Ferulic acid alleviates abnormal behaviors in isolation-reared mice via 5-HT receptor partial agonist activity.

Psychopharmacology (Berl)

Laboratory of Functional Biomolecules and Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka, 573-0101, Japan.

Published: August 2021

AI Article Synopsis

  • Ferulic acid (FA) has shown potential in reducing mental health issues like anxiety and irritability without significant side effects, although its exact mechanism of action remains unclear.
  • The study aims to explore how FA affects mental health by examining its impact on mouse behavior, monoamine levels, and receptor interactions.
  • Results indicated that FA effectively reduces aggressive behaviors and hyperactivity in mice by activating serotonin (5-HT) receptors, with in silico analysis confirming its binding to these receptors.

Article Abstract

Rationale: Preclinical and clinical reports suggest that ferulic acid (FA), a plant-derived phenylpropanoid, is effective against mental health problems such as agitation, anxiety, and irritability in humans, without causing adverse side effects. However, the mechanism of action is unknown.

Objective: The aim of the study is to investigate the mechanism underlying the ameliorative effects of FA on mental health problems such as agitation, anxiety, and irritability, using in vivo behavioral analysis, in vitro pharmacological analysis, and in silico binding analysis.

Methods: The effects of FA (10 mg/kg, 50 mg/kg, and 250 mg/kg) on hyperactivity and aggressive behaviors of isolation-reared mice were examined. The effects of FA (50 mg/kg and 250 mg/kg) on extracellular levels of monoamines such as serotonin (5-HT), dopamine, and noradrenaline were analyzed by in vivo microdialysis. The effects of FA (10-10 M) on 5-HT and 5-HT receptors were analyzed using a luciferase reporter gene assay. Binding of FA to the mouse 5-HT receptor was evaluated by in silico analysis.

Results: The behavioral analysis showed that administration of FA (50 mg/kg) 1 h before experiments significantly alleviated hyperactivity and aggressive behaviors in isolation-reared mice. These alleviative effects were abolished by pretreatment with the 5-HT receptor antagonist WAY-100635 (1 mg/kg). In vivo microdialysis analysis showed that FA (50 mg/kg) did not change extracellular monoamine levels in the prefrontal cortex of mice. The luciferase reporter gene assay indicated that FA activated 5-HT receptors, but not 5-HT receptors, in a dose-dependent manner. The maximal response of 5-HT receptors to FA was weaker than that to 8-hydroxy-2-dipropylaminotetralin (8-OH-DPAT), a 5-HT receptor full agonist. In silico binding analysis showed that FA binds to the orthosteric site of 5-HT receptors.

Conclusion: Taken together, these results suggest that FA ameliorates agitation-, anxiety-, and irritability-like behaviors such as hyperactivity and aggressive behaviors in isolation-reared mice via 5-HT receptor partial agonist activity. These findings support the efficacy of FA on mental health problems that have been suggested in preclinical and clinical practice.

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Source
http://dx.doi.org/10.1007/s00213-021-05839-2DOI Listing

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