The nervous system maintains homeostasis by controlling conditions within healthy limits.
This chapter will cover the different branches of the nervous system.
We will identify and describe the various types of cells found in nervous tissue.
The nervous system has sensory, integrative, and motor functions.
Sensory functions detect changes through sensory receptors.
Integrative functions analyze sensory information, store aspects, and make decisions.
Motor functions respond to stimuli via effectors.
The nervous system is divided into two main divisions:
Central Nervous System (CNS): Brain and spinal cord.
Peripheral Nervous System (PNS): Cranial nerves, spinal nerves, enteric plexuses, and sensory receptors.
The Central Nervous System (CNS) integrates sensory input and initiates motor output.
The Peripheral Nervous System (PNS) is divided into:
Sensory (afferent) division: somatic and special senses.
Motor (efferent) division: somatic nervous system, autonomic nervous system, and enteric plexuses.
Somatic nervous system: controls skeletal muscle.
Autonomic nervous system: controls smooth muscle, cardiac muscle, and glands.
Sympathetic division
Parasympathetic division
Enteric plexuses: control smooth muscle and glands of the digestive canal.
Nervous tissue consists of:
Neurons: Electrically excitable cells that transmit nerve impulses (action potentials).
Neuroglia: Support, protect, and maintain neurons.
Neurons are electrically excitable cells.
A nerve impulse is called an action potential.
Neurons are classified by the number of processes extending from the cell body.
Neurons are classified based on the direction of nerve impulse propagation.
Sensory (afferent) neurons: convey information to the CNS.
Motor (efferent) neurons: convey action potentials from the CNS to effectors (muscles or glands).
Interneurons (association neurons): process sensory information and elicit a motor response; usually multipolar.
Neuroglia are not electrically excitable.
They make up about half the volume of the nervous system.
They can multiply and divide.
There are 6 kinds total (4 in CNS, 2 in PNS).
Astrocytes (protoplasmic and fibrous)
Oligodendrocytes - produce myelin
Microglial cells
Ependymal cells - produces spinal fluid
Schwann cells - produce myelin
Satellite cells
The myelin sheath is produced by Schwann cells (PNS) and oligodendrocytes (CNS).
It surrounds the axons of most neurons.
Gray matter contains neuronal cell bodies, dendrites, unmyelinated axons, and neuroglia. - on the outside in the brain and inside with the spine
White matter contains myelinated axons.
Excitable cells communicate via action potentials (AP) or graded potentials (GP).
Action potentials (AP) allow communication over short and long distances.
Graded potentials (GP) allow communication over short distances only.
Production of an AP or GP depends on:
Resting membrane potential
Existence of certain ion channels
Leak channels: alternate between open and closed; K+ channels are more numerous than Na^+ channels.
Ligand-gated channels: respond to chemical stimuli (ligand binds to receptor).
Mechanically-gated channels: respond to mechanical vibration or pressure stimuli.
Voltage-gated channels: respond to direct changes in membrane potential.
Type of Ion Channel | Description | Location |
---|---|---|
Leak channels | Gated channels that randomly open and close. | Found in nearly all cells, and dendrites, cell bodies, and axons of all types of neurons. |
Ligand-gated channels | Gated channels that open in response to binding of ligand (chemical) stimulus. | Dendrites of some sensory neurons such as pain receptors and dendrites and cell bodies of interneurons and motor neurons. |
Mechanically gated channels | Gated channels that open in response to mechanical stimulus (such as touch, pressure, vibration, or tissue stretching). | Dendrites of some sensory neurons such as touch receptors, pressure receptors, and some pain receptors. |
Voltage-gated channels | Gated channels that open in response to voltage stimulus (change in membrane potential). | Axons of all types of neurons. |
The membrane of a non-conducting neuron is positive outside and negative inside.
Determined by:
Unequal distribution of ions across the plasma membrane and the selective permeability of the neuron’s membrane to Na^+ and K^+.
Most anions cannot leave the cell.
Na^+/K^+ pumps.
Unequal distribution of ions (e.g., sodium, potassium, chloride, phosphate).
Selective permeability of the membrane to Na^+ and K^+ through leak channels.
