Nervous System: Complete Notes
Glial Cells • Action Potential • Conduction of Nerve Impulse • Neurotransmitter Release
CSIR-NET • GATE • DBT • ICMR • MSc Biotechnology📚 Table of Contents / Index
- Introduction to the Nervous System
- Organization of the Nervous System
- Neuron: Structural and Functional Unit
- Glial Cells
- Resting Membrane Potential
- Action Potential
- Ion Channels During Action Potential
- Refractory Period
- Conduction of Nerve Impulse
- Myelination and Saltatory Conduction
- Synapse and Synaptic Transmission
- Release of Neurotransmitters
- Neurotransmitter Receptors
- Excitatory and Inhibitory Synaptic Potentials
- Important Comparisons
- Important Applied Concepts
- Quick Revision Notes
- 10 MCQs with Hidden Answers
- Final Exam-Oriented Summary
1. Introduction to the Nervous System
The nervous system is one of the major regulatory systems of the human body. It receives information from the internal and external environment, processes that information and generates appropriate responses. The nervous system allows an organism to detect changes, integrate sensory information, coordinate movement, regulate physiological functions and participate in higher functions such as learning, memory, emotion and cognition.
Nervous communication is generally rapid because neurons communicate through electrical signals and chemical signals. Electrical changes in the plasma membrane allow information to travel along neurons, while chemical neurotransmitters transmit information across most synapses.
Major functions of the nervous system
- Sensory function: Detects changes in the external and internal environment.
- Integration: Processes and interprets incoming information.
- Motor function: Produces responses through muscles and glands.
- Coordination: Coordinates activities of different organs.
- Homeostasis: Helps maintain stable internal conditions.
- Higher functions: Participates in learning, memory, thought, emotion and consciousness.
- Reflex activity: Produces rapid responses to specific stimuli.
Key Point
The basic functional principle of the nervous system is: receive information → process information → produce an appropriate response.
2. Organization of the Nervous System
Anatomically and functionally, the nervous system can be divided into several interconnected components. The two major anatomical divisions are the central nervous system and peripheral nervous system.
Consists mainly of the brain and spinal cord. It acts as a major site for integration and processing of information.
Includes nerves and ganglia outside the brain and spinal cord. It connects the CNS with receptors, muscles and glands.
Primarily involved in sensory information and voluntary control of skeletal muscles.
Regulates many involuntary functions involving smooth muscle, cardiac muscle and glands.
Functional direction of information
- Afferent pathway: Carries sensory information toward the CNS.
- Efferent pathway: Carries motor commands away from the CNS.
- Sensory neuron: Transmits information from sensory receptors.
- Motor neuron: Transmits signals to effectors.
- Interneuron: Connects neurons within the CNS and participates in integration.
| Division | Main components | Major role |
|---|---|---|
| CNS | Brain and spinal cord | Integration and information processing |
| PNS | Nerves and ganglia | Communication between CNS and body |
| Somatic system | Sensory and skeletal motor pathways | Voluntary movement and sensory function |
| Autonomic system | Sympathetic, parasympathetic and enteric components | Regulation of visceral functions |
3. Neuron: Structural and Functional Unit
The neuron is the principal electrically excitable cell of the nervous system. Neurons are specialized for receiving, integrating and transmitting information. Although neurons differ greatly in size and shape, most contain a cell body and processes specialized for receiving or transmitting signals.
Major parts of a neuron
- Cell body (soma): Contains the nucleus and most metabolic machinery.
- Dendrites: Usually receive synaptic or sensory information.
- Axon: Conducts electrical signals away from the cell body.
- Axon hillock/initial segment: Important region for action-potential initiation in many neurons.
- Axon terminals: Specialized endings involved in communication with another cell.
- Myelin sheath: Insulating structure surrounding many axons.
- Nodes of Ranvier: Gaps between myelinated segments where voltage-gated channels are concentrated.
