Efeitos da Atorvastatina (Citalor®) sobre as sequelas neurohistológicas e comportamentais induzidas por hipoperfusão cerebral crônica em ratos de meia-idade
| Main Author: | |
|---|---|
| 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. |
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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. |
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2015 |
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2015 2018-04-06T19:52:23Z 2018-04-06T19:52:23Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/masterThesis |
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http://repositorio.uem.br:8080/jspui/handle/1/1929 |
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por |
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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 |
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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 |
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