Nervous Tissue & Cell Function Flashcards
Classification of Neuron Morphology
- based on the number of processes extending from the cell body
- Multipolar neurons - have one axon and two or more dendrites.
- Almost all neurons in the CNS are multipolar.
- Bipolar neurons - have one axon and one dendrite.
- Pseudounipolar neurons - have one axon with 2 long processes.
- Most bipolar & pseudounipolar neurons are sensory neurons
- transmit impulses of sensory stimuli from the PNS to the CNS
Description of Neurons
- specialized cells that send & receive signals to/from other cells.
- Communication b/t neurons occurs at synapses.
- Consist of
- Cell body-contains the nucleus and other essential organelles.
- Dendrites-processes that receive inputs to the neuron.
- Axon-transmit signal from cell body to the neuron’s target(s).
- often insulated w/ myelin sheath to speed the rate of AP
Glial cells of CNS:
- Provide structural & metabolic support to neurons during development and in the mature brain.
- Oligodendrocytes - form the myelin sheath around CNS axons.
- Astrocytes: provide scaffolds for growing axons and migrating neurons during development
- maintain appropriate extracellular ion concentration
- contribute to the formation of the blood-brain barrier.
- Microglia - act as macrophages or scavengers in the CNS.
- Ependymal cells - line the fluid-filled cavities (ventricles) of the brain and spinal cord.
Glial cells in the PNS
- Provide structural & metabolic support to neurons during development and in adult
- Schwann cells: myelinate axons of peripheral nerves.
- Role in regeneration following injury to a peripheral nerve axon.
- Satellite cells-surround/support nerve cells in peripheral ganglia
Information Processing in the CNS
- Most CNS neurons act as miniature computational units
- integrate inputs from multiple sources.
- Balance of excitatory & inhibitory inputs
- determines whether the neuron generates an AP
- many presynaptic inputs to postsynaptic cell required to reach threshold & fire an AP
- Components: Many CNS neurons to One CNS neuron
- Synaptic Input: Excitatory and inhibitory inputs
- Transmitters: Various chemical transmitters interacting with a variety of receptor types
- Electrical Activity: Many action potentials firing synchronously –> An AP in the target neuron
Information Processing in the PNS
- postsynaptic skeletal muscle fiber at the NMJ excited by a single presynaptic alpha motor neuron
- Components: One alpha motor neuron to one muscle fiber
- Synaptic Input: Excitatory inputs only
- Transmitters: One chemical transmitter and One receptor type
- Electrical Activity: Action potential in a motor neuron–> Action potential in muscle fiber
Define Synaptic Potential
graded, monophasic changes in postsynaptic membrane potential that are generated at a synapse
Structural Features of the Synapse
- Synapses are intercellular junctions that are specialized for the transmission of nerve impulses.
- Presynaptic neuron (usually axon terminal) releases a chemical substance into the synaptic cleft.
- Chemical substance interacts w/ receptors in membrane of postsynaptic neuron (dendrites or soma)
- Fewer synapses also occur between axons and other axons.
Physiological Properties of Synaptic Potentials
- Release of an excitatory NT depolarizes the postsynaptic membrane.
- This is called an excitatory postsynaptic potential (EPSP).
- Release of an inhibitory neurotransmitter hyperpolarizes the postsynaptic membrane.
- This is called an inhibitory postsynaptic potential (IPSP).
- Size of graded synaptic potential related to amt of transmitter released & density of receptors on postsynaptic membrane.
- Amplitude of graded synaptic potentials can vary at each synapse and over time at a given synapse.
- Graded synaptic potentials spread passively thru membrane of the postsynaptic dendrite & soma
- Graded synaptic potentials decay with time and distance.
- EPSPs at a single synapse are generally subthreshold and will not generate an AP
difference between excitatory and inhibitory postsynaptic potentials.
- Release of an excitatory NT depolarizes the postsynaptic membrane.
- This is called an excitatory postsynaptic potential (EPSP).
- Release of an inhibitory neurotransmitter hyperpolarizes the postsynaptic membrane.
- This is called an inhibitory postsynaptic potential (IPSP).
Types of Integration of Synaptic Input
- AP occurs when multiple subthreshold EPSPs sum to bring the membrane potential to threshold.
- Temporal summation: Consecutive EPSPs at the SAME site add to depolarize toward threshold.
- Spatial Summation: Simultaneous EPSPs at DIFFERENT synapses on the same neuron sum to depolarize the membrane toward threshold.
Principal Site of Synaptic Integration
- The axon hillock of a neuron is the usual site of integration of graded postsynaptic potentials.
- When the sum of graded potentials in a postsynaptic cell is large enough the neuron will generate an AP
- High density of voltage-gated Na+ channels at the axon hillock make it the zone for initiating the AP
Synaptic Connections: Divergence
-One presynaptic neuron synapses on multiple postsynaptic neurons.
-Ex: The sensory signal produced by touching a hot stove
diverges to retract the affected limb & inform higher CNS centers that you touched a hot stove.
Synaptic Connection: Convergence
- multiple axon terminals synapse on the same postsynaptic cell.
