Abstract

Chrysin (5,7-dihydroxyflavone), a nutraceutical flavonoid present in diverse plants, has a backbone structure shared with the flavone backbone, with additional hydroxyl groups that confers its antioxidant properties and effects at the GABAA receptor complex. However, whether these effects are due to the hydroxyl groups is unknown. Here we report the effects of chrysin or the flavone backbone (1 mg/kg) in rats subjected to the elevated plus-maze and the locomotor activity test, as well as in the zebrafish evaluated in light/dark model. Chrysin, but not flavone, increased entries and time in the open arms of the elevated plus-maze, as well as time on white compartment of the light/dark model in zebrafish. These effects were comparable to diazepam, and were devoid of motor effects in both tests, as well as in the locomotor activity test. On the other hand, flavone decreased risk assessment in the light/dark test but increased rearing in the locomotor activity test in rats, suggesting effects threat information gathering; important species differences suggest new avenues of research. It is suggested that the specific effects of chrysin in relation to flavone include more of a mechanism of action in which in addition to its action at the GABAA/benzodiazepine receptor complex also could be involved its free radical scavenging abilities, which require specific research. Preprint: https://doi.org/10.1101/575514; Data and scripts:https://github.com/lanec-unifesspa/chrysin.

Highlights

  • ObjectivesThe aim of the present study was to compare the effects of the nutraceutical flavonoid chrysin and the flavone backbone, using the LDT in zebrafish, as well as the elevated plus-maze

  • The present study demonstrated that 1) the anxiolytic-like effect of the flavonoid chrysin in the rat elevated plus-maze (EPM) and LDT, without locomotor effects, seems to be associated with hydroxyl groups substituted in 5 and 7 positions of the A ring in the flavone backbone; and 2) the flavone backbone is devoid of anxiolytic-like effects in the rat EPM in rats, but decreases risk assessment in the LDT in zebrafish and rearing in the locomotor activity test

  • These results contribute to the knowledge that positions of hydroxyl in the flavone backbone are important structural characteristic to produces its pharmacological action on the central nervous system, and suggest that a comparative approach is best suited to detect conserved drug effects across species that are more likely to be shared with humans

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Summary

Objectives

The aim of the present study was to compare the effects of the nutraceutical flavonoid chrysin and the flavone backbone, using the LDT in zebrafish, as well as the elevated plus-maze

Methods
Results
Conclusion
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