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86 Cards in this Set

  • Front
  • Back

scientific method

observation, replication, interpretation, verification,

areas of neuroscience

molecular, cellular, systems, behavioral, cog

egypt beliefs about brain

knew about brain damage, had hieroglyph, said heart key to soul and memories stores there, discarded the brain

hippocrates

said brain is the center of sensation and intelligence, epilepsy was a brain disease

alcmaion of crotona

described the optic nerve (500BC)

plato

(387BC)believes brain is the center of mental processes

aristotle

(384-322BC) heart was the center intelligence, brain simply cooled the blood

Galen

(AD 130-200) similar view to hippocrates, many dissections, tried to determine the function of the brain structure (doctor to the gladiators, saw lots of body parts)

galens belief about memory formation

beleived that since the cerebrum felt soft, sensations and memory formed here, cerebellum felt hard and thus muscle control here, also that brain receieved sensory info


believed nerves were hollow tubes, humors (vital fluids) flowed to brain ventricles

descartes

(1596-1650) believed in fluid-mechanical theory, but that human abilities came form the "mind" which communicated to brain via pineal gland

grey matter from white matter, peripheral and central divisions, every brain has some general pattern of gyri and sulci

17th and 18th century scientists studied the brain in more detail, distinguished...

grey matter

cell bodies

white matter

nerve fibers, make up nerves

central sulcus

in between the frontal and parietal lobe

sylvian fissure

in between the frontal lobe/parietal lobe and temporal lobe

nerves as wires: electricity stimulates muscle movement, brain generate electricity

19th century views on the the brain, galvani and dubios

dorsal roots

spinal information in

ventral roots

motor info out

localization of function

these scientists (broca, fritsch and hitzig, ferrier, munk) who believed in this theory

Bell (1811)

proposed that motor fibers come from cerebellum and sensory fibers go to cerebrum

Flourens (1823)

used experimental ablation to show bells thing was correct


believed all parts of the cerebrum contributes to all functions (wrong)

Gall (1809)

believed in phrenology, brain divided into 35 regions (wrong)

broca

believed that different functions localized to different areas

fritsch and hitzig

(used dogs and frogs in 1870) showed specific region of brain controlled movement


ferrier did this with monkeys and removal caused paralysis

munk

showed that the occipital lobe required for vision

evolution of nervous system

darwin origin of species, nervous sustems have evolved and are related, different animals better at specific functions

various animals good for studying specific aspects of the nervous system

squid, snail (basic biology of neurons and synaptic transmission


cats, primates-visual system


rate, mice: neuropharmacology and behavioral studies


worm, fruit fly, zebrafish

animal testing considerations

small number actually used, mostly rats and mice


major discoveries


anternative, anesthia review committees

nuerons and glia

2 major cell types

oxygen and glucose

nervous system uses a large amount of these molecules

neurons

only 10-20% of total cells in the the nervous system


0.01- 0.0 mm in diameter (comparable to other cells)

nissl stain

stains all neurons, but only the cell bodies, stained the rough ER on cells

golgi stain

stains all parts of the neuron, but not every neuron

axons and dendrites

2 types of neurites

reticular theory

golgi supported this theory that neurites fuse together like the circulatory system (exception to the cell theory)

cajal

believed that neurites are not continuous and communicate by contact (mostly correct)

soma

cell body, same as for many cells, 20micrometers, nucleus 5-10 micrometers

rough ER

more of this cell structure is in neurons and glia than most other cells

nissl bodies

rough ERs in the neuron

mitochondria

widespread throughout the cytoplasm and presynaptic region, generates ATP and helps provide for the large energy needed by the brain

neuronal membrane

5nm thick


many proteins embedded in it


composition of proteins varies from soma, axon, dendrites

microtubules, microfilaments, neurofilaments (also called intermediate filaments)

types of structures that make up the cytoskeleton

microtubules

20nm diameter


made of polymers of tubulin


not static


associated with other proteins (MAPS)


tau form seen in alzheimers tangles


involved in axoplasmic transport


microfilaments

5nm in diameter


numerous in neurites


made of two thin strands of actin polymers


not static


closely associated with membrane


often in synaptic terminals and dendritic spines

neurofilaments

10nm diameter


strong, helps maintain neuronal shape/structure


form tangle in alzheimers

neurofilaments

can stain for this when looking for degeneration in the form of tangles in the brain

