Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade

Bibliographic Details
Main Author: Zaghi, Gislene Gonçalves Dias
Publication Date: 2015
Format: Master thesis
Language: por
Source: Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
dARK ID: ark:/35916/0013000003gs1
Download full: http://repositorio.uem.br:8080/jspui/handle/1/1929
Summary: Chronic cerebral hypoperfusion (CCH) may be involved in the pathophysiology of neurodegenerative diseases associated with aging, such as Alzheimer's disease and dementia of vascular origin. Prevention or treatment of some risk factors (e.g., chronic hypertension, atherosclerosis, chronic heart diseases, etc.) is the primary recommendation to reduce the prevalence of neurodegenerative diseases associated with chronic cerebrovascular insuficiency. However, once a condition of CCH has been installed, one issue is whether the progression of neuropathological and functional sequelae can be attenuated by some pharmacological treatment. Statins are inhibitors of the enzyme HMG-CoA reductase, the rate-limiting step for the biosynthesis of cholesterol. Apart from their cholesterol-lowering effects, statins exert pleitropic effects including improvement in endothelial function, reduction of oxidative stress and inflammation, suppression of apoptosis in endothelial cells, and stimulation of angiogenesis. This statin-mediated pleiotropism has been suggested to underly the effects of statins in reducing both infarct size and neurological deficits in animal models of stroke. However, whether statins can be beneficial under conditions of CCH has not been investigated. To invstigate whether the treatment with atorvastatin (Citalor®) attenuates the neurodegeneration and memory deficit caused by CCH in middle-aged rats. Intact, middle-aged rats (12-15 months of age) were trained for 15 days to learn a radial maze task, then subjected to 3-stage, 4-vessel occlusion/internal carotid artery (4-VO/ICA) model of chronic cerebral hypoperfusion. Atorvastatin (10 mg/kg, p.o.) was administered for 42 days or 15 days, beginning approximately 5 hours after the first occlusion stage. The performance of retrograde memory was measured 7, 14, 21, 28 and 35 days of 4-VO/ICA. At the end of behavioral tests, the brain was examined for hippocampal and cortical neurodegeneration. Chronic cerebral hypoperfusion caused persistent retrograde amnesia, which was reversed by atorvastatin after both long-term and short-term treatment. This antiamnesic effect of atorvastatin was sustained throughout the experiment, even after discontinuing treatment (15-day treatment group). This effect occurred in the absence of histological neuroprotection. The present data suggest that atorvastatin (and perhaps other statins) represent a potential strategy for the treatment of cognitive sequelae associated with CCH.
id UEM-10_25a20b32b1755362bb1ab095cc367b8d
oai_identifier_str oai:localhost:1/1929
network_acronym_str UEM-10
network_name_str Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
repository_id_str
spelling Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idadeEffects of Atorvastatin (Citalor®) on the behavioral and neurohistological sequelae after chronic cerebral hypoperfusion in middle-aged ratsHipoperfusão cerebal crônica - Atorvastatina, Amnésia retrógrada, Neurodegeneração, Memória - RecuperçãoMiddle-aged ratsChronic cerebral hypoperfusionRetrograde amnesiaNeurodegenerationAtorvastatinMemory recoveryBrazil.Ciências da SaúdeFarmáciaChronic cerebral hypoperfusion (CCH) may be involved in the pathophysiology of neurodegenerative diseases associated with aging, such as Alzheimer's disease and dementia of vascular origin. Prevention or treatment of some risk factors (e.g., chronic hypertension, atherosclerosis, chronic heart diseases, etc.) is the primary recommendation to reduce the prevalence of neurodegenerative diseases associated with chronic cerebrovascular insuficiency. However, once a condition of CCH has been installed, one issue is whether the progression of neuropathological and functional sequelae can be attenuated by some pharmacological treatment. Statins are inhibitors of the enzyme HMG-CoA reductase, the rate-limiting step for the biosynthesis of cholesterol. Apart from their cholesterol-lowering effects, statins exert pleitropic effects including improvement in endothelial function, reduction of oxidative stress and inflammation, suppression of apoptosis in endothelial cells, and stimulation of angiogenesis. This statin-mediated pleiotropism has been suggested to underly the effects of statins in reducing both infarct size and neurological deficits in animal models of stroke. However, whether statins can be beneficial under conditions of CCH has not been investigated. To invstigate whether the treatment with atorvastatin (Citalor®) attenuates the neurodegeneration and memory deficit caused by CCH in middle-aged rats. Intact, middle-aged rats (12-15 months of age) were trained for 15 days to learn a radial maze task, then subjected to 