Multiparametric Mechanistic Profiling of Inotropic Drugs in Adult Human Primary Cardiomyocytes
Autor: | Nathalie Nguyen, Guy Page, Ky Truong, Najah Abi-Gerges, Paul E. Miller, Andrea Ghetti, William Nguyen, Phachareeya Ratchada, Tim Indersmitten |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
Adult
Male Sarcomeres 0301 basic medicine Inotrope Cardiotonic Agents Cardiology lcsh:Medicine 030204 cardiovascular system & hematology Sarcomere Article Contractility Young Adult 03 medical and health sciences 0302 clinical medicine medicine Cluster Analysis Humans Myocyte Myocytes Cardiac lcsh:Science Drug effect Multidisciplinary Drug discovery business.industry lcsh:R Cell Differentiation Middle Aged medicine.disease Chemical biology Myocardial Contraction 030104 developmental biology Therapeutic Area Heart failure Female lcsh:Q business Neuroscience |
Zdroj: | Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | Effects of non-cardiac drugs on cardiac contractility can lead to serious adverse events. Furthermore, programs aimed at treating heart failure have had limited success and this therapeutic area remains a major unmet medical need. The challenges in assessing drug effect on cardiac contractility point to the fundamental translational value of the current preclinical models. Therefore, we sought to develop an adult human primary cardiomyocyte contractility model that has the potential to provide a predictive preclinical approach for simultaneously predicting drug-induced inotropic effect (sarcomere shortening) and generating multi-parameter data to profile different mechanisms of action based on cluster analysis of a set of 12 contractility parameters. We report that 17 positive and 9 negative inotropes covering diverse mechanisms of action exerted concentration-dependent increases and decreases in sarcomere shortening, respectively. Interestingly, the multiparametric readout allowed for the differentiation of inotropes operating via distinct mechanisms. Hierarchical clustering of contractility transient parameters, coupled with principal component analysis, enabled the classification of subsets of both positive as well as negative inotropes, in a mechanism-related mode. Thus, human cardiomyocyte contractility model could accurately facilitate informed mechanistic-based decision making, risk management and discovery of molecules with the most desirable pharmacological profile for the correction of heart failure. |
Databáze: | OpenAIRE |
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