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- Massachusetts
- Boston University
- Biology
- Biology 315
- Widmaier
- Ch 6: Neuronal Signaling and the Structure of the Nervous System
Ch 6: Neuronal Signaling and the Structure of the Nervous System
Biology 315 with Widmaier at Boston University
About this deck
By: Julie Mallon
Created: 2011-02-19
Size: 97 flashcards
Views: 34
Created: 2011-02-19
Size: 97 flashcards
Views: 34
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Neural Tissue
- CNS – brain and spinal cord
- peripheral (PNS) – nerves that connect the brain or spinal cord w/ the bodys muscles, glands, and sense organs
Neuron
neuron structure
- processes – long extensions that connect neurons to each other and perform input/output functions
- cell body = soma
- dendrites – branched outgrowths of the cell body – increase cell SA
- dendritic spines increase SA further
- ribosomes allow it to remodel their shape in response to variation in synaptic activity
axon
- axon - (nerve fiber) extends from body and carries output to target cells
- the region that arises from the cell body is the initial segment (or axon hillock)
- axon branches – collaterals
axon terminals
- releases neurotransmitters from the axon
- chemical messengers diffuse across an extracellular gap to the cell opposite the terminal
- some neurons release messengers from bulging areas along the axon known as varicosities
Schwann cells
- form sections of myelin sheaths along axons in PNS
- gaps in myelin called nodes of Ranvier where the plasma membrane is exposed to extracellular fluid
Axonal transport
- movement of organelles and materials b/w cell body and axon
- depends on rails of microtubule and specialized motor proteins called kinesins and dyneins
- anterograde – from cell body to axon terminals
- retrograde – from terminals to cell body
types of neurons
- afferent – convey info from tissues and organs to the CNS
- efferent – convey info away from the CNS to effector cells (muscle, gland, etc)
- interneurons – connect neurons w/in the CNS
types of neurons cont'd
- per 1 afferent, 10 efferent & 200,000 interneurons
- sensory receptors
- at the ends afferent neurons
- respond to physical and chemical changes in the environment
nerves
- groups of afferent and efferent neurons together with connective tissue and blood vessels in PNS
- CNS – afferent neurons have cell bodies outside of CNS whereas efferent neurons have cell bodies within CNS
synapse
- junction b/w 2 neurons
- communicate by neurotransmitters
- understand differences in the term ‘receptor’
- presynaptic neuron – conducts a signal -> synapse (terminal area)
- postsynaptic neuron – conducts a signal <- synapse (cell body/dendrite area)
Glial cells
90% of the CNS less than 50% of the volume b/c glial cells branch less surround soma, axon and dendrites of neurons provide physical and metabolic support godendrocyte – myelin covering cells
Glial cells cont'd
microglia – immune functions in the CNSependymal cells – line the fluid-filled cavities w/in the brain and spinal cord and regulate the production of cerebrospinal fluidSchwann cells (of the PNS) have most of the same characteristics
astrocyte
regs composition of extracellular fluid in CNS by removing K+ ions & neurotransmitters
stimulates formation of tight juncts b/w cells in capillaries
forms blood-brain barrier to prevent toxins from entering brain
provides glucose & removes NH3
Neural growth and regeneration
stem cells – precursor cells during developmentgrowth cone – a specialized enlargement at the tip of each axon to help it find the right targetmolecules on Glial and embryonic neurons affect pathway of axons
Neural growth and regeneration 2
neurotrophic factors – growth factors for neural tissue
molecules that affect axons when target is reached synapses form apoptosis – where most neurons self-destruct to fine-tune the CNS
Neural growth and regeneration 3
plasticity – the brain in early development have the ability to remodel due to stimulation or injuryaxons in the PNS can regenerate slowlyspinal cord injuries cause apoptosis
Resting membrane potential (RMP)
- potential across plasma membranes
- extracellular voltage = 0 V
- ions collect against the surfaces of the plasma membrane
- most of the fluids (intra/extracellular) are neutral
Magnitude of RMP
- diff in [specific ion] in intra & extracellular fluid
- diff in membrane permeabilities to different ions, reflecting the # of open channels
- equilibrium potent – membrane potent where 2 fluxes become = in magnitude but opp in direction – 0 net flux
Nernst Equation
- equilibrium potential for any ion species (p 144)
- GHK equation – calculate the potential of a membrane (Vm)
- leak K+ channels cause a concentration gradient
- electrogenic pump – moves net charge across the membrane directly causing the potential
Potentials
- depolarized – membrane is < - than resting level
- overshoot – reversal of memb potent polarity – becomes + relative to the outside
- repolarizing – memb potent that was depolarized returns toward RMP
- hyperpolarized – potent is more - than resting level
Graded potential
- changes in potential that are confined to a small region of the membrane
- signal over short distances
- produced when a specific change in the environment acts on a specialized region of the membrane
