Startseite Ameliorative effect of Neera, nonfermented coconut inflorescence sap, on cisplatin-induced renal toxicity by abating oxidative stress
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Ameliorative effect of Neera, nonfermented coconut inflorescence sap, on cisplatin-induced renal toxicity by abating oxidative stress

  • Prabha Silpa , Nair Meera , Edappilly M. Shaji , Muralidharan S. Indu , Balu T. Kuzhivelil und Thekkekara D. Babu ORCID logo EMAIL logo
Veröffentlicht/Copyright: 25. August 2020

Abstract

Objectives

Neera, nonfermented coconut inflorescence sap (NFCIS) from unopened spadix of Cocos nucifera L., is a well-known traditional beverage. But, scientific reports on its health benefits are limited. NFCIS is reported to exhibits free radical scavenging activity, and its chemical composition is found promising. In the present study, the effect of NFCIS on alleviating cisplatin-induced nephrotoxicity was analyzed in mice.

Methods

The renal toxicity was induced by cisplatin (16 mg/kg b.wt. ip) in Swiss albino mice. The antioxidant activity of NFCIS was evaluated by nitric oxide radical scavenging assay and phorbol-12-myristate-13-acetate–induced superoxide radical generation in mice peritoneal macrophages. Total polyphenolic content of sap was determined using Folin–Ciocalteu reagent. The phytochemicals present in NFCIS was identified using Fourier transform infrared (FT-IR) spectroscopy.

Results

NFCIS was found to scavenge nitric oxide (NO) radicals (IC50 = 32 ± 2.47 μL/mL) and shown to inhibit superoxide (SO) generation (53.5 ± 2.1%) in macrophages. High polyphenolic content (193 µg gallic acid/mL) was determined in the sap. The FT-IR spectrum of NFCIS revealed the presence of several phytochemicals indicate its pharmaceutical and nutritional value. Cisplatin-induced hike in urea, creatinine and lipid peroxidation was significantly decreased to 65.16, 87.74 and 53.41% by NFCIS, respectively. Hb (42.37%) and total count (72.81%) were also found to be increased. Additionally, the activity of antioxidant enzymes superoxide dismutase, catalase, glutathione peroxidase and reduced glutathione was enhanced to 53.06, 40, 52.22 and 38.49%, respectively.

Conclusions

Results indicate that NFCIS effectively alleviates cisplatin-mediated renal toxicity by its antioxidant activity.


Corresponding author: Thekkekara D. Babu, Associate professor, Department of Biochemistry, Amala Cancer Research Centre (Recognized Research Centre, University of Calicut), Amala Nagar, Thrissur, 680 555, Kerala, India, Mobile: 9495739939, E-mail:

Acknowledgments

The authors acknowledge the Department of Biochemistry, Amala Cancer Research Centre, Thrissur, Kerala for giving the facilities to carry out the research work.

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Ethical approval: All the animal experiments in the present study was carried out with the prior approval from Institutional Animal Ethics Committee (IAEC/ACRC/16-12/17 dated 19/12/2016) were strictly following the guidelines of Committee for the Purpose of Control and Supervision of Experiments on Animals (CPCSEA).

References

1. Ozen, AE, Pons, A, Tur, JA. Worldwide consumption of functional foods: a systematic review. Nutr Rev 2012;70:472–81. https://doi.org/10.1111/j.1753-4887.2012.00492.x.Suche in Google Scholar PubMed

2. Davis, JM, Murphy, EA, Carmichael, MD. Effects of the dietary flavonoid quercetin upon performance and health. Curr Sports Med Rep 2009;8:206–13. https://doi.org/10.1249/jsr.0b013e3181ae8959.Suche in Google Scholar

3. Das, L, Bhaumik, E, Raychaudhuri, U, Chakraborty, R. Role of nutraceuticals in human health. J Food Sci Technol 2012;49:173–83. https://doi.org/10.1007/s13197-011-0269-4.Suche in Google Scholar PubMed PubMed Central

4. Hasler, CM. Functional foods: benefits, concerns and challenges—a position paper from the American council on science and health. J Nutr 2002;132:3772–81. https://doi.org/10.1093/jn/132.12.3772.Suche in Google Scholar PubMed

