Bitter kola (Garcinia kola) is the African wonder nut that is widely eaten for its medicinal properties. The aim of this study was to investigate the potential genotoxic effects of the aqueous extract of G. kola nuts using the Allium cepa test system. Roots of A. cepa were treated to a series of concentrations, 0 µg/ml, 5.0 µg/ml, 10.0 µg/ml, 25.0 µg/ml and 40.0 µg/ml for a period of 72 hours. The results indicated that percentage growth of roots and mitotic chromosome behaviour was inversely proportional to the concentration of extract. Increase in concentration of extract significantly reduced the number of roots and the length of roots recorded indicating a progressive inhibition of the mitotic activity of the meristematic cells. The mean number of roots (3.2±5.97) and mean length of roots (1.3±0.53cm) were minimum at the highest concentration of extract (40µg/ml). Mitotic index was also minimum (0.44±0.05%) at the highest concentration (40µg/ml) of the G. kola extract. The genotoxicity of the extract was measured using the frequency of chromosomal aberrations which revealed a high frequency of Anaphase chromosomal bridges, Anaphase laggards, sticky chromosomes and nuclear vacuoles. The highest percentage of abnormal cells (3.65±3.49%) was determined for the highest concentration (40µg/ml) of extract. The chromosomal abnormalities were evidences of the action of the aqueous extract on the mitotic spindle and the coiling of chromosomes during anaphase to telophase These results are therefore enough to conclude that G. kola extract possesses cytotoxic and cytogenotoxic properties.
Published in | American Journal of BioScience (Volume 10, Issue 6) |
DOI | 10.11648/j.ajbio.20221006.13 |
Page(s) | 195-200 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2022. Published by Science Publishing Group |
Garcinia kola, Allium cepa, Root Growth, Mitotic Index, Chromosome Aberrations
[1] | Tcheghebe OT, Signe M, Seukep AJ, Tatong FN, 2016. Review on traditional uses, phytochemical and pharmacological profiles of Garcinia kola Heckel. Merit Research Journal of Medicine and Medicinal Sciences, 4 (11): 480-489. |
[2] | Burkil HM, 2004. Useful plants of West Tropical Africa. Royal Botanic Garden; Kew. |
[3] | Eyog-Matig O, Aoudji AKN, Linsoussi C. (2007). Garcinia kola Heckel seeds dormancy-breaking. Applied Ecology and Environmental Research, 5 (1): 63-71. http://www.ecology.uni-corvinus.hu. |
[4] | Adebisi AA, 2004. A case study of Garcinia kola nut production-to-consumption system in J4 area of Omo Forest Reserve, South-west Nigeria.-In: Sunderland, T and Ndoye, O. (eds): Forest Products, livelihood and conservation (Case study of Non-Timber Forest Product Systems), Volume 2 Africa, pp. 115-132. |
[5] | Eleyinmi AF, Bressler DC, Amoo IA, Sporns P, Oshodi AA, 2006. Chemical composition of Bitter cola (Garcinia kola) seed and hulls. Polish Journal of Food and Nutrition Sciences, 15/56 (4): 395-400. |
[6] | Akintonwa Am Essien AR, 1990. Protective effects of Garcinia kola seed extract against paracetamol-induced hepatotoxicity in rats. J. Ethnopharmacol., 29: 207-2011. |
[7] | Adegoke GO, Kumar MV, Sambaiah K, Lokesh BR, 1998. Inhibitory effect of Garcinia kola on the lipid peroxidation in rat liver homogenate. Indian J. Exp. Biol., 36: 907-910. |
