2,240
Views
25
CrossRef citations to date
0
Altmetric
Original Article

Neuroprotective effects of the ethanol stem bark extracts of Terminalia ivorensis in ketamine-induced schizophrenia-like behaviors and oxidative damage in mice

, , &
Pages 2871-2879 | Received 19 Jun 2015, Accepted 12 May 2016, Published online: 02 Jun 2016

References

  • Adiko VA, Barthelemy KA, Félix ZT, Kouamé MA, Coulibali S, Léon AD. 2013. Separation and characterization of phenolic compounds from Terminalia ivoiriensis using liquid chromatography-positive electrospray ionization tandem mass spectroscopy. Afr J Biotechnol. 12:4393–4398.
  • Agbedahunsi JM, IvieAnao CO, Clement OA, Simon LC. 2006. Trypanocidal properties of terminalia ivorensis. Chevalier (Combretaceae). Afr J Tradit Complement Altern Med. 3:51–56.
  • Aguirre-Hernandez E, Gonzalez-Trujano ME, Martinez AL, Moreno J, Kite G, Terrazas T, Soto-Hernandez M. 2010. HPLC/MS and anxiolytic-like effect of quercetin and kaemferol flavonoids from Tilia americana var. maxicana. J Ethnopharmacol. 127:91–97.
  • Andreasen NC. 1990. Methods for assessing positive and negative symptoms of schizophrenia. Mod Probl Pharmacopsychiatry. 24:73–88.
  • Aoyama K, Suh SW, Hamby AM, Liu J, Chan WY, Chen Y, Swanson RA. 2006. Neuronal glutathione deficiency and age-dependent neurodegeneration in the EAAC1 deficient mouse. Nat Neurosci. 9:119–126.
  • Arnt J, Skarsfeldt T. 1998. Do novel antipsychotics have similar pharmacological characteristics? A review of the evidence. Neuropsychopharmacology. 18:63–101.
  • Aultman JM, Moghaddam B. 2001. Distinct contributions of glutamate and dopamine receptors to temporal aspects of rodent working memory using a clinically relevant task. Psychopharmacology (Berl). 153:353–364.
  • Becker A, Grecksch G. 2004. Ketamine-induced changes in rat behaviour: a possible animal model of schizophrenia. Test of predictive validity. Prog Neuropsychopharmacol Biol Psychiatry. 28:1267–1277.
  • Behrens MM, Ali SS, Dugan LL. 2008. Interleukin-6 mediates the increase in NADPH-oxidase in the ketamine model of schizophrenia. J Neurosci. 28:13957–13966.
  • Behrens MM, Sejnowski TJ. 2009. Does schizophrenia arise from oxidative dysregulation of parvalbumininterneurons in the developing cortex? Neuropharmacol. 57:193–200.
  • Benturquia N, Courtin C, Noble F, Marie-Claire C. 2008. Involvement of D1 dopamine receptor in MDMA-induced locomotor activity and striatal gene expression in mice. Brain Res.1211:1–5.
  • Bitanihirwe KY, Tsung-Ung W, Woo MD. 2011. Oxidative stress in schizophrenia: An integrated approach. Neurosci Biobehav Rev. 35:878–893.
  • Bókkon I, Antal I. 2011. Schizophrenia: redox regulation and volume neurotransmission. Curr Neuropharmacol. 9:289–300.
  • Bourin M, Poisson L, Larousse C. 1986. Piracetam interaction with neuroleptics in psychopharmacological tests. Neuropsychobiology. 19:93–96.
  • Buckley PF, Stahl SM. 2007. Pharmacological treatment of negative symptoms of schizophrenia: therapeutic opportunity or cul-de-sac? Acta Psychiatr Scand. 115:93–100.
  • Chatterjee M, Ganguly S, Srivastava M, Palit G. 2011. Effect of ‘chronic’ versus ‘acute’ ketamine administration and its ‘withdrawal’ effect on behavioural alterations in mice: implications for experimental psychosis. Behav Brain Res. 216:247–254.
  • Chatterjee M, Rajkumar V, Surajit G, Gautam P. 2012. Neurochemical and molecular characterization of ketamine-induced experimental psychosis model in mice. Neuropharmacology. 63:1161–1171.
