Protective effect of Moringa oleifera oil against HgCl2-induced hepato- and nephro-toxicity in rats
Abstract:
Background:
Various parts of the Moringa oleifera (M. oleifera) tree are widely accepted to have ameliorative effects against metal toxicity. In the present study, M. oleifeira oil (MO) was tested against HgCl2-induced tissue pathologies and oxidative stress.
Methods:
Male Wistar rats were administered MO (1.798 mg/kg p.o.) or HgCl2 (5 mg/kg body wt) alone or in combination (5 mg/kg HgCl2+1.798 mg/kg MO p.o.) three times per week for 21 days. After exposure and treatment periods, rats were sacrificed; blood collected and the oxidative status of the liver and kidney homogenates were evaluated.
Results:
In the liver, malondialdehyde (MDA) level, glutathione (GSH), and superoxide dismutase (SOD) activities were higher whereas catalase (CAT) activity was lower in the HgCl2 group than in the control group. In the kidney, MDA level, SOD, and CAT activities were higher whereas GSH activity was unchanged in the HgCl2 group compared to the control group. In the liver, MDA level, SOD, and CAT activities were lower in the HgCl2+MO group than in the HgCl2 group. In the kidney, MDA level, SOD and CAT activities were lower in the HgCl2+MO than in the HgCl2 group. Furthermore, Hg-induced increases in creatinine and bilirubin levels as well as the increase in γ-glutamyl transferase, lactate dehydrogenase, and alkaline phosphatase activities were attenuated in the combine exposure group and the animals showed improvement in the histology of the liver and kidney.
Conclusions:
MO decreased the negative effects of Hg-induced oxidative stress in rats.
Acknowledgments
The technical expertise of Messrs Christian Kingsley Nwaugha (Department of Biochemistry, University of Port Harcourt) on animal handling and collection of blood samples is gratefully acknowledged.
Author contributions: S.O.A conceived the study, designed the experiments, and wrote the manuscript. S.B., S.G.E, G.O., and G.A. performed the experiments. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: None declared.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
References
1. Abarikwu SO. Toxic elements and human diseases. In: Lichtfouse E, Schwarzbauer J, Robert D, editors. Pollutant diseases, remediation and recycling. Switzerland: Springer International Publishing, 2013:351–86.10.1007/978-3-319-02387-8_7Suche in Google Scholar
2. Ayensu WK, Tchounwou PB. Microarray analysis of mercury-induced changes in gene expression in human liver carcinoma (HepG2) cells: importance in immune responses. Int J Environ Res Public Health 2006;3:141–73.10.3390/ijerph2006030018Suche in Google Scholar
3. Fossato da Silva DA, Teixeira CT, Scarano WR, Favareto AP, Fernandez CD, Grotto D, et al. Effects of methylmercury on male reproductive functions in Wistar rats. Reprod Toxicol 2011;31:431–9.10.1016/j.reprotox.2011.01.002Suche in Google Scholar
4. Nyland JF, Fairweather D, Shirley DL, Davis SE, Rose NR, Silbergeld EK. Low dose inorganic mercury increases severity and frequency of chronic coxsackievirus-induced autoimmune myocarditis in mice. Toxicol Sci 2012;125:134–43.10.1093/toxsci/kfr264Suche in Google Scholar
5. Martinez CS, Torres JG, Pecanha FM, Anselmo-Franci JA, Vassallo DV, Salaices M, et al. 60-day chronic exposure to low concentrations of HgCl2 impairs sperm quality: Hormonal imbalance and oxidative stress as potential routes for reproductive dysfunction in rats. PLoS One 2014;9:e111202.10.1371/journal.pone.0111202Suche in Google Scholar
6. Myers GJ, Davidson PW. Prenatal methylmercury exposure and children: neurologic, developmental and behavioral research. Environ Health Perpect 1998;106:841–7.10.1289/ehp.98106841Suche in Google Scholar
