Maternal dopamine encodes affective signals of human infants

Mothers are highly responsive to their offspring. In non-human mammals, mothers secrete dopamine in the nucleus accumbens (NAcc) in response to their pups. Yet, it is still unknown which aspect of the offspring behavior elicits dopaminergic responses in mothers. Here, we tested whether infants’ affective signals elicit dopaminergic responses in the NAcc of human mothers. First, we conducted a behavioral analysis on videos of infants’ free play and quantified the affective signals infants spontaneously communicated. Then, we presented the same videos to mothers during a magnetic resonance-positron emission tomography scan. We traced the binding of [(11)C]raclopride to free D(2/3)-type receptors to assess maternal dopaminergic responses during the infant videos. When mothers observed videos with many infant signals during the scan, they had less [(11)C]raclopride binding in the right NAcc. Less [(11)C]raclopride binding indicates that less D(2/3) receptors were free, possibly due to increased endogenous dopamine responses to infants’ affective signals. We conclude that NAcc D(2/3) receptors are involved in maternal responsiveness to affective signals of human infants. D(2/3) receptors have been associated with maternal responsiveness in nonhuman animals. This evidence supports a similar mechanism in humans and specifies infant-behaviors that activate the maternal dopaminergic system, with implications for social neuroscience, development and psychopathology.