Graded potential 2
- charge flows b/w the place of origin and the potential and adjacent regions of the plasma membrane that are at resting potential
- local current is decremental – flow of charge decreases as the distance from the point of origin increases
Graded potential 3
- summation – addition stimuli occur before the graded potential dies, they are added to the depolarization from the first stimulus
- all cells are capable of producing graded potentials
- depolarize or hyperpolarize
Action potential
- large alterations in the membrane potential
- rapid, high frequencies
- excitable membranes – membranes capable of producing APs (neuron and muscle cells, etc)
- excitability - ability to generate
- only excitable membranes can produce APs
Voltage-gated ion channel
- ligand- & mechanically-gated - initial stimulus of an AP
- VG channels allow membrane 2 undergo APs
- Na+ channels have inactivation gates – limits Na+ flux by blocking channel shortly after depolarizing opens it
- Na+ channels opne/close faster than K+
VG ion channel mechanism 1
- depolarizing stimulus - stimulates the opening of VG Na+ channels and Na+ ions add to local membrane depolar
- memb reaches crit threshold potential, depolar becomes a + feedback loop – Na+ causes depolar, opening more channels and more Na+ released
VG ion channel mechanism 2
3. potential is overshot, and its + on the inside and – on the outside
4. membrane potential approaches peak and Na+ permeability declines as inactivation beaks the positive feedback cycle by blocking the open channels
VG ion channel mechanism 3
5. K+ channels open & flux out repolarizes the membrane to RMP - channels go from an inactive to a closed state
6. K+ permeability remains above resting levels and membrane is hyperpolarized toward the K+ equilibrium potent – afterhyperpolarization
VG ion channel mechanism 4
7. when K+ channels close, RMP is restored – K+ causes a neg feedback loop
8. only occur when the initial stimulus plus the current through the Na+ channels it opens are sufficient to elevate the membrane potential beyond the threshold potential
VG ion channel mechansim 5
9. stimuli just strong enough = threshold stimuli
10. < threshold level, + feedbacks cannot start – subthreshold potentials and stimuli
11. APs either occur maximally or not at all – once started they don’t depend on strength of stimuli
10. < threshold level, + feedbacks cannot start – subthreshold potentials and stimuli
11. APs either occur maximally or not at all – once started they don’t depend on strength of stimuli
Refractory periods
- absolute refractory period – when Na+ channels are open or have proceeded to the inactivated state due to an AP
- relative refractory period – with a great stimulus, can last longer & occur during afterhyperpolarization (as channels are closing)
Propogation
- depolar. of adj areas along a neuron to cause more APs
- not conducted decrementally like GPs
- refractory - only move in 1 direction
- not refractory - move in either direction
- salutatory conduction – APs seem to leap from 1 section to the next b/c myelin
Generation of action potentials
- receptor potential – initial depolarization achieved by a GP in afferent neurons
- generated in sensory receptors at peripheral ends
- synaptic potential – depolar is due to GP or synaptic input or a spontaneous change in potential (pacemaker potential)
Synapses
- membrane potent
- depolarized at an excitatory syn
- hyperpolarized at an inhibitory syn
- convergence – 1000s of synapses from diff presyn cells can affect a single postsyn cell
- divergence – a single postsyn cell can affect many other postsyn cells
Electrical synapse
plasma membranes of pre/postsynaptic cells joined by gap junctions depolarizes membrane of the second neuron and continues propagation of the action potential rapid communication b/w cells
Chemical synapse
axon of the presynaptic neuron ends in a swelling that holds synaptic vesicles that contain neurotransmitterspostsynaptic membrane has a high density of intrinsic and extrinsic proteins called the postsynaptic density
Chemical synapse cont'd
synaptic cleft – extracellular space – separates the neurons and prevents direct propagationcotransmitter – if more than one transmitter is releasedusually operates in only one direction
Neurotransmitter release
active zones – presynaptic membrane release regionsrelease is initiated when an action potential reaches the terminal o fthe presynaptic membraneCa2+ flows into the axon terminalvesicles connected to SNARE proteins
Neurotransmitter release cont'd
Ca2+ binds to synaptotagmin proteins that trigger a conformation change in SNARE and releases neurotransmittervesicles either completely fuse with the membrane and are recycled by endocytosis or ‘kiss and run fusion’
Activation of postsynaptic cell
ionotropic receps – ion chnls that are activated receps by neurotransmittersmetabotropic receps – receptors act indirectly on sep ion chnls thru G protein or 2nd messenger
synaptic delay b/w arrival of AP & memb potent changes in the postsyn cell
Activation of postsynaptic cell cont'd
unbound neurotransmitters are removed from the synaptic cleft when theyare actively transported back into the presynaptic axon terminal – reuptakediffuse away from the receptor siteenzymatically transformed into inactive substances
