Pub Date : 2019-03-15Epub Date: 2019-01-17DOI: 10.1007/s40473-019-0170-4
Hestia Moningka, Sarah Lichenstein, Sarah W Yip
Purpose of review: This review provides an overview of the neurobiological mechanisms underlying opioid use disorder (OUD) drawing from genetic, functional and structural magnetic resonance imaging (MRI) research.
Recent findings: Preliminary evidence suggests an association between OUD and specific variants of the DRD2, δ-opioid receptor 1 (OPRD1) and μ-opioid receptor 1 (OPRM1) genes. Additionally, MRI research indicates functional and structural alterations in striatal and corticolimbic brain regions and pathways underlying reward, emotion/stress and cognitive control processes among individuals with OUD.
Summary: Individual differences in genetic and functional and structural brain-based features are correlated with differences in OUD severity and treatment outcomes, and therefore may potentially one day be used to inform OUD treatment selection. However, given the heterogeneous findings reported, further longitudinal research across different stages of opioid addiction is needed to yield a convergent characterization of OUD and improve treatment and prevention.
{"title":"Current understanding of the neurobiology of opioid use disorder: An overview.","authors":"Hestia Moningka, Sarah Lichenstein, Sarah W Yip","doi":"10.1007/s40473-019-0170-4","DOIUrl":"10.1007/s40473-019-0170-4","url":null,"abstract":"<p><strong>Purpose of review: </strong>This review provides an overview of the neurobiological mechanisms underlying opioid use disorder (OUD) drawing from genetic, functional and structural magnetic resonance imaging (MRI) research.</p><p><strong>Recent findings: </strong>Preliminary evidence suggests an association between OUD and specific variants of the DRD2, δ-opioid receptor 1 (OPRD1) and μ-opioid receptor 1 (OPRM1) genes. Additionally, MRI research indicates functional and structural alterations in striatal and corticolimbic brain regions and pathways underlying reward, emotion/stress and cognitive control processes among individuals with OUD.</p><p><strong>Summary: </strong>Individual differences in genetic and functional and structural brain-based features are correlated with differences in OUD severity and treatment outcomes, and therefore may potentially one day be used to inform OUD treatment selection. However, given the heterogeneous findings reported, further longitudinal research across different stages of opioid addiction is needed to yield a convergent characterization of OUD and improve treatment and prevention.</p>","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"6 1","pages":"1-11"},"PeriodicalIF":1.7,"publicationDate":"2019-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-019-0170-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39386638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2019-01-01Epub Date: 2019-08-21DOI: 10.1007/s40473-019-00185-2
Adam Bryant Miller, Tory A Eisenlohr-Moul
Purpose of review: While rates of other medical illnesses have declined over the past several decades, rates of suicide have increased, particularly among adolescents. Prior research on biological underpinnings of suicide risk has remained limited. In this review, we describe a recent model conceptualizing suicide as a failure of biological responses to acute stress. According to this model, youth who fail to mount an adaptive stress response following exposure to a stressor are at acute risk for suicide.
Recent findings: Although much more research is needed, early evidence suggests that abnormal biological responses to acute stress, such as altered autonomic nervous system activity and altered hypothalamic-pituitary-adrenal axis function, may underlie risk for suicide, particularly during the transition to adolescence.
Summary: Overall, initial evidence supports a link between biological responses to acute stress and suicide risk. However, future work that incorporates makers of other biological and environmental systems will sharpen our understanding of who is at suicide risk and when this risk is highest.
