Nigerian Psychoactive Alcoholic Herbal Mixture Impacts Behavioural Performance and Caused Brain Biochemical and Histopathological Alterations in Mice

Kirjoittajat

  • A.M. Ajayi
  • R.O Arasi
  • B Ben-Azu
  • J.C. Godson
  • S. C. Umukoro
  • A.O. Aderibigbe

Avainsanat:

Alcohol herbal beverage, brain, damage, psychoactive behavior

Abstrakti

Psychoactive alcoholic herbal mixture is popularly consumed because of the belief on its stimulant and curative effects. This study investigated the neurobehavioral, biochemical and histopathological consequences following its single and repeated co-administration with ethanol to mice. Mice were assessed for sensorimotor, anxiety and memory functions following acute and repeated administration of alcohol herbal mixture (AHM). Alterations in brain acetylcholineterase, nitrite, reduced glutathione (GSH) and malondialdehyde levels were assessed in striatum, prefrontal cortex (PFC) and hippocampus. Neuronal cells counts were determined in the prefrontal cortex and hippocampal tissues. In the acute study, AHM significantly impaired locomotor activity and motor coordination in mice.  Repeated administration of AHM and AHM combined with ethanol caused significant impairment of locomotor and motor coordination, increased anxiety-like behavior and impaired memory in mice. Acetylcholinesterase activity was significantly increased in the PFC while nitrite level was elevated in the striatum and PFC. There was significant elevation of malondialdehyde and depletion of GSH in all brain regions as well as reduced neuronal cell counts in the PFC and hippocampus. This study showed evidences of behavioral perturbation and brain biochemical changes in mice, hence repeated consumption of alcoholic herbal mixture might produce substance-attributable harm and quicken neurodegenerative diseases in humans

Lähdeviitteet

Bailey, S. M., Patel, V. B., Young, T. A., Asayama, K., & Cunningham, C. C. (2001). Chronic ethanol consumption alters the glutathione/glutathione peroxidase‐1 system and protein oxidation status in rat liver. Alcoholism: Clinical and Experimental Research, 25(5), 726-733.

Bechara, A., Damasio, A. R., Damasio, H., & Anderson, S. W. (1994). Insensitivity to future consequences following damage to human prefrontal cortex. Cognition, 50(1-3), 7-15.

Bowden, S. C., & McCarter, R. J. (1993). Spatial memory in alcohol-dependent subjects: using a push-button maze to test the principle of equiavailability. Brain and cognition, 22(1), 51-62.

Chen, J. J., Schenker, S., & Henderson, G. I. (1997). 4‐hydroxynonenal levels are enhanced in fetal liver mitochondria by in utero ethanol exposure. Hepatology, 25(1), 142-147.

Chikere, E. I., & Mayowa, M. O. (2011). Prevalence and perceived health effect of alcohol use among male undergraduate students in Owerri, South-East Nigeria: a descriptive cross-sectional study. BMC Public health, 11(1), 118.

Coleman, R. A., Young, B. M., Turner, L. E., & Cook, R. T. (2008). A practical method of chronic ethanol administration in mice. In Alcohol (pp. 49-59). Humana Press.

Cook, W. K., Bond, J., & Greenfield, T. K. (2014). Are alcohol policies associated with alcohol consumption in low‐and middle‐income countries?. Addiction, 109(7), 1081-1090.

Correa, M., Manrique, H. M., Font, L., Escrig, M. A., & Aragon, C. M. G. (2008). Reduction in the anxiolytic effects of ethanol by centrally formed acetaldehyde: the role of catalase inhibitors and acetaldehyde-sequestering agents. Psychopharmacology, 200(4), 455-464.

Covas, M. I., Gambert, P., Fitó, M., & de la Torre, R. (2010). Wine and oxidative stress: up-to-date evidence of the effects of moderate wine consumption on oxidative damage in humans. Atherosclerosis, 208(2), 297-304.

