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Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation
The inhibitory effects of perilla oil on the platelet aggregation in vitro and thrombosis in vivo were investigated in comparison with aspirin, a well-known blood flow enhancer. Rabbit platelet-rich plasma was incubated with perilla oil and aggregation inducers collagen or thrombin, and the platelet...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973807/ https://www.ncbi.nlm.nih.gov/pubmed/24707301 http://dx.doi.org/10.5625/lar.2014.30.1.21 |
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author | Jang, Ja-Young Kim, Tae-Su Cai, Jingmei Kim, Jihyun Kim, Youngeun Shin, Kyungha Kim, Kwang-Sei Lee, Sung-Pyo Kang, Myung-Hwa Choi, Ehn-Kyoung Rhee, Man-Hee Kim, Yun-Bae |
author_facet | Jang, Ja-Young Kim, Tae-Su Cai, Jingmei Kim, Jihyun Kim, Youngeun Shin, Kyungha Kim, Kwang-Sei Lee, Sung-Pyo Kang, Myung-Hwa Choi, Ehn-Kyoung Rhee, Man-Hee Kim, Yun-Bae |
author_sort | Jang, Ja-Young |
collection | PubMed |
description | The inhibitory effects of perilla oil on the platelet aggregation in vitro and thrombosis in vivo were investigated in comparison with aspirin, a well-known blood flow enhancer. Rabbit platelet-rich plasma was incubated with perilla oil and aggregation inducers collagen or thrombin, and the platelet aggregation rate was analyzed. Perilla oil significantly inhibited both the collagen- and thrombin-induced platelet aggregations, in which the thromboxane B(2) formation from collagen-activated platelets were reduced in a concentration-dependent manner. Rats were administered once daily by gavage with perilla oil for 1 week, carotid arterial thrombosis was induced by applying 35% FeCl(3)-soaked filter paper for 10 min, and the blood flow was monitored with a laser Doppler probe. Perilla oil delayed the FeCl(3)-induced arterial occlusion in a dose-dependent manner, doubling the occlusion time at 0.5 mL/kg. In addition, a high dose (2 mL/kg) of perilla oil greatly prevented the occlusion, comparable to the effect of aspirin (30 mg/kg). The results indicate that perilla oil inhibit platelet aggregation by blocking thromboxane formation, and thereby delay thrombosis following oxidative arterial wall injury. Therefore, it is proposed that perilla oil could be a good candidate without adverse effects for the improvement of blood flow. |
format | Online Article Text |
id | pubmed-3973807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39738072014-04-04 Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation Jang, Ja-Young Kim, Tae-Su Cai, Jingmei Kim, Jihyun Kim, Youngeun Shin, Kyungha Kim, Kwang-Sei Lee, Sung-Pyo Kang, Myung-Hwa Choi, Ehn-Kyoung Rhee, Man-Hee Kim, Yun-Bae Lab Anim Res Original Article The inhibitory effects of perilla oil on the platelet aggregation in vitro and thrombosis in vivo were investigated in comparison with aspirin, a well-known blood flow enhancer. Rabbit platelet-rich plasma was incubated with perilla oil and aggregation inducers collagen or thrombin, and the platelet aggregation rate was analyzed. Perilla oil significantly inhibited both the collagen- and thrombin-induced platelet aggregations, in which the thromboxane B(2) formation from collagen-activated platelets were reduced in a concentration-dependent manner. Rats were administered once daily by gavage with perilla oil for 1 week, carotid arterial thrombosis was induced by applying 35% FeCl(3)-soaked filter paper for 10 min, and the blood flow was monitored with a laser Doppler probe. Perilla oil delayed the FeCl(3)-induced arterial occlusion in a dose-dependent manner, doubling the occlusion time at 0.5 mL/kg. In addition, a high dose (2 mL/kg) of perilla oil greatly prevented the occlusion, comparable to the effect of aspirin (30 mg/kg). The results indicate that perilla oil inhibit platelet aggregation by blocking thromboxane formation, and thereby delay thrombosis following oxidative arterial wall injury. Therefore, it is proposed that perilla oil could be a good candidate without adverse effects for the improvement of blood flow. Korean Association for Laboratory Animal Science 2014-03 2014-03-24 /pmc/articles/PMC3973807/ /pubmed/24707301 http://dx.doi.org/10.5625/lar.2014.30.1.21 Text en Copyright © 2014 Korean Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jang, Ja-Young Kim, Tae-Su Cai, Jingmei Kim, Jihyun Kim, Youngeun Shin, Kyungha Kim, Kwang-Sei Lee, Sung-Pyo Kang, Myung-Hwa Choi, Ehn-Kyoung Rhee, Man-Hee Kim, Yun-Bae Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title | Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title_full | Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title_fullStr | Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title_full_unstemmed | Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title_short | Perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
title_sort | perilla oil improves blood flow through inhibition of platelet aggregation and thrombus formation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973807/ https://www.ncbi.nlm.nih.gov/pubmed/24707301 http://dx.doi.org/10.5625/lar.2014.30.1.21 |
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