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Electrical Signaling in the Nervous System

The document provides an overview of the nervous system, detailing its structure, including the Peripheral and Central Nervous Systems, and the types of neurons and glial cells involved. It explains the mechanisms of electrical signaling in neurons, including graded and action potentials, as well as the role of the blood-brain barrier and myelin in neuronal function. Additionally, it discusses the importance of ion channels and membrane potentials in the generation and propagation of electrical signals within the nervous system.
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0% found this document useful (0 votes)
10 views17 pages

Electrical Signaling in the Nervous System

The document provides an overview of the nervous system, detailing its structure, including the Peripheral and Central Nervous Systems, and the types of neurons and glial cells involved. It explains the mechanisms of electrical signaling in neurons, including graded and action potentials, as well as the role of the blood-brain barrier and myelin in neuronal function. Additionally, it discusses the importance of ion channels and membrane potentials in the generation and propagation of electrical signals within the nervous system.
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd

INTRO TO:

ELECTRICAL
SIGNALING
NERVOUS SYSTEM

-Consists of:
>The Peripheral Nervous System (PNS)
>The Central Nervous System (CNS) (Acts as the integrating center)
-The Peripheral Nervous system consists of:
>Sensory Division(SENSORS): sends information to CNS through afferent (sensory)
neurons
>Efferent division (RESPONDERS): takes information from the CNS to target cells via
efferent neurons
-Sensory Receptors receive signals and stimulate Sensory Neurons (afferents) and send
information to the CNS
>Sensory Neurons also stimulate the Neurons of the Enteric Nervous System
-The Enteric Nervous System can act autonomously or can be controlled by the CNS through
the autonomic division of the PNS
>Controls Digestive Tract Activity
-Efferent Neurons consists of:
>Autonomic Neurons
>Parasympathetic and Sympathetic neurons which control:
>Cardiac, Smooth muscles, exocrine/endocrine glands
>Adipose Tissue
>Somatic Neurons which control:
>Skeletal Muscles
>Both AUTONOMIC AND SOMATIC Neurons control tissue responses

NEURON ANATOMY
NEURON TYPES:

-Pseudounipolar: have a single process called the axon


>During development, the dendrite fused with the axon
>MOST of the sensory neurons in a human body are pseudounipolar
>Unipolar and Bipolar types can also be sensory neurons
-Bipolar: have two relatively equal fibers extending off the central cell body
-Anaxonic: Anaxonic CNS Interneurons have no apparent axon
-Multipolar: Multipolar CNS Interneurons are highly branched but lack long extensions
>A typical multipolar efferent neuron has 5-7 dendrites, each branching 4-6 times
>A single long axon may branch several times and end at enlarged axon terminals
NEURON ARCHITECTURE:

-Cell Body (Soma): contains the nucleus and other organelles necessary for neuronal function,
including protein synthesis and energy production (POWER SOURCE)
-Dendrites: tree-like extensions that receive signals from other neurons, acting as the neuron’s
main input points (SENSOR)
-Axon: a long, slender projection that transmits signals away from the cell body, carrying
information to other neurons, muscles, or glands (SIGNAL HIGHWAY)
-Myelin Sheath: fatty, insulating layer that surrounds the axon, speeding up the transmission of
electrical signals (HOV LANE)
>Consists of multiple layers of cell membrane
-Axon Terminals: the ends of the axon that form synapses, where signals are transmitted to
other cells
-Synapse: the region where an axon terminal communicates with its postsynaptic target cell
move molecules against their concentration gradient, from an area of low concentration to an
area of high concentration ,using specialized membrane proteins (WHERE TWO NEURONS
MEET) (JUNCTION)
-Node of Ranvier: a section of unmyelinated axon membrane between two Schwann Cells
>Schwann Cell: glial cells that form the myelin sheath on axons outside the brain
SUPPORTING CELLS IN THE NERVOUS SYSTEM

