Influence of Methanol Extract of Dennettia tripetala on Hepatic Redox Homeostasis and Detoxification Pathways in Carbon Tetrachloride–Intoxicated Wistar Rats
Authors
Department of Biochemistry, Prince Abubakar Audu University, Anyigba (Nigeria)
Department of Medical Laboratory Sciences, Edo University, Iyamho (Nigeria)
Integrated Science Department, Kogi State College of Education, Ankpa (Nigeria)
Department of Chemistry, Federal University Lokoja (Nigeria)
Department of Biochemistry, Prince Abubakar Audu University, Anyigba (Nigeria)
Department of Biochemistry, University of Benin (Nigeria)
Article Information
DOI: 10.51584/IJRIAS.2026.11090057
Subject Category: Medical Laboratory Science
Volume/Issue: 11/9 | Page No: 788-798
Publication Timeline
Submitted: 2026-09-13
Accepted: 2026-09-18
Published: 2026-10-09
Abstract
Background: Therapeutic plants are rich sources of bioactive compounds useful in combating various human diseases. This study investigated the in vitro antioxidant activity, gas chromatography–mass spectrometry (GC-MS) profile, and in vivo protective effects of the methanolic leaf extract of Dennettia tripetala in a carbon tetrachloride (CCl₄)-intoxicated rat model.
Methods: Twenty-five male Wistar rats (6–8 weeks old, 150–190 g) were randomly allocated into six groups (n = 5 per group). Group A (normal control) received liquid paraffin (1 mL/kg); Group B (intoxicated control) received 30% CCl₄ in liquid paraffin (1 mL/kg); Group C received silymarin (100 mg/kg) plus CCl₄; Groups D, E and F received the methanolic leaf extract at 100, 200 and 300 mg/kg, respectively, plus CCl₄. Extract or silymarin was administered orally for six consecutive days; CCl₄ was given from day 2 to day 6. Liver function indices (ALT, AST, ALP, total protein, total bilirubin) and antioxidant markers (SOD, CAT, GSH, MDA) were measured. Data were analysed by one-way ANOVA followed by Bonferroni multiple-comparison test (GraphPad Prism 8.0.1) after confirmation that the assumptions of normality and homogeneity of variance were met; p < 0.05 was considered significant. Values are presented as mean ± standard error of the mean (SEM).
Results: The extract exhibited strong free-radical scavenging activity (IC₅₀ = 4.12 µg/mL against DPPH versus 3.33 µg/mL for ascorbic acid; IC₅₀ = 5.00 µg/mL against ABTS versus 3.87 µg/mL for ascorbic acid). GC-MS analysis identified 37 compounds accounting for 99.7% of the total peak area. The major constituents (≥ 2%) were linoleic acid (36.10%), palmitic acid (18.96%), vitamin E (7.15%), stearic acid (6.06%), caryophyllene (4.24%), γ-sitosterol (3.98%), squalene (3.75%), phytol (2.28%) and α-amyrin (2.12%). These compounds are candidate contributors to the observed antioxidant activity. In vivo, CCl₄ significantly elevated serum ALT, AST, ALP and total bilirubin and reduced total protein relative to the normal control (p < 0.05). Concurrent administration of the extract (100–300 mg/kg) significantly attenuated these elevations and restored total protein toward control values (p < 0.05 versus Group B). The extract also significantly increased hepatic SOD, CAT and GSH while decreasing MDA levels compared with the intoxicated control (p < 0.05). Acute oral toxicity testing indicated an LD₅₀ > 3000 mg/kg.
Conclusions: The methanolic leaf extract of D. tripetala demonstrates preclinical hepatoprotective activity against CCl₄-induced oxidative liver injury in rats, consistent with its in vitro antioxidant capacity and the presence of candidate phytochemicals. These findings provide experimental support for further mechanistic and dose–response studies; they do not constitute justification for therapeutic use in humans.