Crabbe, J. C., Metten, P., Yu, C. H., Schlumbohm, J. P., Cameron, A. J., & Wahlsten, D. (2003). Genotypic differences in ethanol sensitivity in two tests of motor incoordination. Journal of Applied Physiology, 95(4), 1338-1351.

Crabbe Jr, J. C., Johnson, N. A., Gry, D. K., Kosobud, A., & Young, E. R. (1982). Biphasic effects of ethanol on open-field activity: sensitivity and tolerance in C57BL/6N and DBA/2N mice. Journal of comparative and physiological psychology, 96(3), 440.

Crocq, M. A. (2007). Historical and cultural aspects of man's relationship with addictive drugs. Dialogues in clinical neuroscience, 9(4), 355.

Cunha-Oliveira, T., Rego, A. C., & Oliveira, C. R. (2008). Cellular and molecular mechanisms involved in the neurotoxicity of opioid and psychostimulant drugs. Brain research reviews, 58(1), 192-208.

Curran, C. P., & Marczinski, C. A. (2017). Taurine, caffeine, and energy drinks: Reviewing the risks to the adolescent brain. Birth defects research, 109(20), 1640-1648.

Das, S. K., & Vasudevan, D. M. (2007). Alcohol-induced oxidative stress. Life sciences, 81(3), 177-187.

Dure, I, Ojo, H. (2015). Paraga craze: The beat goes on despite Ode-Irele tragedy. http://thenationonlineng.net/paraga-craze-the-beat-goes-on-despite-ode-irele-tragedy/. Accessed 12/29/18.

Ellman, G. L., Courtney, K. D., Andres Jr, V., & Featherstone, R. M. (1961). A new and rapid colorimetric determination of acetylcholinesterase activity. Biochemical pharmacology, 7(2), 88-95.

Encomiums, (2017). Paraga consumers applaud its efficacy – in spite of doctors’ warning. http://encomium.ng/paraga-consumers-applaud-its-efficacy-in-spite-of-doctors-warning/. Accessed 12/29/18.

Fernandes, L. M. P., Lopes, K. S., Santana, L. N. S., Fontes-Júnior, E. A., Ribeiro, C. H. M. A., Silva, M. C. F., Monteiro, M. C. (2018). Repeated Cycles of Binge-Like Ethanol Intake in Adolescent Female Rats Induce Motor Function Impairment and Oxidative Damage in Motor Cortex and Liver, but Not in Blood. Oxidative medicine and cellular longevity, 2018.

Fernandez, G. M., & Savage, L. M. (2017). Adolescent binge ethanol exposure alters specific forebrain cholinergic cell populations and leads to selective functional deficits in the prefrontal cortex. Neuroscience, 361, 129-143.

Fowler, A. K., Thompson, J., Chen, L., Dagda, M., Dertien, J., Dossou, K. S. S., ... & Kruman, I. I. (2014). Differential sensitivity of prefrontal cortex and hippocampus to alcohol-induced toxicity. PLoS One, 9(9), e106945.

Fukushiro, D. F., Josino, F. S., Saito, L. P., Berro, L. F., Morgado, F., & Frussa-Filho, R. (2012). Acute and chronic ethanol differentially modify the emotional significance of a novel environment: implications for addiction. International Journal of Neuropsychopharmacology, 15(8), 1109-1120.

Gasbarrini, A., Addolorato, G., Simoncini, M., Gasbarrini, G., Fantozzi, P., Mancini, F., ... & Scaccini, C. (1998). Beer affects oxidative stress due to ethanol in rats. Digestive diseases and sciences, 43(6), 1332-1338.

Green, L. C., Wagner, D. A., Glogowski, J., Skipper, P. L., Wishnok, J. S., & Tannenbaum, S. R. (1982). Analysis of nitrate, nitrite, and [15N] nitrate in biological fluids. Analytical biochemistry, 126(1), 131-138.

Hall, W., Zador, D. (1997). The alcohol withdrawal syndrome. Lancet (London, England) 349: 1897–1900.

