PHYTOCHEMICAL CONSTITUENT, ACUTE AND SUBACUTE TOXICITY STUDIES OF METHANOL EXTRACT OF LAPORTEA AESTUANS LEAF

  • Abiola Adeosun Lead City University, Ibadan
  • A. J. Akamo
  • O. A. Akinloye
  • A. L. A. Shotuyo
Keywords: Bioactive, Phytochemicals, Laportea aestuans, Toxicity Study

Abstract

Laportea aestuans is an African herbaceous weed. This work assessed the bioactive compound content of methanol extract of Laportea aestuans leaf (LALME) and its acute and subacute toxicity effects in Male Wistar rats. According to qualitative and quantitative phytochemical analysis, LALME possesses a significant amount of phenolics, flavonoids, alkaloids, tannin, carotenoids, and anthraquinones. LALME is regarded as safe because it did not cause death in rats when given doses of up to 2,000 mg/kg body weight. LALME at 200 and 400 mg/kg markedly increased (p<0.05) serum activity of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl transferase (GGT). There was a decrease in liver LDH activity in rats administered LALME, but no significant alteration was noticed in the serum of the rats. The total bilirubin concentration in the serum of rats given 200 mg/kg LALME and in the liver of rats administered 200 and 400 mg/kg LALME was significantly higher (p<0.05) than that in the serum and liver of control rats. The serum of rats given LALME had a nearly threefold increase in direct bilirubin compared to control. However, rats administered 200 mg/kg of LALME had an increased serum urea concentration compared to control. When comparing photomicrographs of the liver and kidney of rats given LALME to those of control rats, the liver and kidney of rats given LALME showed minor congestion and renal dissemination, respectively. In conclusion, LALME was found to be safe in acute toxicity; nevertheless, subacute administration may cause variations in

 

References

Adeneye, A. A. (2014). Subchronic and chronic toxicities of African medicinal plants. In "Toxicological survey of African medicinal plants", pp. 99-133. Elsevier.

Akomas, S. C., and Ijioma, S. N. (2015). Beta-adrenergic activity of Laportea aestuans leaves extract on the smooth muscles of the rabbit jejunum. Journal of veterinary and applied sciences 5, 30-35.

Asensi-Fabado, M. A., and Munné-Bosch, S. (2010). Vitamins in plants: occurrence, biosynthesis and antioxidant function. Trends in plant science 15, 582-592.

Bartels, H., Bohmer, M., and Heierli, C. (1972). Serum creatinine determination without protein precipitation. Clin Chim Acta 37, 193–197.

Batt, A.-M., and Ferrari, L. (1995). Manifestations of chemically induced liver damage. Clinical Chemistry 41, 1882-1887.

Chew, W.-L. (1969). monograph of Laportea (Urticaceae). Gard Bull.

de Carvalho, L. M. J., Gomes, P. B., de Oliveira Godoy, R. L., Pacheco, S., do Monte, P. H. F., de Carvalho, J. L. V., Nutti, M. R., Neves, A. C. L., Vieira, A. C. R. A., and Ramos, S. R. R. (2012). Total carotenoid content, α-carotene and β-carotene, of landrace pumpkins (Cucurbita moschata Duch): A preliminary study. Food Research International 47, 337-340.

Englehardt, A. (1970). Measurement of alkaline phosphatase. Aerztl Labor, 16(42), 1.

Essiett, U. A., Edet, N. I., and Bala, D. N. (2011). Phytochemical and physicochemical analysis of the leaves of Laportea aestuans (Linn.) Chew and Laportea ovalifolia (Schumach.) Chew (male and female). Asian Journal of Plant Science and Research, 1, 35-42.

Fabricant, D. S., and Farnsworth, N. R. (2001). The value of plants used in traditional medicine for drug discovery. Environmental health perspectives 109, 69.

Fawcett, J. K., and Scott, J. E. (1960). A rapid and precise method for the determination of urea. J Clin Pathol 13, 158–159.

Focho, D., Ndam, W., and Fonge, B. (2009). Medicinal plants of Aguambu-Bamumbu in the Lebialem highlands, southwest province of Cameroon. African Journal of Pharmacy and Pharmacology 3, 001-013.

Ghadirkhomi, A., Safaeian, L., Zolfaghari, B., Ghazvini, M. R. A., and Rezaei, P. (2016). Evaluation of acute and sub-acute toxicity of Pinus eldarica bark extract in Wistar rats. Avicenna journal of phytomedicine 6, 558.

