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This function is primarily due to the serums high quantities of riboflavin (vitamin B2), which promotes lipolysis while also providing anti-inflammatory properties

This is the case in humans and most other complex species (Wilding, 2001)

The anxiolytic profile comes without sedation at doses up to 400 mg, a property that separates L-theanine from benzodiazepines and most GABAergic anxiolytics [4]

Complicating the matter, administration of ghrelin still leads to cross-desensitization of dopamine-induced Ca 2+ mobilization, and while ghrelin antagonism also reduces this mobilization, it is possible that concurrent cross-sensitization may also occur, which may possibly carry beyond the timeframe of bioavailability of such an antagonist