Telfairia occidentalis Seed Extracts Attenuated Oxidative Stress And Liver Injury In Plasmodium berghei-Infected Mice

Main Article Content

Nsikakabasi E. Sunday
Chinyelu C. Osigwe
Godwin N. Enin
Ugonma F. Uwaeme
Jude E. Okokon

Abstract

TelfairiaoccidentalisHooke. F. (Cucurbitaceae) is a vegetable used medicinally in the treatment of malaria. The seed crude and gradient extracts of T. occidentalis(138 -553 mg/kg) obtained by cold extraction were investigated for antioxidative stress, haematological and hepatoprotective effects in Plasmodium berghei-infected mice using standard curative test. Hematological parameters, oxidative stress markers levels, liver function indices were determined and histopathology of livers of the treated infected mice. Characterisation of the active extract was done using GCMS. The crude and gradient extracts (138-553 mg/kg, p.o.) exerted significant (p<0.05–0.001) antimalarial activity against P. berghei infection with methanol gradient extract having the highest activity. Hematological parameters of the infected treated mice were altered. The extracts treatment significantly (p<0.05) lowered liver enzymes (ALT, AST and ALP), total and conjugated bilirubin and also decreased significantly (p<0.05) total protein and albumin levels of the treated mice relative to control. The seed extracts further improved (p<0.05) the levels of antioxidant enzymes and molecules (CAT, GPx, GST,SOD) of the treated infected mice. The MDA levels of the treated infected mice were reduced (p<0.05) relative to control. Histology of liver sections revealed absence or reductions in pathological features in infected mice treated with crude extract (276 mg/kg), DCM and ethyl acetate gradient extracts compared to untreated infected mice. GCMS analysis of the active gradient extract revealed the presence of polyunsaturated fatty acids and monoterpenes in the active methanol extract. These results suggest that the seed extract possess antimalarial, antioxidative stress and hepatoprotective activities due to it phytochemical constituents


 

Article Details

How to Cite
Sunday, N. E., Osigwe, C. C., Enin, G. N., Uwaeme, U. F., & Okokon, J. E. (2026). Telfairia occidentalis Seed Extracts Attenuated Oxidative Stress And Liver Injury In Plasmodium berghei-Infected Mice. Tropical Journal of Phytochemistry and Pharmaceutical Sciences, 5(5), 568–577. https://doi.org/10.26538/tjpps/v5i5.2
Section
Articles

References

1. World Health Organisation World Malaria Report 2024: Addressing inequity in the global malaria response. Geneva:World Health Organization; 2024. Licence: CC BY-NC-SA 3.0 IGO. https:// www. who.int/teams/global-malariaprogramme/reports/worldmalaria-report-2024

2. Venkatesan P. World Malaria Report 2024. Lancet Microbe 2025; 6: 101073.https://doi.org/: 10.1016/j.lanmic.2025.101073.

3. Okokon, J.E., Augustine, N.B. and Mohanakrishnan, D. Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora, Pharm Biol. 2017; 55(1): 1022-1031. https://doi.org/doi: 10.1080/13880209.2017.1285947

4. Okokon JE, Antia BS, Azare B, Okokon PJ. Antimalarial and antiplasmodial activities of ethanol root extract of Zea mays. Avic J. Phytomed. 2017b;7(3):275-284.PMCID: PMC5511979 PMID: 28748174

5. Okokon JE, Mohanakrishnan D, Dinkar S, Okokon PJ. Antimalarial activities of Zea mays leaf extract in ethanol and selected solvent fractions. J. Herbs, Spices and Med Plants. 2017c;23(4): 334 - 346. https://doi.org/ 10.1080/10496475.2017.1335259

6. Okokon JE, Opara KN, Udobang JA, Bankhede H. In vivo antimalarial and antipyretic activities of leaf extract of Ananas comosus. Trop J. Nat Prod Res. 2019; 3(7): 240-245. https://doi.org/10.26538/tjnpr/v3i7.5

7. William NB, Bassey AL, Offiong AU, Otuekong E, Okokon JE. In vivo antimalarial activities of leaf extract and fractions of Setaria megaphylla (wild.) loes. In Plasmodium berghei infected mice. Trop. J. Nat Prod Res. 2022;6(9):1504-1510. https://doi.org/ 10.26538/tjnpr/v6i9.28

8. Okokon JE, Ekpo AJ, Eseyin OA. Evaluation of in vivo antimalarial activities of ethanolic leaf and seed extracts of Telfairia occidentalis. J. Med Food, 2009;12(3):649-653.https://doi.org/ 10.1089/jmf.2008.0099.