4. Glial Cells
Glial cells, or neuroglia, are non-neuronal cells that provide structural, metabolic, electrical and protective support to neurons. Glia are not simply passive supporting cells. They actively participate in maintaining the neural environment, myelination, immune defense and regulation of neuronal communication.
Major glial cells of the CNS
| Glial cell | Location | Major functions |
|---|---|---|
| Astrocytes | CNS | Support neurons, regulate extracellular ions and neurotransmitters, participate in the blood-brain barrier and metabolic support. |
| Oligodendrocytes | CNS | Form myelin around axons in the CNS. |
| Microglia | CNS | Immune surveillance and phagocytic functions in nervous tissue. |
| Ependymal cells | CNS | Line ventricular and central canal surfaces and participate in cerebrospinal-fluid-related functions. |
Major glial cells of the PNS
- Schwann cells: Form myelin around axons in the peripheral nervous system.
- Satellite cells: Surround neuronal cell bodies in peripheral ganglia and help regulate the local environment.
Oligodendrocyte → CNS myelin
Schwann cell → PNS myelin
Microglia → immune/phagocytic cells of CNS
Astrocytes → structural, metabolic and homeostatic support
Functions of glial cells
- Provide physical support to neurons.
- Maintain extracellular ionic composition.
- Provide metabolic support.
- Produce myelin.
- Participate in repair and immune responses.
- Regulate neurotransmitter concentrations.
- Contribute to the blood-brain barrier.
- Maintain an appropriate environment for neuronal signaling.
5. Resting Membrane Potential
Neurons maintain an electrical potential difference across their plasma membrane. When a neuron is not generating an action potential, its membrane is said to have a resting membrane potential. In many neurons, the resting membrane potential is approximately -70 mV, although the exact value varies among cells.
Why is the inside of the neuron negative?
The resting membrane potential results from unequal distribution of ions across the membrane and selective permeability of the membrane to those ions. Potassium ions (K+) are particularly important because many resting neuronal membranes are relatively permeable to K+.
- K+ concentration is relatively high inside the cell.
- Na+ concentration is relatively high outside the cell.
- Large negatively charged molecules are present inside the cell.
- The membrane has selective permeability to different ions.
- Ion gradients are maintained partly by the Na+/K+-ATPase.
Na+/K+-ATPase
The sodium-potassium pump uses ATP to transport ions against their electrochemical gradients. A typical cycle moves three Na+ ions out of the cell and two K+ ions into the cell.
3 Na+ out
2 K+ in
Uses ATP
The pump is essential for maintaining ion gradients over time, while selective ion permeability makes a major contribution to the immediate resting membrane potential.
6. Action Potential
An action potential is a rapid, transient and regenerative change in membrane potential that allows neurons to transmit information over considerable distances. It is generated when membrane depolarization reaches a critical threshold and activates voltage-gated ion channels.
Major stages of an action potential
- Resting state: Membrane remains near its resting potential.
- Threshold: Sufficient depolarization activates voltage-gated Na+ channels.
- Depolarization: Rapid Na+ influx makes the membrane potential less negative and then positive.
- Peak: Na+ channels become inactivated.
- Repolarization: K+ exits through voltage-gated K+ channels.
- Hyperpolarization: K+ conductance remains elevated temporarily.
- Return to resting state: Ion-channel activity and membrane transport restore the resting condition.
All-or-none principle
Once threshold is reached, an action potential is generated with a characteristic amplitude for that neuron under a given set of conditions. Increasing stimulus strength above threshold does not normally produce a larger action potential. Instead, stronger stimuli can increase the frequency of action potentials.
7. Ion Channels During Action Potential
The action potential depends primarily on voltage-gated Na+ and K+ channels. These channels respond to changes in membrane voltage and undergo characteristic conformational changes.
Voltage-gated Na+ channels
- Open rapidly when membrane depolarization reaches threshold.
- Allow Na+ to move into the neuron.
- Cause the rapid rising phase of the action potential.
- Become inactivated shortly after opening.
- Recovery from inactivation is important for subsequent action potentials.
