13 Functions and channels of the nervous system

Learning Objectives

After reading this section, you should be able to-

  • Describe the general functions of the nervous system
  • Differentiate between the motor (efferent) and sensory (afferent) components of the nervous system
  • List the major ion channels of neurons and describe them as leak (leakage or passive) or voltage-gated channels, mechanically gated channels, or ligand-gated (chemically-gated) channels, and identify where they typically are located on a neuron
  • Describe the physiological basis of the resting membrane potential (RMP) in a neuron including the ion channels involved, the relative ion concentrations, and the electrochemical gradient.

The Central and Peripheral Nervous Systems

The picture you have in your mind of the nervous system probably includes the brain, the nervous tissue contained within the cranium, and the spinal cord, the extension of nervous tissue within the vertebral column. Additionally, the nervous tissue that reach out from the brain and spinal cord to the rest of the body- (nerves) -are also part of the nervous system. We can anatomically divide the nervous system into two major regions: the central nervous system (CNS) is the brain and spinal cord, and the peripheral nervous system (PNS) is the nerves (Figure 13.1). The brain is contained within the cranial cavity of the skull, and the spinal cord is contained within the vertebral canal of the vertebral column. The peripheral nervous system is so named because it is in the periphery—meaning beyond the brain and spinal cord.

 

This diagram shows a silhouette of a human highlighting the nervous system. The central nervous system is composed of the brain and spinal cord. The brain is a large mass of ridged and striated tissue within the head. The spinal cord extends down from the brain and travels through the torso, ending in the pelvis. Pairs of enlarged nervous tissue, labeled ganglia, flank the spinal cord as it travels through the rib area. The ganglia are part of the peripheral nervous system, along with the many thread-like nerves that radiate from the spinal cord and ganglia through the arms, abdomen and legs.
Figure 13.1 – Central and Peripheral Nervous System: The CNS contains the brain and spinal cord, the PNS includes nerves.

Functional Divisions of the Nervous System

In addition to the anatomical divisions listed above, the nervous system can also be divided on the basis of its functions. The nervous system is involved in receiving information about the environment around us (sensory functions, sensation) and generating responses to that information (motor functions, responses) and coordinating the two (integration).

 

Sensation. Sensation refers to receiving information about the environment, either what is happening outside (ie: heat from the sun) or inside the body (ie: heat from muscle activity). These sensations are known as stimuli (singular = stimulus) and different sensory receptors are responsible for detecting different stimuli. Sensory information travels towards the CNS through the PNS nerves in the specific division known as the afferent (sensory) branch of the PNS. When information arises from sensory receptors in the skin, skeletal muscles, or joints, it is transmitted to the CNS using somatic sensory neurons; when information arises from sensory receptors in the blood vessels or internal organs, it is transmitted to the CNS using visceral sensory neurons.

Integration. Stimuli that are detected by sensory structures are communicated to the nervous system where information is processed. In the CNS, information from some stimuli is compared with, or integrated with, information from other stimuli or memories of previous stimuli. Then, a motor neuron is activated to initiate a response from the effector organ. This process during which sensory information is processed and a motor response generated is called integration (Figure 13.2).

Response. The nervous system produces a response in effector organs (such as muscles or glands) due to the sensory stimuli. The motor (efferent) branch of the PNS carries signals away from the CNS to the effector organs. When the effector organ is a skeletal muscle, the neuron carrying the information is called a somatic motor neuron; when the effector organ is cardiac or smooth muscle or glandular tissue, the neuron carrying the information is called an autonomic motor neuron. Voluntary responses are governed by somatic motor neurons and involuntary responses are governed by autonomic motor neurons, which are discussed in the next section.

 

This figure shows the relationship between the peripheral and central nervous system
Figure 13.2 – Nervous System Function: Integration occurs in the CNS where sensory information from the periphery is processed and interpreted. The CNS then creates a motor plan that is executed by the efferent branch working with effector organs.

