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Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester [email protected] PS1000

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Page 1: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

Introduction to Neuroscience

Dr Claire Gibson

School of Psychology, University of [email protected]

PS1000

Page 2: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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1. Functional Neuroanatomy – The Nervous System and Behaviour

2. Development and Plasticity of the Nervous System

Page 3: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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Development of the NS

4 main stages1. Cell proliferation2. Migration3. Differentiation4. Synaptogenesis5. Neuronal cell death6. Synapse rearrangement7. Myelination

….more detailed 7 stages = PS2014/8

Page 4: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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1. Cell Proliferation• 250,000 new cells per minute• Neurogenesis = production of new nerve cells

• Proliferation occurs in the ventricular zone (cells then migrate to final destination)

• Nerve cells themselves do not divide• The cells that produce neurons divide (via mitosis) and =

layer of cells within the ventricular zone• Eventually some cells migrate away from ventricular

zone and begin differentiating into either a neuron or glia cell.

Page 5: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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• Historical opinion - at birth.• But, the human brain weight increases

following birth– simply due to growth in neuronal size, dendrite

branching, increased myelin ???

• NO - Neurogenesis occurs even in adulthood• Neurogenesis is sensitive to experience

– Learning enhances neurogenesis– Social isolation reduces neurogenesis

1. Cell Proliferation – when is it complete?

Page 6: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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• Newly formed neurones migrate from ventricular zone to their final destination

• Radial glial cells• Failure in mechanisms of

migration = behavioural disorders• Cell adhesion molecules (CAMs)

– Promote the adhesion of developing elements of the NS

– Guide migrating cells and growing axons

2. Migration

Page 7: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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3. Differentiation

• Cells reach their final destination – begin to express particular genes

• These enable cells to take on characteristics of a particular neuronal type

• PS2014/8

Page 8: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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4. SynaptogenesisCells undergo extensive growth of axons and dendrites = process

outgrowth and proliferation of synapses (i.e. synaptogenesis)

• Growth cones• Filapodia and lamellipodia – respond to the environment

and pull the growth cone in a particular direction• Chemoattractants• Chemorepellants

• Synaptogenesis occurs rapidly on dendrites and dendritic spines

Page 9: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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5. Neuronal cell death

• Normal part of development

• PS2014/8

Page 10: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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6. Synapse rearrangement

• Not simply elimination• Involves loss of some and formation of others• Human cerebral cortex = net loss of synapses

from late childhood until mid-adolescence

• What determines which synapses are kept and which ones are lost?– Neural activity– Neurotrophic factor = a target-derived chemical that

acts to ‘feed’ neurones

Page 11: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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Development of the NS

• Due to the interaction of intrinsic and extrinsic factors

• Intrinsic (i.e. genes) – originate from within the cell itself

• Extrinsic – originate from outside the developing cell e.g. nutrients, experience

Page 12: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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Genes are the intrinsic factors that influence NS development

• Genome (genotype) • The sum of all the intrinsic genetic information that an

individual possesses• Determined at the moment of fertilisation• Remains constant throughout our lives

• Phenotype• The sum of all the physical characteristics that make up an

individual• Changes constantly as we mature and age• Determined by the interaction of genotype and extrinsic factors

(including experience)

Page 13: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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• So, will two identical twins with identical genotypesa)Have the same phenotype? YES/NO

b)Behave exactly the same? YES/NO

Page 14: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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How does experience modify the NS?

• An individual’s experience during development alters many aspects of behaviour, brain anatomy and neurochemistry

• Much of the change resulting from experience involves reorganisation

• Reorganisation = a shift in connections that changes the function of an area of the brain

• E.g. blind people who read Braille, space in the brain devoted to the index finger increases

• E.g blind people who excel at sound localisation have recruited the unused visual area of their brain to aid in sound localisation

Page 15: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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The ‘plastic’ brain

• So, if experience can ‘reorganise’ the brain = the brain is described as being plastic

• Plasticity = the lifelong ability of the brain to reorganise neural pathways based on new experiences

• Why is this important?• To enable us to learn• As an adaptive mechanism to compensate for lost function

and/or to maximize remaining functions in the event of brain injury.

Page 16: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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Damage and recovery to the CNS

• Scientists are interested in the development of the NS– Hope to find clues about how to repair the NS

when it is damaged by injury, disease or developmental error

– PS2014/8

Page 17: Introduction to Neuroscience Dr Claire Gibson School of Psychology, University of Leicester cg95@le.ac.uk PS1000

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Summary

• Neurogenesis, migration, differentiation, synaptogenesis, neuronal death, synapse rearrangement, myelination

• Intrinsic and extrinsic factors

• Role of experience