MONDAY, Oct. 26, 2015 (HealthDay News) -- The so-called "love hormone" oxytocin may enhance social interactions by triggering production of a marijuana-like molecule in the brain, a new study in mice suggests.
This molecule, anandamide, activates certain receptors in brain cells, resulting in increased motivation and happiness, the researchers explained. THC -- the active ingredient in marijuana -- also activates these receptors.
Based on their results, University of California, Irvine, researchers theorize that manipulating the supply of anandamide -- sometimes called the "bliss hormone" -- might benefit people who have social challenges, including those with autism.
"Our findings open the exciting possibility that drugs that block the degradation of anandamide, which are currently being tested for various anxiety disorders, could give a boost to the brain's own oxytocin and help people with autism socialize more," study leader Daniele Piomelli said in a university news release.
Previous research has linked oxytocin with behaviors that create bonds between people, including hugging, kissing, sex, birth and breast-feeding.
In this study, investigators measured levels of anandamide in the brains of mice that were either isolated or allowed to socialize. They found that social contact boosted production of anandamide, which triggered cannabinoid receptors to reinforce the pleasure of interaction.
When the receptors were blocked, this reinforcement vanished.
The researchers also found that stimulating brain cells that produce oxytocin led to increased production of anandamide, and that blocking anandamide's effects also blocked oxytocin's effects. This suggests that oxytocin reinforces social ties by triggering anandamide production.
In further experiments, the investigators found that preventing anandamide degradation increased the pleasure of social contact for mice.
The study was published online Oct. 26 in the Proceedings of the National Academy of Sciences.
The American Psychological Association has more about oxytocin.
SOURCE: University of California, Irvine, news release, Oct. 26, 2015
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