evaluation of EnXtra™ (standardised extract of Alpinia galanga rhizome) in rats
  18. Ficus glumosa Del. reduces phenylhydrazine-induced hemolytic anaemia and hepatic damage in Wistar rats
  19. Screening of anti-cancerous potential of classical Raudra rasa and modified Raudra rasa modified with hiraka bhasma (nanodiamond) through FTIR & LC-MS analysis
  20. Aqueous extract of Pedalium murex D. Royen ex L. leafy stem protects against lead induced testicular toxicity in Wistar rats
  21. Intrahippocampal co-administration of nicotine and O-acetyl-L-carnitine prevents the H-89-induced spatial learning deficits in Morris water maze
  22. Developmental effects of early-life stress on dopamine D2 receptor and proteins involved in noncanonical D2 dopamine receptor signaling pathway in the prefrontal cortex of male rats
  23. Probiotic administration enhanced antitrypanosomal effects of diminazene aceturate in dogs experimentally infected with Trypanosoma brucei brucei
  24. Acacia arabica (Lam.) Willd. On osteoblastogenesis, osteoblast proliferation, osteoclastic activity, and bone calcium mineralization
  25. GC-MS analysis of curculigo orchiodes and medicinal herbs with cytotoxic, hepatoprotective attributes of ethanolic extract from Indian origin
  26. Biochemical and histopathological evaluation of liver, kidney, and pancreas in normal Sprague Dawley rats administered aqueous extract of beetroot (Beta vulgaris)
  27. The effectiveness of emotional freedom techniques (EFT) on depression of postmenopausal women: a randomized controlled trial
  28. The formulation and efficacy of topical Dorema ammoniacum in treating Melasma: a randomized double-blind, placebo-controlled trial
  29. Impact of inhalation aromatherapy with Damask Rose (Rosa damascena) on stress, anxiety and hemodynamic parameters of patients undergoing coronary angiography: a single blind randomized clinical trial
  30. Hydro-alcoholic extract of Morus nigra reduces fasting blood glucose and HbA1c% in diabetic patients, probably via competitive and allosteric interaction with alpha-glucosidase enzyme; a clinical trial and in silico analysis
  31. Prophylactic management of radiation-induced mucositis using herbal mouthwash in patients with head and neck cancer: an assessor-blinded randomized controlled trial
  32. Implementation science in New Zealand naturopathic practice: a cross-sectional study
  33. Issues of mindfulness implementation for oncology caregivers
  34. Immediate effect of cold mud pack therapy on autonomic variables in primary hypertensive individuals: a randomized trial
  35. Effect of a Persian metabolic diet on the functional dyspepsia symptoms in patients with postprandial distress syndrome: a randomized, double-blind clinical trial
Heruntergeladen am 27.11.2025 von https://www.degruyterbrill.com/document/doi/10.1515/jcim-2022-0099/html
Button zum nach oben scrollen