{"title":"Biological responses to acute stress and suicide: A review and opportunities for methodological innovation.","authors":"Adam Bryant Miller, Tory A Eisenlohr-Moul","doi":"10.1007/s40473-019-00185-2","DOIUrl":"https://doi.org/10.1007/s40473-019-00185-2","url":null,"abstract":"<p><strong>Purpose of review: </strong>While rates of other medical illnesses have declined over the past several decades, rates of suicide have increased, particularly among adolescents. Prior research on biological underpinnings of suicide risk has remained limited. In this review, we describe a recent model conceptualizing suicide as a failure of biological responses to acute stress. According to this model, youth who fail to mount an adaptive stress response following exposure to a stressor are at acute risk for suicide.</p><p><strong>Recent findings: </strong>Although much more research is needed, early evidence suggests that abnormal biological responses to acute stress, such as altered autonomic nervous system activity and altered hypothalamic-pituitary-adrenal axis function, may underlie risk for suicide, particularly during the transition to adolescence.</p><p><strong>Summary: </strong>Overall, initial evidence supports a link between biological responses to acute stress and suicide risk. However, future work that incorporates makers of other biological and environmental systems will sharpen our understanding of who is at suicide risk and when this risk is highest.</p>","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"6 ","pages":"141-150"},"PeriodicalIF":1.7,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-019-00185-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38635082","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2019-01-01Epub Date: 2019-07-25DOI: 10.1007/s40473-019-00180-7
Sara L Weisenbach, Joseph Kim, Dustin Hammers, Kelly Konopacki, Vincent Koppelmans
Purpose of review: This review summarizes recent literature linking Alzheimer's disease (AD) and late life depression (LLD). It describes shared neurobiological features associated with both conditions, as well as factors that may increase resilience to onset and severity of cognitive decline and AD. Finally, we pose a number of future research directions toward improving detection, management, and treatment of both conditions.
Recent findings: Epidemiological studies have consistently shown a significant relationship between LLD and AD, with support for depression as a prodromal feature of AD, a risk factor for AD, and observation of some shared risk factors underlying both disease processes. Three major neurobiological features shared by LLD and AD include neurodegeneration, disruption to cerebrovascular functioning, and increased levels of neuroinflammation. There are also potentially modifiable factors that can increase resilience to AD and LLD, including social support, physical and cognitive engagement, and cognitive reserve.
Summary: We propose that, in the context of depression, neurobiological events, such as neurodegeneration, cerebrovascular disease, and neuroinflammation result in a brain that is more vulnerable to the consequences of the pathophysiological features of AD, lowering the threshold for the onset of the behavioral presentation of AD (i.e., cognitive decline and dementia). We discuss factors that can increase resilience to AD and LLD, including social support, physical and cognitive engagement, and cognitive reserve. We conclude with a discussion of future research directions.
综述的目的:本综述总结了将阿尔茨海默病(AD)和晚年抑郁症(LLD)联系起来的最新文献。它描述了与这两种疾病相关的共同神经生物学特征,以及可能增加对认知能力衰退和阿尔茨海默病发病和严重程度的适应力的因素。最后,我们提出了一些未来的研究方向,以改善这两种疾病的检测、管理和治疗:流行病学研究一直表明,LLD 和 AD 之间存在显著关系,抑郁症是 AD 的前驱特征,是 AD 的风险因素,并且观察到这两种疾病过程中存在一些共同的风险因素。LLD 和 AD 的三大共同神经生物学特征包括神经变性、脑血管功能紊乱和神经炎症水平升高。摘要:我们提出,在抑郁症的背景下,神经生物事件(如神经变性、脑血管疾病和神经炎症)会导致大脑更容易受到注意力缺失症病理生理特征后果的影响,从而降低注意力缺失症行为表现(即认知能力下降和痴呆)发病的阈值。我们讨论了可以提高对注意力缺失症和痴呆症的恢复能力的因素,包括社会支持、身体和认知参与以及认知储备。最后,我们将讨论未来的研究方向。
{"title":"Linking late life depression and Alzheimer's disease: mechanisms and resilience.","authors":"Sara L Weisenbach, Joseph Kim, Dustin Hammers, Kelly Konopacki, Vincent Koppelmans","doi":"10.1007/s40473-019-00180-7","DOIUrl":"10.1007/s40473-019-00180-7","url":null,"abstract":"<p><strong>Purpose of review: </strong>This review summarizes recent literature linking Alzheimer's disease (AD) and late life depression (LLD). It describes shared neurobiological features associated with both conditions, as well as factors that may increase resilience to onset and severity of cognitive decline and AD. Finally, we pose a number of future research directions toward improving detection, management, and treatment of both conditions.