[8] | Tona L, Ngimbi NP, Tsakala M, Mesia K, Cimanga K, Apers S, De Bruyne T, Pieters L, Totte J, Vlietinck AJ, 1999. Antimalarial activity of 20 crude extracts from nine African medicinal plants used in Kinshasa, Congo. Journal of Ethnopharmacology, 68 (1–3): 193-203. https://doi.org/10.1016/S0378-8741(99)00090-2 |
[9] | Farombi EO, Tahnteng JG, Agboola AO, Nwankwo JO, Emerole GO, 2000. Chemoprevention of 2-acetylaminofluorene- induced hepatotoxicity and lipid peroxidation in rats by kolaviron-a Garcinia kola seed extract. Food Chemical Toxicol. 38: 535-541. |
[10] | Farombi EO, Akanni OO, Emerole GO, 2012. Antioxidant and scavenging activities of flavonoid extract (kolaviron) of Garcinia kola seeds in vitro. Pharm. Biol. 91: 129-134. |
[11] | Okunji CO, Ware TA, Hicks RP, Iwu MM, Skanchy DJ, 2002. Capillary electrophoresis determination of biflavanones from Garcinia kola seeds in vitro. Pharm. Biol. 91: 129-134. |
[12] | Iwu MM, Igboko OA, Okunji CO, Tempesta MS, 1990. Antidiabetic and Aldose reductase activities of biflavanones of Garcinia kola. Journal of Pharmancy and Pharmacology, 42: 290-292. http://dx.doi.org/10.111/j.2042-7158.1990.tb05412.x |
[13] | Farombi EO, 2003. African indigenous plants with chemotherapeutic potentials and biotechnological approach to the production of bioactive prophylactic agents. African J. Biotech. 2: 662-671. |
[14] | Labo-Popoola OA, Adaramoye OA, 2015. Garcinia kola (bitter kola): Is truly the wonder seed? African Journal of Sustainable Development, 5 (1): 159-171. |
[15] | Ayuk ET, Duguma B, Franzel S, Kingue J, Mollet M, Tiki-Manga T, Zenkeng P, 1999. Uses, management and economic potentials of Garcinia kola and Ricinodendron heudelotti in the humid lowlands of Cameroon. Journal of Tropical Forest Science, 11 (4): 746-761. |
[16] | Guidje NM, Fankap R, 2001. Utilisation traditionelles de Garcinia lucida et Garcinia kola (Clusiaceae) au Cameroun. Systematic and Geography of plants, 71 (2): 747-758. Doi: 10.2307/3668714. |
[17] | Kanmegne G, Omoko ND, 2008. Germination of Garcinia kola (Heckel) seeds in response to different hormone treatments. Fruits, 63 (08): 155-161. Doi: 10.1051/fruits:2008005. |
[18] | Seino RA, Atonleu MS, Ngnaniyyi A, Dongmo TI, Tchoupou NR, 2020. Cytogenotoxic assessment of the aqueous extract of Citrullus lanatus (Cucurbitaceae) leaves using the spermatogonial germ-line cells of Zonocerus variegatus L. (Orthoptera: Pyrgomorphidae). African Journal of Biological Sciences, 2 (3): 30-36. https://doi.org/10.33472/AFJBS.2.3.2020.30.36. |
[19] | Akwu NA, Naidoo Y, Singh M, 2019. Cytogenotoxic and biological evaluation of the aqueous extracts of Grewia lasiocarpa: An Allium cepa assay. South African Journal of Botany, 125; 371-380. |
[20] | Seino RA, Akongnui T, 2010. Meiotic study of Acrida turrita (Linnaeus 1758), Paracenama luculenta Karsh 1896 and Morphacris fasciata (Thunberg 1815) (Orthoptera: Acrididae). Int. J. Biol. Chem. Sci. 4 (6): 1914 -1921. |
[21] | Sousa SM, Silva PS, Viccini LF, 2010. Cytogenotoxicity of Cymbopogon citratus (DC) Stapf (Lemon grass) aqueous extracts in vegetal test systems. Annals of the Brazilian Academy of Sciences, 82 (2): 305-311. |
[22] | Sadaqa EAA, Mohammed SS, Qari SH, Ali KS, 2016. Genotoxic effect of garlic extracts on root tips of Allium cepa L., IOSR Journal of Pharmacy and Biological Sciences, 11 (2ver.II): 41-44. |
[23] | El-Khodary S, Habib A, Haliem A, 1990. Effect of the herbicide tribunil on root mitosis of Allium cepa. Cytologia, 55: 209-215. |
