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37 Cards in this Set

  • Front
  • Back
What types of cells are there in the brain?
Neurons and glia. Glia are 10 times more common than neurons.
Name the major glia cells (and functions).
Astrocytes (nutritional, scavenger and help in blood-brain behavior) and oligodendroglia (create myelin for axons in the brain -- Schwann cells do this in the rest of the CNS and PNS). Functions of both not fully understood.
Define apoptosis.
Pruning of nerve cells that takes place in maturation to enhance the creation of neuronal pathways.
What can enlarged ventricles indicate?
Hydrocephalus or brain atrophy (ventricles expand to fill the space).
What are the symptoms of NPH?
NPH (Normal Pressure Hydrocephalus) is usually marked by: 1)incontinence, 2)clumsy, wide-based gait, and 3) disorientation including memory problems. The symptoms appear in the OPPOSITE order of Alzheimers (which starts with memory problems and ends with gait problems and incontinence).
What can the cognitive symptoms of NPH be similar to?
Symptoms are often similar to frontal lobe damage. Not surprising because expanding lateral ventricles put pressure on this area. (Cognitive symptoms are disorientation, confusion, apathy, decreased attention, motor slowing, and impaired new learning.)
Name the parts of the hindbrain.
Medulla, Reticular Formation (which encompasses the RAS), Pons, and Cerebellum.
RAS: location, function, and symptoms of lesions.
Reticular Activating System. From upper spinal cord, through medulla into diencephalon (thalamic area). Modulates wakefulness, and alerts organism. Lesions result in somnolence, stupor or coma.
Pons: location, function, and symptoms of lesions.
Inferior to midbrain. Pons and cerebellum coordinate postural and kinesthetic info. Lesions cause motor, sensory and coordination problems.
Cerebellum: location, function, and symptoms of lesions.
Inferoposterior position in brain. Proximal to pons. Primarily motor function. Lesions typically result in dizziness (vertigo, because connected to vestibular system), clumsiness (loss of fine motor control), and nystagmus; but can also disrupt abstract thinking, linguistic processing and other cognitive processes.
Midbrain: location, function, and symptoms of lesions.
Superior to Pons, inferior to Thalamus. Critical area containing RAS necessary for conscious experience. Lesions can result in death.
Thalamus: location, function, and symptoms of lesions.
Together with hypothalamus, most important structures of diencephalon. Relay center for all senses except smell. Lesions can result in loss of body sensation, unilateral inattention (opposite the side of the lesion), and in Korsakoff's syndrome when in dorsomedial nucleus. Memory impairments from thalamic regions characterized by anosognosia.
Hypothalamus: location, function, and symptoms of lesions.
Under the thalamus. Regulates appetite, thirst, and sex drive. Lesions can drive all these one way or the other. Damage to mammillary bodies can affect memory.
Name the components of the basal ganglia.
Caudate nucleus, putamen and globus pallidus (aka lenticular nucleus), amygdala, subthalamic structures, and substantia nigra.
Basal Ganglia: Function and lesions.
Neostriatum (caudate and putamen) translates cognition into action. Lesions primarily affect motor activity, e.g. Parkinson's affects neostriatum resulting in poverty of movement, and Huntington's affects caudate resulting in excessive motor activity.
Limbic System: Function and lesions.
Cingulate gyrus, hippocampus, and (in some systems) amygdala. Emotional memory. Lesions disturb emotional behavior (often anergic effect with loss of fear, etc.)
Amygdala: Location, function and lesions.
Temporal lobe. Direct connection with olfactory bulbs. Damage associated with hypersexuality and decreased aggression (Kluver-Bucy syndrome when uncus also destroyed--inability to learn, excessive eating and hypersexual). Implicated in autism.
Cingulate gyrus: Location, function and lesions.
Superior to corpus callosum. Anterior cingulate senses errors and conflicts during information processing and processes pain; connected to amygdala. Posterior cingulate involved with memory formation; connected to hippocampus.
Hippocampus: Location, function and lesions.
Runs the length of the interior of the temporal lobe, connected to entorhinal cortex, thalamus and fornix. Only sensorimotor skill learning and simple conditioning take place in other brain centers. Basically creates memories that are then stored elsewhere. Lesions usually result in anterograde amnesia. Hippocampus appears to be lateralized (left-verbal, right-spatial).
Name intracerebral pathways.
1) Association fibers (between cortical areas);
2) Commissural fibers (between hemispheres, mainly corpus callosum, also anterior and posterior commissure);
3) Projection fibers (cortical to subcortical and vice versa).
Result of agenesis of corpus callosum.
Typically no noticeable effects, except for slowed performance of intracerebral processing (incorporating visual and linguistic information) including higher order thought.
True or false. Vision from the right eye maps to the left occipital lobe and vice versa.
False. The left field of vision of both eyes maps to the right occipital lobe, and the right field of both eyes maps to the left occipital lobe.
Homonymous hemianopsia.
Lack of vision in both eyes in the same visual field (either right or left).
Scotoma.
Circumscribed field defects in either one or both eyes (pl. scotomata).
True or false. The auditory nerves map just like the optic nerves.
False. The auditory nerves are mainly ipsilateral, although some information is relayed to the opposite temporal lobe.
Lateralization.
Tendency of each hemisphere to specialize. Left towards linear processing (including rapid motor movements). Right towards spatial configuration and symbolic processing.
Apperceptive visual agnosia.
Inability to recognize that seen details are part of a whole object (not a recall problem).
Associative visual agnosia.
Inability to recognize a whole perceived object. Distinguished from a naming problem by the ability to identify an object through other senses.
Balint's syndrome.
Aka simultanagnosia. The inability to perceive more than one object at a time.
Visual neglect.
Aka visual inattention. Usually the result of both occipital damage and right parietal lobe damage.
Prosopagnosia.
Result of bilateral damage to undersides of occipital and temporal lobes (such as incurred in TBI by movement of the brain along the fossa).
The "where" pathway.
Parieto-occipital (dorsal)pathway. Orients an object's location.
The "what" pathway.
Temporo-occipital (ventral)pathway. Names an object.
Apraxia.
More precisely, an inability to perform previously learned, complex motor-skills. The term is also used more generally although this is to be avoided.
Posterior lesions. Right versus left.
Tends to disrupt constructional ability. Left usually interrupts sequenced motor activity necessary for constructional activity. Right usually creates defective spatial imagery.
Astereognosis.
Inability to identify an object by tough. Unilateral lesion in association area posterior to postcentral gyrus usually produces a contralateral effect, though right lesions can affect both sides.
Sensory neglect.
Neglect of one side upon double simultaneous stimulation. Not a perceptual fault. Associated with lesions to posterior association cortex (most often the right).