</p><p><strong>Recent findings: </strong>Epidemiological studies have consistently shown a significant relationship between LLD and AD, with support for depression as a prodromal feature of AD, a risk factor for AD, and observation of some shared risk factors underlying both disease processes. Three major neurobiological features shared by LLD and AD include neurodegeneration, disruption to cerebrovascular functioning, and increased levels of neuroinflammation. There are also potentially modifiable factors that can increase resilience to AD and LLD, including social support, physical and cognitive engagement, and cognitive reserve.</p><p><strong>Summary: </strong>We propose that, in the context of depression, neurobiological events, such as neurodegeneration, cerebrovascular disease, and neuroinflammation result in a brain that is more vulnerable to the consequences of the pathophysiological features of AD, lowering the threshold for the onset of the behavioral presentation of AD (i.e., cognitive decline and dementia). We discuss factors that can increase resilience to AD and LLD, including social support, physical and cognitive engagement, and cognitive reserve. We conclude with a discussion of future research directions.</p>","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"6 3","pages":"103-112"},"PeriodicalIF":2.1,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7597973/pdf/nihms-1535733.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38555805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose of review: To summarize the current literature on the effects of cannabinoids in humans and to discuss the existing literature on the sex- and gender-related differences in the effects of cannabinoids.
Recent findings: Cannabis and its constituent cannabinoids are associated with risk of addiction, cognitive deficits and mood/psychotic disorders. Preclinical and emerging clinical data suggest greater sensitivity to the effects of cannabinoids in women.
Summary: Cannabis is one of the most commonly used drugs with increasing rates of use. Women in particular may be at a greater risk of adverse outcomes given the previously described "telescoping effect" of substance use in women. Human data examining the sex- and gender-related differences in the effects of cannabinoids and factors underlying these differences are very limited. This represents a critical gap in the literature and needs to be systematically examined in future studies.
{"title":"Cannabis Use: Neurobiological, Behavioral, and Sex/Gender Considerations.","authors":"Anahita Bassir Nia, Claire Mann, Harsimar Kaur, Mohini Ranganathan","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose of review: </strong>To summarize the current literature on the effects of cannabinoids in humans and to discuss the existing literature on the sex- and gender-related differences in the effects of cannabinoids.</p><p><strong>Recent findings: </strong>Cannabis and its constituent cannabinoids are associated with risk of addiction, cognitive deficits and mood/psychotic disorders. Preclinical and emerging clinical data suggest greater sensitivity to the effects of cannabinoids in women.</p><p><strong>Summary: </strong>Cannabis is one of the most commonly used drugs with increasing rates of use. Women in particular may be at a greater risk of adverse outcomes given the previously described \"telescoping effect\" of substance use in women. Human data examining the sex- and gender-related differences in the effects of cannabinoids and factors underlying these differences are very limited. This represents a critical gap in the literature and needs to be systematically examined in future studies.</p>","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"5 4","pages":"271-280"},"PeriodicalIF":1.7,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756752/pdf/nihms-1512214.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41214972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2018-12-01Epub Date: 2018-10-30DOI: 10.1007/s40473-018-0168-3
Megha Chawla, Kathleen A Garrison
Purpose of review: Neurobiological studies of tobacco/nicotine use examining genetic, molecular, functional, and behavioral correlates have improved our understanding of nicotine/tobacco dependence and have informed treatment. Recent work extending previously established findings and reporting novel methodologies and discoveries in preclinical and human studies are reviewed.
Recent findings: Recent work in preclinical models has focused on the differential roles of nicotinic receptor subtypes and nicotine's effects on neural systems beyond cortico-striatal dopaminergic pathways, and utilizing advanced methodologies such as pharmacogenetics, optogenetics and rodent fMRI to identify targets for treatment. Likewise, human neuroimaging studies have identified molecular and functional dynamic shifts associated with tobacco/nicotine use that further inform treatment.
