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Plant Foods for Human Nutrition

, Volume 74, Issue 2, pp 204–209 | Cite as

Intake of Heated Leaf Extract of Coriandrum sativum Contributes to Resistance to Oxidative Stress via Decreases in Heavy Metal Concentrations in the Kidney

  • Ryusuke Nishio
  • Hanuna Tamano
  • Hiroki Morioka
  • Azusa Takeuchi
  • Atsushi TakedaEmail author
Original Paper
  • 178 Downloads

Abstract

Coriandrum sativum (coriander) is an annual herb of the Apiaceae family and has been used as a traditional remedy. Here we examined whether heated leaf extract of coriander decreases the concentrations of heavy metals in tissues. Male ddY mice were given a drinking water containing 0.25% of heated leaf extract of coriander for 8 weeks. Eight weeks after the intake, the concentrations of zinc, iron, copper, arsenic, and cadmium were measured in the liver and kidney. The intake of coriander did not modify the concentrations of all heavy metals tested in the liver, but decreased the concentrations of iron, arsenic, and cadmium in the kidney. Because heavy metals can induce oxidative stress, the effect of coriander intake on hydrogen peroxide-induced oxidative stress was compared between slices from the kidney and liver. The slices were immersed in Ringer solution containing 100 μM hydrogen peroxide and aminophenyl fluorescein (APF), a probe for detecting reactive oxygen species (ROS). APF fluorescence was markedly increased in the control kidney slices, while the increase was completely blocked in kidney slices from coriander intake group. In contrast, APF fluorescence was also markedly increased in the control liver slices, while the increase was not blocked by coriander intake. The present study indicates that intake of coriander leaf extract contributes to powerful resistance to oxidative stress in the kidney, probably via decreased concentrations in heavy metals. It is likely that decrease in arsenic concentration to the detection limit is a major factor for the resistance.

Keywords

Arsenic Cadmium Iron Reactive oxygen species Coriandrum sativum 

Notes

Acknowledgements

This work was supported by Nishihara group Inc. (Mishima, Japan).

Compliance with Ethical Standards

Conflict of Interest

The authors declare no conflict of interest.