Voltage-gated K+ channels
- Open more slowly than voltage-gated Na+ channels.
- Allow K+ to move out of the cell.
- Contribute strongly to repolarization.
- May remain open long enough to produce after-hyperpolarization.
| Phase | Main channel event | Major ion movement |
|---|---|---|
| Resting | Voltage-gated channels mostly closed | Dominant resting K+ permeability |
| Depolarization | Voltage-gated Na+ channels open | Na+ enters |
| Peak | Na+ channels become inactivated | Na+ influx decreases |
| Repolarization | Voltage-gated K+ channels are open | K+ exits |
| Hyperpolarization | K+ conductance remains elevated temporarily | Continued K+ efflux |
8. Refractory Period
Following an action potential, the membrane enters a period during which generation of another action potential is either impossible or requires a stronger-than-normal stimulus. This is called the refractory period.
Absolute refractory period
During the absolute refractory period, another action potential cannot normally be initiated regardless of the strength of the stimulus. This is primarily related to the inactivated state of voltage-gated Na+ channels.
Relative refractory period
During the relative refractory period, another action potential can be generated, but a stronger stimulus is required. Persistent K+ conductance and membrane hyperpolarization contribute to this period.
| Feature | Absolute refractory period | Relative refractory period |
|---|---|---|
| Action potential generation | Not normally possible | Possible with stronger stimulus |
| Major mechanism | Na+ channel inactivation | Persistent K+ conductance and membrane hyperpolarization |
| Functional significance | Limits maximum firing frequency | Influences firing threshold after an action potential |
9. Conduction of Nerve Impulse
Once an action potential is generated, the electrical disturbance can propagate along the axon. Local current generated by an active membrane region depolarizes adjacent membrane to threshold, leading to sequential activation of voltage-gated channels.
Important characteristics of impulse conduction
- The action potential is regenerated along the axon.
- Propagation occurs because one active membrane region influences the next region.
- The amplitude of an individual action potential is not progressively reduced along a healthy axon.
- The refractory period helps prevent backward re-excitation of recently activated membrane.
- Myelination greatly increases conduction velocity.
Factors affecting conduction velocity
- Myelination: Myelinated axons generally conduct faster than unmyelinated axons of similar diameter.
- Axon diameter: Larger axons generally have lower internal resistance and conduct impulses more rapidly.
- Temperature: Within physiological limits, temperature can influence channel kinetics and conduction velocity.
10. Myelination and Saltatory Conduction
Myelin is a lipid-rich insulating structure surrounding many axons. It reduces current leakage across the membrane and allows rapid propagation of action potentials.
Myelin-producing cells
| Cell | Location | Function |
|---|---|---|
| Oligodendrocyte | CNS | Myelinates axons in the central nervous system. |
| Schwann cell | PNS | Myelinates axons in the peripheral nervous system. |
Saltatory conduction
In myelinated axons, voltage-gated ion channels are concentrated at the nodes of Ranvier. The electrical signal effectively travels rapidly between successive nodes, a process called saltatory conduction.
- Nodes of Ranvier are exposed regions between myelinated segments.
- Voltage-gated Na+ channels are concentrated at nodes.
- Myelin increases membrane resistance.
- Myelin decreases membrane capacitance.
- Action-potential regeneration occurs at the nodes.
- Saltatory conduction is much faster than continuous conduction in comparable unmyelinated axons.
11. Synapse and Synaptic Transmission
A synapse is a specialized junction through which a neuron communicates with another neuron or an effector cell. Synapses can be electrical or chemical, although chemical synapses are extremely common in the nervous system.
Chemical synapse
A typical chemical synapse consists of a presynaptic terminal, a synaptic cleft and a postsynaptic membrane containing receptors. Neurotransmitters are released from the presynaptic terminal and bind receptors on the postsynaptic cell.
Basic sequence of chemical synaptic transmission
- Action potential reaches the presynaptic terminal.
- Presynaptic membrane depolarizes.
