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Licensed Unlicensed Requires Authentication Published by De Gruyter May 19, 2020

Alterations in histological, biochemical and hematological parameters in Plasmodium berghei NK-65 infected balb/c mice treated with Bridelia ferruginea stem bark extract

  • Olalere Shittu ORCID logo EMAIL logo , Olufunke Adenike Opeyemi , Muritala Kayode Salawu , Abeeb Adio Ashiru , Shadrach Ayodeji Medaiyese , Nnaemeka Asogwa , Kehinde Funmilola Sheba , Rafiu Adebisi Kadir , Olusola Isaac Aremu and Olusola Ajibaye

Abstract

Background

Recent ethnomedicinal studies on Bridelia ferruginea Benth (family Phyllanthaceae) as an antiplasmodial remedy have established its potency as a strong prophylactic and chemosuppressive agent. Human consumption of medicinal herbs without adequate evaluation of its efficacy and safety can result in grave physiological and pathological consequences. Therefore, this study assessed the antiplasmodial bioactivity, biochemical, hematological, histopathological and toxicity profile of the ethanolic stem bark extract of B. ferruginea in mice.

Methods

Ethanolic stem bark extract of B. ferruginea (200, 400 and 800 mg/kg) were orally administered to Plasmodium berghei-infected mice in models and were subsequently observed for mortality, behavioral changes and signs of toxicity. Acute evaluation was experimented at 1,000 mg/kg for 28 days. Occult blood obtained from the euthanized mice were subjected to biochemical and hematological assays. A comprehensive assessment of the histology of the liver and kidney was also ascertained. The median lethal dose (LD50) was determined and extrapolated using the regression equation obtained from the plot of the probits of mortalities (y) and the log of doses (log10C).

Results

Different concentrations of the phytochemical secondary metabolites were revealed. Antiplasmodial bioactivity was established at the 200, 400 and 800 mg/kg of the herbal extract with a dearth in parasitemia at different days post-treatment. The 800 mg/kg group responded by exhibiting a dose-dependent decrease in parasitemia comparable with the chloroquine bi-phosphate group. Significant alterations in the histology of the liver and kidney of the 1,000 mg/kg group was documented. There was a reduction in the titers of LDH, ALT, AST, and urea in the treated group when compared with the control (p < 0.05). Antioxidant profiles were also highly significant with elevation in SOD, GPx, and CAT, but a reduction in MDA. LD50 was established at 424 mg/kg.

Conclusion

B. ferruginea Benth (family Phyllanthaceae) is a potent antiplasmodial, antioxidant, regenerative and ameliorative herbal remedy if administered in controlled dosage.


Corresponding author: Olalere Shittu, Parasitology Unit, Department of Zoology, University of Ilorin, Ilorin, Nigeria, Phone: +234 8033819041, +234 8084717654, E-mail:

Acknowledgments

We express our sincere appreciation to the laboratory staff of Central Research Lab, Tanke, Ilorin for the provision of the assays and bench space. We equally thank Mr. Bolu Ajayi of the Department of Plant Biology, University of Ilorin for identifying to species level the Bridelia ferruginea plant used for this study. This research was an outcome of an in-house financially non-supported study.

  1. Research funding: None declared.

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

  3. 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.

  4. Employment or leadership: None declared.

  5. Honorarium: None declared.

References

1. Garrod LP, Lambert HP, O'Gray F. Antibiotics and chemotherapy, 4th ed. Edinburgh, London and New York: Churchill, Livingstone; 1995.Search in Google Scholar

2. Awodele O, Agbaje E, Ogunkeye F, Kolapo A, Awodele D. Towards integrating traditional medicine (TM) into National Health Care Scheme (NHCS): Assessment of TM practitioners' disposition in Lagos, Nigeria. J Herb Med 2011;1:90–4. https://doi.org/10.1016/j.hermed.2011.09.002.https://doi.org/10.1016/j.hermed.2011.09.002Search in Google Scholar

3. Ekanem J, Kolawole O, Abbah O. Trypanocidal potential of methanolic extract of Bridelia ferruginea benth bark in Rattus novergicus. Afr J Biochem Res 2008;2:45–50. https://doi.org/10.5897/AJBR.https://doi.org/10.5897/AJBRSearch in Google Scholar

