Study Guide for Chapter 3: Structure and Function of Neurons and Synapses
Study Guide: Structure and Function of Neurons and Synapses
Chapter Overview
This study guide covers Chapter 3, covering the structure and function of neurons and synapses as described by OXFORD UNIVERSITY PRESS (2018).
Understanding Neurons
Neuron Doctrine
Definition: Established by Ramon y Cajal, asserts that the brain is made up of many small, discrete individual cells.
Population: Approximately 100 billion neurons are present in the human brain.
Cellular Composition: Neurons, like all other cells, have:
Membrane
Nucleus
Specialized organelles
Structure of Neurons
Neural Membrane
Functions as a boundary between the cell and the external environment, separating intracellular fluid/cytoplasm from extracellular fluid surrounding the neuron.
Uses different chemical compositions of the fluids to facilitate separation.
Phospholipid Membrane: Contains protein structures controlling permeability.
Ion Movement: Channels allow specific ions to move in or out.
Types of Ion Structures in Neurons
Ion Channels
Function: Allow ions to move passively without using energy.
Voltage Dependent Channels: Open and close in response to electrical status of the membrane.
Ion Pumps
Function: Requires energy to move ions across the membrane.
Sodium-Potassium Pumps: Move three sodium ions out while taking in two potassium ions, consuming 20-40% of the brain's energy.
Calcium Pumps: Specifically pump calcium ions out of the neuron.
Cytoskeleton
Provides structural support and maintains the shape of the neuron.
Composition: Made of three types of filaments:
Microtubules (largest, hollow tubes ~25 nm):
Move materials within the cell (e.g., vesicles).
Involved in anterograde (away from soma) and retrograde (towards soma) transport.
Tau Protein: Stabilizes microtubules; elevated levels associated with Alzheimer's disease.
Intermediate Filaments (about 10 nm):
Most common fiber, provide structural support.
Microfilaments (3-5 nm):
Participate in changing the shape and length of structures during development.
Key Components of a Neuron
Nucleus:
Central structure containing the nucleolus, where ribosomes are synthesized.
Ribosomes create proteins alone or with the endoplasmic reticulum (ER).
Endoplasmic Reticulum: Rough ER produces proteins; smooth ER processes proteins which are then sent to the Golgi apparatus.
Mitochondria: Utilize oxygen and transform sugars into ATP, the main energy source for neurons.
Dendrites:
Branching extensions that receive information from other neurons.
Integrate thousands of chemical signals.
Varied shapes with specialized gated ion channels that act as receptor sites for chemicals released from other neurons.
Dendritic Spines: Can change shape based on synaptic activity, contributing to learning and memory; abnormality is associated with autism, schizophrenia, and Alzheimer's.
Soma (Cell Body):
Acts as the neuron’s command center, integrating incoming signals and containing organelles.
Axon:
A single, long extension responsible for conducting neural impulses over distances.
Described as a cable with a diameter of less than 1 µm to about 25 µm.
Types of axons:
Local Circuit Neurons: Short axons communicate with nearby cells.
Projection Neurons: Long axons project to distant areas.
Axon Terminals:
Swellings at the end of axon collaterals that release signals to other neurons.
Involved in neurotransmitter release at synapses.
Axonal Varicosities: Intervals along unmyelinated segments of an axon containing mitochondria and synaptic vesicles.
Neuron Types-Based on Function
Sensory Neurons:
Transmit signals from sensory receptors to the central nervous system (CNS).
Motor Neurons:
Send commands from the CNS to muscles and glands.
Interneurons:
Classified into:
Projection Interneurons: Have long projections to other regions.
Local Interneurons: Stay within a region.
Neuron Types-Based on Shape
Multipolar Neurons:
The most common type in the vertebrate nervous system; serve as motor neurons with many branches extending from the soma.
Examples: Pyramidal cells (cerebral cortex), Purkinje cells (cerebellum).
Bipolar Neurons:
Feature two branches: one axon and one dendrite.
Found in sensory systems like the retina; includes Von Economo Neurons (VENs), specialized bipolar cells.
Unipolar Neurons:
A single branch from the cell body, found in sensory systems involved in touch, temperature, and pain, typically near the spinal cord.
Functional Variations in Neurons
Sensory Neurons: Translate various external and internal stimuli into signals.
Motor Neurons: Transmit commands directly to muscles and glands.
Interneurons: The majority of neurons, acting as bridges between sensory and motor functions.
Glial Cells (Glia)
Total of approximately 360 billion glial cells constitute 80-90% of cells in the CNS, also found in the peripheral nervous system.
Functions: Support neurons by speeding up signaling, regulating chemicals, and modifying connections, help clean debirs and prune synaptic cnxs
Types of Glial Cells:
Macroglia: Large varieties that develop from ectoderm.
Astrocytes: Most common in the CNS, maintain homeostasis, provide support, clean debris, and contribute to the blood-brain barrier.
Microglia: Small cells originating from mesoderm responsible for debris cleanup. They act as the brain's immune system but can damage surrounding cells if activated uncontrollably.
Ependymal Cells: Line ventricles and the spinal canal, moving cerebrospinal fluid and regulating stem cells.
Oligodendrocytes: Myelinate axons in the CNS, supporting structural stability.
Schwann Cells: Myelinate axons in the PNS, with one cell myelinating a single segment of an axon.
Blood-Brain Barrier
A semipermeable barrier formed by endothelial cells in capillaries that protects the brain from toxins in the blood.
Area Postrema: A region in the medulla with a weaker blood-brain barrier to detect poisons and trigger vomiting.
Axons and Dendrites
Dendrites: Receive signals via specialized structures called dendritic spines, which can change shape according to synaptic activity; abnormalities may lead to neurological disorders.
