Levodropropizine suppresses seizure activity in rats with pentylenetetrazol-induced epilepsy.


Journal

Epilepsy research
ISSN: 1872-6844
Titre abrégé: Epilepsy Res
Pays: Netherlands
ID NLM: 8703089

Informations de publication

Date de publication:
02 2019
Historique:
received: 12 08 2018
revised: 03 12 2018
accepted: 28 12 2018
pubmed: 6 1 2019
medline: 19 6 2019
entrez: 6 1 2019
Statut: ppublish

Résumé

Millions of individuals worldwide suffer from epilepsy, and up to 25% of patients have seizures that are resistant to currently available antiepileptic drugs. Hence, there continues to be a need for more seizure medications that are effective yet tolerable. Levodropropizine (LVDP) is an established antitussive drug that, based on preclinical data, may also have antiepileptic activity. We treated rats with either intraperitoneal (IP) LVDP at two different doses or placebo in randomized fashion and then exposed them to IP pentylenetetrazol (PTZ), a potent seizure-inducing compound. We measured the rats' subsequent seizure activity with electroencephalography (EEG), Racine's convulsion scale (RCS) and time to first myoclonic jerk (TFMJ) to determine whether LVDP has antiepileptic properties in our murine model for epilepsy. When compared to placebo, LVDP at both doses significantly suppressed seizure activity. Mean EEG spike wave percentage score decreased from 76.8% (placebo) to 13.1% (lower dose) and 7.6% (higher dose, bothp <  0.0001). RCS decreased from a mean of 5.8 (placebo) to 1.83 (lower dose) and 1.16 (higher dose, both p <  0.05). TFMJ had increased from a mean of 65.1 s (placebo), to 247.3 s (lower dose) and 295.5 s (higher dose, both p <  0.0001). Levodropropizine, a common antitussive drug, suppresses seizure activity in rats with PTZ-induced status epilepticus. Given the ongoing need to find effective therapies for refractory epilepsy, the possibility of using levodropropizine as an antiepilepticshould be further explored.

Sections du résumé

BACKGROUND
Millions of individuals worldwide suffer from epilepsy, and up to 25% of patients have seizures that are resistant to currently available antiepileptic drugs. Hence, there continues to be a need for more seizure medications that are effective yet tolerable. Levodropropizine (LVDP) is an established antitussive drug that, based on preclinical data, may also have antiepileptic activity.
METHODS
We treated rats with either intraperitoneal (IP) LVDP at two different doses or placebo in randomized fashion and then exposed them to IP pentylenetetrazol (PTZ), a potent seizure-inducing compound. We measured the rats' subsequent seizure activity with electroencephalography (EEG), Racine's convulsion scale (RCS) and time to first myoclonic jerk (TFMJ) to determine whether LVDP has antiepileptic properties in our murine model for epilepsy.
RESULTS
When compared to placebo, LVDP at both doses significantly suppressed seizure activity. Mean EEG spike wave percentage score decreased from 76.8% (placebo) to 13.1% (lower dose) and 7.6% (higher dose, bothp <  0.0001). RCS decreased from a mean of 5.8 (placebo) to 1.83 (lower dose) and 1.16 (higher dose, both p <  0.05). TFMJ had increased from a mean of 65.1 s (placebo), to 247.3 s (lower dose) and 295.5 s (higher dose, both p <  0.0001).
CONCLUSIONS
Levodropropizine, a common antitussive drug, suppresses seizure activity in rats with PTZ-induced status epilepticus. Given the ongoing need to find effective therapies for refractory epilepsy, the possibility of using levodropropizine as an antiepilepticshould be further explored.

Identifiants

pubmed: 30610970
pii: S0920-1211(18)30399-1
doi: 10.1016/j.eplepsyres.2018.12.011
pii:
doi:

Substances chimiques

Antitussive Agents 0
Convulsants 0
Propylene Glycols 0
dipropizine U0K8WHL37U
Pentylenetetrazole WM5Z385K7T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-37

Informations de copyright

Copyright © 2018 Elsevier B.V. All rights reserved.

Auteurs

Mumin Alper Erdogan (MA)

Department of Physiology, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Turkey. Electronic address: alpero86@gmail.com.

Dimas Yusuf (D)

Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: dimas.yusuf@alumni.ubc.ca.

Arife Erdogan (A)

Department of Emergency Medicine, Izmir Bozyaka Training and Research Hospital, Izmir, Turkey. Electronic address: arife.erdogan@yahoo.com.

Oytun Erbas (O)

Department of Physiology, Faculty of Medicine, Bilim University, Istanbul, Turkey. Electronic address: oytunerbas2012@gmail.com.

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Classifications MeSH