-Glial Cells: non-neuronal cells that support Neurons and other cells in the nervous syste,
Glial Cells are often found in:
-CENTRAL Nervous System which contains:
>Ependymal Cells: form barriers between compartments, source of neural stem cells
>Astrocytes: source of neural stem cells
>Take up K+ (Potassium), water, neurotransmitters
>Secrete Neurotrophic factors
>Helps form the Blood-Brain Barrier
>Provides Substrates for ATP production
>Microglia (modified immune cells): act as SCAVENGERS
>Oligodendrocytes: form Myelin Sheaths
-PERIPHERAL Nervous System which contains:
>Schwann Cells: form Myelin Sheaths
>Satellite Cells: support cell bodies
-Interneurons: specialized nerve cells that act as intermediaries within the CNS
>Connects sensory and motor neurons
>The MOST ABUNDANT type of neuron in the body
>Found in the Brain and Spinal Cord
>Play a crucial role in integrating sensory information and regulating motor activity

PARALLEL DEVELOPMENT OF NEURAL AND IMMUNE CELLS OF THE CNS


-The Colonization by Yolk Sac-derived macrophages that give rise to microglia and BAM
(Border Associated Macrophages), whereas Neural Progenitors generate Neurons (left)
-At Later Embryonic stages (right), Neural Progenitors additionally produce Oligodendrocytes
and Astrocytes in the Parenchyma while the microglia undergo local differentiation

BLOOD BRAIN BARRIER

-Neurons are protected from harmful substances in the blood because Brain Capillaries are not
leaky
-Astrocyte foot processes promote tight junction formation
-Tight Junctions prevent solute movement between Endothelilal cells

DAMAGED MYELIN
-Damaged Myelin causes a LOSS of Peripheral Motor Control
>When an axon is cut, the section attached to the cell body continues to live
>The section of the axon distal to the cut begins to disintegrate
-Under SOME circumstances, the proximal axon may regrow through the existing sheath of
Schwann Cells and reform a synapse with the proper target (RECONNECTION)

ELECTRICAL SIGNALING IN NEURONS


-The FREQUENCY of action potential firing indicates the strength of the stimulus
>Weak stimulus releases little neurotransmitter:

>Strong stimulus causes more action potentials and releases more neurotransmitter

ELECTRICAL SIGNALING IN NEURONS


GRADED POTENTIAL ACTION POTENTIAL

Signal Type Input Signal Regenerating Conduction Signal

Occurs Where? Usually Dendrites and Cell Trigger zone through Axon
body(Soma)

Gated Ion Mechanically, Chemically, or Voltage-gated channels


Channels Voltage-gated channels
involved

Ions Involved Usually Na+ (Sodium), K Usually Na+ (Sodium) and K


(Potassium), Ca2 (Calcium) (Potassium)

Type of Signal Depolarizing (Na+) or Depolarizing


Hyperpolarizing (Cl)

Strength of Depends on initial stimulus; All-or-none phenomenon; cannot be


Signal can be summed summed

Signal catalyst Entry of ions through gated Above-threshold graded potential at the
channels trigger zone opens ion channels

Unique *No minimum level required to *Threshold stimulus required to initiate


Characteristics initiate *Refractory Period: 2 signals too close
*Two Signals coming close together in time cannot sum
together in time will sum
*Initial Stimulus strength is
indicated by frequency of a
series of action potentials
THE ORIGIN OF MEMBRANE POTENTIALS
-In illustrations, this uneven distribution of charge is often shown by the charge symbols
clustered on each side of the cell membrane

-Membrane Potentials result from Selective Ion Permeability (in this case, K+ ions only)

-Resting Membrane Potentials are stabilized result at EQUILIBRIUM between the diffusion
gradient (from in to out) and the electrical gradient (from out to in)
ELECTROCHEMICAL EQUILIBRIUM
-In this example, the concentration gradient sending K+ (Potassium) out of the cell is exactly
opposed by the electrical gradient pulling K+ into the cell
>This is shown by the arrows that are equal in length but opposite in direction