7. Counter SA, Buchanan LH. Mercury exposure in children: a review. Toxicol Appl Pharmacol 2004;198:209–30.10.1016/j.taap.2003.11.032Suche in Google Scholar
8. Vicente E, Boer M, Netto C, Fochesatto C, Dalmaz C, Siqueira IR, et al. Hippocampal antioxidant system in neonates from methyl mercury-intoxicated rats. Neurotoxicol Teratol 2004;26:817–23.10.1016/j.ntt.2004.08.003Suche in Google Scholar
9. Castoldi AF, Coccini T, Ceccatelli S, Manzo L. Neurotoxicity and molecular effects of methylmercury. Brain Res Bull 2001;55:197–203.10.1016/S0361-9230(01)00458-0Suche in Google Scholar
10. Ung CY, Lam SH, Hlaing MM, Winata CL, Korzh S, Mathavan S, et al. Mercury-induced hepatotoxicity in zebrafish: in vivo mechanistic insights from transcriptome analysis, phenotype anchoring and targeted gene expression validation. BMC Genomics 2010;11:212.10.1186/1471-2164-11-212Suche in Google Scholar PubMed PubMed Central
11. Sharma MK, Kumar M, Kumar A. Protection against mercury-induced renal damage in Swiss albino mice by Ocimum sanctum. Environ Toxicol Pharmacol 2005;19:161–7.10.1016/j.etap.2004.06.002Suche in Google Scholar PubMed
12. Uzunhisarcikli M, Aslanturk A, Kalender S, Apaydin FG, Bas H. Mercuric chloride induced hepatotoxic and hematologic changes in rats: the protective effects of sodium selenite and vitamin E. Toxicol Ind Health 2016;32:1651–62.10.1177/0748233715572561Suche in Google Scholar PubMed
13. Sharma MK, Sharma A, Kumar A, Kumar M. Spirulina fusiforms provides protection against mercuric chloride induced oxidative stress in Swiss albino mice. Food Chem Toxicol 2007;45:2412–9.10.1016/j.fct.2007.06.023Suche in Google Scholar PubMed
14. Al-Said MS, Mothana RA, Al-Yahya MA, Al-Blowi AS, Al-Sohaibani M, Ahmed AF, et al. Edible oils for liver protection: hepatoprotective potentiality of Moringa oleifera seed oil against chemical-induced hepatitis in rats. J Food Sci 2012;77:124–30.10.1111/j.1750-3841.2012.02698.xSuche in Google Scholar
15. Oliveira JTA, Silveira SB, Vasconcelos IM, Cavada BS, Moriera RA. Compositional and nutritional attributes of seeds from the multiple purpose tree Moringa oleifera Lamark. J Sci Food Agric 1999;79:815–20.10.1002/(SICI)1097-0010(19990501)79:6<815::AID-JSFA290>3.0.CO;2-PSuche in Google Scholar
16. Fahey JW. Moringa oleifera: a review of the medical evidence for its nutritional, therapeutic, and prophylactic properties. Part 1. Tree Life J 2005;1:5–19.Suche in Google Scholar
17. Stevens GC, Baiyeri KP, Akinnnagbe O. Ethno-medicinal and culinary uses of Moringa oleifera Lam. in Nigeria. J Med Plants Res 2013;7:799–804.Suche in Google Scholar
18. Maurya SK, Singh AK. Clinical efficacy of Moringa oleifera Lam. stems bark in urinary tract infections. Int Sch Res Notices 2014;2014:906843.10.1155/2014/906843Suche in Google Scholar
19. Rao VA, Devi PU, Kamath R. In vivo radioprotective effect of Moringa Oleifera leaves. Indian J Exp Biol 2001;39:858–63.Suche in Google Scholar
20. Ghasi S, Nwobodo E, Ofili JO. Hypocholesterolemic effects of crude extract of leaf of Moringa oleifera Lam. in high-fat diet fed Wistar rats. J Ethnopharmacol 2000;69:21–25.10.1016/S0378-8741(99)00106-3Suche in Google Scholar
21. Pari L, Kumar NA. Hepatoprotective activity of Moringa oleifera on anti tubercular drug induced liver damage in rats. J Med Food 2002;5:171–7.10.1089/10966200260398206Suche in Google Scholar
22. Fakurazi S, Hairuszah I, Nanthini U. Moringa oleifera Lam. prevents acetaminophen induced liver injury through restoration of glutathione level. Food Chem Toxicol 2008;46:2611–15.10.1016/j.fct.2008.04.018Suche in Google Scholar
23. Caceres AB, Cabrera O, Mirals O, Mollinedo O, Imendia A. Preliminary screening for antimicrobial activity of Moringa oleifera. J Ethnopharmacol 1991;33:213–16.10.1016/0378-8741(91)90078-RSuche in Google Scholar
