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Neuroplasticity in adults

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Presentation on theme: "Neuroplasticity in adults"— Presentation transcript:

1 Neuroplasticity in adults
Domina Petric, MD

2 Synaptogenesis is creation of new synapses.
Synaptogenesis is most active in the early postnatal life up to 3 years. Leonard E. White, PhD, Duke University

3 Brain size in autism spectrum disorder
There is an increased synaptogensis in early postnatal life with brain overgrowth. There is increase in size of frontal and temporal cortex, amygdala and cerebellum in comparisson to the normal brain. The overgrowth of the brain tends to normalize with the time, but aberrant connections remain during the adult life. Leonard E. White, PhD, Duke University

4 There is decrease in rate of synaptogenesis.
Brain size in ADHD There is decrease in rate of synaptogenesis. Frontal and temporal cortex is thinner than in children without ADHD. Leonard E. White, PhD, Duke University

5 Loss of synaptic connections is accelerated in individuals with ADHD.
Gray matter volume There is a reduction in gray matter volume during the childhood and adolescence: loss of synaptic connections. Loss of synaptic connections is accelerated in individuals with ADHD. Leonard E. White, PhD, Duke University

6 White matter volume There is an increase in white matter volume during childhood and adolescence: increase of myelination, increase of axons diameter and/or increase in number of axons. Leonard E. White, PhD, Duke University

7 Overall brain size There is increase in brain size during first decade of life and in second decade of life there is a plato of the brain size. In the third decade of life there is a gradual decline in brain size: gray matter is declining, whilst white matter is expanding. In the fourth decade of life there is a reduction in both gray matter and white matter of brain. Decrase in brain size is due to reduction of myelin (white matter) and reduction of synapses (gray matter). Loss of neurons is pathological and it is not attributable to normal brain aging. Leonard E. White, PhD, Duke University

8 Peripheral nerve injury and regeneration
Injured axon has a significant regenerative capacity. When there is injury to an axon, there will be degeneration of distal parts from the injured site. Macrophages invade the injured region and consume debris. Schwann cells then will proliferate and will create a chanel through wich the regenerating axon will hit his proximal target. Schwann cells are key mediators of regeneration and regrowth of injured axon. They release axon growth-promoting signals and neurotrophins that will activate expression of growth-related genes in neuron body. Leonard E. White, PhD, Duke University

9 Peripheral nerve injury and regeneration
There is never a full functional recovery of injured peripheral nerve. Leonard E. White, PhD, Duke University

10 Excitotoxicity is destruction of neurons due to release of GLUTAMATE.
This can happen during acute injury to the nervous system. Leonard E. White, PhD, Duke University

11 GROWTH FACTOR WITHDRAWAL
Apoptosis stimuli DNA damage HYPOXIA STRESS GROWTH FACTOR WITHDRAWAL Leonard E. White, PhD, Duke University

12 Apoptosis Apoptosis stimuli interupt the normal function of Bcl-2 signal. When Bcl-2 is blocked, cytochrome C is released by mitochondria leading to the activation of CASPASE-9 and CASPASE-3. Apoptosis is then activated: chromosome condensation DNA fragmentation membrane blebbing cytoskeletal changes Leonard E. White, PhD, Duke University

13 Penumbra Penumbra relates to the neurons just peripheral to the injured site in CNS. These neurons will survive. Glial cells proliferate in the site of injury and release chemical signals that have negative effect on the growth and regeneration of survived neurons. Microglia phagocites the debris. Oligodendrocytes then proliferate. Glial cells will form a scar of tissue. Regeneration of axons that run through the white matter of the brain is difficult because of negative glial cells effect on growth and regeneration. Leonard E. White, PhD, Duke University

14 Penumbra Neurons that have axons in gray matter (horizontal axons) will regenerate because they are not that much exposed to suppressive signals of the neuroglia: adaptive plasticity after injury. Leonard E. White, PhD, Duke University

15 Adult neurogenesis Production of new neurons in adult human brain is limited to a special set of stem cells in the basal region of the dentate gyrus of the hippocampus. This is important for learning and creation of new memories. Leonard E. White, PhD, Duke University

16 Literature Leonard E. White, PhD, Duke University Leonard E. White, PhD, Duke University


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