9. Usunobun U, Okpiabhele A.Telfairia occidentalis Hook f. mitigates carbon tetrachloride induced Nephrotoxicity in Rat. J. Appl and Basic Med Sci. 2023; 9(3):130-137. https://doi.org/ 10.61186/rabms.9.3.130.

10. Eseyin, O. A., Ebong, P., Ekpo, A., Igboasoiyi, A., and Oforah, E. Hypoglycemic effect of the seed extract of Telfairia occidentalis in rat. Pak J. Biol Sci. 2007; 10(3), 498–501. http://dx.doi.org/10.3923/pjbs.2007.498.501.

11. Okokon, J. E., Antia, B. S., Dar, A., and Choudhary, M. I. Immunomodulatory, anticancer and antiinflammatory activities of Telfairia occidentalis seed extract and fractions. Int J. Food Nutrition and Safety, 2012a;2(2), 72–85.

12. Osukoya OA, Adegbenro D, Onikanni SA, Ojo OA, OnasanyaA.Antinociceptive and antioxidant activities of the methanolic extract of Telfairia occidentalis seeds. AncSci Life. 2016; 36(2):98-103. https://doi.org/ 10.4103/asl.ASL_142_16

13. Okokon, J. E., Dar, A., and Choudhary, M. I. Chemical constituents and analgesic activity of Telfairia occidentalis. Phytopharmacol. 2012b;3(2), 359–366.

14. Magnus SP, Anagboso MO, Johnny II, Ise UP, Okokon JE. Evaluation of genotoxic and cytotoxic activities of leaf and seed extracts of Telfairiaoccidentalis. J. Comple and Altern Med Res. 2024; 25(3):7-16. https://doi.org/10.9734/JOCAMR/2024/v25i3521

15. Enin GN, Okokon JE, Odokwo BO, Antia BS. Preliminary phytochemical screening and in vivo Inhibitory study of Telfaira occidentalis Hook f. seeds extract on alpha amylase and alpha glucosidase of rats. J Sci and Tech Res. 2023;5(4): 26-35. http://dx.doi.org/ 10.5281/zenodo.10425980

16. Umoh UF, Ubengama EE, Udofia EU, Obasi OI, Okonna UK, Umanah ES, Etefia JE, Okokon JE. HPLC characterization and anti-ulcer effects of methanol seed extract and fractionated components of Telfairia occidentalis in rodents. Nig J. Pharm and ApplSci Res 2025:14 (2): 111-117.https://doi.org/10.60787/nijophasr-v14-i2-622

17. Fabian UA, Anagboso MO, Samuel AE, Okokon JE. Effect of seed extract and fractions of Telfairia occidentalis on liver and kidney functions and histologies of rats with testosterone-induced benign prostatic hyperplasia in rats. J. Comple and Altern Med Res. 2025;26(6):1-18.

18. Ebong AS, Eseyin OA, Etim EI, Okokon JE. Telfairia occidentalis potentiates antiplasmodial activity of artemisinin and amodiaquine combination therapy. Anti-Infective Agents. 2020;18(2): 152-159. https: //doi. org/ 10.2174/2211352517666190206160812

19. Enyiekere VJ, Asanga EE,Okokon JE,Ekeleme CM,Anagboso MO, Ise UP. Fatty acid esters and acyclic monoterpenoid from Justicia insularis leaf fractions attenuated malaria pathogenesis through docking with PFSHMT and PFEMP-1 proteins.Nat Products comm.2024;19(7):1-14.

20. Atanu FO, Idih FM, Nwonuma CO, Hetta HF, Alamery S, Batiha GE. Evaluation of antimalarial potential of extracts from Alstonia boonei and Carica papaya in Plasmodium berghei-infected mice. Evidence-Based Compl and Altern Med. Article ID 2599191, 2021;11. https://doi.org/ 10.1155/2021/2599191

21. Uche FI, GuoX, Okokon JE, Ullah I, Horrocks P, BoatingJ, Huang CG, Li W-W.In vivo efficacy and metabolism of the antimalarial and improved in vitro antiplasmodial activity of novel semisynthetic analogues. Antimicrob Agents Chemother.2020;65(2): doi: 10.1128/aac.01995-20.