24. Bharali R, Tabassum J, Azad MR. Chemomodulatory effect of Moringa oleifera Lam on hepatic carcinogen metabolizing enzymes, antioxidant parameters and skin papillomagenesis in mice. Asian Pac J Cancer Prev 2003;4:131–9.Suche in Google Scholar
25. Dahiru D, Onubiyi JA, Umaru HA. Phytochemical screening and antiulcerogenic effect of Moringa oleifera aqueous leaf extract. African J Trad Complement Alternat Med 2006;3:70–5.10.4314/ajtcam.v3i3.31167Suche in Google Scholar
26. Agrawal ND, Nirala SK, Shukla S, Mathur R. Co-administration of adjuvants along with Moringa oleifera attenuates beryllium induced oxidative stress and histopathological alterations in rats. Pharm Biol 2015;53:1465–73.10.3109/13880209.2014.986685Suche in Google Scholar
27. Mahajan SG, Mali RG, Mehta AA. Protective effect of ethanolic extract of seeds of Moringa oleifera Lam. against inflammation associated with development of arthritis in rats. J Immunotoxicol 2007;4:39–47.10.1080/15476910601115184Suche in Google Scholar
28. Muangnoi C, Chingsuwanrote P, Praengamthanachoti P, Svasti S, Tuntipopipat S. Moringa oleifera pod inhibits inflammatory mediator production by lipopolysaccharide-stimulated RAW 264.7 murine macrophage cell lines. Inflammation 2012;35:445–55.10.1007/s10753-011-9334-4Suche in Google Scholar
29. Tsaknis J, Lalas V, Gergis V, Douroglou V, Spiliotis V. Characterization of Moringa oleifera variety Mbololo seed oil of Kenya. J Agric Food Chem 1999;47:4495–9.10.1021/jf9904214Suche in Google Scholar
30. Ogbunugafor HA, Eneh FU, Ozumba AN, Igwo-Ezikpe MN. Physico-chemical and antioxidant properties of Moringa oleifera Seed Oil. Pakistan J Nutr 2011;10:409–14.10.3923/pjn.2011.409.414Suche in Google Scholar
31. Lalas S, Gortzi O, Athanasiadis V, Tsaknis J, Chinou I. Determination of antimicrobial activity and resistance to oxidation of Moringa peregrina seed oil. Molecules 2012;17:2330–4.10.3390/molecules17032330Suche in Google Scholar
32. Olatosin TM, Akinduko DS, Uche CZ. Evaluation of the hepatoprotective efficacy of Moringa oleifera seed oil on CCl4-induced liver damage in Wistar albino rats. Int J Eng Sci 2013;2:13–18.Suche in Google Scholar
33. El-Desoky GE, Bashandy SA, Alhazza IM, Al-Othman ZA, Aboul-Soud MAM, Yusuf K. Improvement of mercuric chloride-induced testis injuries and sperm quality deteriorations by Spirulina platensis in rats. PLoS One 2013;8:e59177.10.1371/journal.pone.0059177Suche in Google Scholar
34. Pal M, Ghosh M. Studies on comparative efficacy of α-linolenic acid and α-eleostearic acid on prevention of organic mercury-induced oxidative stress in kidney and liver of rat. Food Chem Toxicol 2012;50:1066–72.10.1016/j.fct.2011.12.042Suche in Google Scholar
35. Abarikwu SO, Akiri OF, Durojaiye MA, Alabi AF. Combined effects of repeated administration of Bretmont Wipeout (Glyphosate) and Ultrazin (Atrazine) on testosterone, oxidative stress and sperm quality of Wistar rats. Toxicol Mech Methods 2015;25: 70–80.10.3109/15376516.2014.989349Suche in Google Scholar
36. Sedlak J, Lindsay RH. Estimation of total, protein bound, and non-protein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem 1968;25:192–205.10.1016/0003-2697(68)90092-4Suche in Google Scholar
37. 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;247:3170–5.10.1016/S0021-9258(19)45228-9Suche in Google Scholar
38. Clairborne A. Catalase activity. In: Greewald AR, editor. Handbook of methods for oxygen radical research. Boca Raton: CRC Press, 1995:237–242.Suche in Google Scholar
39. Habig WH, Pabst MJ, Jacob WB. Glutathione S-transferase. The first enzymatic step in mercapturic acid formation. J Biol Chem 1974;249:7130–9.10.1016/S0021-9258(19)42083-8Suche in Google Scholar
40. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ. Protein measurement with Folin phenol reagent. J Biol Chem 1951;193:265–75.10.1016/S0021-9258(19)52451-6Suche in Google Scholar
41. Peixoto NC, Kratz CP, Roza T, Morsch VM, Pereira ME. Effects of HgCl2 on porphobilinogen-synthase (E.C. 4.2.1.24) activity and on mercury levels in rats exposed during different precocious periods of postnatal life. Cell Biol Int 2007;31:1057–62.10.1016/j.cellbi.2007.03.026Suche in Google Scholar
42. Hazelhoff MH, Bulacio RP, Torres AM. Gender related differences in kidney injury induced by mercury. Int J Mol Sci 2012;13:10523–36.10.3390/ijms130810523Suche in Google Scholar
43. de Freitas AS, Funck VR, Rotta Mdos S, Bohrer D, Mörschbächer V, Puntel RL, et al. Diphenyl diselenide, a simple organoselenium compound, decreases methylmercury-induced cerebral, hepatic and renal oxidative stress and mercury deposition in adult mice. Brain Res Bull 2009;79:77–84.10.1016/j.brainresbull.2008.11.001Suche in Google Scholar
44. Tandon SK, Singh, S. Prasad S, Mathur N. Hepatic and renal metallothionein induction by an oral equimolar dose of zinc, cadmium or mercury in mice. Food Chem Toxicol 2001;39:571–7.10.1016/S0278-6915(00)00167-8Suche in Google Scholar
45. Abarikwu SO. Protective effect of quercetin on atrazine induced oxidative stress in the liver, kidney, brain and heart of adult wistar rats. Toxicol Int 2014;21:148–55.10.4103/0971-6580.139794Suche in Google Scholar PubMed PubMed Central
46. Sener G, Sehirli O, Tozan A, Velioğlu-Ovunç A, Gedik N, Omurtag GZ. Ginkgo biloba extract protects against mercury (II)-induced oxidative tissue damage in rats. Food Chem Toxicol 2007;45:543–50.10.1016/j.fct.2006.07.024Suche in Google Scholar PubMed
47. Jadhav SH, Sarkar SN, Patil RD, Tripathi HC. Effects of subchronic exposure via drinking water to a mixture of eight water-contaminating metals: a biochemical and histopathological study in male rats. Arch Environ Contam Toxicol 2007;53:667–77.10.1007/s00244-007-0031-0Suche in Google Scholar PubMed
48. Al-Attar AM. Vitamin E attenuates liver injury induced by exposure to lead, mercury, cadmium and copper in albino mice. Saudi J Biol Sci 2011;18:395–401.10.1016/j.sjbs.2011.07.004Suche in Google Scholar
49. Jin X, Lok E, Caldwell D, Mueller R, Kapal K, Liston V, et al. Dietary fats altered nephrotoxicity profile of methylmercury in rats. J Appl Toxicol 2009;29:126–40.10.1002/jat.1389Suche in Google Scholar
50. Stroo WE, Hook JB. Renal function correlates of methyl mercury intoxication: interaction with acute mercuric chloride toxicity. Toxicol Appl Pharma 1977;42:399–410.10.1016/0041-008X(77)90017-5Suche in Google Scholar
51. Weber TJ, Negash S, Smallwood HS, Ramos KS, Thrall BD, Squier TC. Calmodulin involvement in stress-activated nuclear localization of albumin in JB6 epithelial cells. Biochemistry 2004;43:7443–50.10.1021/bi049731sSuche in Google Scholar PubMed
52. Sheikh A, Yeasmin F, Agarwal S, Rahman M, Islam K, Hossain E, et al. Protective effects of Moringa oleifera Lam. leaves against arsenic-induced toxicity in mice. Asian Pac J Trop Biomed 2014;4:S353–8.10.12980/APJTB.4.201414B44Suche in Google Scholar PubMed PubMed Central
53. Velaga MK, Daughtry LK, Jones AC, Yallapragada PR, Rajanna S, Rajanna B. Attenuation of lead-induced oxidative stress in rat brain, liver, kidney and blood of male Wistar rats by Moringa oleifera seed powder. J Environ Pathol Toxicol Oncol 2014;33:323–37.10.1615/JEnvironPatholToxicolOncol.2014011656Suche in Google Scholar PubMed
54. Gupta R, Kannan GM, Sharma M, Flora SJ. Therapeutic effects of Moringa oleifera on arsenic-induced toxicity in rats. Environ Toxicol Pharmacol 2005;20:456–64.10.1016/j.etap.2005.05.005Suche in Google Scholar PubMed
