Transport of AMPA receptors during long-term potentiation is impaired in rats with hepatic encephalopathy

被引:5
作者
Monfort, Pilar [1 ]
Piedrafita, Blanca [1 ]
Felipo, Vicente [1 ]
机构
[1] Ctr Invest Principe Felipe, Neurobiol Lab, Valencia 46012, Spain
关键词
Hepatic encephalopathy; AMPA receptors; Long-term potentiation; Trafficking; PROTEIN-KINASE-II; RESTORES LEARNING-ABILITY; CHRONIC LIVER-FAILURE; NMDA RECEPTORS; HYPERAMMONEMIA IMPAIRS; GLUTAMATE RECEPTORS; SYNAPTIC PLASTICITY; CEREBELLAR NEURONS; BINDING-SITES; NITRIC-OXIDE;
D O I
10.1016/j.neuint.2009.05.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cognitive function is impaired in patients with hepatic encephalopathy. Learning ability is also impaired in rats with hepatic encephalopathy due to portacaval shunts. Long-term potentiation (LTP) in hippocampus, considered the basis of some forms of learning and memory, is impaired in rats with portacaval shunt. We analyzed the mechanisms by which LTP is impaired in these rats. In control rats, application of the tetanus to induce LTP increases phosphorylation of Thr286 of calcium-calmodulin dependent protein kinase II. This activates the kinase which phosphorylates the GluR1 subunit of AMPA receptors in Ser831 and induces its translocation to the post-synaptic densities. All these steps are completely prevented in rats with hepatic encephalopathy in which the tetanus does not induce phosphorylation of CaMKII or GluR1 nor translocation of this subunit to the post-synaptic membrane. This would explain the impairment in UP in these rats. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:514 / 520
页数:7
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