Inhibition of the renin–angiotensin system prevents seizures in a rat model of epilepsy

Author:

Pereira Marilia G.A.G.1,Becari Christiane2,Oliveira José A.C.3,Salgado Maria Cristina O.2,Garcia-Cairasco Norberto3,Costa-Neto Claudio M.1

Affiliation:

1. Department of Biochemistry and Immunology, Faculty of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, 14049-900, Brazil

2. Department of Pharmacology, Faculty of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, 14049-900, Brazil

3. Department of Physiology, Faculty of Medicine at Ribeirão Preto, University of São Paulo, Ribeirão Preto, 14049-900, Brazil

Abstract

The RAS (renin–angiotensin system) is classically involved in BP (blood pressure) regulation and water–electrolyte balance, and in the central nervous system it has been mostly associated with homoeostatic processes, such as thirst, hormone secretion and thermoregulation. Epilepsies are chronic neurological disorders characterized by recurrent epileptic seizures that affect 1–3% of the world's population, and the most commonly used anticonvulsants are described to be effective in approx. 70% of the population with this neurological alteration. Using a rat model of epilepsy, we found that components of the RAS, namely ACE (angiotensin-converting enzyme) and the AT1 receptor (angiotensin II type 1 receptor) are up-regulated in the brain (2.6- and 8.2-fold respectively) following repetitive seizures. Subsequently, epileptic animals were treated with clinically used doses of enalapril, an ACE inhibitor, and losartan, an AT1 receptor blocker, leading to a significant decrease in seizure severities. These results suggest that centrally acting drugs that target the RAS deserve further investigation as possible anticonvulsant agents and may represent an additional strategy in the management of epileptic patients.

Publisher

Portland Press Ltd.

Subject

General Medicine

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