-Electrophysiology: measuring membrane potentials and currents


-The Resting Membrane Potential is mostly, but not only, due to K+ ions
>Most cells in the human body are about 40 times more permeable to K+ than to Na+
>The resting membrane potential is about -70mV
>The Na-K-ATPase (enzyme) helps maintain the resting membrane potential by
REMOVING Na+ that leaks into the cell and RETURNING K+ that has leaked out
SPREAD OF GRADED POTENTIALS
-Graded potentials decrease in strength as they spread out from the point of origin due to the
current leak out of the cell
GRADED POTENTIALS TRIGGER ZONE
-Graded potentials ACTIVATE the trigger zone above a threshold potentials
-Subthreshold Graded Potential:
>A graded potential starts above threshold (T) at its initiation point but decreases in
strength as it travels through the cell body.
>At the trigger zone, it is below threshold, and therefore, does NOT initiate an Action
Potential

-Suprathreshold Graded Potential:


>A STRONGER stimulus at the same point on the body creates a graded potential that is
still ABOVE Threshold by the time it reaches the trigger zone, so an action potential results
ACTION POTENTIALS
-Action Potentials are self-propagating signals along axons and DO NOT decay over distance
>Graded Potentials decay over distance
-The conduction of an Action Potential down an axon is similar to energy passed along a series
of falling dominoes
>In this snapshot, each domino is in a different phase of falling
>In the axon, each section of membrane is in a different phase of Action Potential
TIME-COURSE OF AN ACTION POTENTIAL
-Changes in ion permeability (Pion) along the axon create ion flow and voltage changes
TIMELINE
1.) Resting Membrane Potential
2.) Depolarizing Stimulus
3.) Membrane depolarizes to threshold
>Voltage-gated Na+ and K+ channels begin to open
4.) Rapid Na+ entry depolarizes cell
5.) Na+ channels close and slower K+ channels open
6.) K+ moves from cell to extracellular fluid
7.) K+ channels remain open and additional K+ leaves the cell; hyperpolarizing it
8.) Voltage-gated K+ channels close; less K+ leaks out of the cell
9.) Cell returns to resting ion permeability and resting membrane potential
FEEDBACK LOOP (The Hodgkin Cycle)
-The depolarization phase of an Action Potential is an example of a positive feed-back loop

-Sodium Entry during an Action Potential creates a positive feedback loop.


>The Positive feedback loop stops when the Na+ channel inactivation gates close
-Action Potentials DO NOT move backward or into the cell body
>They appear to jump from one Node of Ranvier to the next
>Only the nodes have voltage-gated Na+ channels
-Demyelinating disease reduce or block conduction when current leaks out of the previously
insulated regions between the nodes

Common questions

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During an action potential, the opening of voltage-gated Na+ channels causes Na+ to enter the cell, further depolarizing the membrane and leading to the opening of more Na+ channels. This cycle exemplifies a positive feedback loop, as the initial depolarization rapidly drives the process forward . The signal's directionality is ensured by the inactivation of Na+ channels after they open, preventing the action potential from moving backward. Additionally, action potentials appear to jump from one Node of Ranvier to the next, where only these nodes have voltage-gated Na+ channels, ensuring the forward propagation of the signal .

The myelin sheath contributes to the function of signal transmission by insulating the axon and enabling rapid transmission of electrical signals through saltatory conduction. This allows the action potential to 'jump' from one Node of Ranvier to the next, increasing the speed of communication between neurons . If the myelin sheath becomes damaged, as seen in demyelinating diseases, the conduction of electrical signals can be reduced or blocked, causing a loss of peripheral motor control due to current leakage in the previously insulated regions. In some cases, the proximal axon may regrow through the existing sheath and reform a synapse with its target .