Hernández, J. A., López-Sánchez, R. C., & Rendón-Ramírez, A. (2016). Lipids and oxidative stress associated with ethanol-induced neurological damage. Oxidative medicine and cellular longevity, 2016.

Hughes, R. N. (2004). The value of spontaneous alternation behavior (SAB) as a test of retention in pharmacological investigations of memory. Neuroscience & Biobehavioral Reviews, 28(5), 497-505.

Jollow, D. J., Mitchell, J. R., Zampaglione, N. A., & Gillette, J. R. (1974). Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology, 11(3), 151-169.

Jung, M., & Metzger, D. (2010). Alcohol withdrawal and brain injuries: beyond classical mechanisms. Molecules, 15(7), 4984-5011.

Kehinde, O. S., & Adegoke, A. E. (2012). Taking alcohol by deception: an analysis of ethanol concentration of" paraga" an alcoholic herbal mixture in Nigeria. BMC research notes, 5(1), 127.

Kehinde, O. S., & Olusegun, F. F. (2012). Taking alcohol by deception II: Paraga (alcoholic herbal mixture) use among commercial motor drivers in a south-western Nigerian city. BMC research notes, 5(1), 301.

Kliethermes, C. L. (2005). Anxiety-like behaviors following chronic ethanol exposure. Neuroscience & Biobehavioral Reviews, 28(8), 837-850.

Lee, Y. C. A., & Hashibe, M. (2014). Tobacco, alcohol, and cancer in low and high income countries. Annals of global health, 80(5), 378-383.

Lionetto, M. G., Caricato, R., Calisi, A., Giordano, M. E., & Schettino, T. (2013). Acetylcholinesterase as a biomarker in environmental and occupational medicine: new insights and future perspectives. BioMed research international, 2013.

Lukoyanov, N. V., Brandão, F., Cadete-Leite, A., Madeira, M. D., & Paula-Barbosa, M. M. (2000). Synaptic reorganization in the hippocampal formation of alcohol-fed rats may compensate for functional deficits related to neuronal loss. Alcohol, 20(2), 139-148.

Luong, T. N., Carlisle, H. J., Southwell, A., & Patterson, P. H. (2011). Assessment of motor balance and coordination in mice using the balance beam. JoVE (Journal of Visualized Experiments), (49), e2376.

Makanjuola, A. B., Aina, O. F., & Onigbogi, L. (2014). Alcohol and other psychoactive substance use among tanker drivers in Lagos, Nigeria. European Scientific Journal, ESJ, 10(15).

McDaid, J., Abburi, C., Wolfman, S. L., Gallagher, K., & McGehee, D. S. (2016). Ethanol-induced motor impairment mediated by inhibition of α7 nicotinic receptors. Journal of neuroscience, 36(29), 7768-7778.

Melchior, C. L., Glasky, A. J., & Ritzmann, R. F. (1993). A low dose of ethanol impairs working memory in mice in a win-shift foraging paradigm. Alcohol, 10(6), 491-493.

Micallef, M., Lexis, L., & Lewandowski, P. (2007). Red wine consumption increases antioxidant status and decreases oxidative stress in the circulation of both young and old humans. Nutrition Journal, 6(1), 27.

Montoliu, C., Vallés, S., Renau‐Piqueras, J., & Guerri, C. (1994). Ethanol‐induced oxygen radical formation and lipid peroxidation in rat brain: effect of chronic alcohol consumption. Journal of neurochemistry, 63(5), 1855-1862.

Nagababu, E., Rifkind, J. M., Boindala, S., & Nakka, L. (2010). Assessment of antioxidant activity of eugenol in vitro and in vivo. In Free Radicals and Antioxidant Protocols (pp. 165-180). Humana Press.

Obernier, J. A., Bouldin, T. W., & Crews, F. T. (2002). Binge ethanol exposure in adult rats causes necrotic cell death. Alcoholism: Clinical and Experimental Research, 26(4), 547-557.

Ogden, E. J., & Moskowitz, H. (2004). Effects of alcohol and other drugs on driver performance. Traffic injury prevention, 5(3), 185-198.