Keywords
Dennettia tripetala; hepatoprotection; carbon tetrachloride; antioxidant; GC-MS; Wistar rats
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References
1. Abo-elhamd, A.M., Abul-Enein, A.M., Mohammed, S.M., Shalaby, A.S. & Konsowa, A. (2016). Chemical characterization, antioxidant and antihepatotoxicity of Calliandra haematocephala growing in Egypt. Journal of Chemical and Pharmaceutical Research, 8(4), 828–845. [Google Scholar] [Crossref]
2. Adeoti, S.B., Ayedoun, M.A. & Leclercq, P.A. (2000). Essential oil of Dennettia tripetala leaves from Benin. Journal of Essential Oil Research, 12(4), 412–414. [Google Scholar] [Crossref]
3. AlSheikh, H.M.A., Sultan, I., Kumar, V., Rather, I.A., Al-Sheikh, H., Tasleem Jan, A. & Haq, Q.M.R. (2020). Plant-based phytochemicals as possible alternative to antibiotics in combating bacterial drug resistance. Antibiotics, 9(8), 480. [Google Scholar] [Crossref]
4. Anaga, A.O. & Asuzu, I.U. (2011). Glucose uptake-enhancing activity of the ethyl acetate extract of Dennettia tripetala in 3T3-L1 adipocytes. Journal of Complementary and Integrative Medicine, 8(1). [Google Scholar] [Crossref]
5. Ayeni, G., Ejoba, R., Olajide, J.E. & O.S. (2016). Hepatoprotective activity of silymarin in carbon tetrachloride (CCl₄)-intoxicated rats. International Journal of Innovation Research, 4(5), 83–86. [Google Scholar] [Crossref]
6. Bag, A. & Mumtaz, S.M. (2013). Hepatoprotective and nephroprotective activity of hydroalcoholic extract of Ipomoea staphylina leaves. Bangladesh Journal of Pharmacology, 8(3), 263–268. [Google Scholar] [Crossref]
7. Beers, R.F. & Sizer, I.W. (1952). A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. Journal of Biological Chemistry, 195, 133–140. [Google Scholar] [Crossref]
8. Brown, M.B. & Forsythe, A.B. (1974). Robust tests for the equality of variances. Journal of the American Statistical Association, 69(346), 364–367. [Google Scholar] [Crossref]
9. Burkill, H.M. (1995). The useful plants of West Tropical Africa, Vol. 3. Royal Botanic Gardens, Kew. [Google Scholar] [Crossref]
10. Doughari, J.H. (2012). Phytochemicals: extraction methods, basic structures and mode of action as potential chemotherapeutic agents. INTECH Open Access Publisher. [Google Scholar] [Crossref]
11. Ejechi, B.O. & Akpomedaye, D.E. (2005). Activity of essential oil and phenolic acid extracts of pepperfruit (Dennettia tripetala) against some food-borne microorganisms. African Journal of Biotechnology, 4(2), 258–261. [Google Scholar] [Crossref]
12. Gill, L.S. (1992). Ethnomedical uses of plants in Nigeria. Uniben Press, Benin City. [Google Scholar] [Crossref]
13. Gornall, A.G., Bardawill, C.S. & David, M.M. (1949). Determination of serum proteins by means of the biuret reaction. Journal of Biological Chemistry, 177(2), 751–766. [Google Scholar] [Crossref]
14. Guntupalli, M.M.R., Chandana, V.R., Palpu, P. & Annie, S. (2006). Hepatoprotective effects of rubiadin, a major constituent of Rubia cordifolia Linn. Journal of Ethnopharmacology, 103, 484–490. [Google Scholar] [Crossref]
15. Hartman, P.E. (1983). Putative mutagens and carcinogens in foods. IV. Malondialdehyde. Environmental Mutagenesis, 5(4), 603–607. [Google Scholar] [Crossref]
16. Hassan, S.W., Ayeni, G., Wasagu, R.S.U., Umar, R.A., Agaie, B.M. & Farouk, U.Z. (2015). Hepatoprotective effect of leaf extracts of Newbouldia laevis on carbon tetrachloride-intoxicated rats. Journal of Global Biosciences, 4(5), 2258–2281. [Google Scholar] [Crossref]
17. Jendrassik, L. & Gróf, P. (1938). Simplified photometric methods for the determination of bilirubin. Biochemische Zeitschrift, 297, 81–89. [Google Scholar] [Crossref]
