Read the section from pp. 317-322, focusing in particular on the
description of the sensory neurons in the skin (see Figure 10.10 p
319). Chapter 11 provides information about the efferent division
of the peripheral nervous system. Figure 11.9 p. 367
provides a very useful summary of the somatic efferent and
autonomic efferent divisions.
The central nervous system (CNS) consists of the brain and spinal
cord; everything outside of the dura mater is considered the
peripheral nervous system (PNS). The PNS can be divided into two
major divisions based on the way that information flows. The afferent
division consists of neurons that are bringing sensory
information about the periphery toward the CNS, while the
efferent division consists of neurons that
are conveying information away from the CNS, and out to
control muscles and organs in the body. The efferent division is
further divided into the somatic efferent division, which consists
of neurons that control skeletal muscles, and the autonomic
efferent division, which consists of the neurons that control all
other organs (collectively termed viscera).
Spinal nerves are bundles of
axons containing both afferent and efferent axons. But close
to the spinal cord, the axons are separated into dorsal roots (afferent axons) and
ventral roots (efferent
axons).
First let's focus on
the afferent division, as depicted in the figure at right. Afferent neurons have a unique
structure that differs from most other neurons. Their dendrites
(known specifically as sensory dendrites)
are located out in the periphery (many are in the skin). The
sensory dendrites are directly attached to a long axon that
projects into the dorsal spinal cord via the dorsal root. The cell bodies
of afferent neurons are clustered around the dorsal root in the dorsal root ganglion.
The figure at right is a low magnification view of a dorsal root
ganglion (top) adjacent to the spinal cord (bottom). Just visible
at this magnification are the large cell bodies of afferent
neurons (purple circles). The pink material centrally is axons of
the dorsal root.
The image at the left shows a high magnification view of the
dorsal root ganglion. The pink circles are axons of
the dorsal root. The large, pale purple
circles are the cell bodies of the afferent
neurons. The small dark nuclei that surround the
neuronal cell bodies are the nuclei of satellite cells, a type of
glial cell found in the dorsal root ganglia.
Afferent neurons are large cells compared to other cells (compare
the neuronal nuclei with the satellite cell nuclei, for instance).
Besides having a large cell body, the nucleus
of a neuron contains a prominent nucleolus.
This is the organelle located within the nucleus that is
responsible for producing ribosomal RNA. A prominent nucleolus is
a characteristic of cells that engage in a lot of protein
synthesis. (Note that a nucleus and a nucleolus are not
visible in every neuronal cell body; because this is a thin slice
of tissue, and sometimes the plane of section misses certain
elements in a large cell.)
Sensory dendrites may exist as free nerve endings, or they may be encapsulated in specialized connective tissue structures. Free nerve endings are difficult to see in histology slides without special staining mechanisms. However two types of encapsulated touch sensors are readily visible in histological sections of skin: Pacinian corpuscles and Meissner's corpuscles.
Pacinian corpuscles are located in the hypodermis (also known as the subcutaneous layer) of the skin. Their sensory dendrites are encapsulated in concentric layers of connective tissue, so they look a bit like onions. The afferent neurons associated with Pacinian corpuscles are rapidly adapting, (see figure 10.7 p. 316 to understand what occurs in adaptation) so they respond best to vibration.
In this low magnification view, two Pacinian
corpuscles can be seen in the hypodermis. Just to
the left of the Pacinian corpuscles, there are several small
nerves cut in cross section.
The high magnification view at right allows you to see the
concentric layers of connective tissue in the Pacinian corpuscle. A
cross-section of a nerve is seen to the left.
Meissner's corpuscles are located in the upper part of the dermis, just under the epidermis. Meissner's corpuscles sense fine touch. This slide is from the palmar surface of the fingertip (the side where the fingerprint is). Meissner's corpuscles are more abundant in this skin, making it much more sensitive to fine touch.
In this low magnification view, two Meissner's corpuscles are
visible in the part of the dermis that protrudes into the
epidermal layer (called a dermal papilla).
This picture is a high magnification view of the dermal papilla on
the right. The Meissner's
corpuscle is the grayish structure in the center of
the papilla. The sensory dendrites
are embedded in the layers of connective tissue in the Meissner's
corpuscle.
The somatic efferent
division consists of neurons that innervate skeletal muscle. These
somatic motor neurons have
their cell bodies in the ventral horn
of the spinal cord. Their axons leave the spinal cord via
the ventral root. They
synapse onto skeletal muscle cells, where they release the
neurotransmitter acetylcholine. The acetylcholine
acts on nicotinic acetylcholine receptors to cause an
excitatory post synaptic potential. The synapse between a
somatic motor neuron and a skeletal muscle fiber is called the neuromuscular
junction.
