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Ruthenium Complexes as NO Donors for Vascular Relaxation Induction
Nitric oxide (NO) donors are substances that can release NO. Vascular relaxation induction is among the several functions of NO, and the administration of NO donors is a pharmacological alternative to treat hypertension. This review will focus on the physicochemical description of ruthenium-derived...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271244/ https://www.ncbi.nlm.nih.gov/pubmed/25004072 http://dx.doi.org/10.3390/molecules19079628 |
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author | Galvão de Lima, Renata Rodrigues Silva, Bruno Santana da Silva, Roberto Maria Bendhack, Lusiane |
author_facet | Galvão de Lima, Renata Rodrigues Silva, Bruno Santana da Silva, Roberto Maria Bendhack, Lusiane |
author_sort | Galvão de Lima, Renata |
collection | PubMed |
description | Nitric oxide (NO) donors are substances that can release NO. Vascular relaxation induction is among the several functions of NO, and the administration of NO donors is a pharmacological alternative to treat hypertension. This review will focus on the physicochemical description of ruthenium-derived NO donor complexes that release NO via reduction and light stimulation. In particular, we will discuss the complexes synthesized by our research group over the last ten years, and we will focus on the vasodilation and arterial pressure control elicited by these complexes. Soluble guanylyl cyclase (sGC) and potassium channels are the main targets of the NO species released from the inorganic compounds. We will consider the importance of the chemical structure of the ruthenium complexes and their vascular effects. |
format | Online Article Text |
id | pubmed-6271244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62712442018-12-21 Ruthenium Complexes as NO Donors for Vascular Relaxation Induction Galvão de Lima, Renata Rodrigues Silva, Bruno Santana da Silva, Roberto Maria Bendhack, Lusiane Molecules Review Nitric oxide (NO) donors are substances that can release NO. Vascular relaxation induction is among the several functions of NO, and the administration of NO donors is a pharmacological alternative to treat hypertension. This review will focus on the physicochemical description of ruthenium-derived NO donor complexes that release NO via reduction and light stimulation. In particular, we will discuss the complexes synthesized by our research group over the last ten years, and we will focus on the vasodilation and arterial pressure control elicited by these complexes. Soluble guanylyl cyclase (sGC) and potassium channels are the main targets of the NO species released from the inorganic compounds. We will consider the importance of the chemical structure of the ruthenium complexes and their vascular effects. MDPI 2014-07-07 /pmc/articles/PMC6271244/ /pubmed/25004072 http://dx.doi.org/10.3390/molecules19079628 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Galvão de Lima, Renata Rodrigues Silva, Bruno Santana da Silva, Roberto Maria Bendhack, Lusiane Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title | Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title_full | Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title_fullStr | Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title_full_unstemmed | Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title_short | Ruthenium Complexes as NO Donors for Vascular Relaxation Induction |
title_sort | ruthenium complexes as no donors for vascular relaxation induction |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271244/ https://www.ncbi.nlm.nih.gov/pubmed/25004072 http://dx.doi.org/10.3390/molecules19079628 |
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