- Voltage-gated Ca2+ channels open.
- Ca2+ enters the presynaptic terminal.
- Ca2+ promotes synaptic-vesicle fusion with the membrane.
- Neurotransmitter is released into the synaptic cleft.
- Neurotransmitter binds receptors on the postsynaptic membrane.
- Postsynaptic ion channels or signaling pathways are activated.
- The postsynaptic membrane undergoes a change in electrical state.
- Neurotransmitter action is terminated by degradation, reuptake, diffusion or other clearance mechanisms.
12. Release of Neurotransmitters
Neurotransmitter release at a typical chemical synapse is a Ca2+-dependent process. When an action potential arrives at the presynaptic terminal, voltage-gated Ca2+ channels open. Because extracellular Ca2+ concentration is normally higher than intracellular free Ca2+ concentration, Ca2+ enters the terminal.
Role of calcium
- Ca2+ acts as the critical intracellular signal for rapid vesicle fusion.
- Calcium binds specialized proteins associated with synaptic vesicles.
- Vesicles fuse with the presynaptic membrane.
- Neurotransmitter is released by exocytosis.
- The amount of transmitter released is influenced by presynaptic Ca2+ entry.
Action potential → Ca2+ channel opening → Ca2+ influx → vesicle fusion → exocytosis → neurotransmitter release.
Termination of neurotransmitter action
Neurotransmitter signaling must be terminated to allow accurate and controlled communication. Different neurotransmitters are cleared by different mechanisms.
- Reuptake: Transport proteins remove neurotransmitters from the synaptic cleft.
- Enzymatic degradation: Enzymes chemically modify or break down neurotransmitters.
- Diffusion: Some transmitter molecules diffuse away from the synaptic cleft.
- Glial uptake: Glial cells can participate in neurotransmitter clearance.
13. Neurotransmitter Receptors
Neurotransmitters produce their effects by binding to receptors on postsynaptic or presynaptic membranes. Receptors can be broadly divided into ionotropic and metabotropic types.
Ionotropic receptors
Ionotropic receptors are ligand-gated ion channels. Binding of a neurotransmitter directly changes ion-channel activity and can produce rapid postsynaptic responses.
- Directly associated with an ion channel.
- Usually produce rapid responses.
- Often mediate fast synaptic transmission.
Metabotropic receptors
Metabotropic receptors are not themselves ion channels. They generally activate intracellular signaling pathways, often through G proteins. Their effects are usually slower in onset but can be longer-lasting and more modulatory.
- Indirectly influence ion channels or cellular processes.
- Often involve G proteins and second-messenger pathways.
- Responses are generally slower than ionotropic signaling.
- Can amplify and modulate cellular responses.
| Feature | Ionotropic receptor | Metabotropic receptor |
|---|---|---|
| Structure | Ligand-gated ion channel | Usually receptor linked to intracellular signaling pathways |
| Speed | Fast | Usually slower |
| Mechanism | Direct ion-channel opening/closing | Indirect modulation through signaling pathways |
| Duration | Often relatively brief | Can be longer-lasting |
14. Excitatory and Inhibitory Synaptic Potentials
Neurotransmitters can either increase or decrease the probability that the postsynaptic neuron will generate an action potential. The effect depends not simply on the name of the neurotransmitter but on the receptor type, ion permeability and cellular context.
Excitatory postsynaptic potential (EPSP)
An EPSP is a postsynaptic depolarization that generally makes the membrane potential closer to the threshold for action-potential generation.
- Generally depolarizes the postsynaptic membrane.
- Increases the probability of action-potential generation.
- Often involves inward movement of positive ions or reduction in outward positive current.
Inhibitory postsynaptic potential (IPSP)
An IPSP generally reduces the probability of action-potential generation. This may occur through hyperpolarization or by increasing membrane conductance in a way that opposes depolarization.
- Generally decreases neuronal excitability.
- Can involve increased Cl− conductance or K+ conductance, depending on the cell.