axons

unique to neurons


has NO rough ER, but a few ribosomes


must be some ribosomes because some mRNA is transferred to the end of the axon


different proteins in the membrane of this than the soma


can be 1mm to over a meter long


form branches/collaterals (some recurrent)


axon diameter

variable in axons, can range from 1um to 25um (1m in squid)


thicker=faster nerve impulse

axon hillock

beginning of axon, no ribosomes or any other organelles

terminal button/presynaptic axon terminal

end of the axon


no microtubules


many synaptic vesicles


protein rich


many mitochondria

synapse

2 sides pre and post


cleft in between, no direct contact


many drugs and chemicals act here


malfunctions here responsible for many mental disorders


synaptic tranmission

mediated by chemical neurotransmitter

wallerian degeneration

decribes that after the axon is cut, everything beyond the cut dies (axons need the cell body/soma to survive)

fast axoplasmic transport

axonal transport that transmits signals 1000mm per day

slow axoplasmic transport

axonal transport that transmits signals at 1-10 mm per day

anterograde axonal transport

axonal transport where kinesin walks down microtubules


Uses ATP


(fast or slow)

retrograde axonal transport

type of axonal transport along the microtubules


uses dynein


(fast 50-250mm/day)


from end back up

retrograde trasnport

can be used to trace synaptic connections


inect dye into brain and two days later has moved along microtubules and back to reveal syntaptic connections and axon branches

dendrites

come in different shapes and sizes


covered with 1000s of synapses



contain microtubules (fewer microfilaments)

spines

knobs of sides of dendrites


some dendrites covered in these


can change structure depending on type and amount of synaptic input


where many synapses form


correlates between structure and proper function





number of neurites, shape of dendritic tree, connectivity, axon length, neurotransmitter

4 ways to classify neurons

unipolar neurites

type of neurite: a single process with peripheral branch and central branch (one end for both receiving and sending from the soma)


found in sensory ganglia

bipolar neurites

found in the retina/ olfactory bulb (sensory structures


one receiving end and one sending end from the soma

multipolar neurites

have many dendrites, but a single axon


pyramidal cells and stellate cells

two types of dendritic structure classes in the brain

spiny

neurons with all pyramidal cell (some stellate)

Aspinous neurons

neurons with some stellate cells

stellate cell

cell with axon with a star shaped dentritic tree (lots of random dendrites

pyramidal cells in the cortex

cells in the cortex with a pyramid shaped cell body and less crazy dendritic tree

primary sensory neurons

category of neurons that receives input from skin, pain receptors etc

motor neurons

category of neurons that are generally in the spine


send axon out to the skeletal muscle


some are higher up in the brain

interneurons

category of neurons that encompasses most neurons


have sensory input into the spine and synapse out to complete the reflex


many have GABA

golgi type 1 neurons

characterized by axon length


projection neurons


extend between brain regions


long axons


many pyramidal cells

golgi type II neurons

characterized by axon length


local circuit neurons


connect to neurons in the vicinity


short axons


stellate cells

ACh, glutamate, GABA, serotonin, dopamine, opiods, etc

some types of neurotransmitters in the brain

astroctyes, oligodendroctyes, schwann cells,


microglia, ependymal cells

5 types of glia

glia

most of the cells in the brain, thought to be supportive of neuronal function,


some can act as stem cells


can support synapse formation

astrocytes

most numerous glia, provide structural support


remove nerutrans from synaptic cleft


regulate extracellular ion levels


can divide (source of majority of brain tumors)


express neurotransmitter receptors


regulate contents of extracellular space

oligodenrocytes and schwann cells

myelinating glia (2 types)

protoplasmic, fibrous, and muller

two types of astroctyes


protoplasmic

type of astrocyte that is in the grey matter and close to neurons, involved in the blood-brain barrier and metabolism

fibrous

type of astrocyte primarily in the white matter


repairs damaged tissue, may form scars

muller

type of astrocyte found in the retina

oligodendroglia

in the brain and spinal cord


myelinate several axons


has to make a lot of myelin to wrap around axons

schwann cells

myelinate only one axon per cell, one per every internode region


peripheral nervous system ONLY


nodes of ranvier

parts along the axon where Na+ can enter to keep the action potential flowing down the axon


myelination helps nothing to leak out except here where you want it to