Literature DB >> 27131970

Pharmacological inhibition of FAAH activity in rodents: A promising pharmacological approach for psychological-cardiac comorbidity?

Luca Carnevali1, Silvia Rivara2, Eugene Nalivaiko3, Julian F Thayer4, Federica Vacondio2, Marco Mor2, Andrea Sgoifo5.   

Abstract

Numerous studies have documented a link between psychological disorders and cardiac disease. Yet, no systematic attempts have been made to develop pharmacological approaches for mood and anxiety disorders that could also be beneficial for cardiac health. The endocannabinoid system has been implicated in the regulation of stress, emotional behavior and cardiovascular function. General preclinical findings indicate that the endocannabinoid anandamide modulates physiological and behavioral stress responses and may also protect the heart from arrhythmias. Moreover, recent experimental studies suggest that pharmacological enhancement of anandamide signaling via inhibition of its degrading enzyme fatty acid amide hydrolase (FAAH) exerts anxiolytic- and antidepressive-like effects and improves cardiac autonomic function and the electrical stability of the myocardium in rodent models that reproduce aspects of human psychological/cardiac comorbidity. Here we summarize and discuss such experimental findings, which might guide future preclinical studies towards a systematic evaluation of the therapeutic potential of pharmacological approaches that target FAAH activity for the treatment of the comorbidity between psychological disorders and cardiac disease.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Anandamide; Anxiety; Arrhythmias; Autonomic nervous system; Cardiovascular disease; Depression; FAAH; Stress

Mesh:

Substances:

Year:  2016        PMID: 27131970     DOI: 10.1016/j.neubiorev.2016.04.013

Source DB:  PubMed          Journal:  Neurosci Biobehav Rev        ISSN: 0149-7634            Impact factor:   8.989


  6 in total

1.  Stress, behavior and the heart.

Authors:  Andrea Sgoifo; Nicola Montano; Murray Esler; Viola Vaccarino
Journal:  Neurosci Biobehav Rev       Date:  2016-11-09       Impact factor: 8.989

2.  Chronic inhibition of fatty acid amide hydrolase by URB597 produces differential effects on cardiac performance in normotensive and hypertensive rats.

Authors:  Anna Pędzińska-Betiuk; Jolanta Weresa; Marek Toczek; Marta Baranowska-Kuczko; Irena Kasacka; Ewa Harasim-Symbor; Barbara Malinowska
Journal:  Br J Pharmacol       Date:  2017-05-31       Impact factor: 8.739

3.  Involvement of endocannabinoid neurotransmission in the bed nucleus of stria terminalis in cardiovascular responses to acute restraint stress in rats.

Authors:  Lucas Gomes-de-Souza; Leandro A Oliveira; Ricardo Benini; Patrícia Rodella; Willian Costa-Ferreira; Carlos C Crestani
Journal:  Br J Pharmacol       Date:  2016-08-22       Impact factor: 8.739

4.  Social defeat stress causes depression-like behavior with metabolite changes in the prefrontal cortex of rats.

Authors:  Yi-Yun Liu; Xin-Yu Zhou; Li-Ning Yang; Hai-Yang Wang; Yu-Qing Zhang; Jun-Cai Pu; Lan-Xiang Liu; Si-Wen Gui; Li Zeng; Jian-Jun Chen; Chan-Juan Zhou; Peng Xie
Journal:  PLoS One       Date:  2017-04-28       Impact factor: 3.240

5.  Higher trait neuroticism is associated with greater fatty acid amide hydrolase binding in borderline and antisocial personality disorders.

Authors:  Nathan J Kolla; Isabelle Boileau; R Michael Bagby
Journal:  Sci Rep       Date:  2022-01-21       Impact factor: 4.379

6.  Genetic Blockade of NAAA Cell-specifically Regulates Fatty Acid Ethanolamides (FAEs) Metabolism and Inflammatory Responses.

Authors:  Xiaohua Xie; Yitian Li; Sennan Xu; Pan Zhou; Longhe Yang; Yaping Xu; Yan Qiu; Yungang Yang; Yuhang Li
Journal:  Front Pharmacol       Date:  2022-01-07       Impact factor: 5.810

  6 in total

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