The functions of the nervous system—sensation, integration, and response—depend on the functions of the neurons underlying these pathways. To understand how neurons are able to communicate, it is necessary to describe the role of an excitable membrane in generating these signals. The basis of this process is the action potentialAn action potential is a predictable change in membrane potential that occurs due to the opening and closing of voltage gated ion channels on the cell membrane.

Electrically Active Cell MembranesMost cells in the body make use of charged particles (ions) to create electrochemical charge across the cell membrane. In a prior chapter, we described how muscle cells contract based on the movement of ions across the cell membrane. For skeletal muscles to contract, due to excitation–contraction coupling, they require input from a neuron. Both muscle and nerve cells make use of a cell membrane that is specialized for signal conduction to regulate ion movement between the extracellular fluid and cytosol.

As you learned in the chapter on cells, the cell membrane is primarily responsible for regulating what can cross the membrane. The cell membrane is a phospholipid bilayer, so only substances that can pass directly through the hydrophobic core can diffuse through unaided. Charged particles, which are hydrophilic, cannot pass through the cell membrane without assistance (Figure 13.3). Specific transmembrane channel proteins permit charged ions to move across the membrane. Several passive transport channels, as well as active transport pumps, are necessary to generate a transmembrane potential, and an action potential. Of special interest is the carrier protein referred to as the sodium/potassium pump that uses energy to move sodium ions (Na+) out of a cell and potassium ions (K+) into a cell, thus regulating ion concentration on both sides of the cell membrane.

This diagram shows a cross section of a cell membrane. The cell membrane proteins are large, blocky, objects. Peripheral proteins are not embedded in the phospholipid bilayer. The peripheral protein shown here is attached to the outside surface of another protein on the extracellular fluid side. Integral proteins are embedded between the phospholipids of the cell membrane. The transmembrane integral protein extends through both phospholipids layers. The opposite ends of this protein project into the cytosol and the extracellular fluid. A second, smaller integral protein only extends into the inner phospholipid layer. Its opposite end projects into the cytosol. This second protein is, therefore, not a transmembrane protein. The channel protein is cylinder shaped with a hollow internal tube labeled the pore. The sides of the channel protein can bulge inward to close the pore.
Figure 13.3 – Cell Membrane and Transmembrane Proteins: The cell membrane is composed of a phospholipid bilayer and has many transmembrane proteins, including different types of channel proteins that serve as ion channels.

The sodium/potassium pump requires energy in the form of adenosine triphosphate (ATP), so it is also referred to as an ATPase pump. As was explained in the cell chapter, the concentration of Na+ is higher outside the cell than inside, and the concentration of K+ is higher inside the cell than outside. Therefore, this pump works against the concentration gradients for sodium and potassium ions, which is why it requires energy. The Na+/K+ ATPase pump maintains these important ion concentration gradients.

Ion channels are pores that allow specific charged particles to cross the membrane in response to an existing electrochemical gradient. Proteins are capable of spanning the cell membrane, including its hydrophobic core, and can interact with charged ions because of the varied properties of amino acids found within specific regions of the protein channel. Hydrophobic amino acids are found in the regions that are adjacent to the hydrocarbon tails of the phospholipids, where as hydrophilic amino acids are exposed to the fluid environments of the extracellular fluid and cytosol. Additionally, ions will interact with the hydrophilic amino acids, which will be selective for the charge of the ion. Channels for cations (positive ions) will have negatively charged side chains in the pore. Channels for anions (negative ions) will have positively charged side chains in the pore. The diameter of the channel’s pore also impacts the specific ions that can pass through.  Some ion channels are selective for charge but not necessarily for size. These nonspecific channels allow cations—particularly Na+, K+, and Ca2+—to cross the membrane, but exclude anions.

Some ion channels do not allow ions to freely diffuse across the membrane, but are gated instead. A ligand-gated channel opens because a molecule, or ligand, binds to the extracellular region of the channel (Figure 13.4). These channels are usually found on the dendrites of a cell.

