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Can stress make you relax?

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Balligand, Jean-Luc [UCL] Farah, Charlotte [UCL]

(eng) This editorial refers to ‘Stretch-induced compliance: a novel adaptive biological mechanism following acute cardiac load’ by A.M. Leite-Moreira et al., pp. 656–667. Cardiac force adaptations to increased preload are well-known, with a biphasic increase in contractility, i.e. a rapid phase that involves enhanced calcium sensitivity of cardiac myofilaments (the basis of the Frank–Starling mechanism)1 and a delayed phase due to an increased Calcium transient (the basis of the classical Anrep effect).2 Concurrent adaptations of ventricular compliance and diastolic pressure are much less defined. Increased compliance with ensuing fibre and sarcomere stretch (within physiological range of sarcomere length) would allow further recruitment of diastolic reserve to optimize ventricular filling and the adaptation of contractility (according to the earlier mechanisms) in the face of increased venous return (e.g. during exercise). Such phenomena have been proposed in response to paracrine release of myocardial ‘relaxants’ such as natriuretic peptides (NPs) and nitric oxide (NO).3 In this issue of Cardiovascular Research4, Leite-Moreira (father and son) and colleagues now systematically examine the occurrence of stretch-induced compliance adaptation in several animal and human experimental preparations and propose an underlying mechanism. [...]

Document type Article de périodique (Journal article) – Éditorial
Access type Accès libre
Publication date 2018
Language Anglais
Journal information "Cardiovascular Research" - Vol. 114, no. 5, p. 643-644 (2018)
Peer reviewed yes
Publisher Oxford University Press ((United Kingdom) Oxford)
issn 0008-6363
e-issn 1755-3245
Publication status Publié
Affiliations UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique
UCL - (SLuc) Service de médecine interne et maladies infectieuses (MIMI)
Links
  1. Patterson S. W., Starling E. H., On the mechanical factors which determine the output of the ventricles, 10.1113/jphysiol.1914.sp001669
  2. Parmley, Am J Physiol, 224, 1195 (1973)
  3. Paulus W. J., Vantrimpont P. J., Shah A. M., Paracrine Coronary Endothelial Control of Left Ventricular Function in Humans, 10.1161/01.cir.92.8.2119
  4. Leite-Moreira André M, Almeida-Coelho João, Neves João S, Pires Ana L, Ferreira-Martins João, Castro-Ferreira Ricardo, Ladeiras-Lopes Ricardo, Conceição Glória, Miranda-Silva Daniela, Rodrigues Patrícia, Hamdani Nazha, Herwig Melissa, Falcão-Pires Inês, Paulus Walter J, Linke Wolfgang A, Lourenço André P, Leite-Moreira Adelino F, Stretch-induced compliance: a novel adaptive biological mechanism following acute cardiac load, 10.1093/cvr/cvy026
  5. Fish D., Orenstein J., Bloom S., Passive stiffness of isolated cardiac and skeletal myocytes in the hamster, 10.1161/01.res.54.3.267
  6. Kulke M., Fujita-Becker S., Rostkova E., Neagoe C., Labeit D., Manstein D. J., Gautel M., Linke W. A., Interaction Between PEVK-Titin and Actin Filaments: Origin of a Viscous Force Component in Cardiac Myofibrils, 10.1161/hh2201.099453
  7. Cerra M., Pellegrino D., Cardiovascular cGMP-Generating Systems in Physiological and Pathological Conditions, 10.2174/092986707780059715
  8. Kötter Sebastian, Gout Laurence, Von Frieling-Salewsky Marion, Müller Anna Eliane, Helling Stefan, Marcus Katrin, Dos Remedios Cristobal, Linke Wolfgang A., Krüger Martina, Differential changes in titin domain phosphorylation increase myofilament stiffness in failing human hearts, 10.1093/cvr/cvt144
  9. Kruger M., Kotter S., Grutzner A., Lang P., Andresen C., Redfield M. M., Butt E., dos Remedios C. G., Linke W. A., Protein Kinase G Modulates Human Myocardial Passive Stiffness by Phosphorylation of the Titin Springs, 10.1161/circresaha.108.184408
  10. Hammond Joanna, Balligand Jean-Luc, Nitric oxide synthase and cyclic GMP signaling in cardiac myocytes: From contractility to remodeling, 10.1016/j.yjmcc.2011.07.029
  11. Farah Charlotte, Michel Lauriane Y. M., Balligand Jean-Luc, Nitric oxide signalling in cardiovascular health and disease, 10.1038/nrcardio.2017.224
  12. Bishu K., Hamdani N., Mohammed S. F., Kruger M., Ohtani T., Ogut O., Brozovich F. V., Burnett J. C., Linke W. A., Redfield M. M., Sildenafil and B-Type Natriuretic Peptide Acutely Phosphorylate Titin and Improve Diastolic Distensibility In Vivo, 10.1161/circulationaha.111.048520
  13. Prosser Benjamin L., Khairallah Ramzi J., Ziman Andrew P., Ward Christopher W., Lederer W.J., X-ROS signaling in the heart and skeletal muscle: Stretch-dependent local ROS regulates [Ca2+]i, 10.1016/j.yjmcc.2012.11.011
  14. Scotcher Jenna, Prysyazhna Oleksandra, Boguslavskyi Andrii, Kistamas Kornel, Hadgraft Natasha, Martin Eva D., Worthington Jenny, Rudyk Olena, Rodriguez Cutillas Pedro, Cuello Friederike, Shattock Michael J., Marber Michael S., Conte Maria R., Greenstein Adam, Greensmith David J., Venetucci Luigi, Timms John F., Eaton Philip, Disulfide-activated protein kinase G Iα regulates cardiac diastolic relaxation and fine-tunes the Frank–Starling response, 10.1038/ncomms13187
  15. Sequeira Vasco, Najafi Aref, McConnell Mark, Fowler Ewan D., Bollen Ilse A. E., Wüst Rob C. I., dos Remedios Cris, Helmes Michiel, White Ed, Stienen Ger J. M., Tardiff Jil, Kuster Diederik W. D., van der Velden Jolanda, Synergistic role of ADP and Ca2+in diastolic myocardial stiffness : Cross-bridging the gap between energetics and Ca2+, 10.1113/jp270354
  16. Lourenco, Eur J Heart Fail (2017)
  17. Balligand Jean-Luc, Cardiac salvage by tweaking with beta-3-adrenergic receptors, 10.1093/cvr/cvw056
  18. Balligand Jean-Luc, Cardiac beta3-adrenergic receptors in the clinical arena: the end of the beginning : Editorial comment, 10.1002/ejhf.784
Bibliographic reference Balligand, Jean-Luc ; Farah, Charlotte. Can stress make you relax?. In: Cardiovascular Research, Vol. 114, no. 5, p. 643-644 (2018)
Permanent URL http://hdl.handle.net/2078.1/196624