55. Tumer TB, Rojas-Silva P, Poulev A, Raskin I, Waterman C. Direct and indirect antioxidant activity of polyphenol-and isothiocyanate-enriched fractions from Moringa oleifera. J Agric Food Chem 2015;63:1505–13.10.1021/jf505014nSuche in Google Scholar PubMed PubMed Central
©2017 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Editorial
- The double face of light effects: circadian adjustment or disruption
- Review
- Artificial light-at-night – a novel lifestyle risk factor for metabolic disorder and cancer morbidity
- Behavior and Neuroprotection
- Anti-stress effects of a GSK-3β inhibitor, AR-A014418, in immobilization stress of variable duration in mice
- Cardiovascular Function
- Addition of omega-3 fatty acid and coenzyme Q10 to statin therapy in patients with combined dyslipidemia
- Oxidative Stress
- Protective effect of Moringa oleifera oil against HgCl2-induced hepato- and nephro-toxicity in rats
- Effects of peripherally and centrally applied ghrelin on the oxidative stress induced by renin angiotensin system in a rat model of renovascular hypertension
- Investigation of the role of α-lipoic acid on fatty acids profile, some minerals (zinc, copper, iron) and antioxidant activity against aluminum-induced oxidative stress in the liver of male rats
- Metabolism
- The choice of freely preferred cadence by trained nonprofessional cyclists may not be characterized by mechanical efficiency
- Immune Response
- Ascorbic acid does not modulate potassium currents in cultured human lymphocytes
- Phytotherapy
- Anti-inflammatory activity of Elaeagnus angustifolia fruit extract on rat paw edema
- Histopathological and biochemical assessments of Costus afer stem on alloxan-induced diabetic rats
- In vitro inhibition of phosphodiesterase-5 and arginase activities from rat penile tissue by two Nigerian herbs (Hunteria umbellata and Anogeissus leiocarpus)
- Antioxidant and antiproliferative potentials of methanol extract of Xylopia aethiopica (Dunal) A. Rich in PC-3 and LNCaP cells
Artikel in diesem Heft
- Frontmatter
- Editorial
- The double face of light effects: circadian adjustment or disruption
- Review
- Artificial light-at-night – a novel lifestyle risk factor for metabolic disorder and cancer morbidity
- Behavior and Neuroprotection
- Anti-stress effects of a GSK-3β inhibitor, AR-A014418, in immobilization stress of variable duration in mice
- Cardiovascular Function
- Addition of omega-3 fatty acid and coenzyme Q10 to statin therapy in patients with combined dyslipidemia
- Oxidative Stress
- Protective effect of Moringa oleifera oil against HgCl2-induced hepato- and nephro-toxicity in rats
- Effects of peripherally and centrally applied ghrelin on the oxidative stress induced by renin angiotensin system in a rat model of renovascular hypertension
- Investigation of the role of α-lipoic acid on fatty acids profile, some minerals (zinc, copper, iron) and antioxidant activity against aluminum-induced oxidative stress in the liver of male rats
- Metabolism
- The choice of freely preferred cadence by trained nonprofessional cyclists may not be characterized by mechanical efficiency
- Immune Response
- Ascorbic acid does not modulate potassium currents in cultured human lymphocytes
- Phytotherapy
- Anti-inflammatory activity of Elaeagnus angustifolia fruit extract on rat paw edema
- Histopathological and biochemical assessments of Costus afer stem on alloxan-induced diabetic rats
- In vitro inhibition of phosphodiesterase-5 and arginase activities from rat penile tissue by two Nigerian herbs (Hunteria umbellata and Anogeissus leiocarpus)
- Antioxidant and antiproliferative potentials of methanol extract of Xylopia aethiopica (Dunal) A. Rich in PC-3 and LNCaP cells