22. Okokon JE, Mobley R, Edem UA, Bassey AL, Fadayomi I, Horrocks P, Drijfhout F, Li WW. In vitro and in vivo antimalarial activities and chemical profiling of sugarcane leaves. Sci Rep. 2022; 41598 article no: 14391 doi.org/10.1038/s41598-022-14391-8.

23. Okokon JE, Andrew UE, Uwaeme UF, OsigweCC, Ise UP.Effect of Telfairia occidentalis stem extract and fractions on parasitaemia, oxidative stress markers, lipid profile, hematological parameters, liver functionindices and liver histology in Plasmodium berghei infected mice. Asian J. Biochem Gen Mol Med.2025;17(1): 42-57.

24. Tietz WW. Clinical Guide to Laboratory tests. 2nd edn. Sanders Company. Philadelphia, PA. 1990; pp. 554-556

25. Khalid AS, Momodu I, Iduh MU, Shittu BS, Maniru N, Tukur M, Auwal AN, Khalid HS, Zakariyya A. Evaluation of antioxidant and haematological effects of ethanol extract of Saussurea lappa on streptozotocin induced-diabetic Wistar rats. Trop J Phytochem Pharm. Sci. 2024; 3(6):327 – 331. http://www.doi.org/10.26538/tjpps/v3i6.1

26. Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of lowdensity lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem., 1972; 18(6): 499-502.PMID: 4337382.

27. Okokon JE, Davies K, Lekara J, Iwara K, Thomas P, Li W-W. Phytochemical characterization, antihyperglycaemic and antihyperlipidemic activities of Setaria megaphylla in alloxan-induced diabetic rats. Phytomed Plus. 2022; 2(2022):100182.https://doi.org/10.1016/j.phyplu.2021.100182

28. Khan SL, Siddiqui FA. Beta-Sitosterol: As Immunostimulant, Antioxidant and Inhibitor of SARS-CoV-2 Spike Glycoprotein. Arch Pharmacol and Therapeut, 2020;2(1):12-16. https://doi.org/10.33696/Pharmacol.2.014.

29. Waako PJ, Gumede B, Smith P, Folb P I. The in vitro and in vivo Antimalarial activity of Cardiospermum halicacabum L. and Momordica foetida Schumch. Et Thonn. J. Ethnopharmacol. 2005;99(1):137-143. https://doi.org/ 10.1016/j.jep.2005.02.017.

30. Okokon JE, Ekpo AJ, Eseyin OA. Antiplasmodial activity of ethanolic root extract of Telfairia occidentalis. Res J. Parasitol. 2007; 2(2): 94 - 98. https://doi.org/jp.2007.94.98.

31. Melariri, P., Campbell, W., Etusim, P., Smith, P. In vitro and in vivo antimalarial activity of linolenic and linoleic acids and their methyl esters. Adv Stud Biol, 2012;4:333–349.

32. Marei GI, Rabea EI, Badawy ME. In vitro antimicrobial and antioxidant activities of monoterpenes against some food-borne pathogens. J. Plant Protection and Pathol. Mansoura University, 2019;10 (1): 87- 94.

33. Anthony PC, Attih E, Ebong A, Johnson EC, Anthony V, Goodness C, Esenam F, Omotoso A, Asanga EE, After S, Eseyin O.A. Antiplasmodial potential of quercetin and its derivatives: molecular docking, synthesis and in vivo studies. J. Pure and ApplMicrobiol. 2025:19(3):2292-2304. https://doi.org/ 10.22207/JPAM.19.3.55.

34. Guthrow C E, Morris MA, Day JF, Thorpe SR, Baynes JW. Enhanced nonenzymatic glucosylation of human serum albumin in diabetes mellitus. Proc Natl Acad Sci USA.1979; 76(9): 4258-4261. https://doi.org/ 10.1073/pnas.76.9.4258.

35. Onyesom I, Onyemakonor N. Levels of parasitaemia and changes in some liver enzymes among malarial infected patients in Edo-Delta Region of Nigeria. Cur Res J. Biol Sci. 2011; 3(2): 78-81.