4. Njamen D, Nkeh-Chungag B, Tsala E, Fomum Z, Mbanya J, Ngufor G. Effect of Bridelia ferruginea (Euphorbiaceae) leaf extract on sucrose-induced glucose intolerance in rats. Trop J Pharm Res 2012;11:759–65. https://doi.org/10.4314/tjpr.v11i5.9.https://doi.org/10.4314/tjpr.v11i5.9Search in Google Scholar

5. Ekanem J, Kolawole O, Abbah O. Trypanocidal potential of methanolic extracts of Bridelia ferruginea (benth) bark in Rattus novergicus. Afr J Biochem Res 2008;4:45–50. https://doi.org/10.5897/AJBR.https://doi.org/10.5897/AJBRSearch in Google Scholar

6. Mbah C, Akuodor G, Anyalewechi N, Iwuanyanwu T, Osunkwo U. In vivo antiplasmodial activities of aqueous extract ofBridelia ferruginea stem bark against Plasmodium berghei berghei in mice. Pharm Biol 2012;50:188–94. https://doi.org/10.3109/13880209.2011.592537.https://doi.org/10.3109/13880209.2011.592537Search in Google Scholar

7. Nene-Bi S, Traore F, Soro T. Etudes phytochimique et pharmacologique de Bridelia ferruginea Benth (Euphorbiaceae) sur la motricité du Taenia coli de cobaye. Afr Sci 2009;5:305–20. https://www.ajol.info/index.php/afsci/article/view/61745.10.4314/afsci.v5i2.61745Search in Google Scholar

8. Olarewaju OI, Oloyede O, Ojo OA, Onikanni SA, Ajiboye BO. Aqueous Bridelia ferruginea stem bark transaminase activities in Albino rats. Afr J Biochem Res 2014;8:84–7. https://doi.org/10.5897/AJBR.https://doi.org/10.5897/AJBRSearch in Google Scholar

9. De Bruyne T, Cimanga K, Pieters L, Claeys M, Dommisse R, Vlietinck A. Gallocatechim (4-0-7) – Epigallocatechin. A new Biflavonoid isolated from Bridelia ferruginea. Nat Prod Let 1997;11:47–52. https://doi.org/10.1080/10575639708043756.https://doi.org/10.1080/10575639708043756Search in Google Scholar

10. Cimanga K, De Bruyne T, Apers S, Dieters L, Totte J, Kambu K, et al. Complement- inhibiting constituents of Bridelia ferruginea stem bark. Planta Med 1999;65:213–17. https://doi.org/10.12691/ajfn-2-1-3.https://doi.org/10.12691/ajfn-2-1-3Search in Google Scholar

11. Akuodor G, Mbah C, Essien A, Akpan J, Ezeokpo B, Iwuanyanwu T, et al. Ulcer-protective and Antidiarrhoeal effects of the aqueous stem bark extract of Bridelia ferruginea in Rodents. Pharmacol 2012;3:591–7. https://doi.org/10.5567/pharmacologia.2012.591.5.https://doi.org/10.5567/pharmacologia.2012.591.5Search in Google Scholar

12. Olajide OA, Makinde JM, Okpako DT, Awe SO. Studies on the anti-inflammatory and related pharmacological properties of the aqueous extract of Bridelia ferruginea stem bark. J Ethnopharmacol 2000;71:153–60. https://doi.org/10.1016/S0378-8741(99)00201-9.https://doi.org/10.1016/S0378-8741(99)00201-9Search in Google Scholar

13. Mbah C, Akuodor G, Anyalewechi N, Iwuanyanwu T, Osunkwo U. In vivo antiplasmodial activities of aqueous extract of Bridelia ferruginea stem bark against Plasmodium berghei berghei in mice. Pharm Biol 2012;50:188–94. https://www.researchgate.net/publication/288393452_Pharmacological_profile_of_aqueous_extract_of_Bridelia_ferruginea_stem_bark_in_the_relief_of_pain_and_fever/citation/download.10.3109/13880209.2011.592537Search in Google Scholar

14. Mitchell R, Kumar V, Abul K, Fausto N. Robbins Basic Pathology. 8th ed. Vol.7. Philadelphia: Saunders; 2007., pp. 516-522. https://www.scirp.org/(S(vtj3fa45qm1ean45vvffcz55))/reference/ReferencesPapers.aspx?ReferenceID=1402515.Search in Google Scholar