3-stage, 4-vessel occlusion/internal carotid artery (4-VO/ICA) model of chronic cerebral hypoperfusion. Atorvastatin (10 mg/kg, p.o.) was administered for 42 days or 15 days, beginning approximately 5 hours after the first occlusion stage. The performance of retrograde memory was measured 7, 14, 21, 28 and 35 days of 4-VO/ICA. At the end of behavioral tests, the brain was examined for hippocampal and cortical neurodegeneration. Chronic cerebral hypoperfusion caused persistent retrograde amnesia, which was reversed by atorvastatin after both long-term and short-term treatment. This antiamnesic effect of atorvastatin was sustained throughout the experiment, even after discontinuing treatment (15-day treatment group). This effect occurred in the absence of histological neuroprotection. The present data suggest that atorvastatin (and perhaps other statins) represent a potential strategy for the treatment of cognitive sequelae associated with CCH.Hipoperfusão cerebral crônica (HCC) pode estar envolvida na patofisiologia de doenças neurodegenerativas associadas com o envelhecimento, tais como a doença de Alzheimer e demência de origem vascular. A prevenção ou tratamento de alguns fatores de risco (por exemplo, hipertensão crônica, aterosclerose, doenças cardíacas crônicas, etc.) é a principal recomendação para reduzir a prevalência de doenças neurodegenerativas associadas com a insuficiência vascular cerebral crônica. No entanto, uma vez que a condição de HCC tenha sido instalada, uma questão é se a progressão de sequelas neuropatológicas e funcionais podem ser atenuadas por um tratamento farmacológico. As estatinas são inibidores da enzima HMG-CoA redutase, reduzindo a velocidade da biossintese de colesterol. Além do seu efeito de redução dos níveis de colesterol, as estatinas exercem efeitos pleitropicos incluindo melhoria da função endotelial, redução do stress oxidativo e inflamação, supressão da apoptose das células endoteliais e estimulação da angiogénese. Tem se sugerido que estes efeitos pleiotrópicos das estatinas são responsáveis pela redução da dimensão do infarte e dos déficits neurológicos em modelos animais de acidente vascular cerebral. No entanto, se as estatinas podem ser benéficas em condições de HCC ainda não foi investigado. Investigar se o tratamento com atorvastatina (Citalor®) atenua o déficit de memória e a neurodegeneração causada por HCC em ratos de meia-idade. Ratos, de meia-idade (12-15 meses de idade), intactos, foram treinados durante 15 dias para aprender uma tarefa no labirinto radial, em seguida, submetidos ao modelo de hipoperfusão cerebral crônica que consiste na oclusão permanente dos quatro vasos (4-VO/ICA), em três fases. Atorvastatina (10 mg / kg, v.o) foi administrada durante 43 dias ou 15 dias, começando cerca de 5 horas após a primeira fase de oclusão. O desempenho da memória retrógrada foi medido 7, 14, 21, 28 e 35 dias após 4-VO/ICA. No final dos testes comportamentais, o cérebro foi analisado para verificar a neurodegeneração hipocampal e cortical. A hipoperfusão cerebral crônica causou amnésia retrógrada persistente que foi revertida pela atorvastatina tanto no tratamento a longo prazo e a curto prazo. Esta atividade antiamnésica da atorvastatina foi sustentada durante todo o experimento, mesmo após a descontinuação do tratamento (grupo de tratamento de 15 dias). Este efeito ocorreu na ausência de neuroproteção histológica. Os presentes dados sugerem que a atorvastatina (e talvez outras estatinas) representam uma estratégia potencial para o tratamento de sequelas cognitiva associada com HCC.38 fUniversidade Estadual de MaringáBrasilDepartamento de Farmacologia e TerapêuticaPrograma de Pós-Graduação em Ciências FarmacêuticasUEMMaringá, PRCentro de Ciências da SaúdeHumberto MilaniCássia Valério RomaniniMaria Angélica Raffaini Covas Pereira da SilvaZaghi, Gislene Gonçalves Dias2018-04-06T19:52:23Z2018-04-06T19:52:23Z2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesishttp://repositorio.uem.br:8080/jspui/handle/1/1929ark:/35916/0013000003gs1porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)instname:Universidade Estadual de Maringá (UEM)instacron:UEM2018-10-10T18:39:48Zoai:localhost:1/1929Repositório InstitucionalPUBhttp://repositorio.uem.br:8080/oai/requestrepositorio@uem.bropendoar:2018-10-10T18:39:48Repositório Institucional da Universidade Estadual de Maringá (RI-UEM) - Universidade Estadual de Maringá (UEM)false
dc.title.none.fl_str_mv Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
Effects of Atorvastatin (Citalor®) on the behavioral and neurohistological sequelae after chronic cerebral hypoperfusion in middle-aged rats
title Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
spellingShingle Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
Zaghi, Gislene Gonçalves Dias
Hipoperfusão cerebal crônica - Atorvastatina, Amnésia retrógrada, Neurodegeneração, Memória - Recuperção
Middle-aged rats
Chronic cerebral hypoperfusion
Retrograde amnesia
Neurodegeneration
Atorvastatin
Memory recovery
Brazil.