- Contributes to integration of excitatory and inhibitory signals.
Summation
A neuron receives signals from many synapses. Postsynaptic potentials can combine through spatial and temporal summation.
- Spatial summation: Signals from different synaptic locations combine.
- Temporal summation: Repeated signals from the same synapse occur close together in time and combine.
- The axon initial segment integrates the resulting electrical inputs and may initiate an action potential if threshold is reached.
15. Important Comparisons for Competitive Exams
| Concept | Meaning | Key Point |
|---|---|---|
| Neuron | Excitable cell specialized for communication | Generates and transmits electrical signals |
| Glial cell | Non-neuronal support cell | Support, myelination, homeostasis and defense |
| Resting potential | Electrical potential difference across resting membrane | Often around -70 mV in neurons |
| Depolarization | Membrane potential becomes less negative | Na+ influx is important during neuronal action potentials |
| Repolarization | Membrane returns toward negative values | K+ efflux is important |
| Hyperpolarization | Membrane becomes more negative than resting level | Often associated with continued K+ conductance |
| Absolute refractory period | New action potential cannot normally be generated | Na+ channels are inactivated |
| Relative refractory period | New action potential requires stronger stimulus | Often associated with elevated K+ conductance |
| Saltatory conduction | Rapid propagation in myelinated axons | Action potential regenerated at nodes |
| Synapse | Specialized communication junction | Can be chemical or electrical |
| Ionotropic receptor | Ligand-gated ion channel | Fast response |
| Metabotropic receptor | Receptor linked to intracellular signaling | Slower and modulatory response |
16. Important Applied Concepts
Myelin disorders
Proper myelination is essential for rapid and reliable nerve conduction. Damage to myelin can slow or disrupt electrical signal propagation. Disorders affecting CNS myelin and PNS myelin have different cellular and anatomical characteristics.
- CNS myelin is produced by oligodendrocytes.
- PNS myelin is produced by Schwann cells.
- Loss of myelin can reduce conduction velocity.
- Severe disruption of myelin can result in conduction failure.
Ion-channel toxins and drugs
Neuronal excitability depends on voltage-gated ion channels. Substances that interfere with Na+, K+ or Ca2+ channels can substantially alter neuronal signaling.
- Blocking voltage-gated Na+ channels can prevent action-potential propagation.
- Changes in K+ channel function can alter repolarization and excitability.
- Changes in Ca2+ entry can influence neurotransmitter release.
- Ion-channel function is therefore central to neurophysiology and pharmacology.
Synaptic transmission and disease
Abnormalities in neurotransmitter synthesis, release, receptors, reuptake or degradation can affect nervous-system function. Because synaptic communication is highly regulated, even small alterations in signaling pathways can influence neuronal activity.
17. Quick Revision Notes
⭐ Must-Remember Points
- The nervous system receives, integrates and responds to information.
- The CNS consists of the brain and spinal cord.
- The PNS connects the CNS with the rest of the body.
- The neuron is the principal electrically excitable cell of the nervous system.
- Dendrites generally receive information, whereas axons generally transmit information away from the cell body.
- Glial cells support, protect and regulate the neuronal environment.
- Astrocytes provide metabolic and homeostatic support in the CNS.
- Oligodendrocytes form myelin in the CNS.
- Schwann cells form myelin in the PNS.
- Microglia provide immune and phagocytic functions in the CNS.
- Resting neuronal membrane potential is often approximately -70 mV.
- K+ permeability is an important contributor to the resting membrane potential.
- The Na+/K+-ATPase uses ATP.
- Each pump cycle commonly transports 3 Na+ out and 2 K+ in.
- Action potentials are triggered when membrane depolarization reaches threshold.
- Voltage-gated Na+ channels are responsible for the rapid depolarizing phase.
- Voltage-gated K+ channels contribute strongly to repolarization.
- After-hyperpolarization can occur because K+ conductance remains elevated temporarily.
- The absolute refractory period is mainly associated with Na+ channel inactivation.