Axons: Transmit signals; key structures include:
Axon Hillock: Initiates action potentials, lacks myelin coverage.
Myelin Sheath: Insulates electrical signals.
Nodes of Ranvier: Gaps in the myelin facilitating saltatory conduction, where action potentials jump between nodes for faster signal propagation.
Neural Communication
Resting Potential
Definition: The neural membrane has a resting potential of approximately -70 mV due to the concentration of potassium ions inside the cell.
This resting state is maintained to prepare for incoming signals.
Action Potentials
Definition: An action potential is an electrical signal essential for neural communication, generated in the presynaptic neuron.
Sequence of ionic changes occurs across the neural membrane to propagate signals from the axon terminal to the postsynaptic neuron.
Ionic Composition: High sodium and chloride outside and high potassium inside, with the intercellular fluid being more negative than the exterior.
Generating Action Potentials
Action potentials result from the movement of ions across the membrane, creating a difference in charge.
Diffusion: The tendency for molecules to distribute evenly, leading to movement from high to low concentration.
Electrostatic Pressure: Causes attraction of opposite charges and repulsion of like charges, influencing ion movement across membranes.
Propagation of Action Potentials
Action potentials reproduce down the axon, influenced by myelination:
In unmyelinated axons, action potentials are reproduced at each segment.
In myelinated axons, they propagate via saltatory conduction, jumping from node to node, increasing conduction velocity.
Neurotransmitter Release at Synapses
Types of Synapses
Gap Junctions: Allow cells to communicate through shared cytoplasm, contributing to synchronization in brain functions and responding to hormone release.
Chemical Synapses: Wider gaps that utilize neurotransmitters to relay signals, allowing both excitatory and inhibitory interactions, impacting subsequent neuronal firing.
Neurotransmitter Release Mechanism
An action potential reaching an axon terminal triggers neurotransmitter release via exocytosis:
Synaptic vesicles merge with the membrane to release contents into the synaptic gap.
Kiss-and-Run Mechanism: Vesicles partially empty their contents before retreating.
Auto Receptors: Feedback mechanisms for neurotransmitter release and synthesis adjustments.
Receptors:
Ionotropic: Directly influence ion channels upon binding neurotransmitters.
Metabotropic: Initiate longer-term changes through G proteins and second messengers.
Neurotransmitter Deactivation
Neurotransmitters can be deactivated through:
Diffusion away from the synapse.
Enzymatic degradation (e.g., MAOs, AchE).
Reuptake process where pre-synaptic membranes recapture neurotransmitters.
Postsynaptic Potentials
EPSPs (Excitatory Postsynaptic Potentials): Result from depolarization and increase likelihood of action potential firing; produced by open ion channels allowing positive ions in.
IPSPs (Inhibitory Postsynaptic Potentials): Result in hyperpolarization and decrease likelihood of action potential firing; open channels allowing chloride or potassium ions movement.
Summation of Inputs
Action potentials are produced when excitatory inputs exceed inhibitory inputs (spatial summation).
Temporal summation: EPSPs and IPSPs may build up over time at active synapses, influencing action potential generation.
Axo-Axonic Synapses
These synapses modulate neurotransmitter release; if a presynaptic neuron increases release, it is called presynaptic facilitation; if it decreases release, it is presynaptic inhibition.
Axoplasmic Transport
An active process propelling substances along axonal microtubules.
Anterograde Transport: From cell body toward axon terminals.
Retrograde Transport: From axon terminals back to the cell body.
Types and Examples of Neurotransmitters
Small-Molecular-Weight Neurotransmitters:
Synthesized locally at axon terminals (e.g., monoamines, amino acids).
Large-Molecular-Weight Neurotransmitters:
Require synthesis in the cell body (e.g., neuropeptides).
Type | Examples |
|---|---|
Monoamines | Dopamine, norepinephrine, serotonin |
Amino Acids | Glutamate, glycine, GABA |
Peptide Neurotransmitters | Cholecystokinin, somatostatin |
Gases | Nitric oxide, carbon monoxide |
Organic Cation | Acetylcholine |
Drug Interactions and Synaptic Function
Agonists: Enhance neurotransmitter activity.
Antagonists: Reduce neurotransmitter activity.
Synaptic Actions
Reuptake
The process of reabsorbing neurotransmitters back into the presynaptic neuron (e.g., SSRIs inhibit serotonin reuptake).
Enzymatic Degradation
Breakdown of neurotransmitters occurs through enzymatic activity (e.g., MAOs, AchE).
Neuronal Excitation
Neurotransmitters can elicit EPSPs by facilitating the entry of positively charged ions (e.g., ), increasing the chance of neuronal firing.
Type | Duration | Size | Character | Channels Involved |
|---|---|---|---|---|
Action Potential | 1 to 2 msec | About 100 mV | All-or-none | Voltage-dependent Na+, K+ |
EPSPs | 5 to 10 msec | Up to 20 mV | Graded depolarization | Ligand-gated Na+ |
IPSPs | 5 to 10 msec | Up to 15 mV | Graded hyperpolarization | Ligand-gated K+ or Cl− |
Example Questions for Understanding
If a neuron has a resting membrane potential of and undergoes hyperpolarization to , the size of the IPSP is:
3 mV.
If a neurotransmitter binds to a receptor changing the membrane potential from to , it undergoes:
an IPSP.
If the potential changes from to , it undergoes:
an EPSP.
For a neuron’s membrane potential at with a threshold of , how much depolarization is required?
10 mV.
If the membrane potential is at and the threshold is , how much depolarization is necessary?
13 mV (More hyperpolarized membranes require greater depolarization to reach firing threshold).