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Hepatoprotective effects of Quassia amara stem bark against cadmium-induced toxicity in male Wistar rats

  • Olawale O. Obembe EMAIL logo , Taofeek O. Usman and Yinusa Raji
Published/Copyright: February 8, 2021

Abstract

Objectives

The liver is one of the primary biorepositories of cadmium (Cd) and it has been implicated in the pathogenesis of hepatic diseases. Quassia amara stem bark has been reputed to have strong antimalarial, antimicrobial, antiulcerative and amoebicidal properties. This study aims to determine the effects of Q. amara on Cd-induced hepatotoxicity and lipid profile in male Wistar rats.

Methods

The animals were divided into three groups of five animals each. Group 1 served as control while group 2 received Cd (5 mg/kg) for 4 weeks. Prior to Cd treatment, group 3 was treated with Q. amara extract (200 mg/kg) for 2 weeks and received the Q. amara and Cd simultaneously for 4 weeks.

Results

Cadmium caused significant increase in serum total cholesterol and low-density lipoprotein (LDL) as well as increased hepatic malondialdehyde (MDA) when compared with the control group. On the other hand, Cd caused a decrease in serum high-density lipoprotein (HDL) and hepatic superoxide dismutase (SOD) when compared with control. However, treatment with Q. amara prevented Cd-induced changes in the lipid profile, augmented Cd-induced decline in SOD and also ameliorated the Cd-induced increase in MDA. Catalase level was however comparable across the groups.

Conclusions

Q. amara ameliorated the Cd-induced damage to liver by preventing dyslipidemia and oxidative damage in the hepatic tissue.


Corresponding author: Olawale O. Obembe, PhD, Department of Physiology, College of Health Sciences, Osun State University, Osogbo, Nigeria, E-mail:

  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. Informed consent: Not applicable.

  5. Ethical approval: This study was approved by the Ethical Review Committee of Osun State University.

References

1. Egnan, K, Hambridge, T, Kayama, F. WHO Food additive series, Geneva. Cadmium impact assessment of different maximum limits; 2005. p. 35–46.Search in Google Scholar

2. Prozialeck, WC, Edwards, JR. Mechanisms of cadmium-induced proximal tubule injury: new insights with for biomonitoring and therapeutic intervention. J Pharmacol Exp Therap 2012;343:2–12. https://doi.org/10.1124/jpet.110.166769.Search in Google Scholar PubMed PubMed Central

3. Pari, L, Murugavel, P. Diallyltetrasulfide improves cadmium induced alterations of acetylcholinesterase, ATPases and oxidative stress in brain of rats. Toxicology 2007;234:44–50. https://doi.org/10.1016/j.tox.2007.01.021.Search in Google Scholar PubMed

4. Habeebu, SS, Liu, J, Liu, YP, Klaassen, CD. Metallothionein-null mice are more sensitive than wildtype mice to liver injury induced by repeated exposure to cadmium. Toxicol Sci 2000;55:223–32. https://doi.org/10.1093/toxsci/55.1.223.Search in Google Scholar PubMed

5. Hyder, O, Chung, M, Cosgrove, D, Herman, JM, Li, Z, Firoozmand, A, et al.. Cadmium exposure and liver disease among US adults. J Gastrointest Surg 2013;17:1265–73. https://doi.org/10.1007/s11605-013-2210-9.Search in Google Scholar PubMed PubMed Central

6. Andjelkovic, M, Djordjevic, AB, Antonijevic, E, Antonijevic, B, Stanic, M, Kotur-Stevuljevic, J, et al.. Toxic effect of acute cadmium and lead exposure in rat blood, liver, and kidney. Int J Environ Res Public Health 2019;16:274. https://doi.org/10.3390/ijerph16020274.Search in Google Scholar PubMed PubMed Central

7. Samarghandian, S, Azimi-Nezhad, M, Samini, F. Ameliorative effect of saffron aqueous extract on hyperglycemia, hyperlipidemia and oxidative stress on diabetic encephalopathy in streptozotocin induced experimental diabetes mellitus. BioMed Res Int 2014;9:208–57.10.1155/2014/920857Search in Google Scholar PubMed PubMed Central

8. Ognjanovic, BI, Markovic, SD, Pavlovic, SZ, Zikic, RV, Stajn, AS, Saicic, ZS. Effect of chronic cadmium exposure on antioxidant defense system in some tissues of rats: protective effect of selenium. Physiol Res 2008;57:403.10.33549/physiolres.931197Search in Google Scholar PubMed