15. Atawodi S, Bulus T, Ibrahim S, Ameh D, Nok A, Mamman M, Galadima M. In vitro trypanocidal effect of methanolic extracts of some. Nigerian Savannah Plants. Afr J Biotechnol 2003;2:317–21. https://doi.org/10.5897/AJB2003.000-1065.https://doi.org/10.5897/AJB2003.000-1065Search in Google Scholar

16. Atawodi S. Comparative in vitro trypanocidal activities of petroleum ether, chloroform, methanol and aqueous extracts of some Nigerian Savannah Plants. Afr J Biotechnol 2005;2:177–82.Search in Google Scholar

17. Bakoma B, Berke B, Eklu-Gadegbeku K, Agbonon A, Aklikokou K, Gbeassor M, et al. Acute and sub-chronic (28 days) oral toxicity evaluation of hydroethanolic extract of Bridelia ferruginea Benth root bark in male rodent animals. Food Chem Toxicol 2013;52:176–9. https://doi.org/10.1016/j.fct.2012.1.https://doi.org/10.1016/j.fct.2012.1Search in Google Scholar

18. Wintola O, Sunmonu T, Afolayan A. Effect of Aloe ferox Mill. in the treatment of loperamide-induced constipation in Wistar rats. Gastroenterology 2010;10:95–99. https://doi.org/10.1186/1471-230X-10-95.https://doi.org/10.1186/1471-230X-10-95Search in Google Scholar

19. Wintola O, Sunmonu T, Afolayan A. Toxicological evaluation of aqueous extract of Aloe ferox Mill. in loperamide induced constipated rats. Hum Exp toxicol 2010;30:425–31. https://doi.org/10.1186/1471-230X-10-95.https://doi.org/10.1186/1471-230X-10-95Search in Google Scholar

20. Pousset J. Medicinal plants used as a source of raw material for the pharmaceutical industry; problems and prospects. Drug production from natural products. In: Proceeding of the 7th international symposium. Ife, Nigeria: DRPU, Obafemi Awolowo Univ; 1988:37–41 pp. http://www.bioline.org.br/pdf?tc05032.Search in Google Scholar

21. Ajani E, Sabiu S, Bamisaye F, Salami M, Nurain I. Evaluation of tha cute and sub-acute toxicity effect of ethanol leaves extract of Lagenaria brevifoliab(bitter gourd) on hepatic and renal function of rats. J Pharm Biol Sci 2014;9:61–8. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3307184/.Search in Google Scholar

22. Sabiu S, Ashafa O. Toxicological implication and laxative potential of ethanol root extract of Morella serrata in loperamide-induced constiapated wistar rats. Pharmaceut Biol 2016;54:2901–8. https://www.ncbi.nlm.nih.gov/pubmed/27267728.10.1080/13880209.2016.1193885Search in Google Scholar

23. Sunmonu T, Oloyede O. Performance and haematological indices in rats exposed to monocrotophos contamination. Hum Exp Toxicol 2010;29:845–50. https://doi.org/10.1177/0960327110363441.https://doi.org/10.1177/0960327110363441Search in Google Scholar

24. Awodele O, Amagon K, Agbo J, Prasad M. Toxicological evaluation of the aqueous stem bark extract of Bridelia ferruginea (Euphorbiaceae) in rodents. Interdiscip Toxicol 2015;8:89–98. https://doi.org/10.1515/intox-2015-0014.https://doi.org/10.1515/intox-2015-0014Search in Google Scholar

25. Olarewaju O, Oloyede O, Ojo O, Onikanni S. Effects of aqueous extract of Bridelia ferruginea stem bark on some haematological parameters of albino rats. Innovat Pharm Pharmacother 2013;1:70–5. https://www.researchgate.net/scientific-contributions/2030416254_Olarewaju_OI. https://www.researchgate.net/publication/276699570_Protective_effect_of_Irvingia_gabonensis_stem_bark_extract_on_cadmiuminduced_nephrotoxicity_in_rats/citation/download.Search in Google Scholar

26. Olarewaju O, Oloyede O, Ajayi O, Ojo O, Ajiboye B. Toxicity studies of the crude aqueous stem bark extracts of Bridelia ferruginea in Albino rats. Int J Pharm Toxicol Sci 2014;4:19–27. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961903/.Search in Google Scholar