 

These two diagrams each show a channel protein embedded in the cell membrane. In the left diagram, there is a large number of sodium ions (NA plus) and calcium ions (CA two plus) in the extracellular fluid. Within the cytosol, there is a large number of potassium ions (K plus) but only a few sodium ions. In this diagram, the channel is closed. Two ACH molecules are floating in the extracellular fluid. Their label indicates that a neurotransmitter, a ligand, is required to open the ion channel. The neurotransmitter receptor site on the extracellular fluid side of the channel protein matches the shape of the ACH molecules. In the right diagram, the two ACH molecules attach to the neurotransmitter receptor sites on the channel protein. This opens the channel and the sodium and calcium ions diffuse through the channel and into the cytosol, down their concentration gradient. The potassium ions also diffuse through the channel in the opposite direction down their concentration gradient (out of the cell and into the extracellular fluid).
Figure 13.4 – Ligand-Gated Channels: When the ligand, in this case the neurotransmitter acetylcholine, binds to a specific location on the extracellular surface of the channel protein, the pore opens to allow select ions through. The ions, in this case, are cations of sodium, calcium, and potassium.

 

A mechanically-gated channel opens because of a physical distortion of the cell membrane. Many channels associated with the sense of touch are mechanically-gated. For example, as pressure is applied to the skin, mechanically-gated channels on the subcutaneous receptors open and allow ions to enter (Figure 13.5).

These two diagrams each show a channel protein embedded in the cell membrane. In the left diagram, there are a large number of sodium ions in the extracellular fluid, but only a few sodium ions in the cytosol. There is a large number of calcium ions in the cytosol but only a few calcium ions in the extracellular fluid. In this diagram, the channel is closed, as the extracellular side has a lid, somewhat resembling that on a trash can, that is closed over the channel opening. In the right diagram, the mechanically gated channel is open. This allows the sodium ions to flow from the extracellular fluid into the cell, down their concentration gradient. At the same time, the calcium ions are moving from the cytosol into the extracellular fluid, down their concentration gradient.
Figure 13.5 – Mechanically-Gated Channels: When a mechanical change occurs in the surrounding tissue (such as pressure or stretch) the channel is physically opened, and ions can move through the channel, down their concentration gradient.

A voltage-gated channel is a channel that responds to changes in the electrical properties of the membrane in which it is embedded. Normally, the inner portion of the membrane is at a negative voltage. When that voltage becomes less negative and reaches a value specific to the channel, it opens and allows ions to cross the membrane (Figure 13.6).

This is a two part diagram. Both diagrams show a voltage gated channel embedded in the lipid membrane bilayer. The channel contains a sphere shaped gate that is attached to a filament. In the first diagram there are several ions in the cytosol but only one ion in the extracellular fluid. The voltage across the membrane is currently minus seventy millivolts and the voltage gated channel is closed. In the second diagram, the voltage in the cytosol is minus fifty millivolts. This voltage change has caused the voltage gated channel to open, as the small sphere is no longer occluding the channel. One of the ions is moving through the channel, down its concentration gradient, and out into the extracellular fluid.
Figure 13.6 – Voltage-Gated Channels: Voltage-gated channels open when the transmembrane voltage changes around them. Amino acids in the structure of the protein are sensitive to charge and cause the pore to open to the selected ion.

A leak channel is randomly gated, meaning that it opens and closes at random, hence the reference to leaking. There is no actual event that opens the channel; instead, it has an intrinsic rate of switching between the open and closed states. Leak channels contribute to the resting transmembrane voltage of the excitable membrane (Figure 13.7). Voltage-gated and leak channels are generally found along the axon and are involved in maintaining membrane potential, and moving an action potential forward.

This is a two part diagram. Both diagrams show a leakage channel embedded in the lipid membrane bilayer. The leakage channel is cylindrical with a large, central opening. In the first diagram there are several ions in the cytosol but only one ion in the extracellular fluid. No ions are moving through the leakage channel because the channel is closed. In the second diagram, the leakage channel randomly opens, allowing two ions to travel through the channel, down their concentration gradient, and out into the extracellular fluid.
Figure 13.7– Leak Channels: These channels open and close at random, allowing ions to pass through when they are open.

Adapted from Anatomy & Physiology by Lindsay M. Biga et al, shared under a Creative Commons Attribution-ShareAlike 4.0 International License, chapter 12.

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