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Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model
The benefits of lowering blood pressure (BP) are well established for the prevention of cardiovascular disease. While there are a number of pharmaceuticals available for lowering BP, there is considerable interest in using dietary modifications, lifestyle and behaviour changes as alternative strateg...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075663/ https://www.ncbi.nlm.nih.gov/pubmed/35522680 http://dx.doi.org/10.1371/journal.pone.0267567 |
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author | Butts, Christine A. Hedderley, Duncan I. Martell, Sheridan Dinnan, Hannah Middlemiss-Kraak, Susanne Bunn, Barry J. McGhie, Tony K. Lill, Ross E. |
author_facet | Butts, Christine A. Hedderley, Duncan I. Martell, Sheridan Dinnan, Hannah Middlemiss-Kraak, Susanne Bunn, Barry J. McGhie, Tony K. Lill, Ross E. |
author_sort | Butts, Christine A. |
collection | PubMed |
description | The benefits of lowering blood pressure (BP) are well established for the prevention of cardiovascular disease. While there are a number of pharmaceuticals available for lowering BP, there is considerable interest in using dietary modifications, lifestyle and behaviour changes as alternative strategies. Kukoamines, caffeic acid derivatives of polyamines present in solanaceous plants, have been reported to reduce BP. We investigated the effect of orally administered synthetic kukoamine A on BP in the Spontaneously Hypertensive Rat (SHR) laboratory animal model of hypertension. Prior to the hypertension study, we determined the safety of the synthetic kukoamine A in a single oral dose (5 or 10 mg kg(-1) bodyweight) 14-day observational study in mice. No negative effects of the oral administration of kukoamine A were observed. We subsequently investigated the effect of daily oral doses of kukoamine A (0, 5, 10 mg kg(-1) bodyweight) for 35 days using the SHR rat model of hypertension. The normotensive control Wistar Kyoto (WKY) strain was used to provide a baseline for normal BP in rats. We observed no effect of orally administered synthetic kukoamine A on arterial hypertension in this laboratory animal model of hypertension. |
format | Online Article Text |
id | pubmed-9075663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90756632022-05-07 Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model Butts, Christine A. Hedderley, Duncan I. Martell, Sheridan Dinnan, Hannah Middlemiss-Kraak, Susanne Bunn, Barry J. McGhie, Tony K. Lill, Ross E. PLoS One Research Article The benefits of lowering blood pressure (BP) are well established for the prevention of cardiovascular disease. While there are a number of pharmaceuticals available for lowering BP, there is considerable interest in using dietary modifications, lifestyle and behaviour changes as alternative strategies. Kukoamines, caffeic acid derivatives of polyamines present in solanaceous plants, have been reported to reduce BP. We investigated the effect of orally administered synthetic kukoamine A on BP in the Spontaneously Hypertensive Rat (SHR) laboratory animal model of hypertension. Prior to the hypertension study, we determined the safety of the synthetic kukoamine A in a single oral dose (5 or 10 mg kg(-1) bodyweight) 14-day observational study in mice. No negative effects of the oral administration of kukoamine A were observed. We subsequently investigated the effect of daily oral doses of kukoamine A (0, 5, 10 mg kg(-1) bodyweight) for 35 days using the SHR rat model of hypertension. The normotensive control Wistar Kyoto (WKY) strain was used to provide a baseline for normal BP in rats. We observed no effect of orally administered synthetic kukoamine A on arterial hypertension in this laboratory animal model of hypertension. Public Library of Science 2022-05-06 /pmc/articles/PMC9075663/ /pubmed/35522680 http://dx.doi.org/10.1371/journal.pone.0267567 Text en © 2022 Butts et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Butts, Christine A. Hedderley, Duncan I. Martell, Sheridan Dinnan, Hannah Middlemiss-Kraak, Susanne Bunn, Barry J. McGhie, Tony K. Lill, Ross E. Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title | Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title_full | Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title_fullStr | Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title_full_unstemmed | Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title_short | Influence of oral administration of kukoamine A on blood pressure in a rat hypertension model |
title_sort | influence of oral administration of kukoamine a on blood pressure in a rat hypertension model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075663/ https://www.ncbi.nlm.nih.gov/pubmed/35522680 http://dx.doi.org/10.1371/journal.pone.0267567 |
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