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36 Cards in this Set
- Front
- Back
What are the sources of brain damage?
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-brain tumors
-cerebrovascular disorders -infections of the CNS -Neuropsychological Diseases -Contusions -Genetic Syndromes |
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glial tumors
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glial tumors are a type of brain tumors that arise from glial cells in the brain; glial tumors are 40% of brain tumors
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meningiomas
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meningiomas are tumors between the meninges that are often encapsulated and benign (20% of brain tumors are meningiomas)
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metasteses
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metastestes are cancer cells that come from other organs, such as thee lungs, skin, etc. (20% of brain tumors are metastestes)
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cerebral hemorrhage
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A CEREBRAL HEMORRHAGE is a cerebro-vascular disorder (stroke) that is characterized by bleeding in the brain and may be caused by a ruptured aneurysm.(15% of cerebro-vascular disorders are cerebral hemorrhages)
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cerebral ischemia
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CEREBRAL ISCHEMIA
-cerebro-vascular disorder (stroke) -caused by disruption of blood supply -may be caused by a clogged blood vessel -85% of cerebro-vascular disorders are cerebral ischemias (compared to the 15% that are cerebral hemorrhages) |
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cerebro-vascular disorders
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cerebro-vascular disorders- strokes
-cerebral hemorrhage-bleeding in the brain that may be caused by a ruptured aneurysm -cerebral ischemia- disruption of the blood supply that may be caused by a clogged blood vessel (85%) |
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types of cell death
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-apoptosis- programmed cell death
-necrosis- sudden, unexpected cell death |
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apoptosis
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programmed cell death
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necrosis
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sudden, unexpected cell death
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Infections of the CNS
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-syphilis- bacterial infection
-meningitis- bacterial infection/viral infection -rabies- viral infection -herpes- viral infection |
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syphilis
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syphilis is a bacterial infection of the cns
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meningitis
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meningitis is a bacterial/viral infection of the CNS
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rabies
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rabies is a viral infection of the CNS
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herpes
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herpes is a viral infection of the CNS
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Neuropsychological Diseases- name them
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NEUROPSYCHOLOGICAL DISEASES
-Parkinson's disease -Huntingtin's disease -Alzheimer's Disease -Epilepsy -Multiple Sclerosis |
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What system is Parkinson's disease?
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Parkinson's disease is a disease of the extra-pyramidal system
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What system is Huntingtin's Disease?
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Huntington's Disease is a disease of the extra pyramidal system
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Parkinson's disease vs. Huntingon's disease: how often do they occur in the population?
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Parkinson's disease occurs in about 0.5% of the population but Huntington's Disease is much less common than Parkinson's Disease
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Symptoms of Parkinson's disease
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symptoms of parkinson's disease include difficulties initiating voluntary movements, tremor during inactivity, muscle rigidity. Usually no dementia.
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Symptoms of Huntinton's Disease
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Huntington's disease symptoms include:
-uncontrolled rapid movements of the limbs -severe dementia |
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Are their genetic factors in Parkinson's vs Huntington's Diseases?
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Parkinson's disease has no one genetic factor linked to the disease; Huntington's has a clear genetic cause
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Treatment for Parkinson's vs. Huntington's Diseases?
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Parkinson's disease is treated with agonists of the dopamine system; Huntington's disease has no effective treatment
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What causes Alzhemier's disease?
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Alzheimer's disease is caused by amyloid plaques (outside neurons) and neurofibrillary tangles (inside neurons)
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what parts of the brain are most affected in alzheimer's disease?
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-most affected: amygdala, enterohinal cortex, hippocampus
-less affected: prefrontal cortex, posterior parietal cortex, inferior temporal cortex *Note that THE MEDIAL TEMPORAL LOBE IS AFFECTED! The hippocampus and other medial temporal lobe structures are involved in the formation of new memories. |
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Neuronal and transneuronal degeneration following axotomy
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NEURAL DEGENERATION
1. axotomy- the axon of the neuron is cut 2. anterograde degeneration- then, the distal portion of the damaged neuron degenerates 3. retrograde degeneration-then, the proximal portion of the damaged neuron may degenerate 4. transneuronal degeneration- then, neurons that synapsed on the damaged neuron may degenerate and so too may neurons on which the damaged neuron synapsed |
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axotomy
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the axon of a neuron is cut in an axotomy --- this causes neural degeneration (axotomy is followed by anterograde degeneration, retrograde degeneration, & then transneuronal degeneration)
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anterograde degeneration
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-anterograde degeneration (2) happens after the axotomy (1)
-in anterograde degeneration, the distal portion of the damaged neuron degenerates -anterograde degeneration is the second step in neural degeneration (1. axotomy 2. anterograde degeneration 3. retrograde degeneration 4. transneuronal degeneration) |
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retrograde degeneration
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Retrograde degeneration (3 of 4 steps of neural degeneration)
-the proximal portion of the damaged neuron may degenerate and this is called retrograde degeneration |
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transneuronal degeneration
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-transneuronal degeneration is the final (4th) step in neural degeneration (1. axotomy 2. anterograde degeneration 3. retrograde degeneration 4. transneuronal degeneration)
-in transneuronal degeneration, the neurons that synapsed on the damaged neuron may degenerate and so too may neurons on which the damaged neuron synapsed |
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Neural Regeneration: by which cells does this happen?
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Oligodendrocytes (in the CNS): block regeneration
Schwann cells (in the PNS): promote regeneration |
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what happens when a nerve is damaged without severing the schwann cell sheaths?
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When a nerve is damaged without severing the Schwann Cell scheathes (e.g. crushing) individual axons regenerate to their correct targets
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what happens when a nerve is damaged and the severed ends of the Schwann cell sheaths are slightly seperated?
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When a nerve is damaged and the severed ends of the schwann cell sheaths are slightly seperated, individual axons often regenerate up incorrect sheaths
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what happens when a nerve is damaged and the Schwann cell sheaths are widely seperated?
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When a nerve is damaged and the Schwann cell sheaths are widely seperated, there is typically no regeneration
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cells that block regeneration in the CNS
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Oligodendrocytes block regeneration in the CNS
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cells that promote regeneration in the PNS
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Schwann cells promote regeneration in the PNS
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