27. Wells R, Melntyre R, Morgan A. Physiological stress responses in big game fish after exposure: observation on plasma chemistry and blood factors. Comp Biochem Physiol 1986;64A:565–71. https://doi.org/10.1016/0300-9629(86)90366-x.https://doi.org/10.1016/0300-9629(86)90366-xSearch in Google Scholar

28. Tilkian S, Conover M, Tilkian A. Clinical implications of laboratory tests. St Louis, Toronto and_London: C.V. Mosby Company; 1979:3–44; 117–32; 154–9 p.Search in Google Scholar

29. Srilaxmi P, Sareddy G, Kishor P, Setty O, Babu P. Protective effcacy of natansnin, a dibenzoyl glycoside from Salvinia natans against CCl4 induced oxidative stress and cellular degeneration in rat liver. BMC Pharmacol 2010;10:471–2210. https://doi.org/10.1186/1471-2210-10-13.https://doi.org/10.1186/1471-2210-10-13Search in Google Scholar

30. Birben E, Sahiner U, Sackesen C, Erzurum S, Kalayci O. Oxidative stress and antioxidant defense. WAO 2012;5:9–19. https://doi.org/10.1097/WOX.0b013e3182439613.https://doi.org/10.1097/WOX.0b013e3182439613Search in Google Scholar

31. National Institute of Health. NIH guide for the care and use of laboratory animal (Revised). Bethesda, MD: NIH Publication; 1985, vol. 83-23. https://www.nationalacademies.org/.Search in Google Scholar

32. Mfon AG, Dick EA, David-Oku E, Linus AJ, Chukwuma EB. Antimalarial potency of the leaf extract of Aspilia africana (Pers.) CD Adams. Asian Pac J Trop Med 2012;5:126–9. https://doi.org/10.1016/S1995-7645(12)60010-8.https://doi.org/10.1016/S1995-7645(12)60010-8Search in Google Scholar

33. World Health Organization. Malaria. Geneva: World Health Organization; 2010. https://apps.who.int/iris/bitstream/handle/10665/44449/9789241500470_eng.pdf.Search in Google Scholar

34. Lorke D. A new approach to practical acute toxicity testing. Arch Toxicol 1983;54:275–87. https://doi.org/10.4103/0971-6580.121674.https://doi.org/10.4103/0971-6580.121674Search in Google Scholar

35. Misra H, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972;247:3170–5. https://www.ncbi.nlm.nih.gov/pubmed/4623845.10.1016/S0021-9258(19)45228-9Search in Google Scholar

36. Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70–7. https://www.ncbi.nlm.nih.gov/pubmed/13650640.10.1016/0003-9861(59)90090-6Search in Google Scholar

37. Sinha K. Colorimetric assay of catalase. Anal Biochem 1972;47:389–94. https://doi.org/10.1016/0003-2697(72)90132-7.https://doi.org/10.1016/0003-2697(72)90132-7Search in Google Scholar

38. Adisa RA, Sulaimon LA. Assessment of liver antioxidant status and mitochondrial membrane composition of Plasmodium berghei-infected mice treated with selected antimalarials. Acta Biochim Pol 2017;64:485–91. https://www.ncbi.nlm.nih.gov/pubmed/28787466.10.18388/abp.2016_1440Search in Google Scholar PubMed

39. Silva J, Ramos AdS, Machado M, Moura D, Zoraima Neto, Canto-Cavalheiro MM, et al. A review of antimalarial plants used in traditional medicine in communities in Portuguese-Speaking countries: Brazil, Mozambique, Cape Verde, Guinea-Bissau, São Tomé and Príncipe and Angola. Memórias do Inst Oswaldo Cruz 2011;106:142–58. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762011000900019.10.1590/S0074-02762011000900019Search in Google Scholar

40. Adebayo JO, Krettli AU. Potential antimalarials from Nigerian plants: A review. J Ethnopharmacol 2011;133:289–302. https://doi.org/10.1016/j.jep.2010.11.024.https://doi.org/10.1016/j.jep.2010.11.024Search in Google Scholar

41. Kolawole OM, Adesoye AA. Evaluation of antimalarial activity of Bridelia Ferruginea Benth bark. Can J Pure Appl Sci 2010;4:1039–44. https://doi.org/10.1590/S0074-02762011000900019.10.1590/S0074-02762011000900019Search in Google Scholar

