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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282XOn-line version ISSN 1678-4227

Arq. Neuro-Psiquiatr. vol.63 no.4 São Paulo Dec. 2005

http://dx.doi.org/10.1590/S0004-282X2005000600013 

Lovastatin reduces neuronal cell death in hippocampal CA1 subfield after pilocarpine-induced status epilepticus: preliminary results

 

Lovastatina reduz a lesão celular na região CA1 do hipocampo após o status epilepticus induzido pela pilocarpina: resultados preliminares

 

 

Pauline RangelI; Roberta Monterazzo CysneirosII; Ricardo Mario AridaI, II; Marly de AlbuquerqueI; Diego Basile ColugnatiI, II; Carla Alessandra ScorzaII; Esper Abrão CavalheiroII; Fulvio Alexandre ScorzaI, II

ILaboratório de Neurociências, Núcleo de Pesquisas Tecnológicas/Universidade de Mogi das Cruzes (NPT/ UMC), Mogi das Cruzes SP, Brazil
IILaboratório de Neurologia Experimental, Universidade Federal de São Paulo/Escola Paulista de Medicina (UNIFESP/EPM), São Paulo SP, Brazil. FAEP, FAPESP, CNPq and CAPES supported this study

 

 


ABSTRACT

OBJECTIVE: To further characterize the capacity of lovastatin to prevent hippocampal neuronal loss after pilocarpine-induced status epilepticus (SE)
METHOD: Adult male Wistar rats were divided into four groups: (A) control rats, received neither pilocarpine nor lovastatin (n=5); (B) control rats, received just lovastatin (n=5); (C) rats that received just pilocarpine (n=5); (D) rats that received pilocarpine and lovastatin (n=5). After pilocarpine injection (350mg/kg, i.p.), only rats that displayed continuous, convulsive seizure activity were included in our study. Seizure activity was monitored behaviorally and terminated with an injection of diazepam (10 mg/kg, i.p.) after 4 h of convulsive SE. The rats treated with lovastatin received two doses of 20mg/kg via an oesophagic probe immediately and 24 hours after SE induction. Seven days after pilocarpine-induced SE, all the animals were perfused and their brains were processed for histological analysis through Nissl method.
RESULTS: The cell counts in the Nissl-stained sections performed within the hippocampal formation showed a significant cell loss in rats that received pilocarpine and presented SE (CA1= 26.8 ± 13.67; CA3= 38.1 ± 7.2; hilus= 43.8 ± 3.95) when compared with control group animals (Group A: CA1= 53.2 ± 9.63; CA3= 63.5 ± 13.35; hilus= 59.08 ± 10.24; Group B: CA1= 74.3 ± 8.16; CA3= 70.1 ± 3.83; hilus= 70.6 ± 5.10). The average neuronal cell number of CA1 subfield of rats that present SE and received lovastatin (44.4 ± 17.88) was statically significant increased when compared with animals that just presented SE.
CONCLUSION: Lovastatin exert a neuroprotective role in the attenuation of brain damage after SE.

Key words: epilepsy, pilocarpine, lovastatin, hippocampus.


RESUMO

OBJETIVO: Capacidade da lovastatina em prevenir a perda de neurônios hipocampais após o status epilepticus (SE) induzido pela pilocarpina.
MÉTODO:
Ratos adultos Wistar foram divididos em 4 grupos: (A) ratos controles que não receberam pilocarpina nem lovastatina (n=5); (B) ratos controles que receberam somente lovastatina (n=5); (C) ratos que receberam somente pilocarpina (n=5); (D) ratos que receberam pilocarpina e lovastatina (n=5). Após a administração de pilocarpina (350mg/kg, i.p.), somente ratos que evoluíram para o status epilepticus foram incluídos em nosso estudo. A atividade epiléptica foi interrompida com uma injeção de diazepam (10 mg/kg, i.p.) após 4h do início do SE. Os ratos tratados com lovastatina receberam duas doses de 20mg/kg via esofágica, imediatamente e 24 h após a indução do SE. Sete dias após o SE induzido pela pilocarpina, todos os animais foram perfundidos e seus cérebros processados para análise histológica através do método de Nissl.
RESULTADOS: A contagem celular da formação hipocampal mostrou uma significante perda celular nos animais que receberam pilocarpina e apresentaram SE (CA1= 26,8 ± 13,67; CA3= 38,1 ± 7,2; hilus= 43,8 ± 3,95) quando comparados com animais pertencentes ao grupo controle (Grupo A: CA1= 53,2 ± 9,63; CA3= 63,5 ± 13,35; hilus= 59,08 ± 10,24; Grupo B: CA1= 74,3 ± 8,16; CA3= 70,1 ± 3,83; hilus= 70,6 ± 5,10). O número de células neuronais na região CA1 do hipocampo de ratos que apresentaram SE e receberam lovastatina (44,4 ± 17,88) foi estatisticamente maior quando comparado com animais que somente apresentaram SE.
CONCLUSÃO: A lovastatina exerce papel neuroprotetor na atenuação do dano cerebral após o SE.

