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Study M1128

Study name

Zada W 2022

Title

Fatty acid amide hydrolase inhibition and N-arachidonoylethanolamine modulation by isoflavonoids: a novel target for upcoming antidepressants

Overall design

The aim of this study was to explore the therapeutic potential of three specific isoflavonoid compounds (7-hydroxyflavone, biochanin-A, and genistein). Male and female CD1 mice were divided into the following 6 groups (n = 8 in each group): (1) control group, (2) fluoxetine group (fluoxetine treatment at the dose of 10 mg/kg), (3) arachidonyl serotonin group (arachidonyl serotonin treatment at the dose of 5 mg/kg), (4) 7-hydroxyflavone group (7-hydroxyflavone treatment at the dose of 20 mg/kg), (5) biochanin-A group (biochanin-A treatment at the dose of 30 mg/kg), and (6) genistein group (genistein treatment at the dose of 20 mg/kg). Mice underwent 14 consecutive days of intra-peritoneal drug administration, followed by forced swim test. All treatments significantly decreased immobility time in both male and female mice in the forced swim test. LC-MS was used to determine the anandamide concentrations in the prefrontal cortex (n = 4-8 per group per sex).

Study Type

Type3;

Data available

Unavailable

Organism

Mouse; CD1 mouse;

Categories of depression

Healthy individuals; Healthy individuals; Healthy individuals;

Criteria for depression

Forced swimming test

Sample size

60

Tissue

Central; Brain; Prefrontal cortex;

Platform

MS-based; LC-MS: Eksigent Ekspert micro liquid chromatographer 200 with AB SciexQtrap5500 mass spectrometer;

PMID

36029006

DOI

10.1002/prp2.999

Citation

Zada W, VanRyzin JW, Perez-Pouchoulen M, et al. Fatty acid amide hydrolase inhibition and N-arachidonoylethanolamine modulation by isoflavonoids: a novel target for upcoming antidepressants. Pharmacol Res Perspect. 2022 Oct;10(5):e00999.

Metabolite

Anandamide;