Cardioprotective Melatonin: Translating from Proof-of-Concept Studies to Therapeutic Use.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
05 Sep 2019
Historique:
received: 07 08 2019
revised: 29 08 2019
accepted: 04 09 2019
entrez: 8 9 2019
pubmed: 8 9 2019
medline: 29 1 2020
Statut: epublish

Résumé

In this review we summarized the actual clinical data for a cardioprotective therapeutic role of melatonin, listed melatonin and its agonists in different stages of development, and evaluated the melatonin cardiovascular target tractability and prediction using machine learning on ChEMBL. To date, most clinical trials investigating a cardioprotective therapeutic role of melatonin are in phase 2a. Selective melatonin receptor agonists Tasimelteon, Ramelteon, and combined melatonergic-serotonin Agomelatine, and other agonists with registered structures in CHEMBL were not yet investigated as cardioprotective or cardiovascular drugs. As drug-able for these therapeutic targets, melatonin receptor agonists have the benefit over melatonin of well-characterized pharmacologic profiles and extensive safety data. Recent reports of the X-ray crystal structures of MT1 and MT2 receptors shall lead to the development of highly selective melatonin receptor agonists. Predictive models using machine learning could help to identify cardiovascular targets for melatonin. Selecting ChEMBL scores > 4.5 in cardiovascular assays, and melatonin scores > 4, we obtained 284 records from 162 cardiovascular assays carried out with 80 molecules with predicted or measured melatonin activity. Melatonin activities (agonistic or antagonistic) found in these experimental cardiovascular assays and models include arrhythmias, coronary and large vessel contractility, and hypertension. Preclinical proof-of-concept and early clinical studies (phase 2a) suggest a cardioprotective benefit from melatonin in various heart diseases. However, larger phase 3 randomized interventional studies are necessary to establish melatonin and its agonists' actions as cardioprotective therapeutic agents.

Identifiants

pubmed: 31491852
pii: ijms20184342
doi: 10.3390/ijms20184342
pmc: PMC6770816
pii:
doi:

Substances chimiques

Cardiotonic Agents 0
Melatonin JL5DK93RCL

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : FAPESP 2014/50457-0
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 307760/2018-9
Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 301324/2018-22

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Auteurs

Ovidiu Constantin Baltatu (OC)

Center of Innovation, Technology and Education (CITE), School of Health Sciences at Anhembi Morumbi University, Laureate International Universities, Sao Jose dos Campos 12247-016, Brazil. ocbaltatu@anhembi.br.

Sergio Senar (S)

DrTarget, 28806 Madrid, Spain. senars00@gmail.com.

Luciana Aparecida Campos (LA)

Center of Innovation, Technology and Education (CITE), School of Health Sciences at Anhembi Morumbi University, Laureate International Universities, Sao Jose dos Campos 12247-016, Brazil. camposbaltatu@gmail.com.

José Cipolla-Neto (J)

Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-900, Brazil. ocbaltatu@gmail.com.

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Classifications MeSH