Most anions cannot leave the cell.
Sodium-potassium ATPase (pump) maintains the resting membrane potential by pumping 3 Na^+ ions out and 2 K^+ ions into the cell.
Small deviations in resting membrane potential.
Occur in response to the opening of a mechanically-gated or ligand-gated ion channel.
The amplitude of a graded potential depends on the stimulus strength.
Graded potentials can be added together to become larger in amplitude.
An action potential is a sequence of rapidly occurring events that decrease and eventually reverse the membrane potential and eventually restore it to the resting state.
Action Potentials have two phases:
Depolarization
Repolarization
Action potentials can only occur if the membrane potential reaches threshold.
Voltage-gated Na^+ channels open during the depolarizing phase.
Voltage-gated K^+ channels open during the repolarizing phase.
Characteristic | Graded Potentials | Nerve Impulses |
---|---|---|
Origin | Arise mainly in dendrites and cell body. | Arise at trigger zones and propagate along axon. |
Types of channels | Ligand-gated or mechanically gated ion channels. | Voltage-gated channels for Na^+ and K^+. |
Conduction | Decremental (not propagated); permit communication over short distances. | Propagate and thus permit communication over longer distances. |
Amplitude (size) | Depending on strength of stimulus, varies from less than 1 mV to more than 50 mV. | All or none; typically about 100 mV. |
Duration | Typically longer, ranging from several milliseconds to several minutes. | Shorter, ranging from 0.5 to 2 msec. |
Polarity | May be hyperpolarizing (inhibitory) or depolarizing (excitatory). | Always consist of depolarizing phase followed by repolarizing phase and return to resting membrane potential. |
Refractory period | Not present; summation can occur. | Present; summation cannot occur. |
Action potentials must travel from the trigger zone to the axon terminals for communication to occur.
This traveling is called propagation.
Action potentials do not die out; they keep their strength as they spread across the membrane of a neuron.
Continuous conduction: Step-by-step depolarization of each adjacent area of the plasma membrane; occurs in unmyelinated axons.
Saltatory conduction: Nerve impulse jumps from neurofibril node (node of Ranvier) to node; occurs in myelinated axons; faster than continuous conduction.
Axon diameter
Larger diameter axons propagate APs faster.
Amount of myelination
Myelin increases speed of AP propagation.
Temperature
Higher temperature increases speed of AP propagation.
A synapse is the junction between neurons or between a neuron and an effector.
Electrical Synapse
Gap junctions connect cells and allow the transfer of information to synchronize the activity of a group of cells
Chemical Synapse
One-way transfer of information from a presynaptic neuron to a postsynaptic neuron
Nerve impulse arrives at synaptic end bulb of presynaptic neuron.
Depolarization opens voltage-gated Ca^{2+} channels, and Ca^{2+} flows inward.
Increase in Ca^{2+} inside the presynaptic neuron triggers exocytosis of synaptic vesicles.
Neurotransmitter molecules are released into the synaptic cleft.
Neurotransmitter binds to receptors on the postsynaptic neuron.
Opening of ligand-gated channels results in an excitatory or inhibitory postsynaptic potential (EPSP or IPSP).
When summation of EPSPs and IPSPs causes depolarization to threshold, an action potential (nerve impulse) is generated.
Excitatory postsynaptic potentials (EPSP): A depolarizing postsynaptic potential.
Inhibitory postsynaptic potentials (IPSP): A hyperpolarizing postsynaptic potential.
A postsynaptic neuron can receive many signals at once.
Neurotransmitters at chemical synapses cause either an excitatory or inhibitory graded potential
Neurotransmitter receptors have two structures
Ionotropic receptors
Contains a neurotransmitter binding site and ion channel
Metabotropic receptors
Contains a neurotransmitter binding site and is coupled ot a separate ion channel by a G protein
Neurotransmitter can be removed from the synaptic cleft by:
Diffusion
Enzymatic degradation
Uptake into cells
If several presynaptic end bulbs release their neurotransmitter at about the same time, the combined effect may generate a nerve impulse due to summation.
Summation may be spatial or temporal.
Spatial summation: summation of postsynaptic potentials in response to stimuli that occur at different locations in the postsynaptic neuron at the same time.