Ciências da Saúde
Farmácia
title_short Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
title_full Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
title_fullStr Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
title_full_unstemmed Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
title_sort Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
author Zaghi, Gislene Gonçalves Dias
author_facet Zaghi, Gislene Gonçalves Dias
author_role author
dc.contributor.none.fl_str_mv Humberto Milani
Cássia Valério Romanini
Maria Angélica Raffaini Covas Pereira da Silva
dc.contributor.author.fl_str_mv Zaghi, Gislene Gonçalves Dias
dc.subject.por.fl_str_mv Hipoperfusão cerebal crônica - Atorvastatina, Amnésia retrógrada, Neurodegeneração, Memória - Recuperção
Middle-aged rats
Chronic cerebral hypoperfusion
Retrograde amnesia
Neurodegeneration
Atorvastatin
Memory recovery
Brazil.
Ciências da Saúde
Farmácia
topic Hipoperfusão cerebal crônica - Atorvastatina, Amnésia retrógrada, Neurodegeneração, Memória - Recuperção
Middle-aged rats
Chronic cerebral hypoperfusion
Retrograde amnesia
Neurodegeneration
Atorvastatin
Memory recovery
Brazil.
Ciências da Saúde
Farmácia
description Chronic cerebral hypoperfusion (CCH) may be involved in the pathophysiology of neurodegenerative diseases associated with aging, such as Alzheimer's disease and dementia of vascular origin. Prevention or treatment of some risk factors (e.g., chronic hypertension, atherosclerosis, chronic heart diseases, etc.) is the primary recommendation to reduce the prevalence of neurodegenerative diseases associated with chronic cerebrovascular insuficiency. However, once a condition of CCH has been installed, one issue is whether the progression of neuropathological and functional sequelae can be attenuated by some pharmacological treatment. Statins are inhibitors of the enzyme HMG-CoA reductase, the rate-limiting step for the biosynthesis of cholesterol. Apart from their cholesterol-lowering effects, statins exert pleitropic effects including improvement in endothelial function, reduction of oxidative stress and inflammation, suppression of apoptosis in endothelial cells, and stimulation of angiogenesis. This statin-mediated pleiotropism has been suggested to underly the effects of statins in reducing both infarct size and neurological deficits in animal models of stroke. However, whether statins can be beneficial under conditions of CCH has not been investigated. To invstigate whether the treatment with atorvastatin (Citalor®) attenuates the neurodegeneration and memory deficit caused by CCH in middle-aged rats. Intact, middle-aged rats (12-15 months of age) were trained for 15 days to learn a radial maze task, then subjected to 3-stage, 4-vessel occlusion/internal carotid artery (4-VO/ICA) model of chronic cerebral hypoperfusion. Atorvastatin (10 mg/kg, p.o.) was administered for 42 days or 15 days, beginning approximately 5 hours after the first occlusion stage. The performance of retrograde memory was measured 7, 14, 21, 28 and 35 days of 4-VO/ICA. At the end of behavioral tests, the brain was examined for hippocampal and cortical neurodegeneration. Chronic cerebral hypoperfusion caused persistent retrograde amnesia, which was reversed by atorvastatin after both long-term and short-term treatment. This antiamnesic effect of atorvastatin was sustained throughout the experiment, even after discontinuing treatment (15-day treatment group). This effect occurred in the absence of histological neuroprotection. The present data suggest that atorvastatin (and perhaps other statins) represent a potential strategy for the treatment of cognitive sequelae associated with CCH.
publishDate 2015
dc.date.none.fl_str_mv 2015
2018-04-06T19:52:23Z
2018-04-06T19:52:23Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.uem.br:8080/jspui/handle/1/1929
dc.identifier.dark.fl_str_mv ark:/35916/0013000003gs1
url http://repositorio.uem.br:8080/jspui/handle/1/1929
identifier_str_mv ark:/35916/0013000003gs1
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Universidade Estadual de Maringá
Brasil
Departamento de Farmacologia e Terapêutica
Programa de Pós-Graduação em Ciências Farmacêuticas
UEM
Maringá, PR
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Estadual de Maringá
Brasil
Departamento de Farmacologia e Terapêutica
Programa de Pós-Graduação em Ciências Farmacêuticas
UEM
Maringá, PR
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
instname:Universidade Estadual de Maringá (UEM)
instacron:UEM
instname_str Universidade Estadual de Maringá (UEM)
instacron_str UEM
institution UEM
reponame_str Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
collection Repositório Institucional da Universidade Estadual de Maringá (RI-UEM)
repository.name.fl_str_mv Repositório Institucional da Universidade Estadual de Maringá (RI-UEM) - Universidade Estadual de Maringá (UEM)
repository.mail.fl_str_mv repositorio@uem.br
_version_ 1846637203169476608