18. Kakkar, P., Das, B. & Viswanathan, P.N. (1984). A modified spectrophotometric assay of superoxide dismutase. Indian Journal of Biochemistry & Biophysics, 21, 130–132. [Google Scholar] [Crossref]
19. Lee, I.C., Kim, S.H., Baek, H.S., et al. (2014). The involvement of Nrf2 in the protective effects of diallyl disulfide on carbon tetrachloride-induced hepatic oxidative damage and inflammatory response in rats. Food and Chemical Toxicology, 63, 174–185. [Google Scholar] [Crossref]
20. Leitzmann, C. (2016). Characteristics and health benefits of phytochemicals. Complementary Medicine Research, 23(2), 69–74. [Google Scholar] [Crossref]
21. OECD (2001). Guideline for the testing of chemicals. Acute oral toxicity – Up-and-Down Procedure. No. 425. [Google Scholar] [Crossref]
22. Ofem, O.E., et al. (2014). Methanolic extract of Dennettia tripetala leaf normalises abnormal bile secretion in rats during toxic challenge. [Google Scholar] [Crossref]
23. Patterson, J.W. & Lazarow, A. (1955). Determination of glutathione. In: Glick, D. (ed.) Methods of Biochemical Analysis, Vol. 2. Interscience, New York, pp. 259–278. [Google Scholar] [Crossref]
24. Re, R., Pellegrini, N., Proteggente, A., Pannala, A., Yang, M. & Rice-Evans, C. (1999). Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radical Biology and Medicine, 26, 1231–1237. [Google Scholar] [Crossref]
25. Reitman, S. & Frankel, S. (1957). A colorimetric method for the determination of serum glutamic oxaloacetic and glutamic pyruvic transaminases. American Journal of Clinical Pathology, 28, 56–63. [Google Scholar] [Crossref]
26. Shapiro, S.S. & Wilk, M.B. (1965). An analysis of variance test for normality (complete samples). Biometrika, 52(3–4), 591–611. [Google Scholar] [Crossref]
27. Simelane, M.B.C., Lawal, O.A., Djarova, T.G. & Opoku, A.R. (2010). In vitro antioxidant and cytotoxic activity of Gunnera perpensa L. from South Africa. Journal of Medicinal Plants Research, 4(21), 2181–2188. [Google Scholar] [Crossref]
28. Sood, R. (1999). Medical Laboratory Technology: Methods and Interpretations, 5th ed. Jaypee Brothers Medical Publishers. [Google Scholar] [Crossref]
29. Timothy, C.O. & Okere, C.O. (2008). Effect of Dennettia tripetala (Mmimi) seed intake on the IOP of normotensive emmetropic Nigerian Igbos. Journal of the Nigerian Optometric Association, 14(1), 14–17. [Google Scholar] [Crossref]
30. Wang, M.Y., West, B.J., Jensen, C.J., et al. (2002). Morinda citrifolia (Noni): a literature review and recent advances in Noni research. Acta Pharmacologica Sinica, 23(12), 1127–1141. [Google Scholar] [Crossref]
31. Weber, L.W., Boll, M. & Stampfl, A. (2003). Hepatotoxicity and mechanism of action of haloalkanes: carbon tetrachloride as a toxicological model. Critical Reviews in Toxicology, 33(2), 105–136. [Google Scholar] [Crossref]
32. Yang, J., Li, Y., Wang, F. & Wu, C. (2010). Hepatoprotective effects of apple polyphenols on CCl₄-induced acute liver damage in mice. Journal of Agricultural and Food Chemistry, 58(10), 6525–6531. [Google Scholar] [Crossref]
33. Yi, J., Xia, W., Wu, J., et al. (2014). Betulinic acid prevents alcohol-induced liver damage by improving the antioxidant system in mice. Journal of Veterinary Science, 15(1), 141–148. [Google Scholar] [Crossref]
34. Zamzami, M.A., Baothman, O.A.S., Samy, F. & Abo-Golayel, M.K. (2019). Amelioration of CCl₄-induced hepatotoxicity in rabbits by Lepidium sativum seeds. Evidence-Based Complementary and Alternative Medicine, 2019, 5947234. [Google Scholar] [Crossref]
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