  • Coates KM, Flood P. 2001. Ketamine and its preservative, benzethonium chloride, both inhibit human recombinant alpha7 and alpha4beta2 neuronal nicotinic acetylcholine receptors in Xenopus oocytes. Br J Pharmacol. 134:871–879.
  • Coulibaly K, Zirihi GN, N'Guessan K, Djaman AJ. 2006. Botanical study and evaluation of antifungal activity of Terminalia ivorensis and Terminalia superba (Combretaceae) on the growth in vitro of Aspergillus fumigatus. Int J Ph Sci. 2:904–912.
  • Dall’igna OP, Fett P, Gomes MW. 2007. Caffeine and adenosine A(2a) receptor antagonists prevent beta-amyloid (25-35)-induced cognitive deficits in mice . Exp Neurol. 203:241–245.
  • De Oliveira L, Spiazzi CM, Bortolin T. 2009. Different sub-anesthetic doses of ketamine increase oxidative stress in the brain of rats. Prog Neuropsychopharmacol Biol Psychiatry. 33:1003–1008.
  • Do KQ, Cabungcal JH, Frank A, Steullet P, Cuenod M. 2009. Redox dysregulation, neurodevelopment, and schizophrenia. Curr Opin Neurobiol. 19:220–230.
  • Dodd S, Dean O, Copolov DL, Malhi GS, Berk M. 2008. N-Acetylcysteine for antioxidant therapy: pharmacology and clinical utility. Expert Opin Biol Ther. 8:1955–1962.
  • Foli EG. (2009). Terminalia ivorensis A. Chevalier. In: Lemmens RHMJ, Louppe D, OtengAmoako A, editors. Prota 7(2): Timbers/Bois d’œuvre 2. [CD-Rom]. PROTA, Wageningen: Netherlands.
  • Freedman R. 2003. Schizophrenia. N Engl J Med. 349:1738–1749.
  • Geyer MA, Moghaddam B. 2002. Animal models relevant to schizophrenia disorders. Neuropsychopharmacology. 50:690–701.
  • Gornall AG, Bardawill CJ, David MM. 1949. Determination of serum proteins by means of the biuret reaction. J Biol Chem. 177:751–766.
  • Halliwell B. 2006. Oxidative stress and neurodegeneration: where are we now? J Neurochem. 97:1634–1658.
  • Hasselmo ME. 2006. The role of acetylcholine in learning and memory. Curr Opin Neurobiol. 16:710–715.
  • Himi T, Ikeda M, Yasuhara T. 2003. Oxidative neuronal death caused by glutamate uptake inhibition in cultured hippocampal neurons. J Neurosci Res. 71:679–688.
  • Ikonomidou C, Kaindl AM. 2011. Neuronal death and oxidative stress in the developing brain. Antioxid Redox Signal. 14:1535–1550.
  • Irifune M, Shimizu T, Nomoto M. 1991. Ketamine-induced hyperlocomotion associated with alteration of presynaptic component of dopamine neurons in the nucleus accumbens of mice. Pharmacol Biochem Behav. 40:399–407.
  • Iwu MM, Anyawu BN. 1982. Anti-inflammatory and anti-arthritic properties of Terminalia ivorensis. Fitoterapia. 52:25–34.
  • Janaky R, Dohovics R, Saransaari P. 2007. Modulation of [3H]dopamine release by glutathione in mouse striatal slices. Neurochem Res. 32:1357–1364.
  • Javitt DC, Grochowski S, Shelley AM, Ritter W. 1998. Impaired mismatch negativity (MMN) generation in schizophrenia as a function of stimulus deviance, probability, and interstimulus/interdeviant interval. Electroencephalogr Clin Neurophysiol. 108:143–153.
  • Jentsch JD, Roth RH. 1999. The neuropsychopharmacology of phencyclidine: from NMDA receptor hypofunction to the dopamine hypothesis of schizophrenia. Neuropsychopharmacology. 20:201–225.
  • Jollow DJ, Michell JR, Zampaglione N, Gillete J. 1974. Bromobenzene-induced liver necrosis. Protective role of glutathione an evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology. 11:151–169.
