Chapter
14
The
Autonomic Nervous System Objectives
1. Define autonomic
nervous system and list its components.
2. Compare the somatic and autonomic
nervous systems relative to effectors, efferent pathways, and neurotransmitters
released.
3. Compare and contrast the general
functions of the parasympathetic and sympathetic division and the general
effects of each on major body systems.
4. Compare and contrast the general
anatomical features of the parasympathetic and sympathetic divisions.
5. List the cranial and sacral nerves
which carry parasympathetic fibers and the structures they innervate.
6. Describe the sympathetic pathways from
origin to sympathetic chain to structures innervated.
7. Explain the mechanism of referred pain.
8. Describe the two types of cholinergic
receptors with respect to location of receptors and effect of acetylcholine
binding.
9. Describe the two types of adrenergic
receptors with respect to location of receptors and effect of norepinephrine
binding.
10. Explain the mechanisms by which the
drugs neostigmine, tricyclic antidepressants, and beta blockers function.
11. Briefly describe the interactions of
the sympathetic and parasympathetic divisions.
12. Compare and contrast the sympathetic
and parasympathetic divisions with respect to tone, localized vs. diffuse
effects, and unique sympathetic roles.
13. Describe the control centers of
autonomic functions.
14. Define the autonomic disorders of
hypertension and Raynaud's disease.
AUTONOMIC
NERVOUS SYSTEM
Regulates the activities of smooth muscle,
cardiac muscle, and certain glands.
Consists of: visceral efferent neurons,
visceral afferent neurons with receptors
Functionally it operates without conscious
control. The system is regulated by centers in the brain, in particular by the
hypothalamus and medulla oblongata.
Comparison of the Somatic and Autonomic
Systems
Both have motor fibers.
Differ in their effectors, in their
pathways, and in target organ responses to their neurotransmitters.
|
Somatic System |
ANS |
|
Stimulates skeletal muscles |
Stimulates cardiac muscle, smooth muscle, and glands |
|
Motor neuron cell body in CNS, one neuron extends to effector organ. |
Motor unit is 2 neuron chain. Preganglionic neuron cell body in s.c., synapses outside CNS, postganglionic axon extends to the effector organ. |
|
Axons are myelinated. Conduction is fast. |
Preganglionic axons are lightly myelinated. Postganglionic neurons are unmyelinated. Conduction is slower. |
|
All motor neurons secrete acetylcholine at synapse with effector. |
Postganglionic neurons secrete acetylcholine or norepinephrine at synapse with effector. |
|
Response is always excitation. |
Response may be either excitation or inhibition depending on the nature of receptors present on target organ. |
Divisions of the ANS
Two major arms are the:
1. Parasympathetic
2. Sympathetic
Generally they serve the same visceral
organs but cause essentially opposite effects. The two divisions counterbalance
each other's activities .
The parasympathetic system is primarily
concerned with activities that conserve and restore body energy during times of
rest or recovery of the body. ("Resting and digesting system")
Under normal conditions, parasympathetic
impulses to the digestive glands and smooth muscle of the G.I. tract dominate
over sympathetic impulses. Blood pressure, heart and breathing rates are
regulated at low levels, while the GI tract is active after a meal. The skin is
warm and the eye pupils are constricted to protect the retinas.
The sympathetic system mobilizes the body
during extreme situations of stress. The sympathetic division is primarily
concerned with processes involving the expenditure of energy due to either
physical or emotional activities. ("Fight-or-flight system") During
homeostasis, the main function of the sympathetic division is to counteract the
parasympathetic effects just enough to carry out normal processes requiring
energy.
During vigorous exercise, the sympathetic
division promotes certain adjustments. Visceral and/or cutaneous vessels are
constricted, and cardiac and skeletal vessels are dilated shunting blood to the
active muscles.
The bronchioles in the lungs are dilated
to increase ventilation and the liver releases glucose into the blood.
Temporarily nonessential activities are
damped.
Anatomy of the ANS
The two systems are distinguished by:
1. Unique origin sites - parasympathetic
fibers emerge from the cranial and sacral regions of the spinal cord. The
sympathetic fibers originate from the thoracolumbar region of the spinal cord.
2. Different lengths of their fibers:
parasympathetic has long preganglionic and short postganglionic fibers. The
sympathetic has the opposite condition.
3. Location of their ganglia: most
parasympathetic ganglia are located in the visceral effector organs. Sympathetic
ganglia lie close to the spinal cord.
Parasympathetic Division
Originates from cranial and sacral regions
of spinal cord (craniosacral).
The preganglionic axons extend from the
CNS nearly all the way to the target structures where they synapse with
postganglionic neurons located in terminal ganglia that are within or very close
to the target organs.
Short postganglionic axons issue from the
terminal ganglia and run to synapse with effector cells.