42. Amoa Onguéné P, Ntie-Kang F, Lifongo LL, Ndom JC, Sippl W, Mbaze L. The potential of anti-malarial compounds derived from African medicinal plants. Part I: A pharmacological evaluation of alkaloids and terpenoids. Malaria J 2013;12:449.10.1186/1475-2875-12-449Search in Google Scholar

43. Olajide OA, Makinde JM, Awe SO. Effects of the aqueous extract of Bridelia ferruginea stem bark on carrageenan-induced oedema and granuloma tissue formation in rats and mice. J Ethnopharmacol 1999;66:113–17. https://doi.org/10.1016/s0378-8741(99)00006-9.https://doi.org/10.1016/s0378-8741(99)00006-9Search in Google Scholar

44. Mbah CC, Akuodor GC, Anyalewechi NA, Iwuanyanwu TC, Osunkwo UA. In vivo antiplasmodial activities of aqueous extract of Bridelia ferruginea stem bark against Plasmodium berghei berghei in mice. Pharmaceut Biol 2012;50:188–94. https://doi.org/10.3109/13880209.2011.592537.https://doi.org/10.3109/13880209.2011.592537Search in Google Scholar

45. Adebayo JO, Krettli AU. Potential antimalarials from Nigerian plants: a review. J Ethnopharmacol 2011;133:289–302. https://www.sciencedirect.com/science/article/pii/S0378874110008093?via%3Dihub.10.1016/j.jep.2010.11.024Search in Google Scholar PubMed

46. Khozirah S, Noor Rain A, Siti Najila MJ, Imiyabir Z, Madani L. In vitro Antiplasmodial properties of selected plants J Sci Technol 2011;19:11–17. http://psasir.upm.edu.my/id/eprint/40635/1/97.%20In%20vitro%20antiplasmodial%20properties%20of%20selected%20plants%20of%20Sabah.pdf.Search in Google Scholar

47. Akuodor G, Mbah C, Anyalewechi N, Iwuanyanwu TC, Osunkwo U. Pharmacological profile of aqueous extract of Bridelia ferruginea stem bark in the relief of pain and fever. J Med Plants Res 2011;5:5366–9. https://www.researchgate.net/publication/274031044_Pharmacological_profile_of_aqueous_extract_of_Bridelia_ferruginea_stem_bark_in_the_relief_of_pain_and_fever.Search in Google Scholar

48. Singh A, Kumar R. Evaluation of acute toxicity of aqueous extract of Eclipta alba and its effects on liver of male Swiss albino mice. J Herb Med Tox 2011;5:89–95. https://doi.org/10.4103/0253-7613.106437.https://doi.org/10.4103/0253-7613.106437Search in Google Scholar

49. Bakoma B, Berké B, Eklu-Gadegbeku K, Agbonon A, Aklikokou K, Gbeassor M, et al. Acute and sub-chronic (28 days) oral toxicity evaluation of hydroethanolic extract of Bridelia ferruginea Benth root bark in male rodent animals. Food Chem Toxicol 2013;52:176–9. https://www.sciencedirect.com/science/article/pii/S0278691512008289?via%3Dihub.10.1016/j.fct.2012.11.021Search in Google Scholar PubMed

50. Taiwo I, Adewumi O, Odeigah P. Assessment of Bridelia ferruginea benth for its therapeutic potential in pregnancy-induced impaired glucose tolerance in rats. Int Res J Med Biomed Sci 2012;1:49–55. https://www.researchgate.net/publication/335960184_Assessment_of_Bridelia_ferruginea_benth_for_its_therapeutic_potential_in_pregnancy-induced_impaired_glucose_tolerance_in_rats/citation/download.10.14194/ijmbr.118Search in Google Scholar

51. Odunlade A, Taiwo I, Arojojoye O, Lawal T. Hepatotoxicity of aqueous leaf extract of Bridelia ferruginea on the liver of Albino rats. Int J Nat Sci Res 2015;5:57–64. https://www.iiste.org/tag/journal-of-natural-sciences-research-call-for-papers/page/3/.Search in Google Scholar

52. Tamargo J, Le Heuzey J-Y, Mabo P. Narrow therapeutic index drugs: a clinical pharmacological consideration to flecainide. Eur J Clin Pharmacol 2015;71:549–67. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412688/.10.1007/s00228-015-1832-0Search in Google Scholar PubMed PubMed Central

