Hepatoprotective Effect of <I>Ipomoea cairica</I> Leaf Extract against Acetaminophen Hepatotoxic Effect in Rats viz antioxidant and anti-inflammatory activities

Authors

  • Omotayo B. Ilesanmi Department of Biochemistry, Faculty of Science, Federal University Otuoke, Otuoke, Bayelsa State.

DOI:

https://doi.org/10.51412/psnnjp.2025.16

Keywords:

hepatotoxicity, acetaminophen, natural products, oxidative stress, inflammation
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Abstract

Background: Acetaminophen is one of the over-the-counter drugs commonly used by humans as a pain reliever. While it is generally safe at a prescribed dose, misuse and overdose of the drug make it one of the substances linked to liver damage. Ipomoea cairica is one of the medicinal plants reported to be an alternative source of treatment and prevention of toxic effects of chemicals against organ function. This study evaluated the hepatoprotective effect of I. cairica leaf extract against the hepatotoxic effect of acetaminophen in rats.

Methods: Thirty-five male Wistar rats were randomly divided into five groups of seven rats each. I: Normal control; II: orally administered 2000 mg/kg of acetaminophen (ACET); III: orally administered 100 mg/kg Methanolic extract of I. cairica (MEIC) for 14 days before single dose administration of ACET; IV: orally administered 250 mg/kg of MEIC for 14 consecutive days before single dose administration of ACET V: orally administered 250 mg/kg of MEIC for 14 consecutive days. Animals were sacrificed 24 hours after the last administration. Blood was collected and processed for markers of lipidaemia and hepatic function. The liver was excised and processed for antioxidant, oxidative stress, and pro-inflammatory activities

Results: The results showed that ACET (group II) caused a significant increase in the concentration of serum total cholesterol (TC), triglyceride (TG), and low-density lipoprotein (LDL). In contrast, the concentration of HDL was significantly reduced when compared to the rats in the control group. Pretreatment with MEIC at a higher dose was able to prevent the production of malondialdehyde
(MDA) and phosphatidylserine (PC) as well as glutathione (GSH) levels. MEIC also prevented the depletion of SOD and CAT activities by ACET. In addition, ACE overdose elevated the activities of NADPH oxidoreductases, xanthine oxidases, and MPO. However, administration of the two doses of MEIC was able to reverse all the toxic effects of acetaminophen on hepatic tissues.

Conclusion: The results provided scientific proof of the potential of I. cairica to protect against hepatotoxicity that can be linked to the antioxidant and anti-inflammatory activity of the plant.

Author Biography

Omotayo B. Ilesanmi, Department of Biochemistry, Faculty of Science, Federal University Otuoke, Otuoke, Bayelsa State.

Telephone: +2348149962032

References

Abdeen A, Abdelkader A, Abdo M, Wareth G, Aboubakr M, Aleya L, Abdel-Daim M (2019) Protective effect of cinnam on against

acetaminophen-mediated cellular damage and apoptosis in renal tissue. Environmental Science Pollution Research International, 26:240–249. https://doi.org/10.1016/j.jcs.2012.07.014

Abdulrazzaq AM, Badr M, Gammoh O, Abu Khalil AA, Ghanim BY, Alhussainy TM, Qinna NA (2019) Hepatoprotective actions of ascorbic acid, alpha lipoic acid and silymarin or their combination against acetaminophen-induced hepatotoxicity in rats. Medicina, 55(5): 181.

https://doi.org/10.3390/medicina55050181

James LP (2003) Acetaminophen-induced hepatotoxicity. Drug Metabolism and Disposition, 31: 1499 – 1506. https://doi.org/10.1124/dmd.31.12.1499

Nili-Ahmadabadi A, Borzouee Z , Ahmadimoghaddam D, Firozian F, Dastan D (2019) The occurrence of acetaminophen/codeine as an adulterant in herbal analgesic supplements in Hamadan, Iran: A pilot study. Complementary Therapies in Medicine, 42: 223–225. https://doi.org/10.1016/j.ctim.2018.11.018

Hwang K, Hwang Y, Hwang H, Park N (2022) Hepatoprotective Effects of Radish (Raphanus sativus L.) on Acetaminophen-Induced Liver Damage via Inhibiting Oxidative Stress and Apoptosis. Nutrients, 14 (23):5082.https://doi.org/10.3390/nu14235082

Bhaumik A, Saha S, Baishya U, Kashyap G, Kuli B, Rahman F, Sarkar N (2025). Screening of Bioactive Molecules and Phytopharmacological Potential of Ipomoea Cairica: A Comprehensive Review. American Journal of Psychiatric Rehabilitation, 28(1), 210-215.

Ilavenil, S., Al-Dhabi, N. A., Srigopalram, S., Ock Kim, Y., Agastian, P., Baru, R., & Valan Arasu, M. (2016). Acetaminophen induced hepatotoxicity in Wistar rats—A proteomic approach. Molecules, 21(2), 161.

Ilesanmi, O. B., & Adeogun, E. O. (2022). Nephroprotective effect of Ipomoea cairica leaf extract against cadmium-induced renal damage. Nigerian Journal of Biochemistry and Molecular Biology, 37(4):282-288.

Doumas BT, Watson WA, Bigg, HG (1971) Albumin standards and the measurement of serum albumin with bromocresol green, Clinica Chimica Acta, 31(1): 87-96.

Allain CC, Poon LS, Chan CS, Richmond W, Fu PC (1974) Enzymatic determination of total serum cholesterol. Clinical Chemistry, 20:470–5

Fossati P and Prencipe L (1982) Serum Triglycerides Determined Calorimetrically with an Enzyme That Produces Hydrogen Peroxide.

Clinical Chemistry, 28: 2077-2080.