Palavras-chave: epilepsia, pilocarpina, lovastatina, hipocampo.


 

 

Status epilepticus (SE), a neurological emergency characterized by abnormally prolonged seizures, remains an important clinical problem1. Animal models of SE have been used to produce chronic epilepsy, thus suggesting that SE itself is epileptogenic2. The systemic administration of a potent agonist pilocarpine to rats leads to a pattern of repetitive limbic seizures and SE, which can last for up 12 hours3,4. Morphological analysis of hippocampal formation after pilocarpine-induced SE shows an extensive loss of neurons within the hilar area of the dentate gyrus4,5, as well a loss of selective populations of interneurons in areas CA1 and CA3 and in the hilus4. Furthermore, SE-associated cell loss is a critical step that activates a cascade of events leading to mossy fiber sprouting, de novo recurrent excitation of granule cells, culminating in spontaneous recurrent seizures (SRSs)4-6.

Lovastatin, a fungal antibiotic used in hypercholesterolemia treatment, is a competitive inhibitor of HMG-CoA (3-hydroxy-3-methylglutaryl coenzime A reductase), the major regulatory enzyme of de novo cholesterol synthesis7. Recent data reveal that statins reduce vascular inflammatory responses8, promote angiogenesis9, modulate cytokine production10 and decrease oxidative stress11. Furthermore, recent studies have shown that statins reduces the extent of brain damage after ischemic insult12.

Based on this, the purpose of our study was to further characterize the capacity of lovastatin to prevent hippocampal neuronal loss after pilocarpine-induced status epilepticus.

 

METHOD

Adult male Wistar rats (n=20), weighting 200-250g were housed under standard controlled conditions (7:00 AM/7:00 P.M. light/dark cycle; 20-22ºC; 45-55% humidity) with food and water ad libitum were used in our study. The procedures involving the animals and their care at the Neuroscience Laboratory at University of Mogi das Cruzes respected the Institution’s guidelines, which comply with national and international rules and policies. Rats were divided randomly into four groups: (A) control rats, received neither pilocarpine nor lovastatin (n=5); (B) control rats, received just lovastatin (n=5); (C) rats that received just pilocarpine (n=5); (D) rats that received pilocarpine and lovastatin (n=5).

SE were induced according to the procedure described previously4. In brief, 30 minutes after methylscopolamine injection (1mg/kg, s.c - used to reduce peripheral effects of pilocarpine), pilocarpine (350mg/kg, i.p.) was administered to rats. Only rats that displayed continuous, convulsive seizure activity after pilocarpine treatment were included in these studies. Seizure activity was monitored behaviorally and terminated with an i.p. injection of diazepam (10 mg/kg; Roche, Brazil) after 4 h of convulsive SE. Lovastatin was provided by Millenium Pharmacy (São Paulo, Brazil) and was diluted using sterile saline 0,9%. The rats treated with lovastatin received two doses of 20mg/kg via an oesophagic probe immediately and 24 hours after SE induction.

Seven days after pilocarpine-induced SE, the animals were perfused and the brains were processed for histological analysis. Sections cut 20 mm thick were stained according to Nissl method. Cell counts in the Nissl-stained sections, were performed within the hippocampal pyramidal cell layer and the dentate hilus, as previously reported by Mouritzen-Dam13. For each animal, both the right and left hemispheres of three different sections were counted to provide a total of five individuals values per animal. Only cells with evident nucleus and nucleolus were included in the counts. The mean value observed in control rats was considered 100% of normal cell population. Statistical analysis was performed by one-way analysis of variance (ANOVA), followed by post-hoc Dunnett's test; p values of p<0.05 were considered statically significant.

 

RESULTS

Pilocarpine treatment induced the following behavioral changes: akinesia, facial automatisms, and limbic seizures consisting of forelimb clonus with rearing, salivation, and masticatory jaw movements and falling. This type of behavior built up progressively into motor limbic seizures that recurred repeatedly and rapidly and developed into SE. After SE, animals were comatose or unresponsive to their environment and akinetic; behavior returned toward normal over a 3 to 5-day period.