Summary: Nicotine/tobacco use is associated with widespread neural adaptations that are persistent and function to maintain addiction. The continued identification of genetic, molecular, neural, and behavioral endophenotypes related to nicotine/tobacco use, dependence, and addiction will facilitate the development and delivery of personalized treatment.
{"title":"Neurobiological Considerations for Tobacco Use Disorder.","authors":"Megha Chawla, Kathleen A Garrison","doi":"10.1007/s40473-018-0168-3","DOIUrl":"10.1007/s40473-018-0168-3","url":null,"abstract":"<p><strong>Purpose of review: </strong>Neurobiological studies of tobacco/nicotine use examining genetic, molecular, functional, and behavioral correlates have improved our understanding of nicotine/tobacco dependence and have informed treatment. Recent work extending previously established findings and reporting novel methodologies and discoveries in preclinical and human studies are reviewed.</p><p><strong>Recent findings: </strong>Recent work in preclinical models has focused on the differential roles of nicotinic receptor subtypes and nicotine's effects on neural systems beyond cortico-striatal dopaminergic pathways, and utilizing advanced methodologies such as pharmacogenetics, optogenetics and rodent fMRI to identify targets for treatment. Likewise, human neuroimaging studies have identified molecular and functional dynamic shifts associated with tobacco/nicotine use that further inform treatment.</p><p><strong>Summary: </strong>Nicotine/tobacco use is associated with widespread neural adaptations that are persistent and function to maintain addiction. The continued identification of genetic, molecular, neural, and behavioral endophenotypes related to nicotine/tobacco use, dependence, and addiction will facilitate the development and delivery of personalized treatment.</p>","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"5 4","pages":"238-248"},"PeriodicalIF":1.7,"publicationDate":"2018-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-018-0168-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37258375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2018-11-17DOI: 10.1007/s40473-018-0169-2
K. Naish, J. Mackillop, I. Balodis
{"title":"The Concept of Food Addiction: a Review of the Current Evidence","authors":"K. Naish, J. Mackillop, I. Balodis","doi":"10.1007/s40473-018-0169-2","DOIUrl":"https://doi.org/10.1007/s40473-018-0169-2","url":null,"abstract":"","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"5 1","pages":"281-294"},"PeriodicalIF":1.7,"publicationDate":"2018-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-018-0169-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48035995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2018-10-29DOI: 10.1007/s40473-018-0166-5
Jillian E. Hardee, L. Cope, M. Martz, M. Heitzeg
{"title":"Review of Neurobiological Influences on Externalizing and Internalizing Pathways to Alcohol Use Disorder","authors":"Jillian E. Hardee, L. Cope, M. Martz, M. Heitzeg","doi":"10.1007/s40473-018-0166-5","DOIUrl":"https://doi.org/10.1007/s40473-018-0166-5","url":null,"abstract":"","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"5 1","pages":"249-262"},"PeriodicalIF":1.7,"publicationDate":"2018-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-018-0166-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"52800359","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2018-10-26DOI: 10.1007/s40473-018-0165-6
M. Kyrios, Patrick Trotzke, L. Lawrence, D. Fassnacht, K. Ali, Nora M. Laskowski, A. Müller
{"title":"Behavioral Neuroscience of Buying-Shopping Disorder: a Review","authors":"M. Kyrios, Patrick Trotzke, L. Lawrence, D. Fassnacht, K. Ali, Nora M. Laskowski, A. Müller","doi":"10.1007/s40473-018-0165-6","DOIUrl":"https://doi.org/10.1007/s40473-018-0165-6","url":null,"abstract":"","PeriodicalId":36384,"journal":{"name":"Current Behavioral Neuroscience Reports","volume":"5 1","pages":"263-270"},"PeriodicalIF":1.7,"publicationDate":"2018-10-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s40473-018-0165-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45721375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}