  • Krystal JH, Karper LP, Seibyl JP, Freeman GK, Delaney R, Bremner JD. 1994. Subanaesthetic effects of the non-competitive NMDA antagonist, ketamine, in humans: psychotomimetic, perceptual, cognitive, and neuroendocrine responses. Arch Gen Psychiatry. 51:199–214.
  • Lahti AC, Koffel B, LaPorte D, Tamminga CA. 1995. Subanesthetic doses of ketamine stimulate psychosis in schizophrenia. Neuropsychopharmacology. 13:9–19.
  • Larson MK, Walker EF, Compton MT. 2010. Early signs, diagnosis and therapeutics of the prodromal phase of schizophrenia and related psychotic disorders. Expert Rev Neurother. 10:1347–1359.
  • Lavoie S, Murray MM, Deppen P. 2008. Glutathione precursor, N-acetyl-cysteine, improves mismatch negativity in schizophrenia patients. Neuropsychopharmacology. 33:2187–2199.
  • Lawal IO, Uzokwe NE, Igboanugo AB, Adio AF, Awosan EA, Nwogwugwu JO. 2010. Ethno-medicinal information on collation and identification of some medicinal plants in Research Institutes of South-west Nigeria. Afr J Pharm Pharmacol. 4:001–007.
  • Lorke D. 1983. A new approach to practical acute toxicity testing. Arch Toxicol. 54:275–287.
  • Lorrain DS, Baccei CS, Bristow LJ. 2003. Effects of ketamine and N-methyl-d-aspartate on glutamate and dopamine release in the rat prefrontal cortex: modulation by a group II selective metabotropicglutamate receptor agonist LY379268. Neuroscience. 117:697–706.
  • Mahadik SP, Evans D, Lal H. 2001. Oxidative stress and role of antioxidant and omega-3 essential fatty acid supplementation in schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry. 25:463–493.
  • Malcom SA, Sofowora EA. 1969. Antimicrobial activity of selected Niegerian folk remedies and their constituent plants. Lloydia. 32:512–517.
  • Misra HP, Fridovich I. 1972. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 247:3170–3175.
  • Monji A, Kato T, Kanba S. 2009. Cytokines and schizophrenia: microglia hypothesis of schizophrenia. Psychiatry Clin Neurosci. 63:257–265.
  • Monte AS, Greicy CS, Roger SM, Joanna KS, Júnia VS, Rafaela CC. 2013. Prevention and reversal of ketamine-induced schizophrenia related behavior by minocycline in mice: possible involvement of antioxidant and nitrergic pathway. J Psychopharmacol. 11:1032–1043.
  • Mouri A, Noda Y, Noda A, Nakamura T, Tokura T, Yura Y, Nitta A, Furukawa H, Nabeshima T. 2007. Involvement of a dysfunctional sopamine-D1/N-methyl-d-aspartate- NR1 and Ca2+/calmodulin-dependent protein kinase II pathway in the impairment of latent learning in a model of schizophrenia induced by phencyclidine. Mol Pharmacol. 71:1598–1609.
  • Oja SS, Janáky R, Varga V, Saransaari P. 2000. Modulation of glutamate receptor functions by glutathione. Neurochem Int. 37:299–306.
  • Okhawa H, Ohishi N, Yagi K. 1979. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 95:351–358.
  • Omogbiya IA, Solomon U, Aderibigbe AO, Adewale GB. 2013. Jobelyn pretreatment ameliorates symptoms of psychosis in experimental models. J Basic Clin Physiol Pharmacol. 24:331–336.
  • Pavlovic D, Tamburic V, Stojanovic I. 2002. Oxidative stress as marker of positive symptoms in schizophrenia. Facta Univ. 9:157–161.
  • Pazvantoglu O, Selek S, Okay IT. 2009. Oxidative mechanisms in schizophrenia and their relationship with illness subtype and symptom profile. Psychiatry Clin Neurosci. 63:693–700.
  • Picchioni MM, Murray RM. 2007. Schizophrenia. BMJ. 335:91–95.
