4.6 Article

Quercetin Antagonizes the Sedative Effects of Linalool, Possibly through the GABAergic Interaction Pathway

Journal

MOLECULES
Volume 28, Issue 14, Pages -

Publisher

MDPI
DOI: 10.3390/molecules28145616

Keywords

sedative modulatory activity; quercetin; linalool; GABA(A) receptor; molecular docking simulation

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Sedatives are used for calmness or sleepiness in surgery or severe stress. Depression negatively affects emotional well-being and can be treated with anti-depressants. This study evaluated the effects of quercetin and linalool on sleeping mice induced by thiopental sodium and investigated their combined effects using in silico studies.
Sedatives promote calmness or sleepiness during surgery or severely stressful events. In addition, depression is a mental health issue that negatively affects emotional well-being. A group of drugs called anti-depressants is used to treat major depressive illnesses. The aim of the present work was to evaluate the effects of quercetin (QUR) and linalool (LIN) on thiopental sodium (TS)-induced sleeping mice and to investigate the combined effects of these compounds using a conventional co-treatment strategy and in silico studies. For this, the TS-induced sleeping mice were monitored to compare the occurrence, latency, and duration of the sleep-in response to QUR (10, 25, 50 mg/kg), LIN (10, 25, 50 mg/kg), and diazepam (DZP, 3 mg/kg, i.p.). Moreover, an in silico investigation was undertaken to assess this study's putative modulatory sedation mechanism. For this, we observed the ability of test and standard medications to interact with various gamma-aminobutyric acid A receptor (GABA(A)) subunits. Results revealed that QUR and LIN cause dose-dependent antidepressant-like and sedative-like effects in animals, respectively. In addition, QUR-50 mg/kg and LIN-50 mg/kg and/or DZP-3 mg/kg combined were associated with an increased latency period and reduced sleeping times in animals. Results of the in silico studies demonstrated that QUR has better binding interaction with GABA(A) & alpha;3, & beta;1, and & gamma;2 subunits when compared with DZP, whereas LIN showed moderate affinity with the GABA(A) receptor. Taken together, the sleep duration of LIN and DZP is opposed by QUR in TS-induced sleeping mice, suggesting that QUR may be responsible for providing sedation-antagonizing effects through the GABAergic interaction pathway.

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