Lee R and Niemann D (1996) Nutritional Assessment 2nd ed Mosby Missou USA.

Ohkawa H, Ohishi N, Yagi K (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry, 95 (2): 351 – 358. https://doi.org/10.1016/0003-2697(79)90738-3

Beutler E, Duron O, Kelly BM (1963) Improved method for the determination of blood glutathione. The Journal of Laboratory and Clinical Medicine, 61:882–888

Misra HP, Fridovich I (1972) The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. Journal of Biological Chemistry, 247(10):3170-3175.

Luck H (1963) Methods of enzymatic analysis. Enzyme assays in vivo. New York, London: Academic Press.

Montgomery HAC, Dymock JF (1961) The determination of nitrite in water. Analyst, 86:414-416

Hernández-Espinosa DR, Massieu L, Montiel T, Morán J (2019) Role of NADPH oxidase-2 in the progression of the inflammatory response secondary to striatum excitotoxic damage. Journal of Neuro inflammation, 16:91.https://doi.org/10.1186%2Fs12974-019-1478-4

Della CE, Stripe F (1972) The regulation of rat liver xanthine oxidase: Involvement of thiol groups in the conversion of the enzyme activity from dehydrogenase -type D- into oxidase -type O- and purification of the enzyme. Biochemistry Journal, 126: 739 - 745. https://doi.org/10.1042/bj1260739

Battelli MG, Buonamici L, Polito L, Bolognesi A, Stirpe F (1996). Hepatoxicity of ricin, saporin or a saporin immunotoxin: xanthine oxidase activity in rat liver and blood serum. Virchows Archiv: an international journal of pathology, 427 (5), 529–535. https://doi.org/10.1007/BF00199514

Nishikimi M, Appaji N, Yagi K (1972) The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochemical and Biophysical Research Communications, 46 (2): 849 – 854. https://doi.org/10.1016/s0006-291x(72)80218-3

Ilesanmi OB, Inala ER (2022) Hepatoprotective effect of Ipomoea cairica (Convolvulaceae) leaf extract against cadmium chloride induced liver damage. Toxicologie Analytique et Clinique 34 (1), 30-37

Raˇskovi ́c A, Milanovi ́c I, Pavlovi ́c N, ́Cebovi ́c T, Vukmirovi ́c S, Mikov M (2014) Antioxidant activity of rosemary (Rosmarinus officinalis L.) essential oil and its hepatoprotective potential. BMC Complementary and Alternative Medicine, 14 (1): 1 – 9.

https://doi.org/10.1186%2F1472-6882-14-225

Kim SJ, Hyun J (2024) Altered lipid metabolism as a predisposing factor for liver metastasis in MASLD. Molecules and Cells, 47(2): 100010. https://doi.org/10.1016/j.mocell.2024.100010

Deprince A, Haas JT, Staels B (2020) Dysregulated lipid metabolism links NAFLD to cardiovascular disease. Molecular Metabolism, 42: 101092. https://doi.org/10.1016/j.molmet.2020.101092

Gulcin ̇I (2020) Antioxidants and antioxidantmethods: An updated overview. Archives of Toxicology, 94: 651 – 715.

https://doi.org/10.1007/s00204-020-02689-3

Fisher L, Green MD, Harman AW (1982) Levels of acetaminophen and its metabolites in mouse tissues after a toxicdoes. Journal of Pharmacology Experiment and Therapy, 221:407–413

Pigeolet E, Corbisier P, Houbion A, Lambert D, Michiels C, Raes M, Zachary MD, Remacle J (1990) Glutathione peroxidase superoxide

dismutase, and catalase inactivation by peroxides and oxygen derived free radicals. Mechanism of Ageing and Development, 51: 283 – 297. https://doi.org/10.1016/0047-6374(90)90078-t

Zubkova EV, Robaire B (2004) Effect of Glutathione Depletion on Antioxidant Enzymes in the Epididymis, Seminal Vesicles, and Liver and on Spermatozoa Motility in the Aging Brown Norway Rat. Biology of Reproduction, 71: 1002 – 1008).

https://doi.org/10.1095/biolreprod.104.028373

Ilesanmi OB, Akinmoladun AC, Josiah SS, Olaleye MT, Akindahunsi AA (2020) Modulation of key enzymes linked to Parkinsonism and neurologic disorders by Antiaris africana in rotenone-toxified rats. Journal of Basic and Clinical Physiology and Pharmacology, 31 (3): 20190014. https://doi.org/10.1515/jbcpp-2019-0014

Koelsch M, Mallak R, Graham GG, Kajer T, Milligan MK, Nguyen LQ, Davies MJ (2010) Acetaminophen (paracetamol) inhibits myeloperoxidase-catalysed oxidant production and biological damage at therapeutically achievable concentrations. Biochemical Pharmacology, 79 (8): 1156 - 1164. https://doi.org/10.1016/j.bcp.2009.11.024

Tang C, Cen L, Zeng H, Zhang X, Liu P, Chen Y, Xu C (2024) Inhibiting hepatocyte uricacid synthes is and reabsorption ameliorates

acetaminophen-induced acute liver injury in mice. Cellular and Molecular Gastroenterology and Hepatology, 17 (2): 251 - 265.

https://doi.org/10.1016/j.jcmgh.2023.10.005

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Published

2025-05-24

How to Cite

Ilesanmi, O. B. (2025). Hepatoprotective Effect of <I>Ipomoea cairica</I> Leaf Extract against Acetaminophen Hepatotoxic Effect in Rats viz antioxidant and anti-inflammatory activities. The Nigerian Journal of Pharmacy, 59(1), 165–175. https://doi.org/10.51412/psnnjp.2025.16