9. Meena, BM, Divya, K, Haseena, BSK, Sailaja, G, Sandhya, D, Thyagaraju, K. Evaluation of genotoxic and lipid peroxidation effect of cadmium in developing chick embryos. J Environ Anal Toxicol 2014;4:238.Search in Google Scholar

10. Polonsky, J. Quassinoid bitter principle 11. In: HerzGrisebach, WH, Kirby, GW, Tamm, C, editors. Fortschritte der Chemie Organischer Naturstoffe, vol 47. Wien, New York: Springer-Verlag; 1985. pp. 222–64.10.1007/978-3-7091-8790-6_4Search in Google Scholar PubMed

11. Njar, VC, Alao, TO, Okogun, JI, Holland, HL. 2-Methoxycanthin-6-one: a new alkaloid from the stem wood of Quassia amara. Planta Med 1993;59:259–61. https://doi.org/10.1055/s-2006-959664.Search in Google Scholar PubMed

12. Ajaiyeoba, EO, Krebs, HC. Antibacterial and antifungal activities of Quassia undulata and Quassia amara extracts in vitro. Afr J Med Med Sci 2003;32:353–6.Search in Google Scholar

13. Raji, Y, Oloyede, GK. Antiulcerogenic effects and possible mechanism of action of Quassia amara (L. Simaroubaceae) extract and its bioactive principles in rats. Afr J Tradit Complement Altern Med 2012;9:112–9. https://doi.org/10.4314/ajtcam.v9i1.16.Search in Google Scholar PubMed PubMed Central

14. Garcia, GM, Gonzalez, SMC, Pazos, LS. Pharmacologic activity of the aqueous wood extract from Quassia amara (Simurabaceae) on albino rats and mice. Rev Biol Trop 1997:47–50.Search in Google Scholar

15. Obembe, OO, Raji, Y. Reproductive toxicity of Quassia amara extract: action on sperm capacitation and acrosome reaction. Acad J Plant Sci 2012;5:60–9.Search in Google Scholar

16. Maranhao, HM, Vasconcelos, CF, Rolim, LA, Neto, PJ, Neto Jda, C, Filho, RC, et al.. Hepatoprotective effect of the aqueous extract of Simarouba amara Aublet (Simaroubaceae) stem bark against carbon tetrachloride (CCl4)-induced hepatic damage in rats. Molecules 2014;19:17735–46. https://doi.org/10.3390/molecules191117735.Search in Google Scholar

17. World Medical Association, American Physiological Society. Guiding principles for research involving animals and human beings. Am J Physiol Regul Integr Comp Physiol 2002;283:R281–3. https://doi.org/10.1152/ajpregu.00279.2002.Search in Google Scholar

18. Renugadevi, J, Prabu, SM. Cadmium-induced hepatoxicity in rats and the protectice effects of naringenin. Exp Toxicol Pathol 2009;62:171–81. https://doi.org/10.1016/j.etp.2009.03.010.Search in Google Scholar

19. Prabu, SM, Shagirtha, K, Renugadevi, J. Amelioration of cadmium-induced oxidative stress, impairment in lipids and plasma lipoproteins by the combined treatment with quercetin and α-tocopherol in rats. J Food Sci 2010;75:T132–40. https://doi.org/10.1111/j.1750-3841.2010.01757.x.Search in Google Scholar

20. Raji, Y, Bolarinwa, AF. Antifertility activity of Quassia amara in male rats: in vivo study. Life Sci 1997;61:1067–74. https://doi.org/10.1016/s0024-3205(97)00615-2.Search in Google Scholar

21. Obembe, OO, Olopade, JO, Raji, Y. Implication of HongrES1 protein in Quassin-induced male reproductive abnormality. Endocrinol Metab Syndrome 2014;3:128.Search in Google Scholar

22. Rifai, N, Bachorik, PS, Albers, JJ. Lipids, lipoproteins and apolipoproteins. In: Burtis, CA, Ashwood, ER, editors Tietz textbook of clinical chemistry, 3rd ed. Philadelphia: W. Saunders Company; 1999. pp. 809–61.Search in Google Scholar

23. Obembe, OO. Sex hormones and oxidative stress biomarkers of male Wistar rats treated with Moringa oleifera seed fractions. JBRA Assist Reprod 2019;23:408–13. https://doi.org/10.5935/1518-0557.20190047.Search in Google Scholar

