Quercetin-Supplemented Diet Modulates Aluminium Chloride-Induced Neurotoxicity in Fruit Flies

Authors

  • J.A. Saliu Adekunle Ajasin University, Akungba Akoko, Ondo State, Nigeria.
  • N.G. Areola Department of Biochemistry, Adekunle Ajasin University, Akungba Akoko, Ondo State, Nigeria.
  • O.B. Ogunsuyi Federal University of Technology, Akure, Ondo State, Nigeria.

DOI:

https://doi.org/10.26437.ajar.03.2022.6

Abstract

Purpose: Neurotoxicity refers to the potential of a chemical substance, biological or physical agents to induce structural or functional defects in nerve tissue of the brain or peripheral nervous system. This study examined the therapeutic effect of dietary inclusion of Quercetin on Aluminium chloride-induced neurotoxicity in wild-type Fruit flies (Drosophila melanogaster).

Design/ Methodology/ approach: Flies were fed with diet supplements with AlCl3 (40mM) and Quercetin (0.1 and 1.0%) and counted daily throughout their life span. Flies were also raised on a diet supplemented with AlCl3 (40mM) and Quercetin (0.1 and 1.0%) for seven days. Flies were subsequently homogenized, and the activity of Acetylcholinesterase (AChE), Butyrylcholinesterase (BChE), Monoamine Oxidase (MAO), Catalase, and Glutathione-S-transferase (GST) were assayed.

Findings: Regarding the number of days required to reach 50% mortality, dietary inclusions of AlCl3 (40mM) reduced the life span of D.melanogaster more significantly than control flies. Also, Quercetin's 0.1 and 1.0% dietary inclusions significantly reduced AChE, BChE, and Monoamine Oxidase activity compared to the control.

Research Limitation/ Implications: The study focus on the dietary inclusion of Quercetin on Aluminium chloride-induced neurotoxicity in wild-type Fruit flies.

Practical Implication: There was a significant increase in the catalytic activities of GST and catalase in flies fed diet supplemented with 0.1 and 1.0% of Quercetin. However, dietary inclusion of both 0.1 and 1.0% of Quercetin seems tolerable as there was a less significant reduction in life span with a substantial effect on AChE, BChE, MAO activities, and its antioxidant activities compared to control flies.

Originality/ Value: The outcome of this research established that dietary inclusion of 40mM AlCl3 reduced the life span of D.melanogaster. In contrast, dietary inclusion of 0.1 and 1.0% of Quercetin produced some adaptive responses associated with reduction of neurotoxicity and elevated activities of some antioxidant enzymes.

 

Author Biography

J.A. Saliu, Adekunle Ajasin University, Akungba Akoko, Ondo State, Nigeria.

He is a Senior  Lecturer at the Department of Biochemistry at Adekunle Ajasin University, Akungba Akoko, Ondo State, Nigeria.

References

Abolaji, O.A., Kamdem, J.P., Lugokenski, T.H., Nascimento, T.K., Waczuk, E.P., Farombi, E.O., Loreto, E.L. & Rocha, J.B.T. (2014). Involvement of oxidative stress in 4- vinylcyclohexene-induced toxicity in Drosophila melanogaster. Free RadicBiol Med; 71:99–108.

Adedara, I.A., Abolaji, A.O., Rocha, J.B.T. & Farombi, E.O. (2016). DiphenylDiselenide Protects Against Mortality, Locomotor Deficits and Oxidative Stress in Drosophila melanogaster; Model of Aluminium-Induced Neurotoxicity. Neurochem Res. DOI 10.1007/s11064-016

Bilen, J. & Bonini, N.M. (2005). Drosophila as a model for human neurodegenerative disease. Annu. Rev. Genet.; 39: 153–171.

David, A. V. A., Arulmoli, R. & Parasuraman, S. (2016). Overviews of biological importance of quercetin: A bioactive flavonoid. Pharmacognosy Reviews, 10(20), 84.

Ellman, G.L. & Fiches, F.T. (1959). Quantitative determination of peptides by sulfhydryl groups. Arch. Biochem Biophys.; 82: 70-72.