Kinds of chemical synapses effects
kinds of chemical synapses have different effects on the postsynaptic cell
depends on the type of signal transduction mechanism brought into operation with the neurotransmitter and the type of channel it influences
Excitatory chemical
depolar opens channels perme to sml ions (K+ out & Na+ in)excitatory postsynaptic potential (EPSP) - net movement -> depolarspreads decrementally away by local currentonly function - bring the memb potent of postsyn neuron closer to threshold
Inhibitory chemical
hyperpolarizing graded potential called IPSP lessens the likelihood that a postsynaptic cell will depolarize and generate an action potential opens Cl- and K+ channels
Synaptic integration
1 AP isn’t enough to depolarize a neuron 100s of synapses are excited at once memb potent of postysynaptic neuron at any moment is the sum of all synaptic activity affecting it at that moment
Synaptic integration 2
depends on the inputs that predominates – more excitatory inputs than inhibitory inputs yield depolarization change in membrane potential is very short lived before it returns to resting potential
temporal summation
input signals arrive from the same presynaptic cell at different times and the potentials summate due to more ion channels being open
spatial summation
input signals arrive from different presynaptic cells at the same time postsynaptic potentials last longer than action potentials and often occur in bursts
Synaptic strength
variation in signal strength presynaptic terminals don’t release a constant amount of neurotransmitter each time
· if [Ca2+] is high in the terminal, more ions will be released than usual
happens when Ca2+ removal doesn’t occur quickly enough by organelles causes a higher amplitude of EPSP or IPSP
Synaptic strength altered by activation of membrane receptors on term
influences Ca2+ influx into the terminal and therefore the number of neurotransmitter vesicles released associated with a second synaptic ending – an axo-axonic synapse an axon terminal of neuron ends on an axon terminal of another
synaptic strength altered cont'd
the first neuron won’t have a direct effect overall, but it will influence the amount of neurotransmitter released by the neuron it is connected to cause presynaptic inhibition or presynaptic facilitation
autoreceptors
provides feedback to the neuron so it can regulate its output
receptor desensitization
receptor responds once and then fails to respond despite the presence of neurotransmitters Drugs - interfer with or stimulate normal processes in the neuron involved in neurotransmitter synthesis, storage, and release, and in receptor activation diseases also alter synapse mechanisms
presynaptic factors
availability of neurotransmitter availability of precursor molecules amount of the rate limiting enzyme in the pathway for neurotransmitter synthesis axon terminal membrane potential
presynaptic factors cont'd
axon terminal Ca2+
activation of membrane receptos on presynaptic terminal axo-axonic synapses autorecptors other receptors certain drugs and disease, which act via the above mechanisms A-D
postsynaptic factors
immediate post history of electrical state of postsynaptic membrane (excitation or inhibition from temporal or spatial summation) effects of other neurotransmitters or neuromodulators acting on postsynaptic neurons up- or down-regulation and desensitization of receptors certain drugs and diseases
general factors
area of synaptic contact enzymatic destruction of neurotransmitter geometry of diffusion path neurotransmitter reuptake
neuromodulators
elicit complex neuron responses that aren’t EPSP or IPSPs modify the postsynaptic cell’s response to specific neurotransmitters, amplifying or dampening the effectiveness of ongoing synaptic activity may change presynaptic synthesis, release, reuptake, or metabolis of a transmitter
neuromodulators cont'd
alter the effectiveness of the synapse effects occur for much longer than transmitter effects associated with slower events like learning, development, motivational states and sensory or motor activities
Acetylcholine (ACh)
major neurotransmitter in the PNS at the neuromuscular junction and in the brain neurons that release ACh are cholinergic neurons
Acetylcholinesterase
enzyme decreases [ACh]
breaks ACh apart and the small molecules return to be synthesized by cholinergic nicotinic receptors muscarinic receptors neurons degenerate in Alzheimer disease
biogenic amines
synthesized from amino acids and contain an amino group
catecholamines
dopamine norepinephrine (NE) epinephrine contain catechol ring and an amine group broken down by monoamine oxidase (MAO) adrenergic alpha-adrenergic receptors beta-adrenergic receptors
serotonin
produced by tryptophan slow – a neuromodulator excitatory effect on muscles inhibitory effect on sensations
neuropeptides
two or more amino acids linked together by peptide bonds peptidergic neurons endogenous opiods analgesics – relieve pain w/o losing consciousness substance P
gases
nitric oxide carbon monoxide hydrogen sulfide activate proteins
purines
ATP and adenosine
Structure of the NS
- no nerves in CNS
- a group of axons is called a pathway or tract
- one that links R and L halves of the CNS is a commissure
- long pathways carry info b/w brain and SC or two parts of the brain