24. Roopha, PD, Padmalatha, C. Effect of herbal preparation on heavy metal (Cadmium) induced antioxidant system in female Wistar rats. J Med Toxicol 2012;8:101–7.10.1007/s13181-011-0194-ySearch in Google Scholar

25. Hanzlik, RP. Reactivity and toxicity among halogenated methanes and related compounds. Biochem Pharmacol 1981;30:3027–30. https://doi.org/10.1016/0006-2952(81)90488-3.Search in Google Scholar

26. Slater, TF. Biochemical implications of current studies on vitamin E. Ann N Y Acad Sci 1982;393:496–500. https://doi.org/10.1111/j.1749-6632.1982.tb31286.x.Search in Google Scholar

27. Brattin, WJ, Glende, EA, Recknagel, RO. Pathological mechanisms in carbon tetrachloride hepatotoxicity. J Free Radic Biol Med 1985;1:27–38. https://doi.org/10.1016/0748-5514(85)90026-1.Search in Google Scholar

28. Recknagel, RO, Glende, EA, Dolak, JA, Waller, RL. Mechanisms of carbon tetrachloride toxicity. Pharmacol Ther 1989;43:139–54. https://doi.org/10.1016/0163-7258(89)90050-8.Search in Google Scholar

29. Khan, MR, Ahmed, D. Protective effects of Digera. muricata (L.) Mart. on testis against oxidative stress of carbon tetrachloride in rat. Food Chem Toxicol 2009;47:1393–9. https://doi.org/10.1016/j.fct.2009.03.020.Search in Google Scholar PubMed

30. Naik, SR, Panda, VS. Antioxidant and hepatoprotective effects of Ginkgo biloba phytosomes in carbon tetrachloride-induced liver injury in rodents. Liver Intern 2007;27:393–9. https://doi.org/10.1111/j.1478-3231.2007.01463.x.Search in Google Scholar PubMed

31. Mirela, P, Andriana, M, Ilean, D. Oxidative stress and antioxidant status in hypo and hyperthyroidism. In: Mohammed, AE, editor Antioxidant enzyme. InTech Open Access Publishers; 2012. pp. 197–236.Search in Google Scholar

32. Dinvoko-Kotsova, AT. Protection against cancer by plant phenyl propenoids: induction of mammalian anti-carcinogenic enzymes. Mini Rev Med Chem 2002;2:595–610.10.2174/1389557023405558Search in Google Scholar PubMed

33. Lima, RK, Cardoso, MG, Andrade, MA, Guimaraes, PL, Batista, LR, Nelson, DL. Bactericidal and antioxidant activity of essential oils from Myristica. fragrans Houtt and Salvia microphylla H.B.K. J Am Oil Chem Soc 2012;89:523–8. https://doi.org/10.1007/s11746-011-1938-1.Search in Google Scholar

34. Pathak, N, Khandelwal, S. Role of oxidative stress and apoptosis in cadmium induced thymic atrophy and splenomegaly in mice. Toxicol Lett 2007;169:95–108. https://doi.org/10.1016/j.toxlet.2006.12.009.Search in Google Scholar PubMed

35. Badisa, VL, Latinwo, LM, Odewumi, CO, Ikediobi, CO, Badisa, RB, Ayuk-Takem, LT, et al.. Mechanism of DNA damage by cadmium and interplay of antioxidant enzymes and agents. Environ Toxicol 2007;22:141–4. https://doi.org/10.1002/tox.20248.Search in Google Scholar PubMed

36. Bronner, LL, Kanter, DS, Manson, JE. Primary prevention of stroke. New England J Med 1995;333:1392–400. https://doi.org/10.1056/nejm199511233332106.Search in Google Scholar

37. Gorelick, PB, Schneck, M, Berglund, LF, Feinberg, W, Goldstone, J. Status of lipids as a risk factor for stroke. Neuroepidemiology 1997;16:107–15. https://doi.org/10.1159/000109679.Search in Google Scholar PubMed

38. Warlow, C, Dennis, M, VanGijn, J. Stroke. A practical guide to management. Oxford: Blackwell Science Ltd; 1996.Search in Google Scholar

39. Iacob, AO, Choudhury, RP. Targeting HDL-cholesterol to reduce residual cardiovascular risk. Curr Opin Lipidol 2012;23:172–4. https://doi.org/10.1097/mol.0b013e32835135bd.Search in Google Scholar

Received: 2020-05-26
Accepted: 2020-09-08
Published Online: 2021-02-08

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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