Literature DB >> 23831620

Electroacupuncture preconditioning-induced neuroprotection may be mediated by glutamate transporter type 2.

Xiaoling Zhu1, Jinbo Yin, Liaoliao Li, Lei Ma, Hongying Tan, Jiao Deng, Shaoyang Chen, Zhiyi Zuo.   

Abstract

Electroacupuncture has been shown to induce a preconditioning effect in the brain. The mechanisms for this protection are not fully elucidated. We hypothesize that this protection is mediated by excitatory amino acid transporters (EAATs) that have been shown to be neuroprotective. To test this hypothesis, two-month old male Sprague-Dawley rats and EAAT type 3 (EAAT3) knockout mice received or did not receive 30-min electroacupuncture once a day for five consecutive days. They were subjected to a 120-min middle cerebral arterial occlusion (MCAO) at 24h after the last electroacupuncture. Neurological outcome was assessed 2days after the MCAO. Brain tissues were harvested at 24h after the last electroacupuncture for Western blotting. Rats subjected to electroacupuncture at the Baihui acupoint had smaller brain infarct volumes and better neurological deficit scores than control rats. Electroacupuncture increased EAAT type 2 (EAAT2) in the cerebral cortex, tended to increase EAAT3 in the hippocampus, and had no effect on EAAT type 1 expression. Dihydrokainate, an EAAT2 inhibitor, worsened the neurological outcome of rats with electroacupuncture pretreatment. Electroacupuncture pretreatment at the Baihui acupoint increased EAAT2 in the cerebral cortex and improved the neurological outcome of EAAT3 knockout mice. Together, our results suggest that EAAT2 may mediate the electroacupuncture preconditioning-induced neuroprotection.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Brain; EA; EAATs; Electroacupuncture; GAPDH; Glutamate transporter; Ischemia; MCAO; Preconditioning; electroacupuncture; excitatory amino acid transporters; glyceraldehydes 3-phosphate dehydrogenase; middle cerebral arterial occlusion

Mesh:

Substances:

Year:  2013        PMID: 23831620      PMCID: PMC3758789          DOI: 10.1016/j.neuint.2013.06.017

Source DB:  PubMed          Journal:  Neurochem Int        ISSN: 0197-0186            Impact factor:   3.921


  26 in total

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