Glial cells have distinct roles in the central and peripheral nervous systems, mainly supporting neuronal function. In the central nervous system, types such as oligodendrocytes form myelin sheaths, while astrocytes support the blood-brain barrier, regulate extracellular potassium levels, and provide substrates for ATP production . Microglia act as scavengers. In the peripheral nervous system, Schwann cells form myelin sheaths around axons, and satellite cells support cell bodies. These functions are critical for maintaining homeostasis, protecting the nervous systems from damage, and ensuring efficient transmission of electrical signals .

Astrocytes play a crucial role in maintaining the blood-brain barrier by promoting the formation of tight junctions between endothelial cells, which prevents solute movement between cells . This function is critical for neural health as it protects neurons from harmful substances in the blood and maintains a stable environment within the central nervous system, which is essential for proper neural function and prevention of neurotoxic damage . Astrocytes also secrete factors that support neuronal health and metabolism, thereby playing a comprehensive role in neural support and protection.

Graded potentials differ from action potentials in several key aspects. Graded potentials are input signals that can occur in dendrites and the cell body, triggered by mechanically, chemically, or voltage-gated channels, and can be summed or attenuate as they spread. They depend on the initial stimulus and decrease in strength over time due to current leakage . Action potentials, conversely, are generated at the trigger zone and propagated down the axon in an all-or-none fashion. They do not diminish in strength as they travel along the axon due to the regenerative opening of voltage-gated Na+ and K+ channels .

The equilibrium potential in neurons is established through the selective permeability of the cell membrane to specific ions, particularly K+ ions. The resting membrane potential is primarily influenced by the concentration gradient of K+ that promotes its movement out of the cell and the electrical gradient pulling K+ back into the cell . This balance creates a state of electrochemical equilibrium, depicted by arrows of equal length but opposite direction, resulting in a stable resting membrane potential . The Na-K-ATPase helps maintain this potential by actively removing Na+ ions and returning K+ ions, ensuring the membrane's selective permeability supports the equilibrium .

Neurons have distinct architectural differences that correlate with their specific functions. Pseudounipolar neurons, mostly sensory neurons, have a single process that branches into peripheral and central projections, enabling quick signal transmission from sensory receptors to the CNS . Bipolar neurons, with two extensions, are involved in special senses like vision and smell. Anaxonic neurons, lacking a distinct axon, are primarily integrative CNS interneurons . Multipolar neurons, with many dendrites and a long axon, manage complex processing and signal propagation, characteristic of motor and interneurons . The structure of these neurons facilitates their roles in sensory input, information processing, and motor output in the nervous system.

Schwann cells significantly influence neuronal repair processes by guiding regrowth in the peripheral nervous system through myelin sheath formation. After axonal damage, although the distal section of the axon degenerates, the proximal section may regrow through the conduit formed by Schwann cells, potentially restoring its connection with target cells . This repair mechanism supports the regeneration of peripheral nerves, enhancing recovery from injuries, an ability not typically seen in the central nervous system due to a lack of similar supporting cells and environments .

The efferent division of the peripheral nervous system (PNS) consists of autonomic and somatic branches, each controlling different target tissues. The autonomic branch is further divided into parasympathetic and sympathetic neurons, regulating involuntary functions by controlling cardiac and smooth muscles, exocrine/endocrine glands, and adipose tissue, ultimately influencing the body's adaptability to stress or relaxation . In contrast, the somatic branch controls skeletal muscles, managing voluntary movements. This division enables the somatic branch to facilitate conscious and precise movements, while the autonomic branch coordinates physiological responses essential for homeostasis and survival, such as heart rate modulation and digestive enzyme secretion .

The enteric nervous system (ENS) controls the digestive tract's activity and acts autonomously due to its complex network of neurons within the gastrointestinal tract, enabling it to coordinate local reflexes independently of the central nervous system (CNS). However, it is also connected to the CNS through the autonomic division of the peripheral nervous system, allowing it to be modulated by sympathetic and parasympathetic inputs. These connections enable the CNS to exert higher-level control over digestive functions when needed, illustrating the intrinsic and extrinsic regulatory mechanisms of the ENS .

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