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Parental brain

Parental experience, as well as changing hormone levels during pregnancy and postpartum, cause changes in the parental brain. Displaying maternal sensitivity towards infant cues, processing those cues and being motivated to engage socially with her infant and attend to the infant's needs in any context could be described as mothering behavior and is regulated by many systems in the maternal brain. Research has shown that hormones such as oxytocin, prolactin, estradiol and progesterone are essential for the onset and the maintenance of maternal behavior in rats, and other mammals as well. Mothering behavior has also been classified within the basic drives.

Maternal brain
Maternal hormonal effect Different hormone levels in the maternal brain and the overall well being of the mother account for 40%–50% of differences in the mother's attachment to her infant. Oxytocin The levels of oxytocin in the maternal brain correlate with maternal behaviors such as gazing, vocalization, positive affect, affectionate touch and other similar mother-infant relationship behaviors. Estradiol and progesterone High mother-infant attachment correlates with a higher ratio of estradiol/progesterone at the end of pregnancy, than at the beginning. Mothers with high levels of cortisol were also found to be more vocal towards their children. Glucocorticoids Glucocorticoids are not essential for displaying maternal behaviors, but in mothers, the levels of glucocorticoids are elevated as to initiate lactation. Neuroanatomy Different areas/structures of the brain are associated with different factors which contribute to maternal behavior. One's own infant acts as a special stimulus which triggers activation of different areas of the brain. These brain areas together allow for maternal behavior and related systems. The amygdala and medial prefrontal cortex also contain receptors for the hormones which are most likely to be changing behavior at the time of pregnancy, and may be the sites where these changes occur. Increased activity has also been observed in the amygdala as the mother is responding to emotions seen in negative (fearful) faces, positive faces or familiar faces that her baby makes. Primate mothers with damage to the prefrontal cortex have also been associated with disrupted maternal behavior. The dorsolateral prefrontal cortex (DLPFC) plays a role in the attention, cognitive flexibility and working memory of the mother. Postpartum changes Changes in estrogen, oxytocin and prolactin in the early postpartum period cause changes in the structures of the maternal brain. In animal mothers Postpartum, new neuron production is suppressed due to decreased levels of estrogen and increased levels of glucocorticoids in mother rats. Mother-infant interaction is also thought to suppress neurogenesis in the hippocampus postpartum in the rat maternal brain. Maternal experience increases neurogenesis in the subventricular zone (SBZ) which is responsible for producing the neurons of the olfactory bulb. Prolactin is the hormone which mediates the increase in neurogenesis in SBZ. In animals, structures of the mother's brain change postpartum due to the increased interaction of the mother with the infant. The volume of gray matter increases postpartum in the following brain regions: Postpartum increase in gray matter volumes may help the mother activate the motivation to perform maternal behavior in response to cue from their offspring. In human mothers there was a correlation between increased gray matter volume in the substantia nigra and positive emotional feelings towards the infant. Other changes such as menstrual cycle, hydration, weight and nutrition may also be factors which trigger the maternal brain to change during pregnancy and postpartum. Maternal experience alters behaviors which stem from the hippocampus such as enhancing spatial navigation learning and behaviors linked with anxiety. Importantly, less medial prefrontal cortex activity and greater limbic system activity (i.e. entorhinal cortex and hippocampus) were found among these post-traumatically stressed mothers of toddlers compared to mothers of toddlers without PTSD in response to stressful parent-child interactions as well as, within a different sample, in response to menacing adult male-female interactions. In the latter study, this pattern of corticolimbic dysregulation was linked to less observed maternal sensitivity during mother-child play. Decreased ventral-medial prefrontal cortex activity in violence-exposed mothers, in response to viewing their own and unfamiliar toddlers in video-clips of separation versus play, has also been associated with increased PTSD symptoms, parenting stress and decreased methylation of the glucocorticoid receptor gene. Early experiences and shaping Women who had a positive experience involving their family in their childhood are more likely to be more maternally sensitive and provide that same experience for their own children. Mothers that had negative experiences involving their families undergo neurobiological changes which lead to high stress reactivity and insecure attachment. This causes lower maternal responsiveness to their infant's needs. Rat mothers provide high levels of maternal care (licking and grooming) to their offspring if they themselves received high maternal care as a pup from their own mothers. Rat mothers who received low levels of maternal care as pups have lower levels of expression of the glucocorticoid receptor gene and lower synaptic density in the hippocampus. In human mothers, lower hippocampal volume has been associated with a lower ability to regulate emotions and stress, which can be linked with decreased maternal sensitivity as a mother. Mothers with insecure attachments to their own mothers display higher amygdala sensitivity to negative emotional stimuli, like hearing their infant cry. Having more difficulty dealing with stress makes mothers less responsive to their infant's cues. Larger gray matter and increased activations of the following brain areas occur in mothers who had experienced higher quality maternal care as infants: Postpartum depression has also been associated with mothers who received low quality maternal care early in their own life. ==Paternal brain==
Paternal brain
In only 6% of mammalian species, including humans, the father plays a significant role in caring for his young. Similar to the changes that occur in the maternal brain, the same areas of the brain (amygdala, hypothalamus, prefrontal cortex, olfactory bulb etc.) are activated in the father, and hormonal changes occur in the paternal brain to ensure display of parenting behavior. These hormonal changes occur through the father's interaction with the mother and his offspring. In humans, and in other primate species, lower levels of testosterone have been linked to the display of paternal behavior. In animal fathers In father rats, just as in the mother rats, a decrease in neurogenesis in the hippocampus occurs postpartum. Just like in mothers, fathers also have increased levels of glucocorticoids which are thought to suppress the production of new cells in the brain. Changes in neurogenesis in the prefrontal cortex of the paternal brain have been linked in some species to recognition of kin. In human fathers Being exposed to crying babies activates the prefrontal cortex and the amygdala in both fathers and mothers, but not in non-parents. The level of testosterone in the paternal brain correlates with the effectiveness of the father's response to the baby's cry. ==References==
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