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A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart
PURPOSE: Inflammation may contribute to the pathogenesis of specific cardiovascular diseases, but it is uncertain if mediators released during the inflammatory process will affect the continued efficacy of drugs used to treat clinical signs of the cardiac disease. We investigated the role of the com...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699762/ https://www.ncbi.nlm.nih.gov/pubmed/26727203 http://dx.doi.org/10.1371/journal.pone.0146022 |
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author | Khor, Kuan Hua Moore, Tyson A. Shiels, Ian A. Greer, Ristan M. Arumugam, Thiruma V. Mills, Paul C. |
author_facet | Khor, Kuan Hua Moore, Tyson A. Shiels, Ian A. Greer, Ristan M. Arumugam, Thiruma V. Mills, Paul C. |
author_sort | Khor, Kuan Hua |
collection | PubMed |
description | PURPOSE: Inflammation may contribute to the pathogenesis of specific cardiovascular diseases, but it is uncertain if mediators released during the inflammatory process will affect the continued efficacy of drugs used to treat clinical signs of the cardiac disease. We investigated the role of the complement 5a receptor 1 (C5aR1/CD88) in the cardiac response to inflammation or atenolol, and the effect of C5aR1 deletion in control of baseline heart rate in an anesthetized mouse model. METHODS: An initial study showed that PMX53, an antagonist of C5aR1 in normal C57BL6/J (wild type, WT) mice reduced heart rate (HR) and appeared to have a protective effect on the heart following induced sepsis. C5aR1 knockout (CD88-/-) mice had a lower HR than wild type mice, even during sham surgery. A model to assess heart rate variability (HRV) in anesthetized mice was developed to assess the effects of inhibiting the β(1)-adrenoreceptor (β(1)-AR) in a randomized crossover study design. RESULTS: HR and LF Norm were constitutively lower and SDNN and HF Norm constitutively higher in the CD88-/- compared with WT mice (P< 0.001 for all outcomes). Administration of atenolol (2.5 mg/kg) reduced the HR and increased HRV (P< 0.05, respectively) in the wild type but not in the CD88-/- mice. There was no shift of the sympathovagal balance post-atenolol in either strains of mice (P> 0.05), except for the reduced LF/HF (Lower frequency/High frequency) ratio (P< 0.05) at 60 min post-atenolol, suggesting increased parasympathetic tone of the heart due to the effect of atenolol administration. The HR of the WT mice were lower post atenolol compared to the CD88-/- mice (P = 0.001) but the HRV of CD88-/- mice were significantly increased (P< 0.05), compared with WT mice. CONCLUSION: Knockout of the C5aR1 attenuated the effect of β(1)-AR in the heart, suggesting an association between the β(1)-AR and C5aR1, although further investigation is required to determine if this is a direct or causal association. |
format | Online Article Text |
id | pubmed-4699762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46997622016-01-15 A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart Khor, Kuan Hua Moore, Tyson A. Shiels, Ian A. Greer, Ristan M. Arumugam, Thiruma V. Mills, Paul C. PLoS One Research Article PURPOSE: Inflammation may contribute to the pathogenesis of specific cardiovascular diseases, but it is uncertain if mediators released during the inflammatory process will affect the continued efficacy of drugs used to treat clinical signs of the cardiac disease. We investigated the role of the complement 5a receptor 1 (C5aR1/CD88) in the cardiac response to inflammation or atenolol, and the effect of C5aR1 deletion in control of baseline heart rate in an anesthetized mouse model. METHODS: An initial study showed that PMX53, an antagonist of C5aR1 in normal C57BL6/J (wild type, WT) mice reduced heart rate (HR) and appeared to have a protective effect on the heart following induced sepsis. C5aR1 knockout (CD88-/-) mice had a lower HR than wild type mice, even during sham surgery. A model to assess heart rate variability (HRV) in anesthetized mice was developed to assess the effects of inhibiting the β(1)-adrenoreceptor (β(1)-AR) in a randomized crossover study design. RESULTS: HR and LF Norm were constitutively lower and SDNN and HF Norm constitutively higher in the CD88-/- compared with WT mice (P< 0.001 for all outcomes). Administration of atenolol (2.5 mg/kg) reduced the HR and increased HRV (P< 0.05, respectively) in the wild type but not in the CD88-/- mice. There was no shift of the sympathovagal balance post-atenolol in either strains of mice (P> 0.05), except for the reduced LF/HF (Lower frequency/High frequency) ratio (P< 0.05) at 60 min post-atenolol, suggesting increased parasympathetic tone of the heart due to the effect of atenolol administration. The HR of the WT mice were lower post atenolol compared to the CD88-/- mice (P = 0.001) but the HRV of CD88-/- mice were significantly increased (P< 0.05), compared with WT mice. CONCLUSION: Knockout of the C5aR1 attenuated the effect of β(1)-AR in the heart, suggesting an association between the β(1)-AR and C5aR1, although further investigation is required to determine if this is a direct or causal association. Public Library of Science 2016-01-04 /pmc/articles/PMC4699762/ /pubmed/26727203 http://dx.doi.org/10.1371/journal.pone.0146022 Text en © 2016 Khor et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Khor, Kuan Hua Moore, Tyson A. Shiels, Ian A. Greer, Ristan M. Arumugam, Thiruma V. Mills, Paul C. A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title | A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title_full | A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title_fullStr | A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title_full_unstemmed | A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title_short | A Potential Link between the C5a Receptor 1 and the β(1)-Adrenoreceptor in the Mouse Heart |
title_sort | potential link between the c5a receptor 1 and the β(1)-adrenoreceptor in the mouse heart |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699762/ https://www.ncbi.nlm.nih.gov/pubmed/26727203 http://dx.doi.org/10.1371/journal.pone.0146022 |
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