Ghate, N. B., Chaudhuri, D., and Mandal, N. (2013). In vitro antioxidant and free radical scavenging assessment of Tinospora cordifolia stem with DNA protective potential. Int J Pharm Bio Sci 4, 373–388.

Ighodaro, O. M., and Akinloye, O. A. (2017). Anti-diabetic potential of Sapium ellipticum (Hochst) Pax leaf extract in Streptozotocin (STZ)-induced diabetic Wistar rats. BMC complementary and alternative medicine 17, 525.

Kutchan, T. M. (1995). Alkaloid biosynthesis [mdash] the basis for metabolic engineering of medicinal plants. The plant cell 7, 1059.

Lans, C. (2007). Ethnomedicines used in Trinidad and Tobago for reproductive problems. Journal of ethnobiology and ethnomedicine 3, 13.

Mbaveng, A. T., Zhao, Q., and Kuete, V. (2014). Harmful and protective effects of phenolic compounds from African medicinal plants. In "Toxicological Survey of African Medicinal Plants", pp. 577-609. Elsevier.

Mickymaray, S. (2019). Efficacy and mechanism of traditional medicinal plants and bioactive compounds against clinically important pathogens. Antibiotics 8, 257.

Nekvindova, J., Mrkvicova, A., Zubanova, V., Vaculova, A.H., Anzenbacher, P., Soucek, P., Radova, L., Slaby, O., Kiss, I., Vondracek, J. and Spicakova, A., (2020). Hepatocellular carcinoma: gene expression profiling and regulation of xenobiotic-metabolizing cytochromes P450. Biochemical pharmacology, 177, 113912.

Obidike, I., and Salawu, O. (2013). New insights into toxicity and drug testing. Screening of herbal medicines for potential toxicities. INTECH 2013, 64-88.

Organization for Economic Co-operation and Development (OECD) (2001). Acute oral toxicity in animals. . (OECD/OCDE, ed.), Vol. Guideline No. 423., No. 423.

Osagie-Eweka, S. E., Orhue, N., Omogbai, E., and Amaechina, F. (2021). Oral acute and sub-chronic toxicity assessment of aqueous leaf extract of Simarouba glauca DC (Paradise tree). Toxicology reports 8, 239-247.

Ramulondi, M., de Wet, H., and van Vuuren, S. (2019). Toxicology of medicinal plants and combinations used in rural northern KwaZulu-Natal (South Africa) for the treatment of hypertension. Journal of Herbal Medicine 16, 100251.

Reitman, Y., and Frankel, S. (1957). Practical biochemistry in clinical medicine. Am J Clin Path 25, 56.

Schnellmann, R. G. (2008). Toxic responses of the kidney. Cassarett and Doull’s Toxicology. The Basic Science of Poisons, 7th ed. New York (NY): McGraw-Hill Medical Publishing Division, 583-608.

Singleton, V. L., Orthofer, R., and Lamuela-Raventos, R. M. (1999). Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin-Cioalteau Reagents. . Method Enzymol 299, 152-178.

Sofowara, A. (1996). Research on medicinal plants and traditional medicine in Africa. Journal Alternative and Complementary Medicine 2, 365–372.

Soladoye, M. O., and Chukwuma, E. C. (2012). Quantitative phytochemical profile of the leaves of Cissus populnea Guill. & Perr. (Vitaceae)e an important medicinal plant in central Nigeria. Arch Appl Sci Res 4, 200-206.

Trease, E., and Evans, W. C. (1984). "A textbook of Pharmacology," 13/Ed., Baillieritindal, London

Woreta, T. A., and Alqahtani, S. A. (2014). Evaluation of abnormal liver tests. Medical Clinics 98, 1-16.

Zengin, G., Cakmak, Y. S., Guler, G. O., and Aktumsek, A. (2011). Antioxidant properties of methanolic extract and fatty acid composition of Centaurea urvillei DC. subsp. hayekiana Wagenitz. Rec Nat Prod 5, 123–132.

Zhishen, J., Mengcheng, T., and Jianming, . (1999). The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemstry 64, 555–559.

Published
2022-03-31
How to Cite
AdeosunA., AkamoA. J., AkinloyeO. A., & ShotuyoA. L. A. (2022). PHYTOCHEMICAL CONSTITUENT, ACUTE AND SUBACUTE TOXICITY STUDIES OF METHANOL EXTRACT OF LAPORTEA AESTUANS LEAF. FUDMA JOURNAL OF SCIENCES, 6(1), 27 - 32. https://doi.org/10.33003/fjs-2022-0601-880