2010
DOI: 10.1016/j.phymed.2009.10.001
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Tea catechins’ affinity for human cannabinoid receptors

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Cited by 32 publications
(16 citation statements)
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“…Cyanidin and delphinidin, two anthocyanidins found in a wide range of plants, have micromolar affinities for CB 1 [162]. Epigallocatechin-3-O-gallate, the most abundant catechin in tea, also has micromolar affinities for CB 1 [163].…”
Section: Resultsmentioning
confidence: 99%
“…Cyanidin and delphinidin, two anthocyanidins found in a wide range of plants, have micromolar affinities for CB 1 [162]. Epigallocatechin-3-O-gallate, the most abundant catechin in tea, also has micromolar affinities for CB 1 [163].…”
Section: Resultsmentioning
confidence: 99%
“…These include green tea extract-and L-theaninemediated regulation of the secretion of stress hormones that influence cognitive function, including corticosterone [119,120]; EGCG-mediated reduction of amyloid-induced mitochondrial dysfunction [121]; inhibition of glutamate dehydrogenase [122,123], 3,4-dihydroxyphenylalanine decarboxylase [124], and histone acetyltransferase [125]; inhibition of fatty acid synthase by catechins [126,127]; interactions between catechin derivatives and opioid/cannabinoid receptors [128,129]; and L-theanine-mediated modulation of glutamatergic [130], GABAergic [131], dopaminergic [132], and serotoninergic neurotransmission in the brain [132][133][134]. Caffeine is also a psychoactive ingredient of green tea [76] and this stimulates cholinergic neurons by acting as a non-selective antagonist of adenosine A1 and A2A receptors [135].…”
Section: Other Mechanismsmentioning
confidence: 99%
“…Fukuda et al reported that the pigments of green tea leaves had the potential to protect against dioxin toxicity through the suppression of aryl hydrocarbon receptor transformation (36). Moreover, EGCG has been suggested to exert binding properties with human cannabinoid receptors and focal adhesion kinase and insulin-like growth factor-I receptors (37,38). Thus, GTE may prevent the down-regulation of muscarinic receptors in CYP-treated bladders by affecting cholinergic neuronal activity.…”
Section: H]nms and [mentioning
confidence: 99%