5. Gul, K, Singh, AK, Jabeen, R. Nutraceuticals and functional foods: the foods for the future world. Crit Rev Food Sci Nutr 2016;56:2617–27. https://doi.org/10.1080/10408398.2014.903384.Suche in Google Scholar PubMed

6. Gupta, RC, Jain, VK, Shanker, G. Palm sap as a potential starting material for vinegar production. Res Ind 1980;25:5–7.Suche in Google Scholar

7. Hali, R. Bio beverage – coco neera. Indian Coconut J 2013:17–19.Suche in Google Scholar

8. Muralidharan, K, Deepthi, SN. Coconut Neera – the hidden unexplored treasure. Indian Coconut J 2013:4–8.Suche in Google Scholar

9. Asha, S, Ratheesh, M, Jose, SP, Illathu Madhavamenon, K, Sukumaran, S. 12 – NEERA: a nonalcoholic nutritious beverage from unopened inflorescence of coconut palm. In: Grumezescu, AM, Holban, AM, editors. Natural beverages. London: Academic Press; 2019:339–60 pp.10.1016/B978-0-12-816689-5.00012-2Suche in Google Scholar

10. Xia, Q. Chemical composition changes of post-harvest coconut inflorescence sap during natural fermentation. Afr J Biotechnol 2011;10:14999–5005. https://doi.org/10.5897/ajb10.2602.Suche in Google Scholar

11. Borse, BB, Rao, LJM, Ramalakshmi, K, Raghavan, B. Chemical composition of volatiles from coconut sap (neera) and effect of processing. Food Chem 2007;101:877–80. https://doi.org/10.1016/j.foodchem.2006.02.026.Suche in Google Scholar

12. Chen, W, Zhu, Q, Xia, Q, Cao, W, Zhao, S, Liu, J. Reactive oxygen species scavenging activity and DNA protecting effect of fresh and naturally fermented coconut sap. J Food Biochem 2011;35:1381–8. https://doi.org/10.1111/j.1745-4514.2010.00506.x.Suche in Google Scholar

13. Marcocci, L, Maguire, JJ, Droylefaix, MT, Packer, L. The nitric oxide-scavenging properties of Ginkgo biloba extract EGb 761. Biochem Biophys Res Commun 1994;201:748–55. https://doi.org/10.1006/bbrc.1994.1764.Suche in Google Scholar PubMed

14. Ainsworth, EA, Gillespie, KM. Estimation of total phenolic content and other oxidation substrates in plant tissues using Folin-Ciocalteu reagent. Nat Protoc 2007;2:875–7. https://doi.org/10.1038/nprot.2007.102.Suche in Google Scholar

15. Dwivedi, PD, Verma, AS, Ray, PK. Induction of immune rejection of tumors by protein A in mice bearing transplantable solid tissue Dalton’s lymphoma tumors. Immunopharmacol Immunotoxicol 1992;14:105–28. https://doi.org/10.3109/08923979209009215.Suche in Google Scholar

16. Somani, SM, Husain, K, Whitworth, C, Trammell, GL, Malafa, M, Rybak, LP. Dose-dependent protection by lipoic acid against cisplatin-induced nephrotoxicity in rats: antioxidant defense system. Pharmacol Toxicol 2000;86:234–41. https://doi.org/10.1034/j.1600-0773.2000.d01-41.x.Suche in Google Scholar

17. Drabkin, HAADL. Spectrophotometric studies: spectrophotometric constants for common hemoglobin derivatives in human, dog and rabbit blood. J Biol Chem 1932;98:719–33.10.1016/S0021-9258(18)76122-XSuche in Google Scholar

18. Chaudhari, AR, Total leukocyte count. In Chaudhari, AR, editor. A text book of practical physiology. Hyderabad: Paras Medical Publisher; 2000:104–8 pp.Suche in Google Scholar

19. Mehara, E, Vaidya, MC. Handbook of pratical and clinical immunology. New Delhi: CBS Publishers; 1984:44–6 pp.Suche in Google Scholar

20. Bancroff, JD, Cook, HF. A manual of histologic technique. London: Churchill Livingston; 1984:171–8 pp.Suche in Google Scholar

21. Ohkawa, H, Ohishi, N, Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351–8. https://doi.org/10.1016/0003-2697(79)90738-3.Suche in Google Scholar