multisynaptic pathways
can input new info along it long pathways have few synapses have fewer opportunities to gain new info
Similar functioning cell bodies
cell bodies of similar functioning neurons are clustered together
called ganglia (a ganglion) in PNS called nuclei (a nucleus) in CNS
CNS
cerebrum diencephalon brainstem cerebellum
Cerebrum (forebrain)
cerebral hemispheres cerebral cortex – outer shell of grey matter (mostly cell bodies) inner layer of white matter (mostly myelin fiber tracts) underneath is subcortical nuclei (more grey matter) L and R are connected by corpus callosum
Lobes of cerebral cortex
frontal parietal occipital temporal
Cerebral cortex
highly folded, but very thin ridges = gyri or gyrus grooves = sulci or sulcus
6 layers – related to higher cognative function
Cells in CNS
pyramidal cells - major output cells that send axons to other parts of the cortex and CNS nonpyramidal cells - receiving inputs into the cortex and in local processing of info
subcortial nuclei basal nuclei (or basal ganglia)
Cerebral hemispheres
contain the cerebral cortex used in perception, generation of skilled movements, reasoning, learning, and memory contains subcortical nuclei, including those that participate in coordination of skeletal muscle activity contain interconnecting fiber pathways
Thalamus
Diencephalon
acts as a synaptic relay station for sensory pathways on their way to the cerebral cortex participate in control of the skeletal muscle coordination plays a key role in awareness
Hypothalamus
Diencephalon
regulates anterior pituitary gland function regulates water balance participates inregulation of autonomic nervous system regulates eating and drinking behavior
Hypothalamus cont'd
regulates reproductive system reinforeces certain behaviors generates and regulates circadian rhythms regulates body temperature participates in generation of emotional behavior
Diencephalon
Other half of the forebrain
ThalamusHypothalamus
pituitary gland
pineal gland
epithalamus
limbic system
cerebellum
brainstem
limbic system
participates in generation of emotions and emotional behavior plays essential role in most kinds of learning interconnection of white and grey matter connect parts of the CNS together
cerebellum
coordinates movements, including those for posture and balance – not voluntary movements participates in some forms of learning
brainstem
contains all the fibers passing b/w the SC, forebrain, and cerebellumcontains the reticular formation & its various integrating centers, including those for cardiovascular and respiratory activity – essential for life
brainstem cont'd
contains nuclei for cranial nerves III through XIIcranial nerves – innervate muscles, glands and sensory receptors and organsalso: midbrain, pons, medull oblongata4 interconnected cavities - cerebral ventricles
PNS
efferent nerves - move out of the brain
afferent nerves - provide sensory inputs to the brain
efferent nerves
somatic NS – skeletal muscle motor neurons excitation causes contraction of muscle cells cannot be inhibited muscle relaxation is from the inhibition of the motor neurons in the spinal cord consists of a single neuron b/w CNS and skeletal muscle cells
Autonomic NS
- smooth and cardiac muscle
- has 2-neuron chain b/w CNS and effector organ
- can be excitatory or inhibitory
- enteric NS - network of nerves in gastrointestinal tract
- includes sensory neurons and interneurons
Autonomic ganglion
synapse b/w two neurons outside the CNS cells b/w CNS and ganglia are preganglionic neurons cells after ganglia are postganglionic neurons
Sympathetic pathway
fight or flight leave CNS from the thoracic and lumbar regions of the spinal cord ganglia are close to the spinal cord and form sympathetic trunks norepinephrine transmits b/w postganglionic and the effector cell
Parasympatheic pathway
rest or digest leave CNS from the brainstem acetylcholine is the neurotransmitter for both divisions
Receptors
for acetylcholine - nicotinic receptors on postganglionic neurons in autonomic ganglia at neuromuscular junctions of skeletal muscle
muscarinic neurons - smooth, cardiac muscle, glands
Endocrine gland
adrenal medulla releases NEPI and EPI (norepinephrine and epinephrine) hormones
Dual innervation
cardiac muscle allows fine tune control
Meninges
three layers
subarachnoid space b/w arachnoid and pia is filled with cerebrospinal fluid (CSF) all together circulate and absorb cerebrospinal fluid
subarachnoid space b/w arachnoid and pia is filled with cerebrospinal fluid (CSF) all together circulate and absorb cerebrospinal fluid
choroid plexus – produces CSF
blood-brain barrier
allows substances to enter the brain quickly
diffusion of oxygen and glucose regulates composition of extracellular fluidAbout this deck
By: Julie Mallon
Created: 2011-02-19
Size: 97 flashcards
Views: 34
Created: 2011-02-19
Size: 97 flashcards
Views: 34
About StudyBlue
STUDYBLUE makes things that make you better at school.
Things like online flashcards with photos and audio.
Things like personalized quizzes and friendly reminders about when (and what) to study next.
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“I have used this website for three exams, and I see a huge difference in my test results.”
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