Advances in neurobiology最新文献

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Microglia and Sleep Disorders. 小胶质细胞与睡眠障碍
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-55529-9_20
Katherine Picard, Kira Dolhan, Jyoti J Watters, Marie-Ève Tremblay
{"title":"Microglia and Sleep Disorders.","authors":"Katherine Picard, Kira Dolhan, Jyoti J Watters, Marie-Ève Tremblay","doi":"10.1007/978-3-031-55529-9_20","DOIUrl":"https://doi.org/10.1007/978-3-031-55529-9_20","url":null,"abstract":"<p><p>Sleep is a physiological state that is essential for maintaining physical and mental health. Sleep disorders and sleep deprivation therefore have many adverse effects, including an increased risk of metabolic diseases and a decline in cognitive function that may be implicated in the long-term development of neurodegenerative diseases. There is increasing evidence that microglia, the resident immune cells of the central nervous system (CNS), are involved in regulating the sleep-wake cycle and the CNS response to sleep alteration and deprivation. In this chapter, we will discuss the involvement of microglia in various sleep disorders, including sleep-disordered breathing, insomnia, narcolepsy, myalgic encephalomyelitis/chronic fatigue syndrome, and idiopathic rapid-eye-movement sleep behavior disorder. We will also explore the impact of acute and chronic sleep deprivation on microglial functions. Moreover, we will look into the potential involvement of microglia in sleep disorders as a comorbidity to Alzheimer's disease and Parkinson's disease.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"37 ","pages":"357-377"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142103375","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}
引用次数: 0
Microglia Colonization Associated with Angiogenesis and Neural Cell Development. 小胶质细胞定植与血管生成和神经细胞发育有关
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-55529-9_10
G Jean Harry
{"title":"Microglia Colonization Associated with Angiogenesis and Neural Cell Development.","authors":"G Jean Harry","doi":"10.1007/978-3-031-55529-9_10","DOIUrl":"https://doi.org/10.1007/978-3-031-55529-9_10","url":null,"abstract":"<p><p>The temporal and spatial pattern of microglia colonization of the nervous system implies a role in early stages of organ development including cell proliferation, differentiation, and neurovascularization. As microglia colonize and establish within the developing nervous system, they assume a neural-specific identity and contribute to key developmental events. Their association around blood vessels implicates them in development of the vascular system or vice versa. A similar association has been reported for neural cell proliferation and associated phenotypic shifts and for cell fate differentiation to neuronal or glial phenotypes. These processes are accomplished by phagocytic activities, cell-cell contact relationships, and secretion of various factors. This chapter will present data currently available from studies evaluating the dynamic and interactive nature of these processes throughout the progression of nervous system development.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"37 ","pages":"163-178"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142103377","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}
引用次数: 0
Astrocyte Development in the Rodent. 啮齿动物的星形胶质细胞发育
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-64839-7_3
Yajun Xie, Corey C Harwell, A Denise R Garcia
{"title":"Astrocyte Development in the Rodent.","authors":"Yajun Xie, Corey C Harwell, A Denise R Garcia","doi":"10.1007/978-3-031-64839-7_3","DOIUrl":"10.1007/978-3-031-64839-7_3","url":null,"abstract":"<p><p>Astrocytes have gained increasing recognition as key elements of a broad array of nervous system functions. These include essential roles in synapse formation and elimination, synaptic modulation, maintenance of the blood-brain barrier, energetic support, and neural repair after injury or disease of the nervous system. Nevertheless, our understanding of mechanisms underlying astrocyte development and maturation remains far behind that of neurons and oligodendrocytes. Early efforts to understand astrocyte development focused primarily on their specification from embryonic progenitors and the molecular mechanisms driving the switch from neuron to glial production. Considerably, less is known about postnatal stages of astrocyte development, the period during which they are predominantly generated and mature. Notably, this period is coincident with synapse formation and the emergence of nascent neural circuits. Thus, a greater understanding of astrocyte development is likely to shed new light on the formation and maturation of synapses and circuits. Here, we highlight key foundational principles of embryonic and postnatal astrocyte development, focusing largely on what is known from rodent studies.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"39 ","pages":"51-67"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142071734","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}
引用次数: 0
Progress in Structural and Functional In Vivo Imaging of Microglia and Their Application in Health and Disease. 小胶质细胞的结构和功能体内成像及其在健康和疾病中的应用进展。
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-55529-9_5
Alexis Crockett, Martin Fuhrmann, Olga Garaschuk, Dimitrios Davalos
