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Rapamycin reverses status epilepticus-induced memory deficits and dendritic damage.

PloS one | Mar 28, 2013

Cognitive impairments are prominent sequelae of prolonged continuous seizures (status epilepticus; SE) in humans and animal models. While often associated with dendritic injury, the underlying mechanisms remain elusive. The mammalian target of rapamycin complex 1 (mTORC1) pathway is hyperactivated following SE. This pathway modulates learning and memory and is associated with regulation of neuronal, dendritic, and glial properties. Thus, in the present study we tested the hypothesis that SE-induced mTORC1 hyperactivation is a candidate mechanism underlying cognitive deficits and dendritic pathology seen following SE. We examined the effects of rapamycin, an mTORC1 inhibitor, on the early hippocampal-dependent spatial learning and memory deficits associated with an episode of pilocarpine-induced SE. Rapamycin-treated SE rats performed significantly better than the vehicle-treated rats in two spatial memory tasks, the Morris water maze and the novel object recognition test. At the molecular level, we found that the SE-induced increase in mTORC1 signaling was localized in neurons and microglia. Rapamycin decreased the SE-induced mTOR activation and attenuated microgliosis which was mostly localized within the CA1 area. These findings paralleled a reversal of the SE-induced decreases in dendritic Map2 and ion channels levels as well as improved dendritic branching and spine density in area CA1 following rapamycin treatment. Taken together, these findings suggest that mTORC1 hyperactivity contributes to early hippocampal-dependent spatial learning and memory deficits and dendritic dysregulation associated with SE.

Pubmed ID: 23536771 RIS Download

Mesh terms: Animals | Dendrites | Dendritic Spines | Disease Models, Animal | Electroencephalography | Gliosis | Hippocampus | Ion Channels | Male | Maze Learning | Memory Disorders | Microglia | Multiprotein Complexes | Neurons | Phosphorylation | Pilocarpine | Rats | Ribosomal Protein S6 Kinases | Sirolimus | Status Epilepticus | TOR Serine-Threonine Kinases

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Associated grants

  • Agency: NINDS NIH HHS, Id: T32 NS 43124
  • Agency: NINDS NIH HHS, Id: R01 NS49427
  • Agency: NINDS NIH HHS, Id: F32 NS056664
  • Agency: NINDS NIH HHS, Id: T32 NS043124
  • Agency: NINDS NIH HHS, Id: F32 NS 56664
  • Agency: NINDS NIH HHS, Id: R01 NS 39943

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