Effects of brain IKKβ gene silencing by small interfering RNA on P-glycoprotein expression and brain damage in the rat kainic acid-induced seizure model

CNS Neurol Disord Drug Targets. 2014;13(4):661-72. doi: 10.2174/18715273113129990106.

Abstract

Multidrug resistance mediated by over-expression of P-glycoprotein (P-gp) in brain is an important mechanism accounting for the drug-therapy failure in epilepsy. Over-expression of P-gp in epilepsy rat brain may be regulated by inflammation and nuclear factor-kappa B (NF-κB) activation. Inhibitory κ B kinase subunit β (IKKβ) is an up-stream molecular controlling NF-κB activation. With the small interfering RNA (siRNA) technique and kainic acid (KA)-induced rat epileptic seizure model, the present study was aimed to further evaluate the role of NF-κB inhibition, via blocking IKKβ gene transcription, in the epileptic brain P-gp over-expression, seizure susceptibility, and post-seizure brain damage. siRNA targeting IKKβ was administered to rats via intracerebroventricular injection before seizure induction by KA microinjection; scrambled siRNA was used as control. Brain mRNA and protein levels of IKKβ and P-gp were detected by RT-PCR and immunohistochemistry. NF-κB activity was measured by electrophoretic mobility shift assay. Latency to grade III or V seizure onset was recorded, brain damage was evaluated by neuronal cell counting and epileptiform activity was monitored by electroencephalography. IKKβ siRNA pre-treatment inhibited NF-κB activation and abolished P-gp over-expression in KA-induced epileptic rat brain, accompanied by decreased seizure susceptibility. These findings suggested that epileptogenic-induced P-gp over-expression could be regulated by IKKβ through the NF-κB pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
  • Animals
  • Brain / metabolism*
  • Brain / pathology
  • Disease Models, Animal
  • Gene Expression
  • I-kappa B Kinase / genetics*
  • I-kappa B Kinase / metabolism*
  • Kainic Acid
  • Male
  • NF-kappa B / metabolism
  • Neurons / pathology
  • Neurons / physiology
  • RNA Interference*
  • RNA, Small Interfering / metabolism*
  • Rats, Sprague-Dawley
  • Seizures / metabolism*
  • Seizures / pathology
  • Transcription, Genetic

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • NF-kappa B
  • RNA, Small Interfering
  • I-kappa B Kinase
  • Kainic Acid