{"title":"Progress in Structural and Functional In Vivo Imaging of Microglia and Their Application in Health and Disease.","authors":"Alexis Crockett, Martin Fuhrmann, Olga Garaschuk, Dimitrios Davalos","doi":"10.1007/978-3-031-55529-9_5","DOIUrl":"https://doi.org/10.1007/978-3-031-55529-9_5","url":null,"abstract":"<p><p>The first line of defense for the central nervous system (CNS) against injury or disease is provided by microglia. Microglia were long believed to stay in a dormant/resting state, reacting only to injury or disease. This view changed dramatically with the development of modern imaging techniques that allowed the study of microglial behavior in the intact brain over time, to reveal the dynamic nature of their responses. Over the past two decades, in vivo imaging using multiphoton microscopy has revealed numerous new functions of microglia in the developing, adult, aged, injured, and diseased CNS. As the most dynamic cells in the brain, microglia continuously contact all structures and cell types, such as glial and vascular cells, neuronal cell bodies, axons, dendrites, and dendritic spines, and are believed to play a central role in sculpting neuronal networks throughout life. Following trauma, or in neurodegenerative or neuroinflammatory diseases, microglial responses range from protective to harmful, underscoring the need to better understand their diverse roles and states in different pathological conditions. In this chapter, we introduce multiphoton microscopy and discuss recent advances in structural and functional imaging technologies that have expanded our toolbox to study microglial states and behaviors in new ways and depths. We also discuss relevant mouse models available for in vivo imaging studies of microglia and review how such studies are constantly refining our understanding of the multifaceted role of microglia in the healthy and diseased CNS.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"37 ","pages":"65-80"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142103386","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}
引用次数: 0
Neuroimaging Correlates of Functional Outcome Following Pediatric TBI. 小儿创伤性脑损伤后功能结果的神经影像学相关性
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-69832-3_3
Emily L Dennis, Finian Keleher, Brenda Bartnik-Olson
{"title":"Neuroimaging Correlates of Functional Outcome Following Pediatric TBI.","authors":"Emily L Dennis, Finian Keleher, Brenda Bartnik-Olson","doi":"10.1007/978-3-031-69832-3_3","DOIUrl":"https://doi.org/10.1007/978-3-031-69832-3_3","url":null,"abstract":"<p><p>Neuroimaging plays an important role in assessing the consequences of TBI across the postinjury period. While identifying alterations to the brain is important, associating those changes to functional, cognitive, and behavioral outcomes is an essential step to establishing the value of advanced neuroimaging for pediatric TBI. Here we highlight research that has revealed links between advanced neuroimaging and outcome after TBI and point to opportunities where neuroimaging could expand our ability to prognosticate and potentially uncover opportunities to intervene.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"42 ","pages":"33-84"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142455763","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}
引用次数: 0
Rodent Models for ASD Biomarker Development. 开发 ASD 生物标记物的啮齿动物模型。
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-69491-2_8
Henry H C Lee, Mustafa Sahin
{"title":"Rodent Models for ASD Biomarker Development.","authors":"Henry H C Lee, Mustafa Sahin","doi":"10.1007/978-3-031-69491-2_8","DOIUrl":"https://doi.org/10.1007/978-3-031-69491-2_8","url":null,"abstract":"<p><p>Advances in molecular biology and genetics are increasingly revealing the complex etiology of autism spectrum disorder (ASD). In parallel, a number of biochemical, anatomical, and electrophysiological measures are emerging as potential disease-relevant biomarkers that could inform the diagnosis and clinical management of ASD. Rodent ASD models play a key role in ASD research as essential experimental tools. Nevertheless, there are challenges and limitations to the validity and translational value of rodent models, including genetic relevance and cognitive performance differences between humans and rodents. In this chapter, we begin with a brief history of autism research, followed by prominent examples of disease-relevant mouse models enabled by current knowledge of genetics, molecular biology, and bioinformatics. These ASD-associated rodent models enable quantifiable biomarker development. Finally, we discuss the prospects of ASD biomarker development.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"40 ","pages":"189-218"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142674742","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}
引用次数: 0
Structural Brain Imaging Biomarkers of Autism Spectrum Disorder. 自闭症谱系障碍的脑结构成像生物标志物。
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-69491-2_17
David G Amaral, Derek Sayre Andrews, Christine Wu Nordahl
{"title":"Structural Brain Imaging Biomarkers of Autism Spectrum Disorder.","authors":"David G Amaral, Derek Sayre Andrews, Christine Wu Nordahl","doi":"10.1007/978-3-031-69491-2_17","DOIUrl":"https://doi.org/10.1007/978-3-031-69491-2_17","url":null,"abstract":"<p><p>Since the early 1990s, there have literally been thousands of reports related to magnetic resonance imaging of the autistic brain. The goals of these studies have ranged from identifying the earliest biological predictors of an autistic diagnosis to determining brain systems most altered in autistic individuals. Some of the later works attempt to use distinct patterns of brain alterations to help define more homogenous subtypes of autism. Far less work has been done to identify brain changes that are associated with therapeutic interventions. In this chapter, we will touch on all of these efforts as they relate to the general topic of the usefulness of brain imaging as a biomarker of autism.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"40 ","pages":"491-509"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142674745","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}