- During the relative refractory period, a stronger stimulus is usually required.
- Myelination increases the speed of nerve impulse conduction.
- Saltatory conduction occurs in myelinated axons.
- Nodes of Ranvier contain high concentrations of voltage-gated ion channels.
- Larger axon diameter generally increases conduction velocity.
- At a chemical synapse, an action potential reaches the presynaptic terminal.
- Depolarization of the terminal opens voltage-gated Ca2+ channels.
- Ca2+ influx triggers synaptic-vesicle fusion.
- Neurotransmitter is released by exocytosis.
- Neurotransmitters bind receptors on the postsynaptic cell.
- Ionotropic receptors are ligand-gated ion channels.
- Metabotropic receptors generally act through intracellular signaling pathways.
- EPSPs generally increase the probability of action-potential generation.
- IPSPs generally reduce the probability of action-potential generation.
- Spatial summation combines signals from different synaptic locations.
- Temporal summation combines repeated signals occurring close together in time.
- Neurotransmitter action can be terminated by reuptake, enzymatic degradation and diffusion.
18. Nervous System: 10 MCQs
Instructions: Select one option for each question and click Submit Quiz. The correct answers and explanations remain hidden until submission.
🎯 Your Quiz Result
19. Final Exam-Oriented Summary
The nervous system is a highly organized communication network that receives sensory information, processes that information and produces appropriate responses. Neurons are specialized excitable cells that generate electrical signals, while glial cells provide essential support, protection, metabolic regulation, immune functions and myelination.
At rest, neurons maintain an electrical potential difference across their membranes. Ion concentration gradients and selective membrane permeability are fundamental to this resting state. When sufficient depolarization reaches threshold, voltage-gated Na+ channels produce rapid depolarization. Na+ channel inactivation and activation of voltage-gated K+ channels then contribute to repolarization. Continued K+ conductance can produce hyperpolarization.
Action potentials propagate along axons through sequential regeneration of electrical activity. Myelinated axons conduct impulses rapidly by saltatory conduction, in which action potentials are regenerated at the nodes of Ranvier. Oligodendrocytes produce myelin in the CNS, whereas Schwann cells produce myelin in the PNS.
At a typical chemical synapse, an action potential reaches the presynaptic terminal and opens voltage-gated Ca2+ channels. Calcium enters the terminal and triggers synaptic-vesicle fusion. Neurotransmitter is subsequently released into the synaptic cleft, where it binds receptors on the postsynaptic cell.
- Neuron: Main electrically excitable cell.
- Glial cells: Support and regulate neural tissue.
- Astrocytes: CNS support and homeostasis.
- Oligodendrocytes: CNS myelin.
- Schwann cells: PNS myelin.
- Microglia: CNS immune/phagocytic cells.
- Resting potential: Often approximately -70 mV.
- Depolarization: Mainly associated with Na+ influx during a typical neuronal action potential.
- Repolarization: Mainly associated with K+ efflux.
- Absolute refractory period: Na+ channel inactivation is important.
- Relative refractory period: Stronger stimulus is required.
- Saltatory conduction: Rapid conduction in myelinated axons.
- Chemical synapse: Uses neurotransmitter-mediated communication.
- Critical ion for neurotransmitter release: Ca2+.
- Ionotropic receptor: Ligand-gated ion channel.
- Metabotropic receptor: Acts through intracellular signaling pathways.
- EPSP: Generally increases neuronal excitability.
- IPSP: Generally decreases neuronal excitability.
- Spatial summation: Integration of inputs from different locations.
- Temporal summation: Integration of repeated inputs over time.
For CSIR-NET, GATE Biotechnology, DBT-BET, ICMR-JRF and postgraduate examinations, the most important strategy is to connect the concepts rather than memorize them separately: resting potential → threshold → Na+ influx → depolarization → Na+ inactivation → K+ efflux → repolarization → hyperpolarization → refractory period → impulse conduction → Ca2+-dependent neurotransmitter release.
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