Cranial Outflow
Parasympathetic outflow is contained in
several cranial nerves.
1. Oculomotor nerves (III): innervate the
smooth muscles within the eyes that cause the pupils to constrict and the lenses
of the eyes to bulge.
2. Facial nerves (VII): stimulate the
secretory activity of many large glands in the head. Stimulates the nasal glands
and the lacrimal glands.
3. Glossopharyngeal nerves (IX): activate
the parotid salivary glands which lie anterior to the ears.
These three pairs of cranial nerves supply
the entire parasympathetic innervation of the head.
4. Vagus nerves (X): accounts for 90% of
all preganglionic parasympathetic fibers in the body.
The two vagus nerves provide fibers to the
neck and contribute to nerve plexuses that serve virtually every organ in the
thoracic and abdominal cavities. As the vagus nerves pass into the thorax, they
branch to the following plexuses located within or near the organs served:
1. cardiac plexuses: supplying the heart-
slow heart rate.
2. pulmonary plexuses: serve the lungs and
bronchi.
3. esophageal plexuses: supplying the
esophagus.
When the main trunks of the vagus nerves
reach the esophagus, their fibers form the anterior and posterior vagal trunks.
The vagal trunks enter the abdominal cavity and send fibers through the large
aortic plexus. The sympathetic and parasympathetic fibers are intermingled in
these abdominal plexuses.
Organs receiving vagal innervation
include: Liver, stomach, small intestine, kidneys, pancreas, and the proximal
half of the large intestine.
Sacral Outflow
Arises from neurons located in S2-S4.
Innervates the rest of the large intestine and the pelvic organs.
Sympathetic Division
Originates from the thoracolumbar region
of spinal cord. More complex, innervates more organs.
All preganglionic fibers of the
sympathetic division arise from cell bodies of preganglionic neurons located in
spinal cord segments T1-L2. After leaving the spinal cord, the preganglionic
neurons enter the sympathetic chain, which is a sequence of connected ganglia
located adjacent to the vertebral column. Although the sympathetic chain extends
from the neck to the pelvis, the sympathetic fibers arise only from the thoracic
and lumbar cord segments. There are 23 ganglia in each sympathetic chain.
All sympathetic ganglia are close to the
cord, and the postganglionic fibers which run from the ganglion to the organs
they supply, are much longer than the preganglionic fibers.
Visceral Sensory Neurons
Send information concerning chemical
changes, stretch, and irritation of the viscera, and are the first link in
autonomic reflexes. Nearly all the sympathetic and parasympathetic fibers are
accompanied by afferent fibers conducting sensory impulses from glands or
muscular structures.
The fact that visceral pain afferents
travel along the same pathways as somatic pain fibers helps to explain the
phenomenon of referred pain, in which pain stimuli arising in the viscera
are perceived as somatic in origin.
A heart attack may produce a sensation of
pain that radiates to the superior thoracic wall and along the medial aspect of
the left arm. The same spinal segments innervate both the heart and the regions
to which pain signals from heart tissue are referred. The brain interprets most
such inputs as coming from the more common somatic pathway.
Neurotransmitters and Receptors
Major neurotransmitters are: Acetylcholine
(ACh) Norepinephrine (NE)
ACh is released by:
1. all preganglionic axons of both ANS
divisions
2. all parasympathetic postganglionic
axons at synapses with their effectors
ACh-releasing fibers are called
cholinergic fibers.
Most sympathetic postganglionic axons
release NE and are classified as adrenergic fibers.
The effects of ACh and NE on their
effectors are not consistently either excitation or inhibition. The response of
visceral effectors depends not only on the neurotransmitter but also on the
receptors to which they attach.
The two or more kinds of receptors that
exist for each of the neurotransmitters allow these chemicals to exert different
effects at different body targets.
Cholinergic Receptors
The two types of receptors that bind ACh
are named for drugs that bind to them and mimic ACh effects.
1. Nicotinic
2. Muscarinic (mushroom poison)
Muscarine has no effect on nicotinic
receptors, and vice versa.
Nicotinic
receptors are found on:
1. motor end plates of skeletal muscle
cells
2. postganglionic neurons
3. hormone-producing cells of the adrenal medulla
The effect of ACh binding to nicotinic
receptors is always stimulatory.
Muscarinic
receptors occur on all effector cells stimulated by postganglionic cholinergic
fibers - all parasympathetic target organs and a few sympathetic targets. The
effect of ACh binding to muscarinic receptors is inhibitory or stimulatory,
depending on the target organ. Binding of ACh to cardiac muscle receptors slows
heart activity, whereas ACh binding to receptors on smooth muscle of the G.I.
tract cause increased motility.