The figure at right is a low magnification view of a section of
the spinal cord at the sacral level. This tissue is treated with a
stain that causes a black product to associate with myelin, so the
central gray matter is light colored and the outer white matter is
dark. A section from the sacral level will have lots of somatic
motor neuron cell bodies since this region of the spinal cord
innervates the legs. Somatic motor neurons have large cell
bodies and even at this low magnification, you can see some
tan-colored cell bodies in the ventral
horn.
At higher magnification, the cell bodies of the somatic motor neurons can be
seen. The nucleus is just barely visible as a somewhat
lighter region that surrounds the prominent dark nucleolus.
The autonomic
division provides innervation to all other tissues that receive
neural control. Targets of the autonomic nervous system
include cardiac muscle in the heart, smooth muscle in organs and
blood vessels, and secretory cells in the digestive tract.
The organization of the autonomic efferent division is more complex than the somatic efferent division. Information must flow through two neurons as it travels to a target: a preganglionic neuron and a postganglionic neuron. The figure (above right) shows this relationship. The preganglionic neuron has its cell body in the central nervous system, with its axon in the ventral root. The axon travels to an autonomic ganglion, where it forms a synapse with a postganglionic cell. Postganglionic neurons synapse with target cells.
Another complexity is that there are two main autonomic
divisions: the sympathetic division
and the parasympathetic division.
Often a target will receive inputs from both sympathetic and
parasympathetic neurons (dual innervation), with each division
causing an opposite effect. A useful organizing principle is to
remember that sympathetic activity is activated during acutely
stressful situations (the "fight-or-flight" response). For
example, activation of the sympathetic nervous system causes an
increased heart rate, dilation of the pupils, and diversion of
blood flow to skeletal muscles. By contrast, when the body is
"resting and digesting", parasympathetic nervous system activity
dominates. Parasympathetic input reduces heart rate and
promotes digestive processes.
There are also key differences in the anatomical organization of
the sympathetic and parasympathetic divisions. The cell
bodies of parasympathetic preganglionic neurons are located in the
brainstem and the sacral spinal cord. Parasympathetic
preganglionic neurons have long axons because parasympathetic
ganglia are located close to targets. The cell bodies of sympathetic preganglionic neurons
are located in the lateral horn of the
thoracic spinal cord. Sympathetic ganglia
containing sympathetic postganglionic
neurons are for the most part located in a chain of
ganglia close to the spinal cord (the sympathetic
chain ganglia).
Lastly, the sympathetic and parasympathetic postganglionic
neurons release different neurotransmitters at target tissues.
Sympathetic postganglionic neurons release the neurotransmitter norepinephrine (abbreviated NE)*. NE acts on adrenergic receptors.
Parasympathetic postganglionic neurons usually release the
neurotransmitter acetylcholine
(abbreviated ACh)*, which
acts on muscarinic receptors.
Both adrenergic and muscarinic receptors are G-protein coupled receptors (GPCRs) The significance of
this information is that drugs targeting these receptors are used
to affect autonomic activity.
*There are a few exceptions to the rule that sympathetic
postganglionic neurons release NE and that parasympathetic
postganglionic neurons release ACh. In physiology, it seems there
are always exceptions to every rule.
The pupil is the hole in the center of the iris that allows light
to get into the eye. The diameter of the pupil is controlled by
smooth muscles in the iris of the eye. The pupil is in the center
of the eye and appears black, while the iris is the colored
portion that surrounds it. Autonomic control of pupil
diameter is a classic example where the sympathetic and
parasympathetic divisions have antagonistic actions.
Refer to the figure at right. Sympathetic preganglionic
neurons located in the thoracic spinal cord activate
sympathetic postganglionic neurons in the sympathetic
ganglion chain. The sympathetic postganglionic
neurons release NE, which stimulates contraction of
the radial muscles in the iris and causes the pupil to dilate
(get larger). The parasympathetic preganglionic neurons are
located in a nucleus in the midbrain. They travel via a
cranial nerve (the occulomotor nerve) to activate postganglionic
neurons in the ciliary ganglion, which is located just behind the
eye. Parasympathetic postganglionic neurons release
ACh, which stimulates contraction in circular muscles
in the iris and causes the pupil to constrict (get
smaller).