[24] | Camparoto ML. Teixeira RO, Mantovani MS, Vicentini VEP, 2002. Effects of Maytenus licifolia Mart. and Bauhinia candicans infusions on onion root-tip and rat bone-marrow cells. Genetics and Molecular Biology, 25: 85-89. |
[25] | Knoll MF, Silva ACF, Tedesco SB, Canto-Dorow TS, 2006. Effects of Pterocaulon polystachyum DC (Asteraceae) on onion (Allium cepa) root tip cells. Genet. Mol. Biol. 29 (3): 539-542. |
[26] | Lubini G, Facchinetto M, Laughinghouse HD, Paranhos JT, Silva ACF, Tedesco, 2008. Extracts affecting mitotic division in root-tip meristematic cells. Biologia, 63: 647–65. https://doi.org/10.2478/s11756-008-0108-x |
[27] | Fiskejo G, 1997. Allium test for screening chemicals; evaluation of cytologic parametres. In Wang, W., Gorsuchm JW, Hughes, JS (Eds.). Plants for environmental studies. CRC Lewis Publishers, Boca Raton, New York. |
[28] | Bakare AA, Wale-Adeyemo AR, 2004. The potential mutagenic and cytotoxic effects of leachates from domestic wastes and Aba -Eku landfill Nigeria on Allium cepa. J. Nat. Environ. Pollut. Technol. 3: 455-462. |
[29] | Babatunde BB, Bakare AA, 2006. Genotoxicity screening of waste waters from Agbara Industrial Estate, Nigeria, evaluated with Allium cepa test. Pollut. Res. 25: 227-234. |
[30] | Alade A, Olufunsho A, Gbenga A, Herbert ABC, 2009. Mutagenic screening of some commonly used medicinal plants in Nigeria. J. Ethnopharmacol. 125: 461-470. |
[31] | Celik AT, and Aslanturk OS, 2010. Evaluation of cytotoxicity and genotoxicity of Inula viscosa leaf extract with Allium test. J. Biomed. Biotechnol. 2010: 189252. Doi: 10.1155/2010/189252. |
[32] | Erana Y and Ozatab A, 2014. Determination of mutagenic and cytotoxic effects of Limonium globuliferum aqueous extract by Allium, Ames and MTT tests. Rev. Bras. Farmacog, 24: 51-59. |
[33] | Singh P, 2015. Toxic effect of Chromium on genotoxicity and cytotoxicity by use of Allium cepa L. International Journal of Research in Engineering and Applied Sciences, 5 (10). |
[34] | Sutan NA, Soare LC, Mutlu E, Dobre R, Yanik T, Sutan C, 2020. Water quality assessment through cytogenotoxic parametres-a case study of Karaco; ak river, Turkey. Current Trends in Natural Sciences, 9 (17): 23-30. https://doi.org/10.47068/ctns.2020.v9i17.003. |
[35] | Finardi A, Massari LF, Visintin R, 2020. Anaphase Bridges: Not all natural fibres are healthy. Genes, 11 (8), 902. https://doi.org/10.3390/genes11080902. |
[36] | Chan KL, Palmia-Pallag T, Ying S, Hickson ID, 2009. Replication stress induces sister-chromatid bridging at fragile site loci in mitosis. Nat. Cell Biol. 11: 753-760. Doi: 10.1038/ncb1882. |
[37] | Lukas C, Savic V, Bekker-Jensen S, Doil C, Neumann B, Pedersen RS, Grofte M, Chan KL, Hickson ID, Bartek J, Lukas J, 2011. 53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress. Nat. Cell Biol. 13: 243-253. Doi: 10.1038/ncb2201. |
[38] | Pampalona J, Roscioli E, Silkworth WT, Bowden B, Genesca A, Tussel L, Cimini D, 2016. Chromosome bridges maintain kinetochore-microtubule attachment throughout mitosis and rarely break during anaphase. Plos One, 11 (1): e0147420. Doi: 10.1371/journal.pone.0147420. |
[39] | Potapova T, Gorbsky GJ, 2017. The consequences of chromosome segregation errors in mitosis and meiosis. Biology (Basel), 6 (1): 12. Doi: 10.3390/biology6010012. |
