| Literature DB >> 26869041 |
Xiaona Wang1,2, Peng Li2, Jingsheng Liu3, Xunbo Jin2, Lianjun Li2, Dong Zhang4, Peng Sun5.
Abstract
3,3'-Iminodipropionitrile (IDPN), one of the nitrile derivatives, can induce persistent neurotoxicity, and therefore cause dyskinesia and cognitive impairments. Gastrodin, a main bioactive ingredient of Gastrodia elata Blume, is shown to greatly improve cognitive function. The aim of this study was to further determine whether administration of gastrodin can ameliorate IDPN-induced cognitive deficits in the Morris water maze (MWM) and novel object recognition (NOR) task, and to explore the underlying mechanisms. Results showed that exposure to IDPN (100 mg/kg/day, for 8 days) significantly impaired spatial and object recognition memory and that repeated treatment with gastrodin (150 mg/kg/day, for 6 weeks) could effectively alleviate the IDPN-induced cognitive impairments as indicated by increased spatial memory and discrimination ratio in the MWM and NOR tests. Gastrodin treatment also reverted IDPN-induced decreases of γ-aminobutyric acid (GABA) levels and increases of a2 GABAA receptor protein expression in the prefrontal cortex and hippocampus of IDPN-treated rats. These results suggest that gastrodin treatment may provide a novel pharmacological strategy for IDPN-induced cognitive deficits, which was mediated, at least in part, by normalizing the GABAergic system.Entities:
Keywords: 3,3′-Iminodipropionitrile; Cognitive deficits; Gastrodin; a2 GABAA receptor; γ-Aminobutyric acid
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Year: 2016 PMID: 26869041 DOI: 10.1007/s11064-016-1845-9
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996