Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/40968 |
Resumo: | Atherosclerosis is a chronic inflammatory disease of multifactorial origin that occurs in response to endothelial aggression, affecting mainly the intimal layer of medium and large arteries. Type 2 diabetes mellitus is associated with a high rate of atherosclerotic cardiovascular disease. This study aims to analyze the impact, by drug treatment of Cilostazol, which is an antiplatelet drug, on the reduction of the aortic artery thickness of rats induced to develop diabetes through the administration of streptozotocin, compared to a control group without diabetes. The study showed that the time it took for the rat to develop diabetes was 8 weeks, the rats in the group that was administered streptozotocin showed a significant increase in aortic arterial thickness, especially in the intimal layer of the artery. A reduction in the thickness of the intimal layer of the aorta arteries of the rats submitted to treatment with cilostazol was observed, with significant significance when comparing the groups with diabetes and even when comparing the rats that were not induced to diabetes, showing that cilostazol can be a great ally in preventing atherosclerosis. |
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Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis Acción del cilostazol en ratas diabéticas y no diabéticas como prevención de la aterosclerosis Ação do cilostazol em ratos diabéticos e não diabéticos como prevenção daateroscleroseCilostazolAterosclerosisDiabetes mellitus.CilostazolAteroscleroseDiabetes mellitus.CilostazolAtherosclerosisDiabetes mellitus.Atherosclerosis is a chronic inflammatory disease of multifactorial origin that occurs in response to endothelial aggression, affecting mainly the intimal layer of medium and large arteries. Type 2 diabetes mellitus is associated with a high rate of atherosclerotic cardiovascular disease. This study aims to analyze the impact, by drug treatment of Cilostazol, which is an antiplatelet drug, on the reduction of the aortic artery thickness of rats induced to develop diabetes through the administration of streptozotocin, compared to a control group without diabetes. The study showed that the time it took for the rat to develop diabetes was 8 weeks, the rats in the group that was administered streptozotocin showed a significant increase in aortic arterial thickness, especially in the intimal layer of the artery. A reduction in the thickness of the intimal layer of the aorta arteries of the rats submitted to treatment with cilostazol was observed, with significant significance when comparing the groups with diabetes and even when comparing the rats that were not induced to diabetes, showing that cilostazol can be a great ally in preventing atherosclerosis.La aterosclerosis es una enfermedad inflamatoria crónica de origen multifactorial que se presenta en respuesta a la agresión endotelial, afectando principalmente la íntima de las arterias de mediano y gran calibre. La diabetes mellitus tipo 2 se asocia con una alta tasa de enfermedad cardiovascular aterosclerótica. Este estudio tiene como objetivo analizar el impacto del tratamiento farmacológico de Cilostazol, que es un fármaco antiplaquetario, en la reducción del grosor de la arteria aorta en ratas inducidas a desarrollar diabetes mediante la administración de estreptozotocina, en comparación con un grupo control sin diabetes. El estudio mostró que el tiempo que tardó la rata en desarrollar diabetes fue de 8 semanas, las ratas del grupo que recibió estreptozotocina mostraron un aumento significativo en el grosor de la arteria aórtica, principalmente en la capa íntima de la arteria. Se observó una reducción del espesor de la capa íntima de las arterias aortas de ratas sometidas a tratamiento con cilostazol, con significación expresiva al comparar los grupos con diabetes e incluso al comparar las ratas que no fueron inducidas a la diabetes, demostrando que el cilostazol puede ser un gran aliado en la prevención de la aterosclerosis.A aterosclerose é uma doença inflamatória crônica de origem multifatorial que ocorre em resposta à agressão endotelial, acometendo principalmente a camada íntima de artérias de médio e grande calibres. O diabetes mellitus tipo 2 está associado a uma alta taxa de doença cardiovascular aterosclerótica. Esse estudo visa analisar o impacto, pelo tratamento medicamentoso do Cilostazol, que é um medicamento antiplaquetário, na redução da espessura da artéria aorta de ratos induzidos a desenvolver o diabetes por meio da administração de estreptozotocina, comparando com um grupo controle sem diabetes. O estudo mostrou que o tempo que o rato levou para desenvolver o diabetes foi de 8 semanas, os ratos do grupo que foi