Grape seed proanthocyanidin extract inhibits glutamate-induced cell death through inhibition of calcium signals and nitric oxide formation in cultured rat hippocampal neurons

• Published in: BMC neuroscience 2011-08, Vol.12 (1), p.78-78, Article 78
• Main Authors: Ahn, Seo-Hee, Kim, Hee Jung, Jeong, Imju, Hong, Yi Jae, Kim, Myung-Jun, Rhie, Duck-Joo, Jo, Yang-Hyeok, Hahn, Sang June, Yoon, Shin Hee
• Format: Article
• Language: English
• Subjects: Animals; Antioxidants - therapeutic use; Bioflavonoids; Calcium Signaling - physiology; Cell death; Cell Death - drug effects; Cells, Cultured; Disease Models, Animal; Flavones; Flavonoids; Glutamates - pharmacology; Grape Seed Extract - therapeutic use; Health aspects; Hippocampus - drug effects; Hippocampus - metabolism; Hippocampus - pathology; Neurons; Neurons - drug effects; Neurons - metabolism; Neurons - pathology; Nitric Oxide - biosynthesis; Physiological aspects; Proanthocyanidins - therapeutic use; Rats
• ISSN: 1471-2202; 1471-2202
• DOI: 10.1186/1471-2202-12-78

Proanthocyanidin is a polyphenolic bioflavonoid with known antioxidant activity. Some flavonoids have a modulatory effect on [Ca²⁺]i. Although proanthocyanidin extract from blueberries reportedly affects Ca²⁺ buffering capacity, there are no reports on the effects of proanthocyanidin on glutamate-induced [Ca²⁺]i or cell death. In the present study, the effects of grape seed proanthocyanidin extract (GSPE) on glutamate-induced excitotoxicity was investigated through calcium signals and nitric oxide (NO) in cultured rat hippocampal neurons. Pretreatment with GSPE (0.3-10 μg/ml) for 5 min inhibited the [Ca²⁺]i increase normally induced by treatment with glutamate (100 μM) for 1 min, in a concentration-dependent manner. Pretreatment with GSPE (6 μg/ml) for 5 min significantly decreased the [Ca²⁺]i increase normally induced by two ionotropic glutamate receptor agonists, N-methyl-D-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA). GSPE further decreased AMPA-induced response in the presence of 1 μM nimodipine. However, GSPE did not affect the 50 mM K+-induced increase in [Ca²⁺]i. GSPE significantly decreased the metabotropic glutamate receptor agonist (RS)-3,5-Dihydroxyphenylglycine-induced increase in [Ca²⁺]i, but it did not affect caffeine-induced response. GSPE (0.3-6 μg/ml) significantly inhibited synaptically induced [Ca²⁺]i spikes by 0.1 mM [Mg²⁺]o. In addition, pretreatment with GSPE (6 μg/ml) for 5 min inhibited 0.1 mM [Mg²⁺]o- and glutamate-induced formation of NO. Treatment with GSPE (6 μg/ml) significantly inhibited 0.1 mM [Mg²⁺]o- and oxygen glucose deprivation-induced neuronal cell death. All these data suggest that GSPE inhibits 0.1 mM [Mg²⁺]o- and oxygen glucose deprivation-induced neurotoxicity through inhibition of calcium signals and NO formation in cultured rat hippocampal neurons.