Literature DB >> 2153388

Naltrexone potentiates 4-aminopyridine seizures in the rat.

A Mihály1, K Bencsik, T Solymosi.   

Abstract

The effects of a pharmacological blockade of the mu opiate receptors on the manifestation of tonic-clonic seizures were investigated in freely moving animals. 4-aminopyridine, a specific blocker of the neuronal K+ channels was used to produce generalized convulsions. After pretreatment of adult rats with 1 mg/kg naltrexone HCl, 3, 5, 7, 9, 14 mg/kg 4-aminopyridine was injected intraperitoneally, and the latencies of the symptoms generated by 4-aminopyridine were measured. Naltrexone HCl decreased these latencies and enhanced the seizures significantly. The experiments provided further evidence for the existence of a tonic anticonvulsant opioid system in the brain.

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Year:  1990        PMID: 2153388     DOI: 10.1007/bf01251001

Source DB:  PubMed          Journal:  J Neural Transm Gen Sect


  40 in total

1.  Distinct distribution of opioid receptor types in rat lumbar spinal cord.

Authors:  B J Morris; A Herz
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1987-08       Impact factor: 3.000

2.  A preliminary study of beta endorphin during chronic naltrexone maintenance treatment in ex-opiate addicts.

Authors:  T R Kosten; M J Kreek; J Ragunath; H D Kleber
Journal:  Life Sci       Date:  1986-07-07       Impact factor: 5.037

3.  Pharmacological evidence for a protective role of the endogenous opioid system on electroshock-induced seizures in the mouse.

Authors:  S Puglisi-Allegra; S Cabib; A Oliverio
Journal:  Neurosci Lett       Date:  1985-12-04       Impact factor: 3.046

4.  Possible allosteric interaction of 4-aminopyridine with rat brain muscarinic acetylcholine receptors.

Authors:  W S Lai; V Ramkumar; E E el-Fakahany
Journal:  J Neurochem       Date:  1985-06       Impact factor: 5.372

5.  Visualization of opiate receptor upregulation by light microscopy autoradiography.

Authors:  A Tempel; E L Gardner; R S Zukin
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

6.  Convulsant and anticonvulsant effects of opioids: relationship to GABA-mediated transmission.

Authors:  S Sagratella; M Massotti
Journal:  Neuropharmacology       Date:  1982-10       Impact factor: 5.250

7.  Naloxone antagonism of GABA-evoked membrane polarizations in cultured mouse spinal cord neurons.

Authors:  D L Gruol; J L Barker; T G Smith
Journal:  Brain Res       Date:  1980-10-06       Impact factor: 3.252

8.  Naloxone as a GABA antagonist: evidence from iontophoretic, receptor binding and convulsant studies.

Authors:  R Dingledine; L L Iversen; E Breuker
Journal:  Eur J Pharmacol       Date:  1978-01-01       Impact factor: 4.432

9.  Opiate receptor localization in rat cerebral cortex.

Authors:  M E Lewis; A Pert; C B Pert; M Herkenham
Journal:  J Comp Neurol       Date:  1983-05-20       Impact factor: 3.215

10.  Different opioid systems may participate in post-electro-convulsive shock (ECS) analgesia and catalepsy.

Authors:  G Urca; J Yitzhaky; H Frenk
Journal:  Brain Res       Date:  1981-08-31       Impact factor: 3.252

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  7 in total

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3.  Repeated application of 4-aminopyridine provoke an increase in entorhinal cortex excitability and rearrange AMPA and kainate receptors.

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4.  Temporal lobe epileptiform activity following systemic administration of 4-aminopyridine in rats.

Authors:  Maxime Lévesque; Pariya Salami; Charles Behr; Massimo Avoli
Journal:  Epilepsia       Date:  2012-11-28       Impact factor: 5.864

5.  Differential modulation of repetitive firing and synchronous network activity in neocortical interneurons by inhibition of A-type K(+) channels and Ih.

Authors:  Sidney B Williams; John J Hablitz
Journal:  Front Cell Neurosci       Date:  2015-03-18       Impact factor: 5.505

6.  A brain slice experimental model to study the generation and the propagation of focally-induced epileptiform activity.

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7.  The opioid antagonist naltrexone decreases seizure-like activity in genetic and chemically induced epilepsy models.

Authors:  Morgan L Sturgeon; Rachel Langton; Shaunik Sharma; Robert A Cornell; Joseph Glykys; Alexander G Bassuk
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