Phyllanthus amarus Chemical Fractions Defend the Brain and Liver from Oxidative Assault Induced by Plasmodium berghei Malarial Parasite Infection

Main Article Content

Uzuegbu E Ugochukwu
Opajobi Adefunke
Ojugbeli Evelyn
Ikwuazom Okwunna
Ezeh A Caleb
Enudinisu N Gabriel
Onyesom Innocent

Abstract

Phyllanthus amarus is being promoted for treating various ailments, including malaria. While its antiplasmodial properties are documented, little is known about the antioxidant potential of its chemical fractions and their protective effects on the brain and liver. This study aimed to assess the ability of different chemical fractions of Phyllanthus amarus to protect these organs from oxidative damage induced by Plasmodium berghei infection. Crude ethanolic leaf extract and chemical fractions (alkaloids, tannins, saponins, flavonoids, carbohydrates, and anthraquinones) were administered to mice at 150, 300, and 450 mg/kg daily for 21 days. A total of 240 adult Swiss albino mice (20–30g) were divided into 24 groups (n=10/group). On day 22, mice were sacrificed under chloroform anesthesia following an overnight fast. Liver and brain tissues were harvested, homogenized, and centrifuged to obtain supernatant for biochemical analysis of total antioxidant capacity (TAC) and malondialdehyde (MDA). Results revealed that the crude extract and its flavonoid, carbohydrate, and anthraquinone fractions significantly (p<0.05) increased TAC and reduced MDA levels in both liver and brain compared to infected controls. These findings suggest that Phyllanthus amarus, particularly its flavonoid, carbohydrate, and anthraquinone fractions, confers antioxidant protection to the liver and brain during Plasmodium berghei malaria. The observed protective effect may be attributed to the high phenolic content of these fractions. This study demonstrates the bioavailability and antioxidant potential of Phyllanthus amarus and supports its therapeutic role in malaria-associated oxidative stress.

Metrics

Metrics Loading ...

Article Details

How to Cite
Ugochukwu, U. E., Adefunke , O., Evelyn, O., Okwunna, I., Caleb , E. A., Gabriel, E. N., & Innocent, O. (2025). Phyllanthus amarus Chemical Fractions Defend the Brain and Liver from Oxidative Assault Induced by Plasmodium berghei Malarial Parasite Infection. Tropical Journal of Phytochemistry and Pharmaceutical Sciences, 4(5), 210–215. https://doi.org/10.26538/tjpps/v4i5.3
Section
Articles

References

Gullo VP, McAlpine JB, Lam KS, Baker D, Petersen F. Drug discovery from natural products. J Ind Microbiol Biotechnol 2006;33:523–531.

Gazzaneo AS, Burkill HM, Bohn T, Shukla Y. Useful plants of West Tropical Africa. Royal Botanic Garden Kew 2005;2:272–275.

Lukmanul H, Adom GH, Liu P. Antioxidant and free radical scavenging potential of Achillea santolina extracts. Food Chem 2005;104:21–29.

Narsaria N, Mohanty C, Das BK, Mishra SP, Prasad R. Oxidative stress in children with severe malaria. J Trop Pediatr 2012;58:147–150.

Keller CC, Kremsner PG, Hittner JB, Misukonis MA, Weinberg JB, Perkin DJ. Elevated nitric oxide production in children with malaria anemia: hemozoin-induced nitric oxide synthase type 2 transcripts and nitric oxide in blood mononuclear cells. Infect Immun 2004;72:4868–4873.

Sohail M, Kaul A, Raziuddin M, Adak T. Decreased glutathione-S-transferase activity: diagnostic and protective role in vivax malaria. Clin Biochem 2007;40:377–382.

Guha M, Kumar S, Choubey V, Maity P, Bandyopadhyay U. Apoptosis in liver during malaria: role of oxidative stress and implication of mitochondrial pathway. FASEB J 2006;20:439–449.

Atamna H, Ginsburg H. Origin of reactive oxygen species in erythrocytes infected with Plasmodium falciparum. Mol Biochem Parasitol 1993;61:231–234.

Finkel T, Holbrook NJ. Oxidants, oxidative stress, and the biology of ageing. Nature 2000;408:239–247

Pappolla MA, Omar RA, Kim KS, Robakis NK. Immunohistochemical evidence of oxidative stress in Alzheimer's disease. Am J Pathol 1992;140(3):621–628.

Lakenbrink C, Adler R. Herbal vitamins: lead toxicity and developmental delay. Pediatrics 2000;160:600–602.

Halliwell TG, Gao L, Oomah BD. Antioxidant activity in selected fruits, vegetables, and grain products. J Agric Food Chem 1996;46:4113–4117.

Delay ER. Antioxidant activity and phenolic compounds in 32 selected herbs. Food Chem 1993;105:940–949.

Joseph B, Raj SJ. An overview: pharmacognostic property of Phyllanthus amarus Linn. Int J Pharmacol 2011;1:41–48.

Onyesom I, Onumaechi IF, Ehiwario J, Dagana R. Antiplasmodial activity of Phyllanthus amarus preserves renal function. Eur J Med Plants 2015;5:109–116.

