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Neuroprotective effects of oral gallic acid against oxidative stress induced by 6-hydroxydopamine in rats

► In this study we investigated the neuroprotective effect of gallic acid. ► Gallic acid significantly improved the passive avoidance memory deficits in 6-OHDA treated rats. ► Gallic acid strongly protects the rat brain against 6-OHDA-MFB lesion via antioxidant mechanism. Free radical-induced neural...

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Published in:Food chemistry 2013-06, Vol.138 (2-3), p.1028-1033
Main Authors: Mansouri, Mohammad Taghi, Farbood, Yaghoub, Sameri, Maryam Jafar, Sarkaki, Alireza, Naghizadeh, Bahareh, Rafeirad, Maryam
Format: Article
Language:English
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Summary:► In this study we investigated the neuroprotective effect of gallic acid. ► Gallic acid significantly improved the passive avoidance memory deficits in 6-OHDA treated rats. ► Gallic acid strongly protects the rat brain against 6-OHDA-MFB lesion via antioxidant mechanism. Free radical-induced neural damage is implicated in neurodegenerative diseases and antioxidants have protective activity. In the present study, we examined the effect of gallic acid (GA; 50, 100 and 200mg/kg, p.o. for 10days) on memory deficit and cerebral oxidative stress induced by 6-hydroxydopamine (6-OHDA; 8μg/2μL) injected into the medial forebrain bundle (MFB, full nigral lesion) as an animal model of Parkinson’s disease (PD). The results showed that 6-OHDA significantly reduced the passive avoidance memory performance, non-enzymatic (total thiol) and enzymatic [glutathione peroxidase (GPx)] antioxidant contents and increased the level of malondialdehyde (MDA) in the hippocampus and striatum of vehicle-treated group as compared to sham-operated rats. Furthermore, oral administration of GA significantly increased the passive avoidance memory, total thiol and GPx contents and also decreased MDA levels in the above tissues. The results suggest that GA has neuroprotective activity against 6-OHDA-induced oxidative stress via enhancement of cerebral antioxidant defence.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2012.11.022