3 options
Handbook of developmental neurotoxicology / edited by William Slikker Jr., Merle G. Paule, Cheng Wang.
- Format:
- Book
- Language:
- English
- Subjects (All):
- Neurotoxicology--Handbooks, manuals, etc.
- Neurotoxicology.
- Physical Description:
- 1 online resource (xvii, 598 pages) : illustrations, charts
- Edition:
- Second edition.
- Place of Publication:
- London : Academic Press, [2018]
- Summary:
- Handbook of Developmental Neurotoxicology, Second Edition, provides a comprehensive view of the fundamental aspects of neurodevelopment, the pathways and agents that affect them, relevant clinical syndromes, and risk assessment procedures for developmental neurotoxicants. The editors and chapter authors are internationally recognized experts whose collaboration heralds a remarkable advance in the field, bridging developmental neuroscience with the principles of neurotoxicology. The book features eight new chapters with newly recruited authors, making it an essential text for students and professionals in toxicology, neurotoxicology, developmental biology, pharmacology, and neuroscience.- Presents a comprehensive, up-to-date resource on developmental neurotoxicology with updated chapters from the first edition- Contains new chapters that focus on subjects recent to the field- Includes well-illustrated material, with diagrams, charts, and tables- Contains compelling case studies and chapters written by world experts
- Contents:
- Cover
- Title page
- Copyright page
- Contents
- List of Contributors
- Preface and Acknowledgments
- Part I - Cellular and molecular morphogenesis of the nervous system
- Chapter 1 - Brain Morphogenesis and Developmental Neurotoxicology
- I - Introduction
- II - Marr proposed computational models be integrated over three levels
- III - Morphogenetic features emerge from interactions across multiple levels of biological organization
- A - Sensory Pathways Encode Features of Sense Organs and the Environment
- B - Neurovascular Coupling (NVC) is Essential to Brain Connectivity
- C - Engrams Exist at Multiple Structural Levels
- IV - Whole Brain Assessment of Larval Zebrafish Reveals Patterns of Connectivity
- V - Conclusions: morphology informs predictive models of developmental neurotoxicity
- Acknowledgments
- Abbreviations
- References
- Further Reading
- Chapter 2 - Neural Cell Adhesion Molecules in Normal and Abnormal Neural Development
- II - The expression levels of NCAM and PSA-NCAM during the development
- III - Regulating PSA-NCAM expression and cell migration
- IV - Requirement of PSA-NCAM for activity-induced synaptic plasticity
- Chapter 3 - Neurite Development and Neurotoxicity
- A - Molecular Mechanisms Underlying Neurite Growth
- 1 - Applications in Neurotoxicology: Addressing Molecular Mechanisms
- B - Genetic Modulation of Neurite Development
- 1 - Examples of Genetic Modulation by Neurotoxicants
- C - Cell Death Mechanisms and Neurite Development
- 1 - Relevance to Neurotoxicology: Addressing Cell Death Mechanisms
- D - Stem/Progenitor Cells and Neurite Development
- 1 - Applications of Stem Cell Technology for Neurotoxicology
- E - Neurite Growth and State-of-the-Art Techniques
- 1 - Overview
- 2 - High-Content Imaging.
- 3 - Applications Using HCI
- 4 - Three-Dimensional Approaches
- a - Organotypic Culture Technique for Assessing Neurite Growth
- b - 3D Cell Culture
- 5 - Nanotechnology and Neurite Development
- a - Applications of Nanotechnology
- b - Neurotoxicity of Nanomaterials
- 6 - Bioengineering and Neurite Development
- a - De Novo Measurement of Neurite Growth
- b - Bioengineering-Induced Neurotoxicity Related to Neurite Development
- II - Conclusions
- Acknowledgment
- Chapter 4 - Myelin: Structure, Function, Pathology, and Targeted Therapeutics
- II - Myelin architecture and assembly: old and new perspectives
- A - Traditional View of Myelin
- B - Recent Findings: Myelin Structure and Functions
- III - Neuron-glia communication and its regulation
- IV - Myelinating glial cell lineages in peripheral and central nervous systems
- A - Schwann Cells
- B - Oligodendrocytes
- V - Chemical composition of vertebrate myelin
- VI - Dysmyelination: myelin mutant models for dysmyelination
- VII - Demyelination: effect of various factors on developmental myelination
- A - Malnutrition
- B - Thyroid Deficiency
- VIII - Remyelination and CNS disorders: myelin to axonal regeneration
- IX - Newer treatment strategies for myelin disorders
- X - Conclusions
- Part II - Developmental neurobiology/toxicology
- Chapter 5 - Neurotrophic Factors
- I - Neurotrophic factors
- II - Expression pattern and regulation
- III - Neurotrophin receptors
- IV - Neurotrophic factors in cell survival and cell death
- V - Neurotrophins and synaptic plasticity
- VI - Neurotrophins and behavior
- VII - Other neurotrophic factors
- VIII - Clinical correlates to neurodegenerative disorders
- IX - Clinical correlates to psychiatric disorders
- X - Genetic polymorphisms.