36. Orhue NE J, Nwanze EAC. Okafor, A. Serum total protein, albumin and globulin levels in Trypanosoma brucei-infected rabbits: Effect of orally administered Scopariadulcis. Afr J. Biotech. 2005;4(10): 1152-1155. https://doi.org/ 10.4314/ajb.v4i10.71355

37. George BO, Osioma E, Okpoghono J1, Aina OO. Changes in liver and serum transaminases and alkaline phosphatase enzyme activities in Plasmodium berghei infected mice treated with aqueous extract of Aframomum sceptrum. Afr J. Biochem Res. 2011;5(9): 277-281.

38. Uzuegbu UE, Emeka CB. Changes in liver function biomarkers among malaria infected patients in Ikeja Lagos State, Nigeria. Curr Res J. Biol Sci. 2011;3(3): 172-174.

39. Nwanna E, Oboh G. Antioxidant and hepatoprotective properties of polyphenol extracts from Telfairia occidentalis (Fluted Pumpkin) leaves on acetaminophen induced liver damage. Pak J Biol Sci. 2007; 10(16): 2682-2687. https://doi.org/ 10.3923/pjbs.2007.2682.2687.

40. Becker K, Tilley L, Vennerstrom JL, Roberts D, Rogerson S, Ginsburg H. Oxidative stress in malaria parasite-infected erythrocytes: Host-parasite interactions. Int J. Parasitol. 2004; 34(2): 163-189. https://doi.org/10.1016/j.ijpara.2003.09.011.

41. Gora D, Sandhya M, Shiv G, Praveen S. Oxidative stress, α-tocopherol, ascorbic acid and reduced glutathione status in schizophrenics. Ind J. Clin Biochem. 2006; 21: 34–38. https://doi.org/10.1007/BF02912908

42. Guyton A, Hall J. Textook of Medical Physiology. 12th ed. Philadelphia; 2007.

43. Uzuegbu UE, Opajobi AO, Ojugbeli, ET, Ikwuazom OO, Ezeh CA, Enudinisu GN, Onyesom I. Phyllanthus amarus Chemical Fractions Defend the Brain and Liver from Oxidative Assault Induced by Plasmodium berghei Malarial Parasite Infection. Trop J Phytochem Pharm Sci. 2025; 4 (5): 210 – 215 http://www.doi.org/10.26538/tjpps/v4i5.3

44. Malaguarnera L, Musumeci S. The immune response to Plasmodium falciparum malaria. Lancet Infectious Dis. 2002; 2(8): 472478. https://doi.org/ 10.1016/s1473-3099(02)00344-4.

45. Casals-Pascual C, Kai O, Newton CRJ, Peshu N, Roberts DJ. Thrombocytopenia in falciparum malaria is associated with high concentrations of IL-10. Am J. Trop Med and Hyg. 2006; 75(3): 434-436.PMID: 16968917

46. Bero, J., Quetin-Leclercq, J. Natural products published in 2009 from plants traditionally used to treat malaria. Planta Med. 2011; 77(06): 631- 640.doi: 10.1055/s-0030-1250405.

47. Nathawut S, Paveena Y, Srivicha K, Wattana L, Gary B, SornchaiL,Rachane U. Increased fluidity and oxidation of malarial lipoproteins: Relation with severity and induction of endothelial expression of adhesion molecules. Lipids in Health and Dis. 2004: 3: 15. https://doi.org/ 10.1186/1476-511X-3-15.

48. Krishna AP, ChandrikaSuchetha K, ManasaA,Shrikant LP. Variation in common lipid parameters in malaria infected patients. Indian J. Physiol. Pharmacol. 2009;53(3): 271-274.PMID: 20329375.

49. Memon RA, Staprans I, Noor M, Holleran WM, Uchida Y, Moser AH, Feingold KR and Grunfeld C. Infection and inflammation induce LDL oxidation in vivo. Arterioscler Thromb Vasc Biol. 2000; 20: 1536-1542. https://doi.org/ 10.1161/01.atv.20.6.1536.

Similar Articles

<< < 1 2 3 4 5 6 7 8 9 10 > >> 

You may also start an advanced similarity search for this article.