53. Ezike AC, Akah PA, Nnamani EM, Okoli CO, Ojike FU, Eze FS, et al. Studies on the antiulcer and gastrointestinal effects of stem bark extract of Bridelia ferruginea. J Compl Integr Med 2011;8. https://europepmc.org/article/med/22754933. 22754933.10.2202/1553-3840.1507Search in Google Scholar PubMed

54. Kolawole O, Olayode J, Oyewo O, Adegboye A, Kolawole C. Toxicological renal eff ects of Bridelia ferruginea-treated wastewater in rats. Afr J Microbiol Res 2009;3:82–7. https://academicjournals.org/journal/AJMR/article-full-text-pdf/0792C6612243.10.4314/afrrev.v3i1.43586Search in Google Scholar

55. Nene BSA, Zahoui OS, Soro TY. Effects of Bridelia ferruginea Benth. (Euphorbiaceae) aqueous extract on renal function in the rat. Int J Cardiol 2011;152:S62. https://www.ncbi.nlm.nih.gov/pubmed/10432217.10.1016/j.ijcard.2011.08.672Search in Google Scholar

56. Lim AKH. Diabetic nephropathy – complications and treatment. Int J Nephrol Renovascular Dis 2014;7:361–81. https://doi.org/10.2147/IJNRD.S40172.https://doi.org/10.2147/IJNRD.S40172Search in Google Scholar

57. Munuswamy S, Gnanamani A, Deepa G, Sudha M, Madharacheryulu E, Deivanai K. In vivo studies on evaluation of potential toxicity of unspent tannins using albino rats (Rattus novergicus). Food Chem Toxicol 2008;46:2288–2295. https://academicjournals.org/journal/AJMR/article-full-text-pdf/0792C6612243.10.1016/j.fct.2008.03.012Search in Google Scholar PubMed

58. Arika WM, Nyamai DW, Musila MN, Ngugi MP, Njagi ENM. Hematological Markers of In Vivo Toxicity. J Hematol Thromb Dis 2016;4:1–7. https://doi.org/10.4172/2329-8790.1000236.https://doi.org/10.4172/2329-8790.1000236Search in Google Scholar

59. Weingand K, Brown G, Hall R, Davies D, Gossett K, Neptun D, et al. Harmonization of animal clinical pathology testing in toxicity and safety studies. The Joint Scientific Committee for International Harmonization of Clinical Pathology Testing. Fundam Appl Toxicol 1996;29:198–201. https://www.ncbi.nlm.nih.gov/pubmed/8742316.10.1006/faat.1996.0022Search in Google Scholar

60. Okpuzor J, Ogbunugafor H, Kareem GK. Hepatic and hematologic effects of fractions of Globimetula Braunii in normal albino rats. EXCLI Journal 2009;8:182–9. https://www.semanticscholar.org/paper/Hepatic-and-hematologic-effects-of-fractions-of-in-Kareem-Ogbunugafor/e16d3d057f00c5653b0e78d447c8ed6dcd1faf79.Search in Google Scholar

61. Patrick-Iwuanyanwu KC, Onyeike EN, Wegwu MO. Hepatoprotective effects of methanolic extract and fractions of African mistletoe Tapinanthus bangwensis (Engl. & K. Krause) from Nigeria. EXCLI Journal 2010;9:187–94. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698891/.Search in Google Scholar

62. Evaluation of hematological and biochemical activity of ethanolic extract of Zygophyllum simplex Linn. in wistar rats, 2016. Pakistan J Biol Sci: PJBS 9, 179–84. https://doi.org/10.3923/pjbs.2016.179.184.https://doi.org/10.3923/pjbs.2016.179.184Search in Google Scholar

63. Ladokun O, Ojezele M, Arojojoye O. Comparative study on the effects of aqueous extracts of viscum album (mistletoe) from three host plants on hematological parameters in albino rats. Afr Health Sci 2015;15:606–12. https://doi.org/10.4314/ahs.v15i2.38.https://doi.org/10.4314/ahs.v15i2.38Search in Google Scholar

64. Ofem O, Ani E, Eno A. Effect of aqueous leaves extract of Ocimum gratissimum on hematological parameters in rats. Int J Appl Basic Med Res 2012;2:38–42. http://www.ijabmr.org/article.asp?issn=2229-516X;year=2012;volume=2;issue=1;spage=38;epage=42;aulast=Ofem.10.4103/2229-516X.96807Search in Google Scholar PubMed PubMed Central