  • Ponou BK, Teponno RB, Ricciutelli M, Quassinti L, Bramucci M, Lupidi G, Barboni L, Tapondjou LA. 2010. Dimeric antioxidant and cytotoxic triterpenoid saponins from Terminalia ivorensis A. Chev. Phytochemistry. 71:2108–2115.
  • Rujescu D, Bender A, Hartmann AM, Ohl F, Raeder H. 2006. A pharmacological model of psychosis based on N methyl-d-aspartate receptor hypofunction: molecular, cellular, functional and behavioral abnormalities. Biol Psychiatry. 59:721–729.
  • Sallmann S, Juttler E, Prinz S, Petersen N, Knopf U, Weiser T, Schwaninger M. 2000. Induction of interleukin-6 by depolarization of neurons. J Neurosci. 20:8637–8642.
  • Seamans JK, Yang CR. 2004. The principal features and mechanisms of dopamine modulation in the prefrontal cortex. Prog Neurobiol. 74:1–58.
  • Singh RP, Sharad S, Kapur S. 2004. Free radicals and oxidative stress in neurodegenerative diseases: relevance of dietary antioxidants. JIACM. 5:218–225.
  • Sinha KA. 1971. Colorimetric assay of catalase. Anal Biochem. 47:389–394.
  • Sorce S, Schiavone S, Tucci P, Colaianna M, Jaquet V, Cuomo V, Dubois-Dauphin M, Trabace L, Krause KH. 2010. The NADPH oxidase NOX2 controls glutamate release: a novel mechanism involved in psychosis-like ketamine responses. J Neurosci. 30:11317–11325.
  • Steullet P, Neijt HC, Cuénod M, Do KQ. 2006. Synaptic plasticity impairment and hypofunction of NMDA receptors induced by glutathione deficit: relevance to schizophrenia. Neuroscience. 137:807–819.
  • Swerdlow NR, Braff DL, Taaid N, Geyer MA. 1994. Assessing the validity of an animal model of deficient sensorimotor gating in schizophrenic patients. Arch Gen Psychiatry. 51:139–154.
  • Turetsky BI, Calkins ME, Light GA, Olincy A, Radant AD, Swerdlow NR. 2007. Neurophysiological endophenotypes of schizophrenia: the viability of selected candidate measures. Schizophr Bull. 33:69–94.
  • Umbricht D, Schmid L, Koller R, Vollenweider FX, Hell D, Javitt DC. 2000. Ketamine-induced deficits in auditory and visual context-dependent processing in healthy volunteers: Implications for models of cognitive deficits in schizophrenia. Arch Gen Psychiatry. 57:1139–1147.
  • Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J. 2007. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol. 39:44–84.
  • Varga V, Jenei Z, Janaky R. 1997. Glutathione is an endogenous ligand of rat brain N-methyl-a-aspartate (NMDA) and 2-amino-3-hydroxy-5-methyl-4-isoxazolepropionate (AMPA) receptors. Neurochem Res. 22:1165–1171.
  • Wang Y, Zhang H, Yuan Q. 2013. Purification, antioxidant activity and protein-precipitating capacity of punicalin from pomegranate husk. Food Chem. 138:437–443.
  • Wood SJ, Yücel M, Pantelis C, Berk M. 2009. Neurobiology of schizophrenia spectrum disorders: the role of oxidative stress. Ann Acad Med Singapore. 38:396–396.
  • Yamada K, Noda Y, Hasegawa T, Komori Y, Nikai T, Sugihara H, Nabeshima T. 1996. The role of nitric oxide in dizocilpine-induced impairment of spontaneous alternation behavior in mice. J Pharm Exp Ther. 276:460–466.
  • Zhang Y, Behrens MM, Lisman JE. 2008. Prolonged exposure to NMDAR antagonist suppresses inhibitory synaptic transmission in prefrontal cortex. J Neurophysiol. 100:959–965.
  • Zhang M, Zhao Z, He L, Wan C. 2010. A meta-analysis of oxidative stress markers in schizophrenia. Sci China Life Sci. 53:112–124.
  • Zijia Z, Liping L, Jeffrey M, Tao W, Zhengtao W. 2009. Antioxidant phenolic compounds from walnut kernels (Juglansregia L). Food Chem. 113:160–165.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.