administrado a estreptozotocina apresentaram significativo aumento da espessura arterial aórtica, principalmente na camada intimal da artéria. Foi observada uma redução na espessura da camada intima das artérias aorta dos ratos submetidos ao tratamento com cilostazol, com expressiva significância na comparação dos grupos com diabetes e até mesmo na comparação dos ratos que não foram induzidos ao diabetes, evidenciando que o cilostazol pode ser um gande aliado na prevenção da aterosclerose.Research, Society and Development2023-04-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4096810.33448/rsd-v12i4.40968Research, Society and Development; Vol. 12 No. 4; e12812440968Research, Society and Development; Vol. 12 Núm. 4; e12812440968Research, Society and Development; v. 12 n. 4; e128124409682525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/40968/33450Copyright (c) 2023 Douglas Felipe Silva; Elise Souza dos Santos Reis; Adriana Yuriko Koga; Diego José Schebelski; Mario Augusto Cray da Costahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSilva, Douglas FelipeReis, Elise Souza dos Santos Koga, Adriana Yuriko Schebelski, Diego José Costa, Mario Augusto Cray da 2023-04-21T18:13:32Zoai:ojs.pkp.sfu.ca:article/40968Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2023-04-21T18:13:32Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis Acción del cilostazol en ratas diabéticas y no diabéticas como prevención de la aterosclerosis Ação do cilostazol em ratos diabéticos e não diabéticos como prevenção daaterosclerose |
title |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
spellingShingle |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis Silva, Douglas Felipe Cilostazol Aterosclerosis Diabetes mellitus. Cilostazol Aterosclerose Diabetes mellitus. Cilostazol Atherosclerosis Diabetes mellitus. |
title_short |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
title_full |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
title_fullStr |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
title_full_unstemmed |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
title_sort |
Action of cilostazol in diabetic and non-diabetic rats as prevention of atherosclerosis |
author |
Silva, Douglas Felipe |
author_facet |
Silva, Douglas Felipe Reis, Elise Souza dos Santos Koga, Adriana Yuriko Schebelski, Diego José Costa, Mario Augusto Cray da |
author_role |
author |
author2 |
Reis, Elise Souza dos Santos Koga, Adriana Yuriko Schebelski, Diego José Costa, Mario Augusto Cray da |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Silva, Douglas Felipe Reis, Elise Souza dos Santos Koga, Adriana Yuriko Schebelski, Diego José Costa, Mario Augusto Cray da |
dc.subject.por.fl_str_mv |
Cilostazol Aterosclerosis Diabetes mellitus. Cilostazol Aterosclerose Diabetes mellitus. Cilostazol Atherosclerosis Diabetes mellitus. |
topic |
Cilostazol Aterosclerosis Diabetes mellitus. Cilostazol Aterosclerose Diabetes mellitus. Cilostazol Atherosclerosis Diabetes mellitus. |
description |
Atherosclerosis is a chronic inflammatory disease of multifactorial origin that occurs in response to endothelial aggression, affecting mainly the intimal layer of medium and large arteries. Type 2 diabetes mellitus is associated with a high rate of atherosclerotic cardiovascular disease. This study aims to analyze the impact, by drug treatment of Cilostazol, which is an antiplatelet drug, on the reduction of the aortic artery thickness of rats induced to develop diabetes through the administration of streptozotocin, compared to a control group without diabetes. The study showed that the time it took for the rat to develop diabetes was 8 weeks, the rats in the group that was administered streptozotocin showed a significant increase in aortic arterial thickness, especially in the intimal layer of the artery. A reduction in the thickness of the intimal layer of the aorta arteries of the rats submitted to treatment with cilostazol was observed, with significant significance when comparing the groups with diabetes and even when comparing the rats that were not induced to diabetes, showing that cilostazol can be a great ally in preventing atherosclerosis. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-04-05 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/40968 10.33448/rsd-v12i4.40968 |
url |
https://rsdjournal.org/index.php/rsd/article/view/40968 |
identifier_str_mv |
10.33448/rsd-v12i4.40968 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/40968/33450 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 12 No. 4; e12812440968 Research, Society and Development; Vol. 12 Núm. 4; e12812440968 Research, Society and Development; v. 12 n. 4; e12812440968 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052621452738560 |