Temporal summation: summation of postsynaptic potentials in response to stimuli that occur at the same location in the postsynaptic neuron but at different times.
Structure | Functions |
---|---|
Dendrites | Receive stimuli through activation of ligand-gated or mechanically gated ion channels; in sensory neurons, produce generator or receptor potentials; in motor neurons and interneurons, produce excitatory and inhibitory postsynaptic potentials (EPSPS and IPSPs). |
Cell body | Receives stimuli and produces EPSPs and IPSPs through activation of ligand-gated ion channels. |
Junction of axon hillock and initial segment of axon | Trigger zone in many neurons; integrates EPSPs and IPSPs and, if sum is depolarization that reaches threshold, initiates a nerve impulse. |
Axon | Propagates nerve impulses from initial segment (or from dendrites of sensory neurons) to axon terminals in self-regenerating manner; impulse amplitude does not change as it propagates along axon. |
Axon terminals and synaptic end bulbs (or varicosities) | Inflow of Ca^{2+} caused by depolarizing phase of nerve impulse triggers exocytosis of neurotransmitter from synaptic vesicles. |
Small molecule neurotransmitters
Acetylcholine
Amino acids
Biogenic amines
ATP and other purines
Nitric oxide
Carbon monoxide
Neuropeptides
Substance P
Enkephalins
Endorphins
Dynorphins
Hypothalamic releasing and inhibiting hormones
Angiotensin II
Cholecystokinin
Substance | Description |
---|---|
Substance P | Found in sensory neurons, spinal cord pathways, and parts of brain associated with pain; enhances perception of pain. |
Enkephalins | Inhibit pain impulses by suppressing release of substance P; may have role in memory and learning, control of body temperature, sexual activity, and mental illness. |
Endorphins | Inhibit pain by blocking release of substance P; may have role in memory and learning, sexual activity, control of body temperature, and mental illness. |
Dynorphins | May be related to controlling pain and registering emotions. |
Hypothalamic releasing and inhibiting hormones | Produced by hypothalamus; regulate release of hormones by anterior pituitary. |
Angiotensin II | Stimulates thirst; may regulate blood pressure in brain. As a hormone, causes vasoconstriction and promotes release of aldosterone, which increases rate of salt and water reabsorption by kidneys. |
Cholecystokinin (CCK) | Found in brain and small intestine; may regulate feeding as a “stop eating” signal. As a hormone, regulates pancreatic enzyme secretion during digestion, and contraction of smooth muscle in gastrointestinal tract. |
Neuropeptide Y | Stimulates food intake; may play a role in the stress response. |
A neural circuit is a functional group of neurons that process specific types of information.
Types of circuits
Simple series
Diverging
Converging
Reverberating
Parallel after-discharge
Although the nervous system exhibits plasticity, neurons have a limited ability to regenerate themselves
Plasticity – the capability to change based on experience
Regenerate – the capability to replicate or repair
In the CNS, there is little or no repair due to:
Inhibitory influences from neuroglia, particularly oligodendrocytes
Absence of growth-stimulating cues that were present during fetal development
Rapid formation of scar tissue
In the PNS repair is possible if the cell body is intact, Schwann cells are functional, and scar tissue formation does not occur too rapidly
Steps involved in the repair process are:
Chromatolysis
Wallerian degeneration
Formation of a regeneration tube
Autoimmune disease that causes progressive destruction of myelin sheath
Cause is unclear; may be genetic and/or environmental
Symptoms include muscle weakness, abnormal sensations and double vision
Several types of depression
Major depression
Dysthymia
Bipolar depression (manic-depressive illness)
Seasonal affective disorder (SAD)
Common feelings are lack of interest in activities, sadness, helpless and possibly suicidal thoughts
Commonly treated through selective serotonin reuptake inhibitors (SSRIs)
Epilepsy
Short, recurrent attacks of motor, sensory or psychological function
Initiated by abnormal synchronous electrical discharges from the millions of neurons in the brain
Excitotoxicity
Destructions of neurons through prolonged activation of excitatory synaptic transmission
Caused by high levels of glutamine in CNS interstitial fluid