22. John, AB, Steven, DA. Methods in enzymology. New York: Academic Press; 1978.Suche in Google Scholar

23. McCord, JM, Fridovich, I. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). J Biol Chem 1969;244:6049–55.10.1016/S0021-9258(18)63504-5Suche in Google Scholar

24. Beers, RF, Sizer, IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 1952;195:133–40.10.1016/S0021-9258(19)50881-XSuche in Google Scholar

25. Hafeman, DG, Sunde, RA, Hoekstra, WG. Effect of dietary selenium on erythrocyte and liver glutathione peroxidase in the rat. J Nutr 1974;104:580–7. https://doi.org/10.1093/jn/104.5.580.Suche in Google Scholar

26. Moron, MS, Depierre, JW, Mannervik, B. Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochim Biophys Acta 1979;582:67–78. https://doi.org/10.1016/0304-4165(79)90289-7.Suche in Google Scholar

27. Jose, SP, Asha, S, Krishnakumar, IM, Ratheesh, M, Savitha, S, Sandya, S, et al. Nephro-protective effect of a novel formulation of unopened coconut inflorescence sap powder on gentamicin induced renal damage by modulating oxidative stress and inflammatory markers. Biomed Pharmacother 2017;85:128–35. https://doi.org/10.1016/j.biopha.2016.11.117.Suche in Google Scholar PubMed

28. Hartmann, JT, Fels, LM, Knop, S, Stolt, H, Kanz, L, Bokemeyer, C. A randomized trial comparing the nephrotoxicity of cisplatin/ifosfamide-based combination chemotherapy with or without amifostine in patients with solid tumors. Invest N Drugs 2000;18:281–9. https://doi.org/10.1023/a:1006490226104.10.1023/A:1006490226104Suche in Google Scholar

29. Sastry, J, Kellie, SJ. Severe neurotoxicity, ototoxicity and nephrotoxicity following high-dose cisplatin and amifostine. Pediatr Hematol Oncol 2005;22:441–5. https://doi.org/10.1080/08880010590964381.Suche in Google Scholar

30. Sharma, S. Protective effect of exacum lawii on cisplatin-induced oxidative renal damage in rats. Phcog Mag 2018;13:S807–16. https://doi.org/10.4103/pm.pm_209_17.Suche in Google Scholar

31. Divya, MK, Lincy, L, Raghavamenon, AC, Babu, TD. Ameliorative effect of Apodytes dimidiata on cisplatin-induced nephrotoxicity in Wistar rats. Pharm Biol 2016;54:2149–57. https://doi.org/10.3109/13880209.2016.1149494.Suche in Google Scholar

32. Purena, R, Seth, R, Bhatt, R. Protective role of Emblica officinalis hydro-ethanolic leaf extract in cisplatin induced nephrotoxicity in rats. Toxicol Rep 2018;5:270–7. https://doi.org/10.1016/j.toxrep.2018.01.008.Suche in Google Scholar

33. Chen, X, Wang, J, Fu, Z, Zhu, B, Wang, J, Guan, S, et al. Curcumin activates DNA repair pathway in bone marrow to improve carboplatin-induced myelosuppression. Sci Rep 2017;7. https://doi.org/10.1038/s41598-017-16436-9.Suche in Google Scholar

34. Campbell, PI, al-Nasser, IA. Renal insufficiency induced by cisplatin in rats is ameliorated by cyclosporin A. Toxicology 1996;114:11–7. https://doi.org/10.1016/s0300-483x(96)03411-7.Suche in Google Scholar

35. Chen, HL, Lan, XZ, Wu, YY, Ou, YW, Chen, TC, Wu, WT. The antioxidant activity and nitric oxide production of extracts obtained from the leaves of Chenopodium quinoa Willd. Biomedicine 2017;7:13. https://doi.org/10.1051/bmdcn/2017070424.Suche in Google Scholar PubMed PubMed Central

36. Pandey, KB, Rizvi, SI. Plant polyphenols as dietary antioxidants in human health and disease. Oxid Med Cell Longev 2009;2:270–8. https://doi.org/10.4161/oxim.2.5.9498.Suche in Google Scholar PubMed PubMed Central

Received: 2020-01-29
Accepted: 2020-04-22
Published Online: 2020-08-25

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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