Title : Sleep Promoting Effect of Luteolin in Mice via Adenosine A1 and A2A Receptors.

Pub. Date : 2019 Nov 1

PMID : 31646844






4 Functional Relationships(s)
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1 On the other hand, the hypnotic effect of 3 mg/kg of luteolin was almost completely blocked by caffeine, an antagonist for both adenosine A1 and A2A receptor (A1R and A2AR), 8-Cyclopentyl-1,3-dipropylxanthine (DPCPX), an A1R antagonist, and SCH-58261, an A2AR antagonist. Luteolin adenosine A2a receptor Mus musculus
2 On the other hand, the hypnotic effect of 3 mg/kg of luteolin was almost completely blocked by caffeine, an antagonist for both adenosine A1 and A2A receptor (A1R and A2AR), 8-Cyclopentyl-1,3-dipropylxanthine (DPCPX), an A1R antagonist, and SCH-58261, an A2AR antagonist. Luteolin adenosine A2a receptor Mus musculus
3 From the binding affinity assay, we have found that luteolin significantly binds to not only A1R but also A2AR with IC50 of 1.19, 0.84 mug/kg, respectively. Luteolin adenosine A2a receptor Mus musculus
4 From these results, it has been suggested that luteolin has hypnotic efficacy through A1R and A2AR binding. Luteolin adenosine A2a receptor Mus musculus