We next analyzed the qualitative morphological changes in the hippocampus associated with lovastatin treatment and SE. In the control animals (Fig 1A, 1B), the Nissl staining of hippocampal formation and dentate gyrus showed integrity of all cells layers. In contrast, animals that received just pilocarpine and presented SE (Fig 1C) we observed a significant cell loss in hippocampal subfields CA1, CA3 and hilus of dentate gyrus. Interesting, the structural analysis of the brains from animals that presented SE and received lovastatin (Fig 1D) was similar when compared with animals in the control group.

 

 

From a quantitative point of view, Fig 2 shows cell counts in the Nissl-stained sections performed within the hippocampal pyramidal cell layer (CA1 and CA3) and the dentate hilus. A significant cell loss was observed in rats that received pilocarpine and presented SE (CA1= 26.8 ± 13.67; CA3= 38.1 ± 7.2; hilus= 43.8 ± 3.95) when compared with control group animals (Group A: CA1= 53.2 ± 9.63; CA3= 63.5 ± 13.35; hilus= 59.08 ± 10.24; Group B: CA1= 74.3 ± 8.16; CA3= 70.1 ± 3.83; hilus= 70.6 ± 5.10). The average neuronal cell number of CA1 subfield of rats that present SE and received lovastatin (44.4 ± 17.88) was statistically significant increased when compared with animals that just presented SE. It is therefore of interest that the cells in CA3 subfield and hilus of rats that present SE and received lovastatin (CA3= 50.14 ± 15.33; hilus= 52.20 ± 18.71) tended to be relatively protect when compared with animals that just received pilocarpine and presented SE.

 

 

DISCUSSION

This study evaluated the effects of lovastatin administration in rats after pilocarpine-induced SE. We demonstrated that lovastatin treatment was able to prevent hippocampal neuronal loss in CA1 subfield after an epileptic insult. In these lines, our results are in agreement with a recent study that reported an effective neuroprotective action of statins after an acute brain injury14.

Reactive oxygen species (ROS) are a part of normal human metabolism; however, when produced in excess, ROS can cause tissue injury including lipid peroxidation, DNA damage and enzyme inactivation8. ROS is a common denominator among acute neurological conditions8,15, including epilepsy16,17. In the pilocarpine model, there is a involvement of excitotoxic neuronal injury18 and ROS production has been considered to be a part of mechanisms involved with glutamatergic excitotoxicity in vitro15 and in vivo16,17,19. Moreover, it was demonstrated that lovastatin treatment inhibits free radical injury20. Thus, this antioxidant effect of statins could explain the neuroprotective properties found in our study.

There is one classical argument supporting a possible role of nitric oxide (NO) in convulsive phenomena: excitatory amino acids, such as N-methyl-D- aspartate (NMDA) and kainate, are known to be potent convulsants21, and the activation of NMDA receptors is accompanied by the formation of NO22. In fact, the role of NO in epileptogenesis has been examined in a number of studies, suggesting to be a proconvulsive endogenous substance23,24. Furthermore, some studies have revealed that statins inhibit the production of NO in brain parenchyma10, indicating that statins, secondarily, may play the role of an anticonvulsant substance, does not promoting glutamate-mediated neurotoxicity. Other possibility is that the inhibition of brain endothelial nitric oxide synthase (eNOS) leads to increased blood pressure25, which, in turn, may affect the excitability of central nervous system26; however, it was demonstrated that statins are able to upregulate eNOS27, may be pivotal in enhance cerebral arterial vasodilator responses, decreasing with this, the firing threshold.

Finally, anti-inflammatory effects of statins could also contribute to neuroprotection after pilocarpine-induced SE observed in our study. The pathological alterations that occur in the hippocampus following prolonged seizures begin within hours and cause changes that last throughout life. Moreover, several studies has implicated a number of cytokines in seizure-related hippocampal pathology28,29. Interestingly, Pahan and colleagues10 have been shown that lovastatin reduces the induction of inflammatory mediators. Taken together, lovastatin treatment may provide an important approach to suppression of the inflammatory responses after SE induced by pilocarpine.

Based on these facts, our preliminary results support previous evidence that statins reduces neuronal death after an acute brain insult. Future studies are needed to gain a better understanding of these and other possible mechanisms of lovastatin during epileptogenesis

Acknowledgements - The authors would like to thank Hilda S. Reis for her help with histological techniques and Jaqueline Botelho her help in cell counts analysis. FAEP, FAPESP, CNPq and CAPES supported this study.

 

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Received 30 May 2005, received in final form 27 July 2005. Accepted 19 August 2005.

 

 

Dr. Fulvio Alexandre Scorza - Rua Botucatu 862 - Ed. Leal Prado, Disciplina de Neurologia Experimental / UNIFESP/EPM - 04023-900 São Paulo SP - Brasil. E-mail: scorza.nexp@epm.br

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