O’Keefe, J. H., Bhatti, S. K., Bajwa, A., DiNicolantonio, J. J., & Lavie, C. J. (2014). Alcohol and cardiovascular health: the dose makes the poison… or the remedy. In Mayo Clinic Proceedings (Vol. 89, No. 3, pp. 382-393). Elsevier.

Parry, C. D., Patra, J., & Rehm, J. (2011). Alcohol consumption and non‐communicable diseases: epidemiology and policy implications. Addiction, 106(10), 1718-1724.

Ramezani, A., Goudarzi, I., Lashkarboluki, T., Ghorbanian, M. T., Abrari, K., & Salmani, M. E. (2012). Role of oxidative stress in ethanol-induced neurotoxicity in the developing cerebellum. Iranian journal of basic medical sciences, 15(4), 965.

Rasmussen, D. D., Mitton, D. R., Green, J., & Puchalski, S. (2001). Chronic daily ethanol and withdrawal: 2. Behavioral changes during prolonged abstinence. Alcoholism: Clinical and Experimental Research, 25(7), 999-1005.

Rehm, J., Baliunas, D., Borges, G. L., Graham, K., Irving, H., Kehoe, T., ... & Roerecke, M. (2010). The relation between different dimensions of alcohol consumption and burden of disease: an overview. Addiction, 105(5), 817-843.

Robins, M. T., Lu, J., & Van Rijn, R. M. (2016). Unique behavioral and neurochemical effects induced by repeated adolescent consumption of caffeine-mixed alcohol in C57BL/6 Mice. PloS one, 11(7), e0158189.

Romano, E., Torres-Saavedra, P., Voas, R. B., & Lacey, J. H. (2014). Drugs and alcohol: their relative crash risk. Journal of studies on alcohol and drugs, 75(1), 56-64.

Ruiz, P. (2000). Comprehensive textbook of psychiatry (Vol. 1, pp. 938-950). B. J. Sadock, & V. A. Sadock (Eds.). Philadelphia: lippincott Williams & wilkins.

Sarkaki, A., Fathimoghaddam, H., Mansouri, S. M. T., Shahram Korram, M., Saki, G., & Farbood, Y. (2014). Gallic acid improves cognitive, hippocampal long-term potentiation deficits and brain damage induced by chronic cerebral hypoperfusion in rats. Pakistan Journal of Biological Sciences, 17(8), 978-990.

Seun Opejobi (2015) Man dies in Lagos after taking local gin. Published. http://dailypost.ng/2015/07/15/. Assessed 09/01/19.

Sircar, R., Basak, A. K., & Sircar, D. (2009). Repeated ethanol exposure affects the acquisition of spatial memory in adolescent female rats. Behavioural brain research, 202(2), 225-231.

Snopek, L., Mlcek, J., Sochorova, L., Baron, M., Hlavacova, I., Jurikova, T., ... & Sochor, J. (2018). Contribution of red wine consumption to human health protection. Molecules, 23(7), 1684.

Trullas, R., & Skolnick, P. (1993). Differences in fear motivated behaviors among inbred mouse strains. Psychopharmacology, 111(3), 323-331.

Vytal, K. E., Cornwell, B. R., Arkin, N. E., Letkiewicz, A. M., & Grillon, C. (2013). The complex interaction between anxiety and cognition: insight from spatial and verbal working memory. Frontiers in human neuroscience, 7, 93.

Watling, K. J. (1998). The RBI handbook of receptor classification and signal transduction RBI. Natick, Mass.

World Health Organization. (2009). Global health risks: mortality and burden of disease attributable to selected major risks. Geneva: World Health Organization

Julkaistu

2020-08-05

Numero

Osasto

Original Articles

Viittaaminen

Nigerian Psychoactive Alcoholic Herbal Mixture Impacts Behavioural Performance and Caused Brain Biochemical and Histopathological Alterations in Mice. (2020). African Journal of Biomedical Research, 23(2), 255-265. https://www.ojshostng.com/index.php/ajbr/article/view/59

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