[40] | Ly P, Brunner SF, Shoshani O, Kim DH, Lan W, Pyntikova T, Flanagan AM, Behjati S, Page DC, Campbell PJ, Cleverland DW, 2019. Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements. Nat. Genet., 51 (4): 705-715. Doi: 10.1038/s41588-019-0360-8. |
[41] | Gordon DJ, Resio B, Pellman D, 2012. Causes and consequences of aneuploidy in cancer. Nature Reviews Genetics. 13 (3): 189-203. Doi: 10.1038/nrg3123. |
[42] | Bavle RM, 2016. Nuclear vacuolization: Giant lochkern-like cells. J. Oral Maxillofac Pathol. 20 (3): 339-341. Doi: 40.4103/0973-029X.190895. |
[43] | Aravinthan A, Verma S, Coleman N, Davies S, Allison M, Alexander G, 2012. Vacuolation in hepatocyte nuclei is a marker of senescence. J. Clin. Pathol. 65 (6): 557-5560. Doi: 10.1136/jclinpath-2011-200641. |
[44] | Badr A, 1983. Mitodepressive and Chromotoxic activities of two herbicides in Allium cepa. Cytologia, 48 (3): 451-457. https://doi.org/10.1508/cytologia.48.451. |
[45] | Sudhakar R, Ninge Gowda KN, Venu G, 2001. Mitotic abnormalities induced in silk dyeing industry effluents in the cells of Allium cepa. Cytologia, 66: 235-239. |
[46] | Hassan G, Yassein A, 2014. Cytogenotoxicity evaluation of water contaminated with some textile azo dyes using rapid markers and chromosomal aberrations of onion (Allium cepa) root cells. Egyptian Journal of Genetics and Cytology, 43: 39-57. |
[47] | Prajitha V, Thoppil JE, 2016. Cytotoxic and apoptotic activities of extract of Amaranthus spinosus L. in Allium cepa and human erythrocytes. Cytotechnology, 69: 123-133. |
[48] | Tuesher JM, Beck CR, Spencer L, Yeremy B, Shi Y, Anderson RJ, Golsteyn RM, 2021. Extracts prepared from a Canadian toxic plant induce light-dependent perinuclear vacuoles in human cells. Toxins, 13 (138): 1-15. https://doi.org/10.3390/toxins130201 |
[49] | Vellaikkannu S, Chathlingathe SV, Subramani M, Gupta P, 2017. Genotoxicity of pesticides to onion root tip Meristematic cells. International Journal of Botany Studies, 2 (4): 202-23. |
APA Style
Seino Richard Akwanjoh, Ngnaniyyi Abdoul, Endum Lucas Akacha, Dongmo Tonleu Ingrid. (2022). Cytogenotoxicity of the Aqueous Extract of Bitter Kola (Garcinia kola: Clusiaceae) Using Allium cepa Assay. American Journal of BioScience, 10(6), 195-200. https://doi.org/10.11648/j.ajbio.20221006.13
ACS Style
Seino Richard Akwanjoh; Ngnaniyyi Abdoul; Endum Lucas Akacha; Dongmo Tonleu Ingrid. Cytogenotoxicity of the Aqueous Extract of Bitter Kola (Garcinia kola: Clusiaceae) Using Allium cepa Assay. Am. J. BioScience 2022, 10(6), 195-200. doi: 10.11648/j.ajbio.20221006.13
@article{10.11648/j.ajbio.20221006.13, author = {Seino Richard Akwanjoh and Ngnaniyyi Abdoul and Endum Lucas Akacha and Dongmo Tonleu Ingrid}, title = {Cytogenotoxicity of the Aqueous Extract of Bitter Kola (Garcinia kola: Clusiaceae) Using Allium cepa Assay}, journal = {American Journal of BioScience}, volume = {10}, number = {6}, pages = {195-200}, doi = {10.11648/j.ajbio.20221006.13}, url = {https://doi.org/10.11648/j.ajbio.20221006.