- Converging inputs on the postsynaptic cell can be inhibitory and/or excitatory signals.
- The postsynaptic cell integrates the converging inputs chiefly by spatial summation.
Synaptic Connections: Axoaxonic Synapses
- Type 1: Presynaptic axon terminal synapses on the initial segment (unmyelinated) of the postsynaptic axon
- Type 2: Presynaptic axon terminal synapses on the axon terminal of a 2nd neuron that is presynaptic to the soma or dendrite of a 3rd neuron
- The presynaptic axon terminal modulates the entry of Ca2+ ions into the postsynaptic axon terminal
- Modulation of Ca2+ entry regulates the amount of NT released by the postsynaptic terminal
Presynaptic Facilitation:
- NT released at axoaxonic synapse increases entry of Ca2+ into axon terminal of postsynaptic neuron
- This increases the amt of transmitter released from postsynaptic neuron
- generates a larger PSP in dendrites or soma of the 3rd neuron
Presynaptic Inhibition
- NT released at axoaxonic synapse decreases entry of Ca2+ into axon terminal of postsynaptic neuron
- Decreases the amt of NT released from the postsynaptic neuron
- generates a smaller PSP in dendrites or soma of the 3rd neuron
Feed forward Processes
- Information flows unidirectionally through a series of neurons.
- Excitation: excitatory neurons project to other excitatory neurons, which, in turn, excite other neurons
- Neuron A excites Neuron B which excites Neuron C
- Inhibition: excitatory neurons activate inhibitory neurons, which then inhibit adjacent populations of excitatory neurons
- Neuron A excites Neuron B which inhibits Neuron C
Disinhibition
- Four neurons connected in series:
- Neurons 1 and 4 are excitatory
- Neurons 2 and 3 are inhibitory.
- Excitation of Neuron 2 by 1 inhibits Neuron 3.
- Decreased firing by Neuron 3 releases Neuron 4 from inhibition
- Result of disinhibition is to increase the activity level of Neuron 4.
- Comparable to a “double negative,”
- inhibition (by Neuron 2) of an inhibitory interneuron (Neuron 3) results in facilitation of activity of its target (Neuron 4).
Retrograde Reaction Following Neuron Damage
- Morphological reaction of proximal axon, cell body and dendrites of a damaged nerve
- Reaction occurs in the direction opposite of conduction
- The primary retrograde reaction occurs at the neuronal cell body.
- swelling of the cell body and nucleus
- displacement of nucleus from center of cell to eccentric location.
- dispersion of Nissl substance into homogeneous particles of decreased basophilia (chromatolysis)
- Ribosome-studded endoplasmic reticulum are dispersed and replaced with polyribosomes.
Anterograde Reaction Following Neuron Damage
- Morphological reaction of the axon, its myelin sheath and axon terminals distal to the injury site
- Reaction occurs in the direction of conduction
- Also termed Wallerian degeneration
- Involves degeneration & clearance of the axon, myelin sheath & axon terminals distal to the injury site
- allows for potential regeneration of the injured axon.
- Schwann cells near the injured nerve dedifferentiate & divide.
- Schwann cells & macrophages phagocytose the degenerative debris in PNS injury
- In CNS this is done by microglia, astrocytes and macrophages.
PNS Nerve Regeneration
- able to repair, including restoring functionally useful connections.
- After injury, tips of proximal stumps swell & experience some retrograde degeneration
- once the debris is cleared, it begins to sprout axons
- presence of growth cones can be detected
- Growth cones sprout initially at the nearest Node of Ranvier of the proximal segment
- must grow across injury & into Schwann cell guidance tunnels
- Growing axons contact Schwann cells forming columns
- second wave of Schwann cell proliferation occurs.
- Schwann cells from 2nd proliferation form guidance tunnels along the former course of the axon.
- Elongating axons innervate target tissue, myelinate and functional recovery occurs.
- Axon growth rates can reach 2 mm/day in small nerves & 5 mm/day in large nerves.
- The growth rate is determined by the slow anterograde transport rate (1 -6 mm/day).
Factors That Influence PNS regeneration and reinnervation
Type of Nerve Injury
- crush: more regeneration b/c endoneurial sheath remain intact.
- transection: continuity of axoplasm lost
- regeneration more difficult because of misalignment of axons
- if suture ends of nerve together, chance of recovery increases
Site of Injury:
-The closer to target site the nerve is damaged the greater the likelihood for regeneration.
Age
-younger = regenerative activity is greater
CNS Neuron Regeneration Capability
- axonal regeneration is typically abortive.
- axons initially sprout from the proximal axon
- regrowth is limited by several factors:
- Loss of molecules that promote axonal growth
- laminin and fibronectin persist in PNS but are absent in CNS
- Expression of molecules that inhibit axonal growth.
- Inhibitory glycoproteins in myelin processes of oligodendroglia.
- Not in Schwann cells.
- Oligodendroglia do not form “guidance tunnels”.
- Glial cells release cytokines that decrease axonal growth.
- Development of glial scar at injury site impedes growth of axons due to proteoglycan production that inhibits sprouting.