65. Nigatu D, Mekbib A, Asfaw D, Eyasu M, Wondwossen E, Bekesho G. Assessment of hematological, biochemical and histopathological effects of acute and sub-chronic administration of the aqueous leaves extract of Thymus schimperi in rats. J Clin Toxicol 2016;6. https://doi.org/10.4172/2161-0495.1000286.https://doi.org/10.4172/2161-0495.1000286Search in Google Scholar

66. Ola-Davies OE, Olukole S., Amoo OA. Haematological and serum biochemical variables in rats treated with ethanol extract of the root of Moringa oleifera. Afr J Biomed Res 2014;17:31–5. https://www.researchgate.net/publication/306107787.Search in Google Scholar

67. Ogbunugafor H, Igwo-Ezikpe M, Igwilo I, Ozumba N, Adenekan S, Ugochukwu C, et al. In vitro and in vivo evaluation of antioxidant properties of Moringa Oleifera ethanolic leaves extract and effect on serum lipid indices in rat. Macedonian J Med Sci 2012;15:397–403. http://www.mjms.mk/Online/MJMS_2012_5_4/MJMS.1857-5773.2012-0240.pdf.10.3889/MJMS.1857-5773.2012.0240Search in Google Scholar

68. Erslev A. Humoral regulation of red cell production. Blood 1953;8:349 https://www.ncbi.nlm.nih.gov/pubmed/13032205.10.1182/blood.V8.4.349.349Search in Google Scholar

69. Okwu DE, Ukanwa N. Isolation and characterization of flavonoids chalcones and anthocynidines from Bridelia ferruginea benth. Chem Sin 2010;1:21–8. https://www.researchgate.net/publication/265033845.Search in Google Scholar

70. Kareem K, Kareem S, Adeyemo O, Egberongbe R. In vitro antimicrobial properties of Bridelia ferruginea on some clinical isolates. Agric Biol J N Am 2010;1:416–20. https://journals.sagepub.com/doi/10.1177/1934578X1801301207.10.5251/abjna.2010.1.3.416.420Search in Google Scholar

71. Osman CP, Ismail NH. Antiplasmodial anthraquinones from medicinal plants: the chemistry and possible mode of actions. Nat Prod Commun 2018;13. https://doi.org/10.1177/1934578X1801301207.https://doi.org/10.1177/1934578X1801301207Search in Google Scholar

72. Khan W, Subhan S, Shams DF, Afridi SG, Ullah R, Shahat AA, et al. Antioxidant potential, phytochemicals composition, and metal contents of Datura alba. BioMed Res Int 2019;2019:1–8. https://www.hindawi.com/journals/bmri/2019/2403718/.10.1155/2019/2403718Search in Google Scholar PubMed PubMed Central

73. Engwa GA., November 7th 2018. Free radicals and the role of plant phytochemicals as antioxidants against oxidative stress-related diseases. Phytochemicals: Source of Antioxidants and Role in Disease Prevention. Source of Antioxidants and Role in Disease Prevention, Toshiki Asao and Md Asaduzzaman, IntechOpen, pp. 49–74. https://doi.org/10.5772/intechopen.76719. Available from: https://www.intechopen.com/books/phytochemicals-source-of-antioxidants-and-role-in-disease-prevention/free-radicals-and-the-role-of-plant-phytochemicals-as-antioxidants-against-oxidative-stress-related.https://doi.org/10.5772/intechopen.76719Search in Google Scholar

74. Olarewaju O, Oloyede O. Aqueous Bridelia ferruginea stem bark transaminase activities in albino rats. Afr J Biochem Res 2014;8:84–7. https://academicjournals.org/journal/AJBR/article-abstract/3AF6D8544720.10.5897/AJBR2013.0738Search in Google Scholar

75. Ajiboye T, Abdussalam F, Adeleye A, Iliasu G, Ariyo F, Adediran Z, et al. Bridelia ferruginea promotes reactive oxygen species detoxification in N-nitrosodiethylamine-treated rats. J Diet Suppl 2013;10:210–28. https://pubs.acs.org/doi/10.1021/jf00039a005.10.3109/19390211.2013.822451Search in Google Scholar PubMed

Received: 2018-11-23
Accepted: 2020-02-19
Published Online: 2020-05-19

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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