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Protective Effect of Gallic Acid in Experimental Model of Ketamine-induced Psychosis: Possible Behaviour, Biochemical, Neurochemical and Cellular Alterations

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Specialty Pharmacology
Date 2017 Jun 4
PMID 28577133
Citations 14
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Abstract

Gallic acid has been reported to possess a number of psychopharmacological activities. These activities are attributed to the antioxidant potential due to the presence of phenolic moeity. The present study was carried out to investigate the protective effects of gallic acid in an experimental model of ketamine-induced psychosis in mice. Ketamine (50 mg/kg, i.p.) was used to induce stereotyped psychotic behavioural symptoms in mice. Behavioural studies (locomotor activity, stereotype behaviour, immobility duration and memory retention) were carried out to investigate the protective of gallic acid on ketamine-induced psychotic symptoms, followed by biochemical and neurochemical changes and cellular alterations in the brain. Chronic treatment with gallic acid for 15 consecutive days significantly attenuated stereotyped behavioural symptoms in mice. Biochemical estimations revealed that gallic acid reduced the lipid peroxidation and restored the total brain proteins. Furthermore, gallic acid remarkably reduced the dopamine levels, AChE activity and inflammatory surge (serum TNF-α), and increased the levels of GABA and increased glutathione in mice. The study revealed that gallic acid could ameliorate psychotic symptoms and biochemical changes in mice, indicating protective effects in psychosis.

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References
1.
Lull M, Block M . Microglial activation and chronic neurodegeneration. Neurotherapeutics. 2010; 7(4):354-65. PMC: 2951017. DOI: 10.1016/j.nurt.2010.05.014. View

2.
Keefe R, Silva S, Perkins D, Lieberman J . The effects of atypical antipsychotic drugs on neurocognitive impairment in schizophrenia: a review and meta-analysis. Schizophr Bull. 1999; 25(2):201-22. DOI: 10.1093/oxfordjournals.schbul.a033374. View

3.
Dhingra M, Dhingra S, Kumria R, Chadha R, Singh T, Kumar A . Effect of trimethylgallic acid esters against chronic stress-induced anxiety-like behavior and oxidative stress in mice. Pharmacol Rep. 2014; 66(4):606-12. DOI: 10.1016/j.pharep.2014.01.004. View

4.
Mosley R, Benner E, Kadiu I, Thomas M, Boska M, Hasan K . Neuroinflammation, Oxidative Stress and the Pathogenesis of Parkinson's Disease. Clin Neurosci Res. 2007; 6(5):261-281. PMC: 1831679. DOI: 10.1016/j.cnr.2006.09.006. View

5.
LOWE I, Robins E, EYERMAN G . The fluorometric measurement of glutamic decarboxylase and its distribution in brain. J Neurochem. 1958; 3(1):8-18. DOI: 10.1111/j.1471-4159.1958.tb12604.x. View