- XI - Neurotrophins as therapeutic agents
- Chapter 6 - Serotonin Signaling as a Target for Craniofacial Embryotoxicity
- I - Introduction-Serotonin and Embryonic Development
- II - Serotonin signal transduction
- A - Serotonin Release and Selective Serotonin Reuptake Inhibitors
- B - Serotonin Receptors and Receptor Antagonists
- III - Role of serotonin in development
- A - Placental Transfer of Serotonin
- B - Serotonin and Craniofacial Development
- C - Embryonic Precursors of the Facial Skeleton
- D - Serotonin and Neural Crest Cells
- E - Importance of Proper Orofacial Osteogenesis to Orofacial Development
- F - Serotonin and Bone Development
- IV - Conclusions
- Chapter 7 - Neurotoxic and Neurotrophic Effects of GABAergic Agents on the Developing Brain
- II - The GABAergic system during development
- III - GABAergic agents and consequences of perturbations of GABAergic system development
- IV - Animal models of GABAergic system perturbation
- V - In vitro and cell-based models of GABAergic system perturbation during neurodevelopment
- VI - Bioinformatic and computational approaches
- VII - Protecting the developing GABAergic system: prospects for the future
- Chapter 8 - Neural Stem Cell Biology and Application to Developmental Neurotoxicity Assessment
- I - Neural stem cells in the developing brain
- II - Neural stem cells in the adult brain
- III - NSCs-derived from embryonic stem cells and induced pluripotent stem cells
- IV - Application of NSCs to developmental neurotoxicity assessments
- A - Status of Developmental Neurotoxicity Tests
- B - Considerations on the Utilization of NSCs as an In Vitro Model for DNT Assessment
- V - Conclusions
- Further Reading.
- Chapter 9 - Apoptosis as a Mechanism of Developmental Neurotoxicity
- II - Molecular Mechanisms of Apoptosis in the Developing Nervous System
- III - Physiological Roles of Apoptosis in Neurodevelopment
- IV - Chemical-Induced Apoptosis
- A - Anesthetics
- B - Polychlorinated Biphenyls
- C - Zinc
- Chapter 10 - Periods of Susceptibility: Interspecies Comparison of Developmental Milestones During Ontogenesis of the Central Ne...
- II - Overview of central nervous system development
- A - Neural Tube Formation
- B - Cellular Components of the Neural Plate
- C - Primary Neurulation
- D - Formation of Cerebral Vesicles
- E - Secondary Neurulation
- F - Intramural Development and Nuclei
- III - Developmental milestones
- A - Externally Observed Central Nervous System Developmental Milestones
- B - Internally Observed Central Nervous System Developmental Milestones
- C - Developmental Milestones Related to Myelination
- D - Developmental Milestones of Cerebral Cortex
- Chapter 11 - Modeling the Neurovascular Unit In Vitro and In Silico
- II - Animal models of BBB development and function
- III - Cell-based models
- IV - Static three-dimensional (3D) models
- V - Organotypic culture models (OCMs) and microphysiological systems(MPS)
- VI - Implementing in vitro BBB models for DNT
- VII - In silico models: BBB permeability
- VIII - In silico models: virtual NVU
- IX - Summary and conclusions
- Chapter 12 - Zebrafish as a Model for Developmental Biology and Toxicology
- II - Developmental biology
- A - Gastrulation
- B - Organogenesis
- C - Neurodevelopment
- D - Neurulation
- E - Neurogenesis
- F - Eye
- G - Brain.
- H - Behavior
- III - Developmental toxicology
- A - Assessments and Chemicals Screened
- 1 - Fish Embryo Acute Toxicity (FET) Test
- 2 - Morphological Screens
- 3 - Behavioral Assays
- B - Advancements
- IV - Concordance with mammalian models
- Chapter 13 - Using Caenorhabditis elegans to Study Neurotoxicity
- II - Studies of specific neurotoxins
- A - Manganese
- B - Selenium
- C - Methylmercury
- D - Other Toxins
- III - Anesthetic-induced neurotoxicity
- Part III - Synaptogenesis and neurotransmission
- Chapter 14 - Human 3D In Vitro Models for Developmental Neurotoxicity
- I - Developmental neurotoxicity represents a societal testing need
- II - The current testing approach for DNT in vivo and in vitro does not satisfy our needs
- III - The process of developing in vitro strategies for DNT
- IV - The development of a reproducible BMPS for modeling neurodevelopment and testing its perturbation
- V - Ongoing developments of the mini-brain
- VI - Conclusions
- Chapter 15 - Ontogeny of Monoamine Neurotransmitters
- II - Innervation of terminal fields
- A - Ontogeny of Dopaminergic Innervation
- B - Ontogeny of Noradrenergic Innervation
- C - Ontogeny of Serotonergic Innervation
- III - Neurochemical synaptogenesis
- A - Neurotransmitter Content
- 1 - Dopamine
- 2 - Norepinephrine
- 3 - Serotonin
- B - Biosynthetic Enzymes
- 1 - Tyrosine Hydroxylase
- 2 - Dopamine β-Hydroxylase (DβH)
- 3 - Tryptophan Hydroxylase (TPH)
- C - Reuptake Systems
- 1 - High-Affinity DA Uptake
- 2 - High-Affinity NE Uptake
- 3 - High-Affinity 5-HT Uptake
- D - Monoaminergic Receptors
- 1 - Dopaminergic Receptors
- 2 - Noradrenergic Receptors
- 3 - Serotonergic Receptors.
- a - Developmental neurotoxicity of amphetamine-type stimulants.
- Notes:
- Includes bibliographical references and indexes.
- Description based on print version of record.
- ISBN:
- 0-12-809394-3
The Penn Libraries is committed to describing library materials using current, accurate, and responsible language. If you discover outdated or inaccurate language, please fill out this feedback form to report it and suggest alternative language.