引用次数: 0
The Roles of Endogenous Opioids in Placebo and Nocebo Effects: From Pain to Performance to Prozac. 内源性阿片类药物在安慰剂和安慰剂效应中的作用:从疼痛到表现再到百忧解
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-45493-6_10
Patrick L Kerr, John M Gregg
{"title":"The Roles of Endogenous Opioids in Placebo and Nocebo Effects: From Pain to Performance to Prozac.","authors":"Patrick L Kerr, John M Gregg","doi":"10.1007/978-3-031-45493-6_10","DOIUrl":"10.1007/978-3-031-45493-6_10","url":null,"abstract":"<p><p>Placebo and nocebo effects have been well documented for nearly two centuries. However, research has only relatively recently begun to explicate the neurobiological underpinnings of these phenomena. Similarly, research on the broader social implications of placebo/nocebo effects, especially within healthcare delivery settings, is in a nascent stage. Biological and psychosocial outcomes of placebo/nocebo effects are of equal relevance. A common pathway for such outcomes is the endogenous opioid system. This chapter describes the history of placebo/nocebo in medicine; delineates the current state of the literature related to placebo/nocebo in relation to pain modulation; summarizes research findings related to human performance in sports and exercise; discusses the implications of placebo/nocebo effects among diverse patient populations; and describes placebo/nocebo influences in research related to psychopharmacology, including the relevance of endogenous opioids to new lines of research on antidepressant pharmacotherapies.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"35 ","pages":"183-220"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141316455","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}
引用次数: 0
Depression, Cancer, Inflammation, and Endogenous Opioids: Pathogenic Relationships and Therapeutic Options. 抑郁症、癌症、炎症和内源性阿片类药物:致病关系与治疗方案》。
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-45493-6_21
Jennifer Hancock, Cristian Sirbu, Patrick L Kerr
{"title":"Depression, Cancer, Inflammation, and Endogenous Opioids: Pathogenic Relationships and Therapeutic Options.","authors":"Jennifer Hancock, Cristian Sirbu, Patrick L Kerr","doi":"10.1007/978-3-031-45493-6_21","DOIUrl":"10.1007/978-3-031-45493-6_21","url":null,"abstract":"<p><p>Endogenous opioids and their associated receptors form a system that maintains survival by positively reinforcing behaviors that are vital to life. Cancer and cancer treatment side effects capitalize on this system pathogenically, leading to maladaptive biological responses (e.g., inflammation), as well as cognitive and emotional consequences, most notably depression. Psychologists who treat people with cancer frequently find depression to be a primary target for intervention. However, in people with cancer, the etiology of depression is unique and complex. This complexity necessitates that psycho-oncologists have a fundamental working knowledge of the biological substrates that underlie depression/cancer comorbidity. Building on other chapters in this volume pertaining to cancer and endogenous opioids, this chapter focuses on the clinical applications of basic scientific findings.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"35 ","pages":"435-451"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141316478","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}
引用次数: 0
Endorphins, Sexuality, and Reproduction. 内啡肽、性和生殖。
Advances in neurobiology Pub Date : 2024-01-01 DOI: 10.1007/978-3-031-45493-6_20
Marjan Khajehei
{"title":"Endorphins, Sexuality, and Reproduction.","authors":"Marjan Khajehei","doi":"10.1007/978-3-031-45493-6_20","DOIUrl":"10.1007/978-3-031-45493-6_20","url":null,"abstract":"<p><p>Beta-endorphin is secreted from the hypothalamus and pituitary in both mother and newborn. The placenta produces numerous pituitary hormones from the third month of pregnancy, one of which is βE. It has been suggested that βE has a role in the appetitive and precopulatory phase of sexual behavior in animals. An increase in endorphin levels during sexual activity in humans may contribute to attachment and bonding between partners, but contradictory reports in the literature question the association between sexuality and βE levels. The level of βE also increases during pregnancy, rises in early labor, peaks in late labor, and drops in the postpartum period. This fluctuation provides natural analgesia, raises the pain threshold, decreases the sensation of pain, or suppresses pain, and decreases fear levels during labor and birth. Beta-endorphin also protects the fetus from hypoxia during labor and birth and potential neural damage by aiding blood flow to the brain under hypoxic conditions. It has been suggested that a variety of pharmacologic and nonpharmacologic complementary therapies, when used in pregnancy, labor, and birth, activate the opioid receptors in the CNS and alter the sensation of pain during labor and birth, affect the mother-child attachment and affect sexual function. These studies report contradictory results that will be discussed in this chapter.</p>","PeriodicalId":7360,"journal":{"name":"Advances in neurobiology","volume":"35 ","pages":"397-433"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141316484","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}
引用次数: 0
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