Standard Research Journal of Pharmacy
and Pharmacology Vol1
(2): 025-033,
August 2014
Copyright © 2014 Standard Research Journals
Author(s) retain the copy right of this article
Author(s) agree that this article remain permanently open
access under the terms of the Creative Commons Attribution
License 4.0 International License |
Research
Article
Renin-angiotensin system inhibitors potentiate the
anticonvulsant activity of valproate in the mouse
pilocarpine-induced seizures model
*1Amina
Mahdy, 2Rehab R Hegazy and 3Heyam S
Ali
1Department
of Pharmacology and Toxicology, Dubai Pharmacy College,
Dubai, United Arab Emirates
2Department
of Pharmacology, Medical Division, National Research Centre,
Cairo, Egypt
3Department
of Pharmaceutics, Dubai Pharmacy College, Dubai, United Arab
Emirates
*Corresponding Author E-mail:
aminamahdy@yahoo.com;
Tel:
+971505596663, +971502099830
Accepted 23 August 2014 |
Systemic inhibition of the
renin-angiotensin-aldosterone system (RAAS) has been
recently suggested to participate in the regulation of
seizures susceptibility. The purpose of the current study
was to evaluate the effect of lisinopril and valsartan as
RAAS modifiers on the protective action of the antiepileptic
sodium valproate (VPA) against pilocarpine-induced
convulsions in mice. Male albino mice were used in the
study, and were grouped into five groups, viz., normal
control group, seizures control group (seizures induced with
pilocarpine), VPA-treated group and groups treated with
combination of VPA with either lisinopril or valsartan.
Lisinopril and valsartan were given orally for three (3)
consecutive days including the day of seizure induction
while VPA was injected in the three treatment groups 30
minutes before pilocarpine injection. All animals were
observed for three (3) hours to assess the seizure severity
and the latency to the onset of seizures. Death rate over
the next twenty four (24) hours was recorded. Brain
specimens from survivors were taken and examined
pathologically. Treatment with either lisinopril or
valsartan potentiated the effect of VPA in reducing the
seizure severity, prolonged the onset of seizures, reduced
the brain insult and decreased the mortality rate. Both
agents did not influence plasma concentration of VPA
excluding pharmacokinetic interactions. It is concluded that
RAAS inhibition combined to VPA treatment may hold a
potential for the cure of pathologies such as epilepsy.
Keywords: Epilepsy, seizures, lisinopril, valsartan,
valproate, pilocarpi |
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