Source:http://linkedlifedata.com/resource/pubmed/id/19272430
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-5-11
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pubmed:abstractText |
Seizures and status epilepticus induce an excessive production of reactive oxygen species leading to oxidative stress. Vitamin E, a classic antioxidant, has a neuroprotective effect on rats with seizures by regulating reactive oxygen species production. The activity of chaperone-mediated autophagy, a selective pathway for the degradation of cytosolic proteins in lysosomes, is enhanced during oxidative stress. Whether chaperone-mediated autophagy is induced during status epilepticus is not established. To address this problem, we used pilocarpine to elicit status epilepticus in rats. Lysosome-associated membrane protein 2a was used to estimate chaperone-mediated autophagy. We showed that compared to control animals, lysosome-associated membrane protein 2a at lysosomal membranes increased significantly in rats at 8 h, 16 h, and 24 h after induction of status epilepticus, which directly correlated with chaperone-mediated autophagy activity. Since reactive oxygen species are believed to be important in the pathogenesis of status epilepticus and are essential for the process of chaperone-mediated autophagy, we also sought to determine if pretreatment with vitamin E reduced chaperone-mediated autophagy. Pretreatment with vitamin E reduced oxidative stress and partially inhibited chaperone-mediated autophagy in brain at 24 h after status epilepticus versus vehicle. Taken together, these data show that chaperone-mediated autophagy is increased in rats with pilocarpine-induced status epilepticus through upregulation of de novo synthesis of lysosome-associated membrane protein 2a. Antioxidants such as vitamin E may partially inhibit activated chaperone-mediated autophagy.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antioxidants,
http://linkedlifedata.com/resource/pubmed/chemical/Lysosomal-Associated Membrane...,
http://linkedlifedata.com/resource/pubmed/chemical/Molecular Chaperones,
http://linkedlifedata.com/resource/pubmed/chemical/Pilocarpine,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Vitamin E
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1873-7544
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
16
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pubmed:volume |
161
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
73-7
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pubmed:meshHeading |
pubmed-meshheading:19272430-Animals,
pubmed-meshheading:19272430-Antioxidants,
pubmed-meshheading:19272430-Autophagy,
pubmed-meshheading:19272430-Hippocampus,
pubmed-meshheading:19272430-Lysosomal-Associated Membrane Protein 2,
pubmed-meshheading:19272430-Male,
pubmed-meshheading:19272430-Molecular Chaperones,
pubmed-meshheading:19272430-Oxidative Stress,
pubmed-meshheading:19272430-Pilocarpine,
pubmed-meshheading:19272430-RNA, Messenger,
pubmed-meshheading:19272430-Rats,
pubmed-meshheading:19272430-Rats, Wistar,
pubmed-meshheading:19272430-Status Epilepticus,
pubmed-meshheading:19272430-Up-Regulation,
pubmed-meshheading:19272430-Vitamin E
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pubmed:year |
2009
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pubmed:articleTitle |
Vitamin E inhibits activated chaperone-mediated autophagy in rats with status epilepticus.
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pubmed:affiliation |
Department of Neurology, Qilu Hospital of Shandong University, Jinan 250012, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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