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajbio.20221006.13}, abstract = {Bitter kola (Garcinia kola) is the African wonder nut that is widely eaten for its medicinal properties. The aim of this study was to investigate the potential genotoxic effects of the aqueous extract of G. kola nuts using the Allium cepa test system. Roots of A. cepa were treated to a series of concentrations, 0 µg/ml, 5.0 µg/ml, 10.0 µg/ml, 25.0 µg/ml and 40.0 µg/ml for a period of 72 hours. The results indicated that percentage growth of roots and mitotic chromosome behaviour was inversely proportional to the concentration of extract. Increase in concentration of extract significantly reduced the number of roots and the length of roots recorded indicating a progressive inhibition of the mitotic activity of the meristematic cells. The mean number of roots (3.2±5.97) and mean length of roots (1.3±0.53cm) were minimum at the highest concentration of extract (40µg/ml). Mitotic index was also minimum (0.44±0.05%) at the highest concentration (40µg/ml) of the G. kola extract. The genotoxicity of the extract was measured using the frequency of chromosomal aberrations which revealed a high frequency of Anaphase chromosomal bridges, Anaphase laggards, sticky chromosomes and nuclear vacuoles. The highest percentage of abnormal cells (3.65±3.49%) was determined for the highest concentration (40µg/ml) of extract. The chromosomal abnormalities were evidences of the action of the aqueous extract on the mitotic spindle and the coiling of chromosomes during anaphase to telophase These results are therefore enough to conclude that G. kola extract possesses cytotoxic and cytogenotoxic properties.}, year = {2022} }
TY - JOUR T1 - Cytogenotoxicity of the Aqueous Extract of Bitter Kola (Garcinia kola: Clusiaceae) Using Allium cepa Assay AU - Seino Richard Akwanjoh AU - Ngnaniyyi Abdoul AU - Endum Lucas Akacha AU - Dongmo Tonleu Ingrid Y1 - 2022/12/15 PY - 2022 N1 - https://doi.org/10.11648/j.ajbio.20221006.13 DO - 10.11648/j.ajbio.20221006.13 T2 - American Journal of BioScience JF - American Journal of BioScience JO - American Journal of BioScience SP - 195 EP - 200 PB - Science Publishing Group SN - 2330-0167 UR - https://doi.org/10.11648/j.ajbio.20221006.13 AB - Bitter kola (Garcinia kola) is the African wonder nut that is widely eaten for its medicinal properties. The aim of this study was to investigate the potential genotoxic effects of the aqueous extract of G. kola nuts using the Allium cepa test system. Roots of A. cepa were treated to a series of concentrations, 0 µg/ml, 5.0 µg/ml, 10.0 µg/ml, 25.0 µg/ml and 40.0 µg/ml for a period of 72 hours. The results indicated that percentage growth of roots and mitotic chromosome behaviour was inversely proportional to the concentration of extract. Increase in concentration of extract significantly reduced the number of roots and the length of roots recorded indicating a progressive inhibition of the mitotic activity of the meristematic cells. The mean number of roots (3.2±5.97) and mean length of roots (1.3±0.53cm) were minimum at the highest concentration of extract (40µg/ml). Mitotic index was also minimum (0.44±0.05%) at the highest concentration (40µg/ml) of the G. kola extract. The genotoxicity of the extract was measured using the frequency of chromosomal aberrations which revealed a high frequency of Anaphase chromosomal bridges, Anaphase laggards, sticky chromosomes and nuclear vacuoles. The highest percentage of abnormal cells (3.65±3.49%) was determined for the highest concentration (40µg/ml) of extract. The chromosomal abnormalities were evidences of the action of the aqueous extract on the mitotic spindle and the coiling of chromosomes during anaphase to telophase These results are therefore enough to conclude that G. kola extract possesses cytotoxic and cytogenotoxic properties. VL - 10 IS - 6 ER -