References

  1. 1.
    Chung RT (2017) Detoxification effects of phytonutrients against environmental toxicants and sharing of clinical experience on practical applications. Environ Sci Pollut Res Int 24:8946–8956.  https://doi.org/10.1007/s11356-015-5263-3 CrossRefGoogle Scholar
  2. 2.
    Laribi B, Kouki K, M’Hamdi M, Bettaieb T (2015) Coriander (Coriandrum sativum L.) and its bioactive constituents. Fitoterapia 103:9–26.  https://doi.org/10.1016/j.fitote.2015.03.012 CrossRefGoogle Scholar
  3. 3.
    Sahib NG, Anwar F, Gilani AH, Hamid AA, Saari N, Alkharfy KM (2013) Coriander (Coriandrum sativum L.): a potential source of high-value components for functional foods and nutraceuticals—a review. Phytother Res 27:1439–1456.  https://doi.org/10.1002/ptr.4897 Google Scholar
  4. 4.
    Gray AM, Flatt PR (1999) Insulin-releasing and insulin-like activity of the traditional anti-diabetic plant Coriandrum sativum (coriander). Br J Nutr 81:203–209.  https://doi.org/10.1017/S0007114599000392 CrossRefGoogle Scholar
  5. 5.
    Cioanca O, Hritcu L, Mihasan M, Hancianu M (2013) Cognitive-enhancing and antioxidant activities of inhaled coriander volatile oil in amyloid β (1–42) rat model of Alzheimer’s disease. Physiol Behav 120:193–202.  https://doi.org/10.1016/j.physbeh.2013.08.006 CrossRefGoogle Scholar
  6. 6.
    Al-Mofleh IA, Alhaider AA, Mossa JS, Al-Sohaibani MO, Rafatullah S, Qureshi S (2006) Protection of gastricmucosal damage by Coriandrum sativum L. pretreatment in Wistar albino rats. Environ Toxicol Pharmacol 22:64–69.  https://doi.org/10.1016/j.etap.2005.12.002 CrossRefGoogle Scholar
  7. 7.
    Mani V, Parle M, Ramasamy K, Majeed AB (2011) Removal of memory deficits by Coriandrum sativum leaves in mice. J Sci Food Agric 91:186–192.  https://doi.org/10.1002/jsfa.4171 CrossRefGoogle Scholar
  8. 8.
    Rakhshandeh H, Sadeghnia HR, Ghorbani A (2012) Sleep-prolonging effect of Coriandrum sativum hydro-alcoholic extract in mice. Nat Prod Res 26:2095–2098.  https://doi.org/10.1080/14786419.2011.613388 Google Scholar
  9. 9.
    Puthusseri B, Divya P, Lokesh V, Neelwarne B (2012) Enhancement of folate content and its stability using food grade elicitors in coriander (Coriandrum sativum L.). Plant Foods Hum Nutr 67:162–170.  https://doi.org/10.1007/s11130-012-0285-1 CrossRefGoogle Scholar
  10. 10.
    Sharma V, Kansal L, Sharma A (2010) Prophylactic efficacy of Coriandrum sativum (coriander) on testis of lead-exposed mice. Biol Trace Elem Res 136:337–354.  https://doi.org/10.1007/s11130-012-0285-1 CrossRefGoogle Scholar
  11. 11.
    Velaga MK, Yallapragada PR, Williams D, Rajanna S, Bettaiya R (2014) Hydroalcoholic seed extract of Coriandrum sativum (coriander) alleviates lead-induced oxidative stress in different regions of rat brain. Biol Trace Elem Res 159:351–363.  https://doi.org/10.1007/s12011-014-9989-4 CrossRefGoogle Scholar
  12. 12.
    Aga M, Iwaki K, Ueda Y, Ushio S, Masaki N, Fukuda S, Kimoto T, Ikeda M, Kurimoto M (2001) Preventive effect of Coriandrum sativum (Chinese parsley) on localized lead deposition in ICR mice. J Ethnopharmacol 77:203–208.  https://doi.org/10.1016/S0378-8741(01)00299-9 CrossRefGoogle Scholar
  13. 13.
    Karunasagar D, Krishna MV, Rao SV, Arunachalam J (2005) Removal and preconcentration of inorganic and methyl mercury from aqueous media using a sorbent prepared from the plant Coriandrum sativum. J Hazard Mater 118:133–139.  https://doi.org/10.1016/j.jhazmat.2004.10.021 CrossRefGoogle Scholar
  14. 14.
    Omura Y, Beckman SL (1995) Role of mercury (Hg) in resistant infections & effective treatment of Chlamydia trachomatis and herpes family viral infections (and potential treatment for cancer) by removing localized hg deposits with Chinese parsley and delivering effective antibiotics using various drug uptake enhancement methods. Acupunct Electrother Res 20:195–229CrossRefGoogle Scholar
  15. 15.
    Omura Y, Shimotsuura Y, Fukuoka A, Fukuoka H, Nomoto T (1996) Significant mercury deposits in internal organs following the removal of dental amalgam, & development of pre-cancer on the gingiva and the sides of the tongue and their represented organs as a result of inadvertent exposure to strong curing light (used to solidify synthetic dental fillingmaterial) & effective treatment: a clinical case report, along with organ representation areas for each tooth. Acupunct Electrother Res 21:133–160CrossRefGoogle Scholar
  16. 16.
    Gaur N, Kukreja A, Yadav M, Tiwari A (2017) Assessment of phytoremediation ability of Coriander sativum for soil and water co-contaminated with lead and arsenic: a small-scale study. 3 Biotech:196.  https://doi.org/10.1007/s13205-017-0794-6
  17. 17.
    Chakraborti D, Rahman MM, Mukherjee A, Alauddin M, Hassan M, Dutta RN, Pati S, Mukherjee SC, Roy S, Quamruzzman Q, Rahman M, Morshed S, Islam T, Sorif S, Selim M, Islam MR, Hossain MM (2015) Groundwater arsenic contamination in Bangladesh-21 years of research. J Trace Elem Med Biol 31:237–248.  https://doi.org/10.1016/j.jtemb.2015.01.003 CrossRefGoogle Scholar
  18. 18.
    Rashid MH, Rahman MM, Correll R, Naidu R (2018) Arsenic and other elemental concentrations in mushrooms from Bangladesh: health risks. Int J Environ Res Public Health 15(5), pii:E919.  https://doi.org/10.3390/ijerph15050919
  19. 19.
    Meharg AA, Raab A (2010) Getting to the bottom of arsenic standards and guidelines. Environ Sci Technol 44:4395e4399.  https://doi.org/10.1021/es9034304 CrossRefGoogle Scholar
  20. 20.
    Meharg AA, Zhao FJ (2012) Arsenic and rice. Springer, Dordrecht.  https://doi.org/10.1017/S0014479712000713 CrossRefGoogle Scholar
  21. 21.
    Meharg AA, Williams PN, Deacon CM, Norton GJ, Hossain M, Louhing D, Marwa E, Lawgalwi Y, Taggart M, Cascio C, Haris P (2014) Urinary excretion of arsenic following rice consumption. Environ Pollut 194:181–187.  https://doi.org/10.1016/j.envpol.2014.07.031 CrossRefGoogle Scholar
  22. 22.
    Jomova K, Jenisova Z, Feszterova M, Baros S, Liska J, Hudecova D, Rhodes CJ, Valko M (2011) Arsenic: toxicity, oxidative stress and human disease. J Appl Toxicol 31:95–107.  https://doi.org/10.1002/jat.1649 Google Scholar
  23. 23.
    Jomova K, Valko M (2011) Advances in metal-induced oxidative stress and human disease. Toxicology 283:65–87.  https://doi.org/10.1016/j.tox.2011.03.001 CrossRefGoogle Scholar
  24. 24.
    Wu X, Cobbina SJ, Mao G, Xu H, Zhang Z, Yang L (2016) A review of toxicity and mechanisms of individual and mixtures of heavy metals in the environment. Environ Sci Pollut Res Int 23:8244–8259.  https://doi.org/10.1007/s11356-016-6333-x CrossRefGoogle Scholar

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© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Department of Neurophysiology, School of Pharmaceutical SciencesUniversity of ShizuokaShizuokaJapan

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