Adrenergic Receptors
Two classes: 1. alpha 2. beta
Organs that respond to NE display one or
both types of receptor. Generally, NE binding to an alpha receptor is
stimulatory, while the binding to beta receptors is inhibitory. Notable
exception includes binding of NE to beta receptors of cardiac muscle which
causes increased heart activity.
Effects of Drugs
Knowing the location of the various
receptors is very important clinically because it allows specific drugs to be
prescribed to obtain the desired blocking of stimulatory effects on selected
target organs.
The anti-ACh drug, neostigmine, inhibits
the enzyme acetylcholinesterase preventing the breakdown of ACh and allowing it
to accumulate in the synapses. Used as a treatment for myasthenia gravis, a
condition in which skeletal muscle activity is impaired for lack of ACh
stimulation.
Tricyclic antidepressants help to relieve
depression because they prolong the activity of NE on the post synaptic
membrane.
Adrenergic blockers that attach
specifically to the beta receptors of cardiac muscle (beta-blockers)
(acebutolol) are used when the goal is to reduce heart rate and prevent
arrhythmias in patients without interfering with other sympathetic effects.
Interactions of the Autonomic Divisions
Most visceral organs receive dual
innervation. Both ANS divisions are partially active, producing a dynamic
antagonism that allows visceral activity to be very precisely controlled. One
division usually exerts the predominant effects in given circumstances.
Antagonistic effects are most clearly seen on the activity, of the heart,
respiratory system and the G.I. organs.
The sympathetic division increases both
respiratory and heart rates while inhibiting digestion and elimination during
times of high stress. When the emergency is passed, the parasympathetic division
restores heart and breathing rates to resting levels and then attends to
processes that refuel the body cells and discard wastes.
Sympathetic and Parasympathetic Tone
With few exceptions, the vascular system
is entirely innervated by sympathetic fibers that keep the blood vessels in a
continual state of partial constriction. When faster blood delivery is needed,
these fibers cause the vessels to constrict and blood pressure to rise. When
blood pressure is to be decreased, the vessels are allowed to dilate.
Drugs (phentolamine) that interfere with
the activity of these vasomotor fibers are often used to treat hypertension.
During circulatory shock or when more
blood must be provided to meet the increased needs of working skeletal muscles,
blood vessels serving the skin and abdominal viscera are strongly constricted.
This "blood shunting" helps to maintain circulation to vital organs or
enhance blood delivery to skeletal muscles.
The parasympathetic effects normally
dominate the heart and smooth muscles of the digestive and urinary tract organs.
The parasympathetic division prevents unnecessary heart acceleration and also
determines the normal activity levels of the digestive and urinary tracts. The
sympathetic division can override these effects during times of stress.
Unique Roles of the Sympathetic
Division
Regulates many functions not subject to
parasympathetic influence. For example, the adrenal medulla, the sweat glands
and arrector pili muscles of the skin, the kidneys, and most of the blood
vessels receive only sympathetic fibers.
Localized Verses Diffuse Effects
Parasympathetic division exerts
short-lived, localized control over its effectors. However, when the sympathetic
division is activated, it responds in a diffuse and highly interconnected way.
Its effects are also much longer lasting.
This reflects three phenomena:
1. NE is inactivated more slowly than ACh
2. NE which acts through a second
messenger system, exerts its effects more slowly.
3. When the sympathetic division is
mobilized, small amounts of NE (15%) and larger amounts of epinephrine (85%) are
secreted into the blood by the adrenal medullary cells. These effects continue
for several minutes until the hormones are destroyed by the liver.
Control of Autonomic Functioning
Although the ANS is not usually considered
to be under voluntary control, its activities are regulated. Several levels of
CNS controls exist - in the spinal cord, brain stem, hypothalamus, and cerebral
cortex..
The brain stem appears to exert the most
direct influence over the ANS functions. Most sensory impulses involved in
eliciting these autonomic reflexes are delivered to the brain stem via the vagus
nerve afferents.
The main or overall integration center of
the ANS is the hypothalamus. The hypothalamus contains centers that coordinate
heart activity, blood pressure, body temperature, water balance, and endocrine
activity. It also contains centers that help mediate various emotional states
and biological drives. The hypothalamus serves as the keystone of the emotional/
visceral brain, and it is through its centers that emotions influence ANS
functioning and behavior.
Homeostatic Imbalances
The ANS is involved in nearly every
important process that goes on within the body. Most autonomic disorders reflect
exaggerated or deficient controls of smooth muscle activity. Two examples are
hypertension and Raynaud's disease.
Hypertension may result from an overactive
sympathetic nervous system response promoted by continual high levels of stress.
It is always serious because it increases the workload on the heart, and it
increases the wear and tear on the artery walls.
Raynaud's disease is characterized by
intermittent attacks during which the skin of the fingers and toes becomes pale,
then cyanotic and painful. Commonly caused by exposure to cold, it is thought to
be an exaggerated vasoconstriction response in the affected body region.