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      Mothers with substance addictions show reduced reward responses when viewing their own infant's face : Reduced Reward Response in Maternal Addiction

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          Abstract

          <p id="d1684975e364">Maternal addiction constitutes a major public health problem affecting children, with high rates of abuse, neglect, and foster care placement. However, little is known about the ways in which substance addiction alters brain function related to maternal behavior. Prior studies have shown that infant face cues activate similar dopamine‐associated brain reward regions to substances of abuse. Here, we report on a functional MRI study documenting that mothers with addictions demonstrate reduced activation of reward regions when shown reward‐related cues of their own infants. Thirty‐six mothers receiving inpatient treatment for substance addiction were scanned at 6 months postpartum, while viewing happy and sad face images of their own infant compared to those of a matched unknown infant. When viewing happy face images of their own infant, mothers with addictions showed a striking pattern of decreased activation in dopamine‐ and oxytocin‐innervated brain regions, including the hypothalamus, ventral striatum, and ventromedial prefrontal cortex—regions in which increased activation has previously been observed in mothers without addictions. Our results are the first to demonstrate that mothers with addictions show reduced activation in key reward regions of the brain in response to their own infant's face cues. <i>Hum Brain Mapp 38:5421–5439, 2017</i>. © <b>2017 Wiley Periodicals, Inc.</b> </p>

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          Most cited references53

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          The neural basis of addiction: a pathology of motivation and choice.

          A primary behavioral pathology in drug addiction is the overpowering motivational strength and decreased ability to control the desire to obtain drugs. In this review the authors explore how advances in neurobiology are approaching an understanding of the cellular and circuitry underpinnings of addiction, and they describe the novel pharmacotherapeutic targets emerging from this understanding. Findings from neuroimaging of addicts are integrated with cellular studies in animal models of drug seeking. While dopamine is critical for acute reward and initiation of addiction, end-stage addiction results primarily from cellular adaptations in anterior cingulate and orbitofrontal glutamatergic projections to the nucleus accumbens. Pathophysiological plasticity in excitatory transmission reduces the capacity of the prefrontal cortex to initiate behaviors in response to biological rewards and to provide executive control over drug seeking. Simultaneously, the prefrontal cortex is hyperresponsive to stimuli predicting drug availability, resulting in supraphysiological glutamatergic drive in the nucleus accumbens, where excitatory synapses have a reduced capacity to regulate neurotransmission. Cellular adaptations in prefrontal glutamatergic innervation of the accumbens promote the compulsive character of drug seeking in addicts by decreasing the value of natural rewards, diminishing cognitive control (choice), and enhancing glutamatergic drive in response to drug-associated stimuli.
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            Drug-evoked synaptic plasticity in addiction: from molecular changes to circuit remodeling.

            Addictive drugs have in common that they target the mesocorticolimbic dopamine (DA) system. This system originates in the ventral tegmental area (VTA) and projects mainly to the nucleus accumbens (NAc) and prefrontal cortex (PFC). Here, we review the effects that such drugs leave on glutamatergic and GABAergic synaptic transmission in these three brain areas. We refer to these changes as drug-evoked synaptic plasticity, which outlasts the presence of the drug in the brain and contributes to the reorganization of neural circuits. While in most cases these early changes are not sufficient to induce the disease, with repetitive drug exposure, they may add up and contribute to addictive behavior. Copyright © 2011 Elsevier Inc. All rights reserved.
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              The role of the right temporoparietal junction in social interaction: how low-level computational processes contribute to meta-cognition.

              Accumulating evidence from cognitive neuroscience indicates that the right inferior parietal cortex, at the junction with the posterior temporal cortex, plays a critical role in various aspects of social cognition such as theory of mind and empathy. With a quantitative meta-analysis of 70 functional neuroimaging studies, the authors demonstrate that this area is also engaged in lower-level (bottom-up) computational processes associated with the sense of agency and reorienting attention to salient stimuli. It is argued that this domain-general computational mechanism is crucial for higher level social cognitive processing.
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                Author and article information

                Journal
                Human Brain Mapping
                Hum. Brain Mapp.
                Wiley
                10659471
                November 2017
                November 2017
                July 26 2017
                : 38
                : 11
                : 5421-5439
                Affiliations
                [1 ]Department of Obstetrics and Gynecology; Baylor College of Medicine; Houston Texas United States
                [2 ]Department of Pediatrics and Menninger Department of Psychiatry and Behavioral Sciences; Baylor College of Medicine; Houston Texas United States
                [3 ]Center for Reproductive Psychiatry, Pavilion for Women, Texas Children's Hospital; Houston Texas United States
                [4 ]Institute of Psychiatry, Psychology and Neuroscience, King's College London; London United Kingdom
                [5 ]Yale Child Study Center, Yale University School of Medicine; New Haven Connecticut United States
                [6 ]Departments of Psychiatry and Neuroscience and the National Center on Addiction and Substance Abuse (CASAColumbia); Yale University School of Medicine; New Haven Connecticut United States
                [7 ]Connecticut Mental Health Center; New Haven Connecticut United States
                [8 ]Stead Family Department of Pediatrics; University of Iowa Carver College of Medicine; Iowa City Iowa United States
                Article
                10.1002/hbm.23731
                5763911
                28746733
                d02aefe7-f13c-4a29-9b89-e997c5962dfd
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1.1

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