Uzuegbu UE, Opajobi OA, Utalor JE, Elu CO, Onyesom I. Cytotoxicity and antiplasmodial activity of alkaloid extracts prepared from eight African medicinal plants used in Nigeria. Thai J Pharm Sci 2020;44:237–244.

Onyesom I, Uzuegbu UE, Mordi JC, Moses FP. Alkaloid extract of Phyllanthus amarus (Stone Breaker) and associated antiplasmodial activity in experimental mice. Niger J Biochem Mol Biol 2019;34:1–7.

Kumar KB, Kuttan R. Chemopreventive activity of an extract of Phyllanthus amarus against cyclophosphamide-induced toxicity in mice. Phytomedicine 2005;7:494–500.

Mbagwu HOC, Jackson C, Jackson I, Ekpe G, Eyaekop U, Essien G. Evaluation of the hypoglycemic effect of aqueous extract of Phyllanthus amarus in alloxan-induced diabetic albino rats. Int J Pharm Biomed Res 2011;2(3):158–160

Oshomoh EO, Uzama-Avenbuan O. Quantitative Phytochemical Composition and Bioactive Constituents of Ethanolic Extract of Phyllanthus amarus (Schum. et Thonn) Leaves. Eur J Agric Food Sci 2020;2(5):1-5

Ujah OF, Mohammad YY, Dewua CM. Quantification, Antioxidant and Free Radical Scavenging Potentials of Polyphenols from Crude Extracts of Phyllanthus amarus Leaves. ChemSearch J 2021;12(1):1-8.

Oshomoh EO, Uzama-Avenbuan O. Quantitative Phytochemical Composition and Bioactive Constituents of Ethanolic Extract of Phyllanthus amarus (Schum. et Thonn) Leaves. Eur J Agric Food Sci 2020;2(5):1-5

Umar HA, Usman H, Abubakar MB, Mohammed BF, Babakura M, Sule MA. Isolation and Characterisation of Hydrolysable Tannin from Ethyl Acetate Portion of the Aerial Part of Phyllanthus amarus Schum. & Thonn. Asian J Appl Chem Res 2019;2(3-4):1-10

Oshomoh EO, Uzama-Avenbuan O. Quantitative Phytochemical Composition and Bioactive Constituents of Ethanolic Extract of Phyllanthus amarus (Schum. et Thonn) Leaves. Eur J Agric Food Sci 2020;2(5):1-5.

Miller NJ, Rice-Evans CA. Factors influencing the antioxidant activity determined by the ABTS⁺• radical cation assay. Free Radical Research. 1997;26(3):195–199

Halliwell B, Gutteridge JMC. Free Radicals in Biology and Medicine. 3rd ed. Oxford: Oxford University Press; 1999

Halliwell B, Grooeveld M. The measurement of free radical reactions in humans. FEBS Lett 1987;213:9–14.

Aruoma OI. Nutrition and health aspects of free radicals and antioxidants. Food Chem Toxicol 1994;32:671–683.

Madsen HL, Bertelsen G. Spices as antioxidants. Trends Food Sci Technol 1995;6:271–277

Pokorny J. Natural antioxidants for food use. Trends Food Sci Technol 1991;2:223–227.

Chidinma M. Iheanacho, Paschal C. Akubuiro, Vincent O. Imieje, Osayemwenre Erharuyi, Kennedy O. Ogbeide, Arthur N. Jideonwo, Abiodun Falodun. Evaluation of the antioxidant activity of the stem bark extracts of Anacardium occidentale (Linn) Anacardiaceae. Tropical Journal of Phytochemistry and Pharmaceutical Sciences 2023; 2(2):65–69.

Kulkanium AG, Suryaka AN, Sardeshmukh AS, Rathi DB. Studies on biochemical changes with special reference to oxidant and antioxidant in malaria patients. Indian J Clin Biochm 2003;18:136–149.

Upadhyay DN, Vyas RK, Sharma ML, Soni Y, Rajnee S. Comparison in serum profile of peroxidation (MDA) and non-enzymatic antioxidants (vit. E and C) among patients suffering from Plasmodium falciparum and vivax malaria. J Portfolio Manag 2011;25:96–100.

Das BS, Nanda NK. Evidence for erythrocyte lipid peroxidation in acute falciparum malaria. Trans R Soc Trop Med Hyg 1999;93:58–62.

Egwunyenga AO, Isamah G, Nmorsi OP. Lipid peroxidation and ascorbic acid levels in Nigerian children with acute falciparum malaria. Afr J Biotechnol 2004;3:560–563.

Lim Y, Murtijaya J. Antioxidant properties of Phyllanthus amarus extracts as affected by different drying methods. Food Sci Technol 2007;40:1664–1669.

Igwe CU, Nwaogu LU, Ujuwondu CO. Assessment of the hepatic effects, phytochemical and proximate compositions of Phyllanthus amarus. Afr J Biotechnol 2007;6:728–731.

Pier-Giorgio P. Flavonoids as antioxidants. J Nat Prod 2000;63:1035–1042.

Baghiani A, Charef N, Djarmouni M, Saadeh HA, Arrar L, Mubarak MS. Free radical scavenging and antioxidant effects of some anthraquinone derivatives. Medicinal Chemistry. 2011;7(6):639–644.