Green, A.L., & Haughton, T.M. (1961). A colourimetric method for the estimation of monoamine oxidase. Biochem J; 78: 172-175.

Habig, W., Pabst, M., & Jakoby, W. (1981): Colorimetric determination of Glutathion S Transferase. J. Biol. Chem; (249): 7130-7139

Karlik, S.J., Eichhorn, G.L., Lewis, P.N., & Crapper, D.R. (1980). Interaction of aluminium species with deoxyribonucleic acid. Biochemistry; 19:5991–5998.

Khanna, P. & Nehru, B. (2007). Antioxidant enzymatic system in neuronal and glial cells enriched fractions of rat brain after aluminium exposure. Cell.Mol. Neurobiol.; 27: 959 –969.

Klafki, H.W., Staufenbiel, M., Kornhuber, J. & Wiltfang, J. (2006.) Therapeutic approaches to Alzheimer's disease. Brain; 129 (11): 2840–2855.

Kumar, V., Bal, A. & Gill, K.D. (2009). Susceptibility of mitochondrial superoxide dismutase to aluminium induced oxidative damage. Toxicology; 255: 117–123.

Lankoff, A., Banasik, A., Duma, A., Ochniak, E., Lisowska, H., Kuszewski, T., Gozdz, S. & Wojcik, A. (2006). A comet assay study reveals that aluminium induces DNA damage and inhibits the repair of radiation-induced lesions in human peripheral blood lymphocytes. Toxicol. Lett.; 161: 27–36.

Middaugh, J., Hamel, R., Jean-Baptiste, G., Beriault, R., Chenier, D., & Appanna, V.D. (2005). Aluminium triggers decreased aconitase activity via Fe–S cluster disruption and the overexpression of isocitrate dehydrogenase and isocitratelyase: a metabolic network mediating cellular survival. J. Biol. Chem.; 280: 3159 –3165.

Miu, A.C., Benga, O.(2006). Aluminium and Alzheimer’s disease: a new look. J. Alzheimers Dis.; 10: 179 –201.

Oyanagi, K. (2005). The nature of the parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam and magnesium deficiency. Parkinsonism Relat. Disord. 11 suppl; 1: S17–S23.

Rand, M.D., (2010). The growing potential for Drosophila in Neurotoxicology.

NeurotoxicolTeratol; 32:74‐83.

Savory, J., Herman, M.M., & Ghribi, O. (2006). Mechanisms of aluminium induced neurodegeneration in animals: Implications for Alzheimer’s disease. J. Alzheimers Dis.; 10: 135–144.

Savory, J., Rao, J.K., Huang, Y., Letada, P.R., & Herman, M.M. (1999). Age-related hippocampal changes in Bcl-2: Bax ratio, oxidative stress, redox-active iron and apoptosis associated with aluminium-induced neurodegeneration: increased susceptibility with ageing. Neurotoxicology; 20: 805– 817.

Sinha, B.B., Peterson, G.A. & Whitny, R.R. (1972). Nuclear change and Distribution of isotone. Pairs Phys. Rev; C6:1657-1663.

Valko, M., Leibfritz, D., Moncol, J., Cronin, M.T., Mazur, M. & Telser, J. (2007). Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol; 39 (1): 44–84.

Walton, J.R. (2007). An aluminium-based rat model for Alzheimer’s disease exhibits oxidative damage, inhibition of PP2A activity, hyperphosphorylated tau, and granulovacuolar degeneration. J. Inorg. Biochem.; 101:1275–1284.

Ward, R.J., Zhang, Y. & Crichton, R.R. (2001). Aluminium toxicity and iron homeostasis. J. Inorg. Biochem.; 87: 9 –14.

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Published

2022-04-03

How to Cite

Saliu, J., Areola , N., & Ogunsuyi , O. (2022). Quercetin-Supplemented Diet Modulates Aluminium Chloride-Induced Neurotoxicity in Fruit Flies. AFRICAN JOURNAL OF APPLIED RESEARCH, 8(1), 85–96. https://doi.org/10.26437.ajar.03.2022.6