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Chapter Five Development and Plasticity of the Brain. Development of the Brain. Growth and Differentiation of the Vertebrate Brain Early Beginnings CNS begins to form at two weeks gestation Development of the neural tube (figure 5.2) At birth, brain weighs 350g, at one year 1,000g
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Development of the Brain Growth and Differentiation of the Vertebrate Brain Early Beginnings CNS begins to form at two weeks gestation Development of the neural tube (figure 5.2) At birth, brain weighs 350g, at one year 1,000g Growth and Development of Neurons Proliferation-production of new cells Migration-move toward final destination Differentiation-form axons and dendrites Myelination-addition of insulating sheath
Figure 5.2 Early development of the human central nervous systemThe brain and spinal cord begin as folding lips surrounding a fluid-filled canal. The stages shown occur at approximately age 2 to 3 weeks.
Figure 5.3 Human brain at five stages of developmentThe brain already shows an adult structure at birth, although it continues to grow during the first year or so. Video
Development of the Brain Determinants of Neuron Survival Must make correct connections Must receive support from nerve growth factor neurotrophins act in several ways early in development cause cells to survive and grow increase the branching of incoming axons decrease pain and increase regrowth of damaged axons apoptosis-programmed cell death that occurs when connections are not reinforced Competition Among Axons as a General Principle We produce redundant synapses the most successful axons and combinations survive
Development of the Brain Pathfinding by Axons Chemical Pathfinding by Axons Example: Weiss and the grafted salamander leg Specificity of Axon Connections Example: Sperry and the rotated eye of newt Chemical Gradients cell surface molecule chemical attractants Neurotrophins
Figure 5.7 Summary of Sperry’s experiment on nerve connections in newtsAfter he cut the optic nerve and inverted the eye, the optic nerve axons grew back to their original targets, not to the targets corresponding to the eye’s current position.
Development of the Brain Fine-Tuning by Experience Effects of Experience on Dendritic Branching Enriched environments increase dendritic branching Generation of New Neurons stem cells in the interior of the brain scientists have observed new cells in hippocampus and cerebral cortex
Development of the Brain Effects of Experience on Human Brain Structures Example: music training on temporal lobe development Example: somatosensory cortex in violin players Combinations of Chemical and Experiential Effects
Development of the Brain The Vulnerable Developing Brain Fetal Alcohol Syndrome decreased alertness, hyperactivity, varying degrees of mental retardation, motor problems, heart defects, and facial abnormalities Fetal Nicotine Exposure low birthweight, SIDS, decreased intelligence, hyperactivity Fetal Cocaine Exposure decrease in IQ and language skills
Recovery of Function After Brain Damage Causes of Human Brain Damage closed head injury-sharp blow to the head resulting from a fall, an automobile accident, a sports accident, an assault, or other sudden trauma that does not actually puncture the brain stroke-loss of normal blood flow to a brain area ischemia-blood clot or other obstruction closes an artery hemorrhage-when an artery ruptures tissue plasminogen activator-breaks up blood clots
Figure 5.20 Mechanisms of neuron death after stroke Procedures that can preserve neurons include removing the blood clot, blocking excitatory synapses, stimulating inhibitory synapses, blocking the flow of calcium and zinc, and cooling the brain.
Recovery from Brain Damage Adjustments and Potential Recovery After Brain Damage Learned Adjustments in Behavior-making better use of unimpaired abilities Diaschisis-decreased activity of surviving neurons after other neurons are damaged The Regrowth of Axons peripheral axons can regrow axons will only regrow very short distances axons regrow better in the young
Recovery from Brain Damage Adjustments and recovery cont’d Sprouting-when nearby, uninjured cells form new branches to the vacant synapses Denervation Supersensitivity-heightened sensitivity to a neurotransmitter after the destruction of an incoming axon Reorganized Sensory Representations and the Phantom Limb Effects of Age Older people do not recover as well as younger people, although, there is a delicate balance here because the very young brain is also more vulnerable
Figure 5.25 Collateral sprouting A surviving axon grows a new branch to replace the synapses left vacant by a damaged axon.
Figure 5.27 Demonstration of denervation supersensitivity Injecting 6-OHDA destroys axons that release dopamine on one side of the brain. Later amphetamine stimulates only the intact side of the brain because it cannot cause axons to release dopamine on the damaged side.Apomorphine stimulates the damaged side more strongly because it directly stimulates dopamine receptors, which have become supersensitive on that side.
Recovery from Brain Damage Therapies Behavioral Interventions Physical therapy Occupational therapy Speech therapy Drugs Nimodipine-prevents calcium from entering cells gangliosides-promote the restoration of damaged brains through unknown mechanisms progesterone-women with brain injury recover better than men and especially if the damage occurs when progesterone levels are high during their cycle
Recovery from Brain Damage Therapies Brain Grafts Used for Parkinson’s Disease Currently Experimental