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GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated

BACKGROUND: Incretin therapies appear to provide cardioprotection and improve cardiovascular outcomes in patients with diabetes, but the mechanism of this effect remains elusive. We have previously shown that glucagon-like peptide (GLP)-1 is a coronary vasodilator and we sought to investigate if thi...

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Autores principales: Aetesam-ur-Rahman, Muhammad, Giblett, Joel P., Khialani, Bharat, Kyranis, Stephen, Clarke, Sophie J., Zhao, Tian X., Braganza, Denise M., Clarke, Sarah C., West, Nick E. J., Bennett, Martin R., Hoole, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088691/
https://www.ncbi.nlm.nih.gov/pubmed/33932990
http://dx.doi.org/10.1186/s12872-021-02030-5
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author Aetesam-ur-Rahman, Muhammad
Giblett, Joel P.
Khialani, Bharat
Kyranis, Stephen
Clarke, Sophie J.
Zhao, Tian X.
Braganza, Denise M.
Clarke, Sarah C.
West, Nick E. J.
Bennett, Martin R.
Hoole, Stephen P.
author_facet Aetesam-ur-Rahman, Muhammad
Giblett, Joel P.
Khialani, Bharat
Kyranis, Stephen
Clarke, Sophie J.
Zhao, Tian X.
Braganza, Denise M.
Clarke, Sarah C.
West, Nick E. J.
Bennett, Martin R.
Hoole, Stephen P.
author_sort Aetesam-ur-Rahman, Muhammad
collection PubMed
description BACKGROUND: Incretin therapies appear to provide cardioprotection and improve cardiovascular outcomes in patients with diabetes, but the mechanism of this effect remains elusive. We have previously shown that glucagon-like peptide (GLP)-1 is a coronary vasodilator and we sought to investigate if this is an adenosine-mediated effect. METHODS: We recruited 41 patients having percutaneous coronary intervention (PCI) for stable angina and allocated them into four groups administering a specific study-related infusion following successful PCI: GLP-1 infusion (Group G) (n = 10); Placebo, normal saline infusion (Group P) (n = 11); GLP-1 + Theophylline infusion (Group GT) (n = 10); and Theophylline infusion (Group T) (n = 10). A pressure wire assessment of coronary distal pressure and flow velocity (thermodilution transit time—Tmn) at rest and hyperaemia was performed after PCI and repeated following the study infusion to derive basal and index of microvascular resistance (BMR and IMR). RESULTS: There were no significant differences in the demographics of patients recruited to our study. Most of the patients were not diabetic. GLP-1 caused significant reduction of resting Tmn that was not attenuated by theophylline: mean delta Tmn (SD) group G − 0.23 s (0.27) versus group GT − 0.18 s (0.37), p = 0.65. Theophylline alone (group T) did not significantly alter resting flow velocity compared to group GT: delta Tmn in group T 0.04 s (0.15), p = 0.30. The resulting decrease in BMR observed in group G persisted in group GT: − 20.83 mmHg s (24.54 vs. − 21.20 mmHg s (30.41), p = 0.97. GLP-1 did not increase circulating adenosine levels in group GT more than group T: delta median adenosine − 2.0 ng/ml (− 117.1, 14.8) versus − 0.5 ng/ml (− 19.6, 9.4); p = 0.60. CONCLUSION: The vasodilatory effect of GLP-1 is not abolished by theophylline and GLP-1 does not increase adenosine levels, indicating an adenosine-independent mechanism of GLP-1 coronary vasodilatation. Trial registration: The local research ethics committee approved the study (National Research Ethics Service-NRES Committee, East of England): REC reference 14/EE/0018. The study was performed according to institutional guidelines, was registered on http://www.clinicaltrials.gov (unique identifier: NCT03502083) and the study conformed to the principles outlined in the Declaration of Helsinki. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02030-5.
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spelling pubmed-80886912021-05-03 GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated Aetesam-ur-Rahman, Muhammad Giblett, Joel P. Khialani, Bharat Kyranis, Stephen Clarke, Sophie J. Zhao, Tian X. Braganza, Denise M. Clarke, Sarah C. West, Nick E. J. Bennett, Martin R. Hoole, Stephen P. BMC Cardiovasc Disord Research Article BACKGROUND: Incretin therapies appear to provide cardioprotection and improve cardiovascular outcomes in patients with diabetes, but the mechanism of this effect remains elusive. We have previously shown that glucagon-like peptide (GLP)-1 is a coronary vasodilator and we sought to investigate if this is an adenosine-mediated effect. METHODS: We recruited 41 patients having percutaneous coronary intervention (PCI) for stable angina and allocated them into four groups administering a specific study-related infusion following successful PCI: GLP-1 infusion (Group G) (n = 10); Placebo, normal saline infusion (Group P) (n = 11); GLP-1 + Theophylline infusion (Group GT) (n = 10); and Theophylline infusion (Group T) (n = 10). A pressure wire assessment of coronary distal pressure and flow velocity (thermodilution transit time—Tmn) at rest and hyperaemia was performed after PCI and repeated following the study infusion to derive basal and index of microvascular resistance (BMR and IMR). RESULTS: There were no significant differences in the demographics of patients recruited to our study. Most of the patients were not diabetic. GLP-1 caused significant reduction of resting Tmn that was not attenuated by theophylline: mean delta Tmn (SD) group G − 0.23 s (0.27) versus group GT − 0.18 s (0.37), p = 0.65. Theophylline alone (group T) did not significantly alter resting flow velocity compared to group GT: delta Tmn in group T 0.04 s (0.15), p = 0.30. The resulting decrease in BMR observed in group G persisted in group GT: − 20.83 mmHg s (24.54 vs. − 21.20 mmHg s (30.41), p = 0.97. GLP-1 did not increase circulating adenosine levels in group GT more than group T: delta median adenosine − 2.0 ng/ml (− 117.1, 14.8) versus − 0.5 ng/ml (− 19.6, 9.4); p = 0.60. CONCLUSION: The vasodilatory effect of GLP-1 is not abolished by theophylline and GLP-1 does not increase adenosine levels, indicating an adenosine-independent mechanism of GLP-1 coronary vasodilatation. Trial registration: The local research ethics committee approved the study (National Research Ethics Service-NRES Committee, East of England): REC reference 14/EE/0018. The study was performed according to institutional guidelines, was registered on http://www.clinicaltrials.gov (unique identifier: NCT03502083) and the study conformed to the principles outlined in the Declaration of Helsinki. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02030-5. BioMed Central 2021-05-01 /pmc/articles/PMC8088691/ /pubmed/33932990 http://dx.doi.org/10.1186/s12872-021-02030-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Aetesam-ur-Rahman, Muhammad
Giblett, Joel P.
Khialani, Bharat
Kyranis, Stephen
Clarke, Sophie J.
Zhao, Tian X.
Braganza, Denise M.
Clarke, Sarah C.
West, Nick E. J.
Bennett, Martin R.
Hoole, Stephen P.
GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title_full GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title_fullStr GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title_full_unstemmed GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title_short GLP-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
title_sort glp-1 vasodilatation in humans with coronary artery disease is not adenosine mediated
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088691/
https://www.ncbi.nlm.nih.gov/pubmed/33932990
http://dx.doi.org/10.1186/s12872-021-02030-5
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